The CENTER-TBI Core dataset is a large dataset containing over 2,500 variables.
The main structure of the e-CRF consists of data related to:
Click to access the detailed structure. Within the structure, you can access the corresponding e-CRF forms.
We have been developing Frequency Tables for the CENTER-TBI data. These Frequency Tables do not lend themselves to analyses of the CENTER-TBI data, but serve to provide some orientating insight into the availability and distribution of data in the CENTER-TBI dataset. The Frequency Tables are available here.
For further insight into the CENTER-TBI dataset we also refer to the descriptive core paper of our Consortium:
Case-mix, care pathways, and outcomes in patients with traumatic brain injury in CENTER-TBI: a European prospective, multicentre, longitudinal, cohort study
Ewout W Steyerberg, Eveline Wiegers, Charlie Sewalt, Andras Buki, Giuseppe Citerio, Véronique De Keyser et al.
Lancet Neurol. 2019 Oct; 18 (10): 923-934. Doi: 10.1016/S1474-4422(19)30232-7
The complete list of CENTER-TBI variables available with their corresponding description is available below:
| Variable | Label | Lookup values | Description |
|---|---|---|---|
| AIS.InjAIS | AIS | 5 == 5 6 == 6 3 == 3 4 == 4 2 == 2 1 == 1 0 == 0 |
In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. This is the AIS score for body regions as specified by AIS.InjBodyRegion. |
| AIS.InjBodyRegion | Body region | 1 == Externa 12 == Pelvic Girdle 11 == Lower Extremities 10 == Upper Extremities 9 == Lumbar Spine 8 == Abdomen/Pelvic Contents 7 == Thoracic Spine 6 == Thorax/Chest 5 == Face 3 == Brain Injury 4 == Cervical Spine 2 == Head and Neck-Other |
Injuries and their severity are recorded according to a (modification of) the AIS. The AIS recognizes 6 main body regions. We included a further subdivision for some body regions, resulting in a total of 12 regions. For example, spine is not considered separately in the original AIS classification, but included under neck/chest and abdomen regions. For TBI, however, we considered it important to record spine separately. |
| AIS.InjDescription | Description of injury | 55 == Pelvic Girdle: Other 54 == Lower Extremities: Other 53 == Upper Extremities: Other 52 == Thoracic Spine: Other 51 == Externa: Other 50 == Pelvic Girdle: Hip dislocation 49 == Pelvic Girdle: Hip fracture 48 == Pelvic Girdle: Pelvic fracture 47 == Lower Extremities: Fibula fracture 46 == Lower Extremities: Metatarsal/tarsal fracture (toe fracture) 45 == Lower Extremities: Calcaneus fracture 44 == Lower Extremities: Ankle fracture 43 == Lower Extremities: Tibia fracture 42 == Lower Extremities: Tibia plateau fracture 41 == Lower Extremities: Femoral fracture 40 == Upper Extremities: Finger 39 == Upper Extremities: Hand 38 == Upper Extremities: Dislocation 37 == Upper Extremities: Radial and/or ulnar fracture 36 == Upper Extremities: Humerus fracture 35 == Lumbar Spine: Other 34 == Lumbar Spine: Sacral fracture 33 == Lumbar Spine: Dislocation 32 == Lumbar Spine: Fracture 31 == Abdomen/Pelvic Contents: Other 29 == Abdomen/Pelvic Contents: Kidney contusion 30 == Abdomen/Pelvic Contents: Retroperitoneal hematoma 28 == Abdomen/Pelvic Contents: Perforating abdominal injury 27 == Abdomen/Pelvic Contents: Liver rupture 26 == Abdomen/Pelvic Contents: Spleen rupture 25 == Thoracic Spine: Dislocation 24 == Thoracic Spine: Fracture 23 == Thorax/Chest: Other 22 == Thorax/Chest: Hemato-thorax 21 == Thorax/Chest: Pneumo-thorax 20 == Thorax/Chest: Aorta dissection 19 == Thorax/Chest: Cardiac contusion 18 == Thorax/Chest: Lung contusion 17 == Thorax/Chest: Rib fracture 16 == Face: Other 15 == Face: Zygomatic arch fracture 14 == Face: Orbital fracture 13 == Face: Maxillo-facial fracture le Fort III 12 == Face: Maxillo-facial fracture le Fort II 11 == Face: Maxillo-facial fracture le Fort I 10 == Cervical Spine: Other 9 == Cervical Spine: Dislocation 8 == Cervical Spine: Fracture 6 == Brain Injury: Other 5 == Brain Injury: ASDH 4 == Brain Injury: Diffuse Injury 2 == Brain Injury: Contusions 3 == Brain Injury: EDH 7 == Head and Neck-Other: Specify in comments box 1 == Brain Injury: Concussion |
List of body regions with 55 subcategories describing the injury. |
| AIS.InjDesOther | Other description of injury (please specify) | Free text specifying the injury when AIS.InjDescription is "other" | |
| Biomarkers.AliquotID1 | Biomarker Aliquot 1 | Biomarker Aliquot 1: Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials. | |
| Biomarkers.AliquotID2 | Biomarker Aliquot 2 | Biomarker Aliquot 2: Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials. | |
| Biomarkers.AliquotID3 | Biomarker Aliquot 3 | Biomarker Aliquot 3: Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials. | |
| Biomarkers.AliquotID4 | Biomarker Aliquot 4 | Biomarker Aliquot 4: Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials. | |
| Biomarkers.AliquotID5 | Biomarker Aliquot 5 | Biomarker Aliquot 5: Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials. | |
| Biomarkers.AliquotID6 | Biomarker Aliquot 6 | Biomarker Aliquot 6: Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials. | |
| Biomarkers.AliquotID7 | Biomarker Aliquot 7 | Biomarker Aliquot 7: Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials. | |
| Biomarkers.AliquotID8 | Biomarker Aliquot 8 | Biomarker Aliquot 8: Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials. | |
| Biomarkers.CentrifugationDate | Centrifugation date of the Biomarker sample | Centrifugation Date of the Biomarker sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Biomarkers.CentrifugationTime | Centrifugation time of the Biomarker sample | Centrifugation Time of the Biomarker sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Biomarkers.CollectionDate | Collection date of the Biomarker sample | Collection Date of the Biomarker sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Biomarkers.CollectionTime | Collection time of the Biomarker sample | Collection Time of the Biomarker sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Biomarkers.FreezerMinusEightyDate | Date the Biomarker sample was stored in a -80 freezer | All processed samples should be stored at -80°C with a needle to freezer time preferably within 2 hours. This variable reflects the date and time that the biomarker sample was stored in a minus 80 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Biomarkers.FreezerMinusEightyTime | Time the Biomarker sample was stored in a -80 freezer | All processed samples should be stored at -80°C with a needle to freezer time preferably within 2 hours. This variable reflects the date and time that the biomarker sample was stored in a minus 80 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Biomarkers.FreezerMinusTwentyDate | Date the Biomarker sample was stored in a -20 freezer | All processed samples should be stored at -80°C with a needle to freezer time preferably within 2 hours. However, if a -80°C freezer was not immediately accessible, samples could be temporarily (max 48 hours) stored in a minus 20°C non-frost-free freezer. This variable reflects the date and time that the biomarker sample was stored in a minus 20 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Biomarkers.FreezerMinusTwentyTime | Time the Biomarker sample was stored in a -20 freezer | All processed samples should be stored at -80°C with a needle to freezer time preferably within 2 hours. However, if a -80°C freezer was not immediately accessible, samples could be temporarily (max 48 hours) stored in a minus 20°C non-frost-free freezer. This variable reflects the date and time that the biomarker sample was stored in a minus 20 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Biomarkers.GFAP | Glial fibrillary acidic protein [GFAP] | Assay results for Glial fibrillary acidic protein [GFAP] - measured with an ultrasensitive immunoassay using digital array technology (Single Molecule Arrays, SiMoA)-based Human Neurology 4-Plex B assay (N4PB) run on the SR-X benchtop assay platform (Quanterix Corp., Lexington, MA) at the University of Florida (Gainesville, Florida). | |
| Biomarkers.NFL | Neurofilament protein-light (NFL) | Assay results for Neurofilament protein-light (NFL) - measured with an ultrasensitive immunoassay using digital array technology (Single Molecule Arrays, SiMoA)-based Human Neurology 4-Plex B assay (N4PB) run on the SR-X benchtop assay platform (Quanterix Corp., Lexington, MA) at the University of Florida (Gainesville, Florida). | |
| Biomarkers.NSE | Neuron-specific enolase (NSE) | Assay results for Neuron-specific enolase (NSE) - measured with a clinical-use automated system, using an electrochemiluminescence immunoassay kit (ECLIA) (Elecsys S100 and Elecsys NSE assays) run on the e 602 module of Cobas 8000 modular analyzer (Roche Diagnostics, Mannheim, Germany) at the University of Pecs (Pecs, Hungary). | |
| Biomarkers.S100B | S100 calcium binding protein B (S100B) | Assay results for S100 calciumbinding protein B (S100B) - measured with a clinical-use automated system, using an electrochemiluminescence immunoassay kit (ECLIA) (Elecsys S100 and Elecsys NSE assays) run on the e 602 module of Cobas 8000 modular analyzer (Roche Diagnostics, Mannheim, Germany) at the University of Pecs (Pecs, Hungary). | |
| Biomarkers.SampleId | Sample identifier for the Biomarker sample | Per patient 1x 9ml blood sample was collected in a serum separator tube. After 45 minutes (+/- 15) of coagulation at room temperature, it was centrifuged at 1500g for 10 minutes. 8x0,5ml of serum was then aliquoted into barcoded 1,8ml cryovials (see also Biomarkers.AliquotID) | |
| Biomarkers.Tau | T-TAU | Assay results for T-TAU - measured with an ultrasensitive immunoassay using digital array technology (Single Molecule Arrays, SiMoA)-based Human Neurology 4-Plex B assay (N4PB) run on the SR-X benchtop assay platform (Quanterix Corp., Lexington, MA) at the University of Florida (Gainesville, Florida). | |
| Biomarkers.UCH-L1 | Ubiquitin C-terminal hydrolase ubiquitin C-terminal hydrolase L1 (UCH-L1) | Assay results for Ubiquitin C-terminal hydrolase ubiquitin C-terminal hydrolase L1 (UCH-L1) - measured with an ultrasensitive immunoassay using digital array technology (Single Molecule Arrays, SiMoA)-based Human Neurology 4-Plex B assay (N4PB) run on the SR-X benchtop assay platform (Quanterix Corp., Lexington, MA) at the University of Florida (Gainesville, Florida). | |
| Brainmonitoring.DataAvailable | Data available (parameters monitored) | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.DataCollectionSoftware | Software used to collect HR data | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.DataEndTime | Data processing end time | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. Contains the time when the high resolution processing ended. This time has been adjusted to the midnight preceding the injury . | |
| Brainmonitoring.DataProcessingSoftware | Software used to process data | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.DataStartTime | Data processing start time | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. Contains the time when the high resolution processing started. This time has been adjusted to the midnight preceding the injury . | |
| Brainmonitoring.DateTimeFormat | Time format for data processing | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.Duration | Duration of data processing | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.FormatVersion | Version of data format | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.HDF5URL | HDF5 file name | File name of the high resolution ICU file. These files can be shared upon request. To request access please contact the CENTER-TBI office. | |
| Brainmonitoring.InvalidValue | Code for invalid value | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| CentralHaemostasis.AnnexinV_single_CD105_Annex_measurement | Measurement of CD105- and AnnexinV-positive microparticles | Measurement of CD105- and AnnexinV-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (single positive Annexin V+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.AnnexinV_single_CD42b_Annex_measurement | Measurement of CD42b- and AnnexinV-positive microparticles | Measurement of CD42b- and AnnexinV-positive microparticles for quantification of platelet-derived microparticles (PDMP) - results for platelet-derived microparticles (PDMP) (single positive Annexin V+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine PDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD105_AnnexinV_double_CD105_Annex_measurement | Measurement of CD105- and AnnexinV-positive (double) microparticles | Measurement of CD105- and AnnexinV-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (double positive CD105+/Annexin V+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD105_CD142_double_CD105_CD142_measurement | Measurement of CD105- and CD142-positive (double) microparticles | Measurement of CD105- and CD142-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (double positive CD105+/CD142+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD105_CD62E_double_CD105_CD62E_measurement | Measurement of CD105- and CD62e-positive (double) microparticles | Measurement of CD105- and CD62e-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (double positive CD105+/CD62e+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke.. | |
| CentralHaemostasis.CD105_single_CD105_Annex_measurement | Measurement of CD105- and AnnexinV-positive microparticles | Measurement of CD105- and AnnexinV-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (single positive CD105+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD105_single_CD105_CD142_measurement | Measurement of CD105- and CD142-positive microparticles | Measurement of CD105- and CD142-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (single positive CD105+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD105_single_CD105_CD62E_measurement | Measurement of CD105- and CD62e-positive microparticles | Measurement of CD105- and CD62e-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (single positive CD105+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD142_single_CD105_CD142_measurement | Measurement of CD105- and CD142-positive microparticles | Measurement of CD105- and CD142-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (single positive CD142+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD42b_AnnexinV_double_CD42b_Annex_measurement | Measurement of CD42b- and AnnexinV-positive (double) microparticles | Measurement of CD42b- and AnnexinV-positive microparticles for quantification of platelet-derived microparticles (PDMP) - results for platelet-derived micro-particles (double positive for CD42b+/Annexin V+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine PDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD42b_CD62p_double_CD42b_CD62p_measurement | Measurement of CD42b- and CD62p-positive (double) microparticles | Measurement of CD42b- and CD62p-positive microparticles for quantification of platelet-derived microparticles (PDMP) - results for platelet-derived microparticles (PDMP) (double positive CD42b+/CD62p+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine PDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD42b_single_CD42b_AnnexV_measurement | Measurement of CD42b and AnnexinV positive microparticles | Measurement of CD42b and AnnexinV positive microparticles for quantification of platelet-derived microparticles (PDMP) - results for platelet-derived microparticles (PDMP) (single positive CD42b+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine PDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD42b_single_CD42b_CD62p_measurement | Measurement of CD42b- and CD62p-positive microparticles | Measurement of CD42b- and CD62p-positive microparticles for quantification of platelet-derived microparticles (PDMP) - results for platelet-derived microparticles (PDMP) (single positive CD42b+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine PDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD62E_single_CD105_CD62E_measurement | Measurement of CD105- and CD62e-positive microparticles | Measurement of CD105- and CD62e-positive microparticles for quantification of endothelial derived microparticles (EDMP) - results for endothelial derived microparticles (EDMP) (single positive CD62e+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine EDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CD62p_single_CD42b_CD62p_measurement | Measurement of CD42b- and CD62p-positive microparticles | Measurement of CD42b- and CD62p-positive microparticles for quantification of platelet-derived microparticles (PDMP) - results for platelet-derived microparticles (PDMP) (single positive CD62p+) - using flow cytometry techniques. Citrated plasma sample was centrifuged for 20 min at 2,500 x g at RT. Supernatants were used to determine PDMP. Run on the BD Accuri C6 Plus flow cytometer (BD Biosciences; Heidelberg, Germany) at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.CentrifugationDate | Centrifugation date of the Central Haemostasis sample | Centrifugation Date and Time of the central haemostatis sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| CentralHaemostasis.CentrifugationTime | Centrifugation time of the Central Haemostasis sample | Centrifugation Date and Time of the central haemostatis sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| CentralHaemostasis.CitrateAliquotID1 | Central Haemostasis citrate aliquot 1 | Central Haemostasis citrate aliquot 1: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml and 1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.SampleID) | |
| CentralHaemostasis.CitrateAliquotID2 | Central Haemostasis citrate aliquot 2 | Central Haemostasis citrate aliquot 2: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml and 1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.SampleID) | |
| CentralHaemostasis.CitrateAliquotID3 | Central Haemostasis citrate aliquot 3 | Central Haemostasis citrate aliquot 3: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml and 1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.SampleID) | |
| CentralHaemostasis.CitrateAliquotID4 | Central Haemostasis citrate aliquot 4 | Central Haemostasis citrate aliquot 4: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml and 1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.SampleID) | |
| CentralHaemostasis.CitrateAliquotID5 | Central Haemostasis citrate aliquot 5 | Central Haemostasis citrate aliquot 5: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml and 1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.SampleID) | |
| CentralHaemostasis.CitrateAliquotID6 | Central Haemostasis citrate aliquot 6 | Central Haemostasis citrate aliquot 6: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml and 1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.SampleID) | |
| CentralHaemostasis.CitrateAliquotID7 | Central Haemostasis citrate aliquot 7 | Central Haemostasis citrate aliquot 7: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml and 1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.SampleID) | |
| CentralHaemostasis.CoagulationparameterFibrinogen_mg_dl | Assay results for standard coagulation test (Fibrinogen) | Assay results for standard coagulation test (Fibrinogen) - using a high sensitivity thromboplastin reagent (RecombiPasTin 2G (HemosIL®), Werfen, Bedford, USA) based on recombinant human tissue factor (RTF) for quantitative determination in citrated plasma of Prothrombin time (PT) and Fibrinogen. Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 276-471 Reference: HemosIL® package insert | |
| CentralHaemostasis.CoagulationparameterINR | Assay results for standard coagulation test (INR) | Assay results for standard coagulation test (INR) - using a high sensitivity thromboplastin reagent (RecombiPasTin 2G (HemosIL®), Werfen, Bedford, USA) based on recombinant human tissue factor (RTF) for quantitative determination in citrated plasma of Prothrombin time (PT) and Fibrinogen. Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. | |
| CentralHaemostasis.CoagulationparameterPTT_sec | Assay results for standard coagulation test (PTT) | Assay results for standard coagulation test (PTT) - using the HemosIL® APTT-SP kit (Werfen, Bedford, USA). Run on the ACL TOP CTS 700 (Werfen; Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 23-36 Reference: HemosIL® package insert | |
| CentralHaemostasis.CoagulationparameterQuick_procent | Assay results for standard coagulation test (Quick) | Assay results for standard coagulation test (Quick) - using a high sensitivity thromboplastin reagent (RecombiPasTin 2G (HemosIL®), Werfen, Bedford, USA) based on recombinant human tissue factor (RTF) for quantitative determination in citrated plasma of Prothrombin time (PT) and Fibrinogen. Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 70-130 Reference: HemosIL® package insert | |
| CentralHaemostasis.CoagulationparameterThrombintime_sec | Assay results for standard coagulation test (Thrombin Time) | Assay results for standard coagulation test (Thrombin Time) - using the HemosIL® Thrombin Time kit (Werfen, Bedford, USA). Fibrinogen in the citrated plasma sample is converted to fibrin by the addition of purified bovine thrombin and the time required to form the clot is measured. Run on the ACL TOP CTS 700 (Werfen; Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 10-17 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_Antithrombin_procent | Assay results for standard coagulation test (Antithrombin) | Assay results for standard coagulation test (Antithrombin) - Antithrombin in human citrated plasma measured with an automated chromogenic assay technology using the HemosIL® aliquid Antithrombin kit (Werfen, Bedford, USA). Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 83-128 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_Ddimers_ug_l | Assay results for standard coagulation test (D-Dimers) | Assay results for standard coagulation test (D-Dimers) - using the HemosIL® D-Dimer Controls kit (Werfen, Bedford, USA). Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 0-232 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_FactorIX_procent | Assay results for standard coagulation test (Factor IX) | Assay results for standard coagulation test (Factor IX) - human plasma immunodepleted of factor IX for the quantitaive determination of factor IX activity based on activated partial thromboplastin time (APTT) assay - using factor IX deficient plasma (Werfen, Barcelona, Spain). Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 65-150 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_FactorVIII_procent | Assay results for standard coagulation test (Factor VIII) | Assay results for standard coagulation test (Factor VIII) - using a Coamatic factor VIII kit (Chromogenix, Bedford, USA) for chromogenic determination of factor VIII activity in human citrated plasma. Run on the ACL TOP CTS 700 (Werfen; Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 50-150 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_FactorV_procent | Assay results for standard coagulation test (Factor V) | Assay results for standard coagulation test (Factor V) - human plasma immunodepleted of factor V for the quantitaive determination of factor V activity based on the prothrombin time (PT) assay - using factor V deficient plasma (Werfen, Bedford, USA). Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 62-139 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_FactorXIIIAg_procent | Assay results for standard coagulation test (Factor XIII) | Assay results for standard coagulation test (Factor XIII) - measured with Chromogenix factor XIII Antigen kit (Chromogenix, Bedford, USA) based on an automated latex enhanced immunoassay techniques. Run on the ACL TOP CTS 700 (Werfen; Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 75.2-154.8 Reference: Chromogenix® package insert | |
| CentralHaemostasis.Coagulationparameter_Plasminogen_procent | Assay results for standard coagulation test (Plasminogen) | Assay results for standard coagulation test (Plasminogen) - Plasminogen in human citrated plasma measured with an automated chromogenic assay technology using the HemosIL® Plasminogen kit (Werfen, Bedford, USA). Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 80-133 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_ProteinC_procent | Assay results for standard coagulation test (Protein C) | Assay results for standard coagulation test (Protein C) - Protein C in human citrated plasma measured with an automated chromogenic assay technology using the HemosIL® Protein C kit (Werfen, Bedford, USA). Run on the ACL TOP CTS 700 (Werfen; Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 70-140 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_ProteinS_procent | Assay results for standard coagulation test (Protein S) | Assay results for standard coagulation test (Protein S) - using the HemosIL® Protein S Activity kit (Werfen, Bedford, USA). Determination of the functional acitivty of free Protein S by measuring the degree of prolongation of a prothrombin time in the presence of recombinant human tissue factor, phospholipids, calcium ions and protein C. Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 63.5-149 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_vWFAg_A_B_AB_procent | Assay results for standard coagulation test (von Willebrand Factor Antigen) in patients with bloodtype A, B and AB | Assay results for standard coagulation test (von Willebrand Factor Antigen) in citrated plasma samples in patients with bloodtype A, B and AB - measured with the HemosIL® von Willebrand Antigen kit (Werfen, Bedford, USA) based on an automated latex enhanced immunoassay technique. Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 66-176 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_vWFAg_BT_0_procent | Assay results for standard coagulation test (von Willebrand Factor Antigen) in patients with bloodtype 0 | Assay results for standard coagulation test (von Willebrand Factor Antigen) in citrated plasma samples in patients with bloodtype 0 - measured with the HemosIL® von Willebrand Antigen kit (Werfen, Bedford, USA) based on an automated latex enhanced immunoassay technique. Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 42-141 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_vWFA_BT_0_procent | Assay results for standard coagulation test (von Willebrand Factor Activity) in patients with bloodtype 0 | Assay results for standard coagulation test (von Willebrand Factor Activity) in citrated plasma samples in patients with bloodtype 0 - measured with the HemosIL® von Willebrand Activity kit (Werfen, Bedford, USA) based on an automated latex enhanced immunoassay technique. Run on the ACL TOP CTS 700 (Werfen; Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 40-126 Reference: HemosIL® package insert | |
| CentralHaemostasis.Coagulationparameter_vWFA_BT_A_B_AB_procent | Assay results for standard coagulation test (von Willebrand Factor Activity) in patients with bloodtype A, B and AB | Assay results for standard coagulation test (von Willebrand Factor Activity) in citrated plasma samples in patients with bloodtype A, B and AB - measured with the HemosIL® von Willebrand Activity kit (Werfen, Bedford, USA) based on an automated latex enhanced immunoassay technique. Run on the ACL TOP CTS 700 (Werfen, Barcelona, Spain). Coagulationparameter were performed by the Institute of Transfusion Medicine (ITM), Cologne-Merheim Medical Centre. Normal range: 49-163 Reference: HemosIL® package insert | |
| CentralHaemostasis.CollectionDate | Collection date of the Central Haemostatis sample | Collection Date and Time of the central haemostatis sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| CentralHaemostasis.CollectionTime | Collection time of the Central Haemostatis sample | Collection Date and Time of the central haemostatis sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| CentralHaemostasis.EDTAAliquotID1 | Central Haemostasis EDTA aliquot 1 | Central Haemostasis EDTA aliquot 1: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml an d1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.CitrateAliquotID) | |
| CentralHaemostasis.EDTAAliquotID2 | Central Haemostasis EDTA aliquot 2 | Central Haemostasis EDTA aliquot 2: The Haemostasis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood inot 1x 2.7ml potassium EDTA tube and 1x 10ml an d1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostasis.CitrateAliquotID) | |
| CentralHaemostasis.Fibrinolysisregulator_Antiplasmin_Prozent | Assay results for Antiplasmin | Assay results for Antiplasmin - measured with a colorimetric assay technology (STA-Stachrom®-TAFI-Kit, Stago; France). Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). Normal range: 80-120 Reference: STA-Stachrom®-TAFI-Kit package insert | |
| CentralHaemostasis.Fibrinolysisregulator_TAFI_procent | Assay results for Thrombin-Activatable Fibrinolysis Inhibitor (TAFI) | Assay results for Thrombin-Activatable Fibrinolysis Inhibitor (TAFI) -measured with a colorimetric assay technology (STA-Stachrom-TAFI-Kit, Stago; France). Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). Detection limit of Stachrom-TAFI-Kit: 5-195 | |
| CentralHaemostasis.Fibrinolysis_FibrinogenMonomer_ug_ml | Assay results for fibrin monomers | Assay results for fibrin monomers -using an immunoturbidimetric determination technology (STA - Liatest FM-Kit, Stago; France). Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). Reference interval of Liatest FM-Kit of 6 | |
| CentralHaemostasis.FreezerMinusEightyDate | Date the Central Haemostasis sample was stored in a -80 freezer | All processed haemostatis samples should be stored at -80°C with a needle to freezer time preferably within 2 hours. This variable reflects the date and time that the sample was stored in a minus 80 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| CentralHaemostasis.FreezerMinusEightyTime | Time the Central Haemostasis sample was stored in a -80 freezer | All processed haemostatis samples should be stored at -80°C with a needle to freezer time preferably within 2 hours. This variable reflects the date and time that the sample was stored in a minus 80 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| CentralHaemostasis.FreezerMinusTwentyDate | Date the Central Haemostasis sample was stored in a -20 freezer | All processed haemostatis samples should be stored at -80°C with a needle to freezer time preferably within 2 hours. However, if a -80°C freezer was not immediately accessible, samples could be temporarely (max 48 hours) stored in a minus 20°C non-frost-free freezer. This variable reflects the date and time that the sample was stored in a minus 20 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| CentralHaemostasis.FreezerMinusTwentyTime | Time the Central Haemostasis sample was stored in a -20 freezer | All processed haemostatis samples should be stored at -80°C with a needle to freezer time preferably within 2 hours. However, if a -80°C freezer was not immediately accessible, samples could be temporarely (max 48 hours) stored in a minus 20°C non-frost-free freezer. This variable reflects the date and time that the sample was stored in a minus 20 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| CentralHaemostasis.PAI1_ng_ml | Assay results for Plasminogen-activator-inhibitor-1 (PAI-1) | Assay results for Plasminogen-activator-inhibitor-1 (PAI-1) - using an ELISA Duo Set Kit from R&D Systems (Minneapolis, USA) based on the sandwich principle according to manufacturer’s instructions. EDTA plasma samples were used. Run on the EPOCH 2 (BioTek; Winooski, USA) microplate reader at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.SampleId | Sample identifier for the Central Haemostasis sample | The Haemostatis samples are complementary to the routine hospital tests and performed only in a selected number of sites. This involved the collection of blood into 1x 2.7ml potassium EDTA tube and 1x 10ml and 1x 5 ml sodium-citrate tubes (only for a limited number of ADM and ICU patients in selected sites). Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU patients (no potassium EDTA sample at these sampling points). Tubes were centrifuged at 1500g for 10 minutes after collection. 7x 1ml citrate plasma was then aliquoted into 1.8ml cryovials (see also CentralHaemostatis.CitrateAliquotID) | |
| CentralHaemostasis.Syndecan1_pg_ml | Assay results for Syndecan-1 | Assay results for Syndecan-1 - using an ELISA Duo Set Kit from R&D Systems (Minneapolis, USA) based on the sandwich principle according to manufacturer’s instructions. EDTA plasma samples were used. Run on the EPOCH 2 (BioTek; Winooski, USA) microplate reader at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CentralHaemostasis.Thrombingeneration_ETP_nm_min | Assay results for endogenous thrombin potential in citrated plasma (ETP) | Assay results for endogenous thrombin potential (ETP) (STG®-BleedScreen, Stago, France) in citrated plasma - using a fluorogenic method (ST Genesia analyzer; Stago, France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_ETP_procent | Assay results for endogenous thrombin potential in citrated plasma (ETP) | Assay results for endogenous thrombin potential (ETP) (STG®-BleedScreen, Stago, France) in citrated plasma - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_LagTime_min | Assay results for quantitative determination of thrombin generation in citrated plasma (Lag Time) | Assay results for quantitative determination of thrombin generation (STG®-BleedScreen, Stago, France) in citrated plasma (Lag Time) - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_LagTime_ratio | Assay results for quantitative determination of thrombin generation in citrated plasma (Lag Time) | Assay results for quantitative determination of thrombin generation (STG®-BleedScreen, Stago, France) in citrated plasma (Lag Time) - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_PeakHeight_nm | Assay results for quantitative determination of thrombin generation in citrated plasma (Peak height) | Assay results for quantitative determination of thrombin generation (STG®-BleedScreen, Stago, France) in citrated plasma (Peak Height) - using a fluorogenic method (ST Genesia analyzer Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_PeakHeight_procent | Assay results for quantitative determination of thrombin generation in citrated plasma (Peak height) | Assay results for quantitative determination of thrombin generation (STG®-BleedScreen, Stago, France) in citrated plasma (Peak Height) - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_StartTail_min | Assay results for quantitative determination of thrombin generation in citrated plasma (Start Tail) | Assay results for quantitative determination of thrombin generation in citrated plasma (Start Tail) - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_StartTail_ratio | Assay results for quantitative determination of thrombin generation in citrated plasma (Start Tail) | Assay results for quantitative determination of thrombin generation in citrated plasma (Start Tail) - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_TimetoPeak_min | Assay results for quantitative determination of thrombin generation in citrated plasma (Time to Peak) | Assay results for quantitative determination of thrombin generation in citrated plasma (Time to Peak) - using a fluorogenic method (ST Genesia analyzer; Stago, France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_TimetoPeak_ratio | Assay results for quantitative determination of thrombin generation in citrated plasma (Time to Peak) | Assay results for quantitative determination of thrombin generation in citrated plasma (Time to Peak) - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_Vel_Index_nm_min | Assay results for quantitative determination of thrombin generation in citrated plasma (Velocity Index) | Assay results for quantitative determination of thrombin generation in citrated plasma (Velocity Index) - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Thrombingeneration_Vel_Index_procent | Assay results for quantitative determination of thrombin generation in in citrated plasma (Velocity index) | Assay results for quantitative determination of thrombin generation in in citrated plasma (Velocity index) - using a fluorogenic method (ST Genesia analyzer, Stago; France) - triggered by a low concentration of tissue factor. Measurement were performed at the Ludwig Boltzman Institute (Salzburg, Vienna). | |
| CentralHaemostasis.Timepoints | Timepoint | ||
| CentralHaemostasis.UsedCitratAliquot1_Microparticles | Sample identifier for the used citrat aliquot 1 (Microparticles) | ||
| CentralHaemostasis.UsedCitratAliquot1_ThrombinFibrinregu | Sample identifier for the used citrat aliquot 1 (Thropmbin/Fibrin) | ||
| CentralHaemostasis.UsedCitratAliquot2_Microparticles | Sample identifier for the used citrat aliquot 2 (Microparticles) | ||
| CentralHaemostasis.UsedCitratAliquot2_ThrombinFibrinregu | Sample identifier for the used citrat aliquot 1 (Thropmbin/Fibrin) | ||
| CentralHaemostasis.UsedCitrateAliquot_Coagulationparameter | Sample identifier for the used citrat aliquot (Coagulation parameter) | ||
| CentralHaemostasis.UsedEDTAAliquot1_ELISA | Sample identifier for the used EDTA aliquot 1 | ||
| CentralHaemostasis.UsedEDTAAliquot2_ELISA | Sample identifier for the used EDTA aliquot 2 | ||
| CentralHaemostasis.VECadherin_ng_ml | Assay results for VE-Cadherin | Assay results for VE-Cadherin - using an ELISA Duo Set Kit from R&D Systems (Minneapolis, USA) based on the sandwich principle according to manufacturer’s instructions. EDTA plasma samples were used. Run on the EPOCH 2 (BioTek; Winooski, USA) microplate reader at Institute for Research in Operative Medicine (IFOM, Cologne, Germany), University Witten/Herdecke. | |
| CTMRI.CTAcuteSubdurHema | Intracranial lesions: Acute subdural haematoma | 0 == No 1 == Small 2 == Large (mass) 88 == Unknown |
Assessment by clinician/investigator whether or not in his/her interpretation an acute subdural hematoma is present. Also, the size (not quantified) is requested to be estimated. |
| CTMRI.CTAngulation | Angulation | 1 == No angulation (volume scan) 2 == Orbital-meatal line 99 == Other |
This variable describes if a CT scan is performed with or without angulation. There are three options: no angulation (volume scan), orbital-meatal line and other. There is a risk of different interpretation, since there was no definition. |
| CTMRI.CTBasalCisternsAbsentCompressed | Basal cisterns absent compressed | 0 == No 1 == Yes |
Assessment by clinician/investigator whether or not in his/her interpretation the basal cisterns are compressed. |
| CTMRI.CTContusion | Intracranial lesions: Contusion | 0 == No 1 == Small 2 == Large (mass) 88 == Unknown |
Assessment by clinician/investigator whether or not in his/her interpretation an intracerebral hematoma/contusion is present. Also, the size (not quantified) is requested to be estimated. |
| CTMRI.CTDeprSkullFract | Depressed skull fracture | 0 == No 1 == Closed 2 == Open (compound) |
Assessment by clinician/investigator whether or not in his/her interpretation a depressed skull fracture is present. In addition, when present, clinician/investigator has to document whether the fracture is associated with an open wound or not (compound vs closed) |
| CTMRI.CTDone | CT done or not | This variable is populated when a CT has been made. Intent to perform a CT was an inclusion criterium for the study. All Images performed have been uploaded to the Imaging repository at Icometrix. Central review of initial and follow-up scans has been done by icometrix. Data of Central review are recorded separately. The variables below capture results of basic scoring by Investigators - these scores inform clinical decision making! | |
| CTMRI.CTERReason | Reason for CT (ER only) | 1 == GCS <= 14 2 == GCS = 15 + risk factors 3 == Head wound 4 == Exclusion of abnormalities prior to discharge 5 == Suspicion of maxillofacial injury 99 == Other 88 == Unknown |
WHY question: reason for performing CT; only applicable to initial scan (presentation). |
| CTMRI.CTERReasonOther | Other reason for CT (ER only) | Specification, only applicable if "CTMRI.CTERReason" was "other" | |
| CTMRI.CTExtraduralHema | Intracranial lesions: Extradural haematoma | 0 == No 1 == Small 2 == Large (mass) 88 == Unknown |
Assessment by clinician/investigator whether or not in his/her interpretation an acute extradural/epidural hematoma is present. Also, the size (not quantified) is requested to be estimated. |
| CTMRI.CTICLesionDAI | Intracranial lesions: Small hyper dense lesions (DAI) | 0 == No 1 == Yes 88 == Unknown |
Assessment by clinician/investigator whether or not in his/her interpretation diffuse axonal injury is present. |
| CTMRI.CTIschemia | Ischemia | 1 == Single arterial territory 2 == Multiple territories 3 == Hemisphere 0 == No |
Assessment by clinician/investigator whether or not in his/her interpretation ischemia is present. Only applicable for clinical follow-up CT, not applicable to initial CT. In addition, the severity, in terms of how many arterial territories have ischemia, is requested to be answered. |
| CTMRI.CTManuf | CT scanner manufacturer | HITA == Hitachi GE == GE CARE == Carestream AGFA == Agfa KONI == Konica Minolta PHIL == Philips SIEM == Siemens TOSH == Toshiba 99 == Other |
This variable describes the CT scans manufacturer. |
| CTMRI.CTMidlineShift | Midline shift present | 0 == No 1 == Yes |
Assessment by Investigator |
| CTMRI.CTMidlineShiftMeasure | Midline shift | Assessment by Investigator | |
| CTMRI.CTMRICompleteStatus | CTMRI form complete status | NOSTART == Not Started PRO == In Process COM == Complete NOT == Queries Outstanding INCPT == Incompletable - Pt Factors INCNOSHOW == Incompletable - No Show |
This variable is populated when the CRF status is "complete". |
| CTMRI.CTMRIDate | Date of imaging | Date of Imaging captured in CRF | |
| CTMRI.CTMRITime | Time of imaging | Time of imaging captured in CRF | |
| CTMRI.CTNoOpMotiv | Motivation for not scheduling operation | 0 == No surgical lesion 1 == Lesion present, but Acceptable/good neurologic condition 2 == Lesion present, but Guideline adherence 3 == Lesion present, but Little/no mass effect 4 == Lesion present, but Not hospital policy 5 == Lesion present, but Extremely poor prognosis 6 == Lesion present, but Brain Death 7 == Lesion present, but Old age 8 == Lesion present, but Wish family, relative or Legal representative 99 == Lesion present, but Other 88 == Unknown |
WHY question: documents reason for not having an indication for (intra)cranial surgery. |
| CTMRI.CTNoOpMotivOther | Specify 'other' motivation for not scheduling operation | Specification, only applicable if "CTMRI.CTNoOpMotiv" was "other" | |
| CTMRI.CTPatientLocation | Patient location at time of CT | ED == ER ADMIS == Ward/Admission ICU == ICU |
This variable describes the in-hospital location of the patient when the CT-scan was performed and was not meant to describe the location of the CT-scanner. Three options: ER, Ward/Admission, ICU |
| CTMRI.CTReason | Main reason for CT scan | SFU == Standard follow-up POC == Post-operative control CD == Clinical deterioration IICP == (Suspicion of) Increasing ICP LOP == Lack of improvement ICUADM99 == Other ICUADM88 == Unknown |
This variable contains the main reason why a CT-scan, during hospital stay, was performed. One of following options: standard follow-up, post-operative control, clinical deterioration, (suspicion of) increasing ICP, lack of improvement, unknown, other (specified in CTMRI.CTReasonOther) The reason for making an early CT-scan/ER scan can be found in: CTMRI.CTERReason |
| CTMRI.CTReasonOther | Specify 'other' main reason for CT scan | This variable contains the main reason why a CT-scan, during hospital stay, was performed. When the "other" option was selected in variable CTMRI.CTReason, investigators could write the reason in this free text variable. The reason for making an early CT-scan/ER scan can be found in: CTMRI.CTERReason | |
| CTMRI.CTRiskFactorsERAgeGreatrThanEqual60 | Risk factors: Age >= 60 | This variable describes the presence of risk factors (here: age greater than or equal to 60 years) for structural abnormalities on an early CT/MRI. Information for this variable was meant to be only entered for early CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERAlterationOfConsc | Risk factors: Alteration of consciousness | This variable describes the presence of risk factors (here: alteration of consciousness) for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERAnticoagTx | Risk factors: Anticoagulant Tx | This variable describes the presence of risk factors (here: use of anticoagulant Tx ) for structural abnormalities on an early CT/MRI. Information for this variable was meant to be only entered for early CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERAnyNeuroDef | Risk factors: Any neurological deficit | This variable describes the presence of risk factors (here: 'any neurological deficit') for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERClinSignsOfFractSkullBaseVault | Risk factors: Clinical signs of fracture skull base or vault | This variable describes the presence of risk factors (here: 'clinical signs of fracture skull base or vault') for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15+risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERContusionFace | Risk factors: Contusion of the face | This variable describes the presence of risk factors (here: 'contusion of the face') for structural abnormalities on an early CT/MRI. Information for this variable was meant to be only entered for early CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERFallFromAnyElev | Risk factors: Fall from any elevation | This variable describes the presence of risk factors (here: fall from any elevation) for structural abnormalities on an early CT/MRI. Information for this variable was meant to be only entered for early CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERHeadache | Risk factors: Headache | This variable describes the presence of risk factors (here: headache) for structural abnormalities on an early CT/MRI. Information for this variable was meant to be only entered for early CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERIntoxication | Risk factors: Intoxication | This variable describes the presence of risk factors (here: intoxication) for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15+risk factors". However due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERLOC | Risk factors: Loss of consciousness | This variable describes the presence of risk factors (here: loss of consciousness) for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsEROther | Risk factors: Other | This variable describes the presence of risk factors (other reason, not specified elsewhere) for structural abnormalities on an early CT/MRI. Information for this variable was meant to be only entered for early CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsEROtherTxt | Specify other risk factors | This variable describes the presence of risk factors (other reason, not specified elsewhere: textfield) for structural abnormalities on an early CT/MRI. Information for this variable was meant to be only entered for early CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERPhysEvidTraumaHeadSkull | Risk factors: Physical evidence of trauma to head/skull | This variable describes the presence of risk factors (here: physical evidence of trauma to head/skull) for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERPTAGreatrThanEqual4hrs | Risk factors: PTA >= 4 hours | This variable describes the presence of risk factors (here: PTA >= 4 hours) for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERSeizure | Risk factors: Seizure | This variable describes the presence of risk factors (here: seizure) for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERSignsFacialFract | Risk factors: Signs of facial fracture | This variable describes the presence of risk factors (here: signs of facial fracture) for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERVomit | Risk factors: Vomiting | This variable describes the presence of risk factors (here: vomiting) for structural abnormalities on an initial/ER CT/MRI. Information for this variable was meant to be only entered for initial/ER CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTRiskFactorsERVulnRoadUser | Risk factors: Vulnerable road user (pedestrian or cyclist) | This variable describes the presence of risk factors (here: vulnerable road users, like pedestrians or cyclists) for structural abnormalities on an early CT/MRI. Information for this variable was meant to be only entered for early CT, when CTMRI.CTERReason = "GCS = 15 + risk factors". However, due to the e-CRF lay-out, it will also be populated for patients with CTMRI.CTERReason is not "GCS = 15 + risk factors" or patients with an MRI. | |
| CTMRI.CTScannerType | Type of CT scanner | 320 == 320-slice 256 == 256-slice 128 == 128-slice 64 == 64-slice 32 == 32-slice 16 == 16-slice 99 == Other |
This variable specifies the type of CT-scanner by the number of slices. |
| CTMRI.CTSchedForOp | Scheduled for operation | 0 == No 1 == Yes |
Whether or not the patient is scheduled for (intra)cranial surgery. The main aim here is to capture whether the clinical team taking care of the patient sees a neurosurgical indication. |
| CTMRI.CTSubarachnoidHem | Subarachnoid hemorrhage | 0 == No 1 == Basal 2 == Cortical 3 == Basal and Cortical |
Assessment by clinician/investigator whether or not in his/her interpretation subarachnoid hemorrhage is present. In addition, the location of the hemorrhage is requested to be answered. |
| CTMRI.CTType | Type of CT done (PCT, CTA, CCT, NCCT) | NCCT == Non-contrast CT CCT == Contrast CT CTA == CT Angiography PCT == Perfusion CT |
This variable describes the type of CT scan that has been made. Multiple options can be selected from: Non-contrast CT, Contrast CT, CT Angiography, Perfusion CT. |
| CTMRI.CTYesOpMotiv | Motivation for scheduling operation | 1 == Emergency/life saving 2 == Clinical deterioration 3 == Mass effect on CT 4 == Radiological progression 5 == (Suspicion of) raised ICP 6 == Guideline adherence 7 == To prevent deterioration 8 == Depressed skull fracture 99 == Other |
WHY question: documents reason for having an indication for (intra)cranial surgery. |
| CTMRI.CTYesOpMotivOther | Specify 'other' motivation for scheduling operation | Free text if "CTMRI.CTYesOpMotiv" was marked as 'Other'. Relates to the WHY question: documents reason for having an indication for (intra)cranial surgery. | |
| CTMRI.IcometrixImageId | Icometrix image ID | Identifier generated for an imaging experiment when images are uploaded from site It's recommended to use: Imaging.CRFIcometrixImageId | |
| CTMRI.IcometrixPassedQA | Passed QA in Icometrix | 1 == Yes 0 == No |
Reflects if images uploaded from site passed QA of icometix. It's recommended to use: Imaging.CRFIcometrixPassedQA |
| CTMRI.IcometrixQADateTime | Icometrix QA Date/Time | Date and time when central QA was done | |
| CTMRI.IcometrixUploadDateTime | Date/Time of image upload to Icometrix | Date and time when the images were uploaded from site | |
| CTMRI.InitialDataIcometrix | Data initially loaded from Icometrix | Reflects if the imaging data was initially loaded from Icometrix into the e-CRF (if not, it means the data in the e-CRF was entered manually by the study nurse) It's recommended to use "Imaging.CRFInitialDataIcometrix" | |
| CTMRI.MRIDone | MRI done or not | This variable is populated when an MRI has been made. MR studies according to study protocol have been performed by selected sites. In addition, results of any MR performed for clinical reasons are captured in the e-CRF. Many of these clinical MR's have also been uploaded to Icometrix. | |
| CTMRI.MRIERReason | Reason for MRI (ER only) | ER4 == ER only: Suspicion spinal cord lesion ER2 == ER only: Suspicion non-metal foreign object ER3 == ER only: Instead of CT (limiting radiation exposure) ER1 == ER only: Discrepancy between clinical symptomatology and (lack of) CT abnormalities 99 == Other 88 == Unknown |
This variable contains the main reason why an MRI, ultra-early MR (within 72 hrs), was performed. Possible options are ER only: Discrepancy between clinical symptomatology and (lack of) CT abnormalities; suspicion nonmetal foreign object; instead of CT (limiting radiation exposure); suspicion spinal cord lesion; unknown; other (further specified in text field CTMRI.MRIERReasonOther. Reasons for clinical MRI's can be found in variable CTMRI.MRIReason |
| CTMRI.MRIERReasonOther | Other reason for MRI (ER only) | This variable contains the main reason why an MRI, ultra-early MR (within 72 hrs), was performed, when in CTMRI.MRIERReason, the "other" option was chosen. This is a free text field. Reasons for clinical MRI's can be found in variable CTMRI.MRIReason | |
| CTMRI.MRIManuf | MRI manufacturer | 99 == Other TOSH == Toshiba GE == GE PHIL == Philips SIEM == Siemens |
This variable describes the MRI-scan manufacturer. It's recommended to use "Imaging.CRFMRIManuf" |
| CTMRI.MRIPatientLocation | Patient location at time of MRI | ICU == ICU ED == ER ADMIS == Ward/Admission |
This variable describes the in-hospital location of the patient when the MRI-scan was performed and was not meant to describe the location of the MRI-scanner. Three options: ER, Ward/Admission, ICU |
| CTMRI.MRIReason | Main reason for MRI scan | STUDYPROT == Study protocol 88 == Unknown 99 == Other ICUADM1 == Discrepancy between CT and clinical condition ICUADM2 == Standard Care ICUADM3 == Detection of brainstem lesions |
This variable contains the main reason why an MRI, during hospital stay, was performed. One of following options must be selected: discrepancy between CT and clinical condition, standard care, detection of brainstem lesions, study protocol, unknown, other (specified in CTMRI.MRIReasonOther). The reason for making an early MRI/ER MRI scan can be found in: CTMRI.MRIERReason It's recommended to use Imaging.CRFMRIReason |
| CTMRI.MRIReasonOther | Specify 'other' main reason for MRI scan | This variable contains the main reason why an MRI, during hospital stay, was performed, when in the variable CTMRI.MRIReason, the option "other" was chosen. This is a text field. The reason for making an early MRI/ER MRI scan can be found in: CTMRI.MRIERReason It's recommended to use Imaging.CRFMRIReasonOther | |
| CTMRI.MRIResultPreExistAbnorm | Pre-existing abnormalities | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there are pre-existing abnormalities present on MRI scan (yes, no, unknown). Assessment by investigator and or physician. It’s recommended to use Imaging.CRFMRIResultPreExistAbnorm |
| CTMRI.MRIResultTraumaticAbnorm | Traumatic abnormalities | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there are traumatic abnormalities present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRIResultTraumaticAbnorm |
| CTMRI.MRIScannerStrength | Scanner strength | This variable describes the MRI scanner strength. This is a text field. It’s recommended to use Imaging.CRFMRIScannerStrength | |
| CTMRI.MRISequences | MRI sequences (T1, T2 FLAIR, DWI, GRE, SWI, DTI, MRSI, PWI) | T1 == T1 T2 == T2 FLAIR == FLAIR DWI == DWI GRE == GRE SWI == SWI DTI == DTI MRSI == MRSI PWI == PWI 99 == Other |
This variable describes the MRI sequence. Options are: T1, T2, FLAIR, DWI, GRE, SWI, DTI, MRSI, PWI, Other. Multiple options can be selected. It’s recommended to use Imaging.CRFMRISequences |
| CTMRI.MRITraumAbnormASDH | ASDH | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there is an acute subdural hematoma present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormASDH |
| CTMRI.MRITraumAbnormContusion | Contusions | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there is a contusion present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormContusion |
| CTMRI.MRITraumAbnormDAI | DAI | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there is DAI (diffuse axonal injury) present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAI |
| CTMRI.MRITraumAbnormDAILesionLocBrainstem | Brainstem | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there is a brain stem lesion present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAILesionLocBrainstem |
| CTMRI.MRITraumAbnormDAILesionLocCorpusCallosum | Corpus Callosum | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there is a corpus callosum lesion present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAILesionLocCorpusCallosum |
| CTMRI.MRITraumAbnormDAILesionLocDiffuseWhiteMatter | Diffuse white matter | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there is a lesion in diffuse white matter present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAILesionLocDiffuseWhiteMatter |
| CTMRI.MRITraumAbnormDAINumLesions | Number of lesions | 1 == 1 2 == 2 3 == 3 4 == 4 5 == >= 5 |
This variable describes how many DAI lesions are present on MRI scan (1,2,3,4,>=5). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAINumLesions |
| CTMRI.MRITraumAbnormEDH | EDH | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there is an epidural hematoma present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormEDH |
| CTMRI.MRIType | Type of MRI done (MRI, MRA) | MRA == MRA MRI == MRI |
This variable describes the type of MRI scan that has been made. Options are: MRI, MRA It’s recommended to use Imaging.CRFMRIType |
| CTMRI.Timepoint | Timepoint | MR Early == MR Early CT Post-Op == CT Post-Op CT Early == CT Early CT Followup == CT Followup |
This variable describes the timepoint of imaging. Options are: CT Early, CT Followup, CT PostOp, MR Early CT early is considered "first CT". A central review was performed on all CT's. When a Central review is not available this can be due to: - Scan uninterpretable - Scan not available/performed/uploaded Reasons for scan not being available included: o Scan performed in referring hospital and images not available o Pediatric patient and MR performed instead of CT (reducing radiation risk) o Patient too uncooperative to undergo scan, and no indication for sedation. |
| CTMRI.XRayDone | X-ray angiography done | This variable is populated when an X-ray angiography has been done. | |
| DailyTIL.TILCCSFDrainageVolume | CSF volume drained | Specification of volume drained, only applicable if "DailyTIL.TILCSFDrainage" was "yes" | |
| DailyTIL.TILCSFDrainage | CSF Drainage | 0 == No 1 == Yes |
Daily TIL: reflects if CSF drainage occurred yes or no |
| DailyTIL.TILDailyPhysConcSatisfNotDone | Daily physician concerns for 9 aspects | Daily physician concerns are documented for 9 aspects rated on a scale of 1 (not concerned) to 10 (very concerned) | |
| DailyTIL.TILDate | Date of TIL assessment | Interpretation of ICP is not possible without knowledge on the level of therapy intensity employed for ICP control and/or for CPP management. TIL can be recorded in great detail and has commonly been performed on an hourly basis. Such detailed recording however, is resource intensive. Further, ICU practices have changed with most high grade interventions (such as metabolic suppression and temperature manipulation) now being used in a continuous fashion over periods of days or at least a large fraction of a day. Other discrete interventions (such as surgical decompression) happen as a single threshold event rather than as a repeated treatment. Given this context, the use of hourly recording of therapy intensity may be less relevant and there are doubts as to whether the data provided by hourly recording of TIL justifies the investment in time, particularly in the context of an increased (and probably increasing) burden of data collection in other areas (such as imaging and biomarkers). We therefore decided to record the therapy intensity level on a daily basis, under the presumption that this will offer a transparent and useful approach with the benefit of a lower burden than when hourly recording is performed. A novel TIL was developed to this purpose, which requires further validation. Preliminary data have been reported by Zuercher et al: Reliability and Validity of the Therapy Intensity Level Scale: Analysis of Clinimetric Properties of a Novel Approach to Assess Management of Intracranial Pressure in Traumatic Brain Injury; J Neurotrauma. 2016 Oct 1;33(19):1768-1774. Epub 2016 Feb 11. The specified treatment modalities and categories are compatible with the pediatric TIL proposed by Shore et al.: Shore P, Adelson PD, Kochanek P, et al. Reliability and validity of the pediatric intensity level of therapy (pilot) scale: A measure of the use of intracranial pressure-directed therapies. Crit Care Med. 2006;34:1981-1987. Possible chasnges in TIL over a 24 hr period are captured in the reporting of "hourly" values at 4 hr intervals. | |
| DailyTIL.TILDobutamineDose | Dobutamine | Indicates the total dose of dobutamine administered (in mg.) if applicable. Calculated over a 24-hour period | |
| DailyTIL.TILDopamineDose | Dopamine | Indicates the total dose of dopamine administered (in mg.) if applicable. Calculated over a 24-hour period | |
| DailyTIL.TILFactorsCaloricIntakeEnteralKcal | Enteral caloric intake (please specify) | Daily TIL: reflects the caloric intake via Enteral route in Kcal | |
| DailyTIL.TILFactorsCaloricIntakeParenKcal | Parenteral caloric intake (please specify) | Daily TIL: reflects the caloric intake via Parenteral route in Kcal | |
| DailyTIL.TILFactorsCaloricIntakeRouteEnteral | Enteral caloric intake | The variables "parenteral" and "enteral route" are used to document if the patient received enteral feeding or not and if so, what the total number of Kcal was given by each route. | |
| DailyTIL.TILFactorsCaloricIntakeRouteParen | Parenteral caloric intake | The variables "parenteral" and "enteral route" are used to document if the patient received enteral feeding or not and if so, what the total number of Kcal was given by each route. | |
| DailyTIL.TILFactorsCoagHemoglobAfterOtherUnitAmt | Level of hemoglobin after transfusion in another unit than the standard g/dL | Reflects the level of hemoglobin after transfusion in another unit than the standard g/dL (together with "DailyTIL.TILFactorsCoagHemoglobAfterOtherUnitSpecify") | |
| DailyTIL.TILFactorsCoagHemoglobAfterOtherUnitSpecify | Unit used for level of hemoglobin after transfusion (in another unit than the standard g/dL) | 1 == mmol/L 99 == Other |
Reflects the level of hemoglobin after transfusion in another unit than the standard g/dL (together with "DailyTIL.TILFactorsCoagHemoglobAfterOtherUnitAmt") |
| DailyTIL.TILFactorsCoagHemoglobBeforeOtherUnitAmt | Level of hemoglobin before transfusion in another unit than the standard g/dL | Reflects the level of hemoglobin before transfusion in another unit than the standard g/dL (together with "DailyTIL.TILFactorsCoagHemoglobBeforeOtherUnitSpecify") | |
| DailyTIL.TILFactorsCoagHemoglobBeforeOtherUnitSpecify | Unit used for level of hemoglobin before transfusion (in another unit than the standard g/dL) | 1 == mmol/L 99 == Other |
Reflects the level of hemoglobin before transfusion in another unit than the standard g/dL (together with "DailyTIL.TILFactorsCoagHemoglobBeforeOtherUnitAmt") |
| DailyTIL.TILFactorsCoagulation | Coagulation status checked | 0 == No 1 == Yes, for clinical reasons 2 == Yes, according to study protocol 88 == Unknown |
A maximum of 4 "types" of treatment (drop down box) can be selected and entered under treatment 1-4. Details on volume/dose of the products administered should correspond to treatment 1-4 and be entered in the variable volume 1-4. |
| DailyTIL.TILFactorsCoagulationHemoglobinAfter | Hemoglobin level after transfusion | Reflects the level of hemoglobin after transfusion in the standard unit (g/dL) | |
| DailyTIL.TILFactorsCoagulationHemoglobinAfterNotDone | Level of hemoglobin after transfusion not recorded | Intended to document hemoglobin levels after blood transfusion, this variable would indicate that hemoglobin levels were not documented after transfusion; however, some investigators may have also marked this for patients who did not receive a blood transfusion | |
| DailyTIL.TILFactorsCoagulationHemoglobinBefore | Hemoglobin level before transfusion | Reflects the level of hemoglobin before transfusion in the standard unit (g/dL) | |
| DailyTIL.TILFactorsCoagulationHemoglobinBeforeNotDone | Level of hemoglobin before transfusion not recorded | Intended to be only applicable in case the patient received a blood transfusion, however various investigators may have entered "not done", also for patient who did not receive a transfusion | |
| DailyTIL.TILFactorsCoagulationType1 | (1) Coagulation product / treatment | 1 == Packed red blood cell concentrates (pRBCs) 2 == Fresh whole blood 3 == Fresh frozen plasma (FFP) 4 == Freeze dried plasma / lypholized plasma 5 == Platelet concentrates 6 == PCC (prothrombin complex concentrates) 7 == Fibrinogen concentrate 8 == Albumine 9 == Recombinant factor FVIIa 10 == Tranexamic acid (TXA) 11 == Cryoprecipitate 12 == Desmopression (DDAVP) 13 == Factor XIII 14 == Calcium |
Reflects the details on volume/dose of the products administered |
| DailyTIL.TILFactorsCoagulationType2 | (2) Coagulation product / treatment | 1 == Packed red blood cell concentrates (pRBCs) 2 == Fresh whole blood 3 == Fresh frozen plasma (FFP) 4 == Freeze dried plasma / lypholized plasma 5 == Platelet concentrates 6 == PCC (prothrombin complex concentrates) 7 == Fibrinogen concentrate 8 == Albumine 9 == Recombinant factor FVIIa 10 == Tranexamic acid (TXA) 11 == Cryoprecipitate 12 == Desmopression (DDAVP) 13 == Factor XIII 14 == Calcium |
Reflects the details on volume/dose of the products administered |
| DailyTIL.TILFactorsCoagulationType3 | (3) Coagulation product / treatment | 1 == Packed red blood cell concentrates (pRBCs) 2 == Fresh whole blood 3 == Fresh frozen plasma (FFP) 4 == Freeze dried plasma / lypholized plasma 5 == Platelet concentrates 6 == PCC (prothrombin complex concentrates) 7 == Fibrinogen concentrate 8 == Albumine 9 == Recombinant factor FVIIa 10 == Tranexamic acid (TXA) 11 == Cryoprecipitate 12 == Desmopression (DDAVP) 13 == Factor XIII 14 == Calcium |
Reflects the details on volume/dose of the products administered |
| DailyTIL.TILFactorsCoagulationType4 | (4) Coagulation product / treatment | 1 == Packed red blood cell concentrates (pRBCs) 2 == Fresh whole blood 3 == Fresh frozen plasma (FFP) 4 == Freeze dried plasma / lypholized plasma 5 == Platelet concentrates 6 == PCC (prothrombin complex concentrates) 7 == Fibrinogen concentrate 8 == Albumine 9 == Recombinant factor FVIIa 10 == Tranexamic acid (TXA) 11 == Cryoprecipitate 12 == Desmopression (DDAVP) 13 == Factor XIII 14 == Calcium |
Reflects the details on volume/dose of the products administered |
| DailyTIL.TILFactorsCoagulationVolume1 | (1) Coagulation product volume | Reflects the details on volume/dose of the products administered | |
| DailyTIL.TILFactorsCoagulationVolume2 | (2) Coagulation product volume | Reflects the details on volume/dose of the products administered | |
| DailyTIL.TILFactorsCoagulationVolume3 | (3) Coagulation product volume | Reflects the details on volume/dose of the products administered | |
| DailyTIL.TILFactorsCoagulationVolume4 | (4) Coagulation product volume | Reflects the details on volume/dose of the products administered | |
| DailyTIL.TILFactorsGenSuppCareDone | Blood transfusion, blood products or treatment of coagulopathy received | 1 == Yes 0 == No |
Reflects whether the patient received any blood transfusion, blood products and treatment of coagulopathy. |
| DailyTIL.TILFactorsGlucoseManagement | Glucose management | 0 == No specific therapy 1 == Prophylactic 2 == Insulin administration to correct hyperglycemias 3 == Tight glycemic control (targeting blood glucose levels of 80-110mg/dL [4.4-6.1mmol/L]) |
Indicates whether glucose management was applied and if so, which therapy used (prophylactic, insulin administration of tight glycemic control). |
| DailyTIL.TILFever | Treatment of fever (temperature > 38 degree Celsius or spontaneous temperature of 34.5 degree Celsius) | 0 == No 1 == Yes |
Records for the Daily TIL whether there was treatment of fever (temperature <38°C) or spontaneous temperature of 34.5°C |
| DailyTIL.TILFeverHypothermia | Hypothermia below 35 degree Celsius | 0 == No 1 == Yes |
Records for the Daily TIL whether there was hypothermia below 35°C |
| DailyTIL.TILFeverMildHypothermia | Mild hypothermia for ICP control with a lower limit of 35 degree Celsius | 0 == No 1 == Yes |
Records for the Daily TIL whether there was mild hypothermia for ICP control with a lower limit of 35°C. |
| DailyTIL.TILFluidBalanceNotDone | Fluid balance not done | Indicates that the Fluid Balance was not done. | |
| DailyTIL.TILFluidCalcStartDate | Date calculation started | Start date Fluid Balance calculation. | |
| DailyTIL.TILFluidCalcStartTime | Time calculation started | Start Time Fluid Balance calculation. | |
| DailyTIL.TILFluidCalcStopDate | Date calculation stopped | Stop date Fluid Balance calculation. | |
| DailyTIL.TILFluidCalcStopTime | Time calculation stopped | Stop Time Fluid Balance calculation. | |
| DailyTIL.TILFluidColloids | Were colloids administered? | 0 == No 1 == Yes 88 == Unknown |
Indicates whether colloids were administered with regard to Fluid Balance. |
| DailyTIL.TILFluidColloidsTotalVolume | Total volume colloids | Total volume of colloids administered (in ml) | |
| DailyTIL.TILFluidColloidsType | Type of colloid | 1 == Albumin 5% 2 == Albumin 20% 3 == Dextran 4 == Gelatin (e.g. gelofusion) 5 == HES (hydroxyethyl starches) 6 == Tetrastarches (e.g. HES 130/04) |
Type of colloids administered |
| DailyTIL.TILFluidIn | Fluids in | Recorded preferably over 24-hour period, exact details to be derived from start and stop date/time for calculation | |
| DailyTIL.TILFluidLoading | Fluid loading for maintenance of cerebral perfusion | 0 == No 1 == Yes |
Records for the Daily TIL whether there was fluid loading for maintenance of cerebral perfusion. |
| DailyTIL.TILFluidLoadingVasopressor | Vasopressor therapy required for management of cerebral perfusion | 0 == No 1 == Yes |
Records for the Daily TIL whether there was vasopressor therapy required for management of cerebral perfusion |
| DailyTIL.TILFluidOutCSFDrain | CSF drainage | Daily TIL - Number of fluid out: CSF drainage in ml | |
| DailyTIL.TILFluidOutGastric | Gastic loss | Daily TIL - Number of fluid out: Gastic loss in ml | |
| DailyTIL.TILFluidOutOther | Fluid out | Daily TIL - Number of fluid out: other fluid (than Urine, Gastic loss or CSF drainage) in ml | |
| DailyTIL.TILFluidOutUrine | Urine | Daily TIL - Number of fluid out: Urine in ml | |
| DailyTIL.TILFluidsRenalReplacement | Need for renal replacement therapy | 0 == No 1 == Yes |
Indicates for the fluid balance whether there was a need for renal replacement therapy. |
| DailyTIL.TILHyperosmolarThearpy | Hyperosmolar therapy with mannitol up to 2 g/kg/24 hours | 0 == No 1 == Yes |
Records for the Daily TIL whether there was Hyperosmolar therapy with mannitol up to 2 g/kg/24 hours |
| DailyTIL.TILHyperosomolarTherapyHigher | Hyperosmolar therapy with hypertonic saline > 0.3 g/kg/24 hours | 0 == No 1 == Yes |
Records for the Daily TIL whether there was Hyperosmolar therapy with hypertonic saline > 0.3 g/kg/24 hours |
| DailyTIL.TILHyperosomolarTherapyHypertonicLow | Hyperosmolar therapy with hypertonic saline up to 0.3 g/kg/24 hours | 0 == No 1 == Yes |
Records for the Daily TIL whether there was Hyperosmolar therapy with hypertonic saline up to 0.3 g/kg/24 hours |
| DailyTIL.TILHyperosomolarTherapyMannitolGreater2g | Hyperosmolar therapy with mannitol > 2 g/kg/24 hours | 0 == No 1 == Yes |
Records for the Daily TIL whether there was Hyperosmolar therapy with mannitol > 2 g/kg/24 hours |
| DailyTIL.TILHypertonicSalineDose | Hypertonic saline | Indicates the total dose of hypertonic saline administered (in g.) if applicable. Calculated over a 24-hour period. | |
| DailyTIL.TILHyperventilation | Mild hypocapnia for ICP control [PaCO2 4.6 - 5.3 kPa (35 - 40 mmHg)] | 0 == No 1 == Yes |
Records for the Daily TIL whether there was Mild hypocapnia for ICP control [PaCO2 4.6 - 5.3 kPa (35 - 40 mmHg)] |
| DailyTIL.TILHyperventilationIntensive | Intensive hypocapnia for ICP control [PaCO2 < 4.0 kPa (30 mmHg)] | 0 == No 1 == Yes |
Records for the Daily TIL whether there was Intensive hypocapnia for ICP control [PaCO2 < 4.0 kPa (30 mmHg)] |
| DailyTIL.TILHyperventilationModerate | Moderate hypocapnia for ICP control [PaCO2 4.0 - 4.5 kPa (30 - 35 mmHg)] | 0 == No 1 == Yes |
Records for the Daily TIL whether there was Moderate hypocapnia for ICP control [PaCO2 4.0 - 4.5 kPa (30 - 35 mmHg)] |
| DailyTIL.TILICPSurgery | Intracranial operation for progressive mass lesion, not scheduled on admission | 1 == Yes 0 == No |
Records for the Daily TIL whether there was an intracranial operation for progressive mass lesion, not scheduled on admission |
| DailyTIL.TILICPSurgeryDecomCranectomy | Decompressive craniectomy | 0 == No 1 == Yes |
Records for the Daily TIL whether there was a Decompressive Craniectomy |
| DailyTIL.TILMannitolDose | Mannitol | Indicates the total dose of Mannitol administered (in g.) if applicable. Calculated over a 24-hour period | |
| DailyTIL.TILNoradrenalineDose | Noradrenaline | Indicates the total dose of Noradrenaline administered (in mg.) if applicable. Calculated over a 24-hour period | |
| DailyTIL.TILOtherDose | Other vasopressor's dosage (please specify) | Indicates the dose (in mg.) of other vasopressors drugs administered (if applicable) | |
| DailyTIL.TILOtherTxt | Other vasopressor (please specify) | Indicates which other vasopressors drugs was administered (if applicable) | |
| DailyTIL.TILOtherVaso | Were there other vasopressors used? | 0 == No 1 == Yes |
Indicates whether any other Vasopressor drug was administered (other than Dobutamine, Dopamine, Noradrenaline or Phenylephrine) |
| DailyTIL.TILPhenylephrineDose | Phenylephrine | Indicates the total dose of phenylephrine administered (in mg.) if applicable. Calculated over a 24-hour period | |
| DailyTIL.TILPhysicianConcernsContusionpregression | To what extent does contusion progression concern the treating physician regarding this specific patient's current condition? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to contusion progression. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianConcernsCPP | To what extent does CPP concern the treating physician regarding this specific patient's current condition? | 2 == 2 1 == 1 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to CPP. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianConcernsEpilepsy | To what extent does epilepsy concern the treating physician regarding this specific patient's current condition? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to epilepsy. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianConcernsFocalSwelling | To what extent does focal swelling concern the treating physician regarding this specific patient's current condition? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to focal swelling. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianConcernsHematomaProgression | To what extent does hematoma progression concern the treating physician regarding this specific patient's current condition? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to hematoma progression. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianConcernsHypoperfusion | To what extent does suspected hypoperfusion concern the treating physician regarding this specific patient's current condition? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to suspected hypoperfusion. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianConcernsICP | To what extent does ICP concern the treating physician regarding this specific patient's current condition? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to ICP. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianConcernsIntracranialInfection | To what extent does intracranial infection concern the treating physician regarding this specific patient's current condition? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to intracranial infections. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianConcernsVasospasm | To what extent does vasospasm concern the treating physician regarding this specific patient's current condition? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Reflects daily the physician concern and satisfaction with regard to vasospasm. Scales from 1 (not concerned) to 10 (very concerned) |
| DailyTIL.TILPhysicianOverallSatisfaction | Overall, how satisfied is the physician with the clinical course of this patient? | 0 == Not at all 1 == Slightly 2 == Moderately 3 == Quite 4 == Very |
This variable aims to capture the overall satisfaction of the physician with the clinical course of this patient; "not at all satisfied" would indicate that the patient did much more poorly than expected; "very satisfied" would indicate that the patient did much better than expected. Physician satisfaction should be assessed on a daily basis, |
| DailyTIL.TILPhysicianOverallSatisfactionSurvival | Overall, what are the short term survival chances of the patient as per the physician? | 1 == Much worse 2 == A little worse 3 == Unchanged 4 == A little better 5 == Much better |
This variable aims to capture the opinion of the treating physician as to whether the short time survival change have chnged in comparision to the previous assessment |
| DailyTIL.TILPhysicianSatICP | How satisfied are you with the ICP control obtained? | 77 == N/A (no ICP monitoring) 1 == Not at all 2 == Slightly 3 == Moderate 4 == Quite 5 == Very |
Documents physician satisfaction with ICP control |
| DailyTIL.TILPosition | Head elevation for ICP control | 0 == No 1 == Yes |
Records for the Daily TIL whether there was head elevation for ICP control |
| DailyTIL.TILPositionNursedFlat | Nursed flat (180 degree) for CPP management | 0 == No 1 == Yes |
Records for the Daily TIL whether there was a patient position of Nursed flat (180°C) for CPP management |
| DailyTIL.TILReasonForChange | Reason for change in treatment over this day | 0 == No change 1 == Intensified: Clinical deterioration 2 == Intensified:Suspicion of increased of ICP (not measured) 3 == Intensified:Increased ICP (documented) 4 == Intensified:Clinical decision to target other mechanism 5 == Intensified:Change of doctor (different shift) 6 == Decreasing:Clinical improvement 7 == Decreasing:Adequate control over ICP 8 == Decreasing:Upper treatment limit reached/past 9 == Decreasing:Further treatment considered futile 10 == Decreasing:Change of doctor (different shift) |
Reflects the reason for change in TIL therapy over the day. |
| DailyTIL.TILSedation | Sedation (low dose as required for mechanical ventilation) | 1 == Yes 0 == No |
Records for the Daily TIL whether there was sedation (low dose as required for mechanical ventilation) |
| DailyTIL.TILSedationHigher | Higher dose sedation for ICP control (not aiming for burst supression) | 0 == No 1 == Yes |
Records for the Daily TIL whether there was a higher dose sedation for ICP control (not aiming for burst supression) |
| DailyTIL.TILSedationMetabolic | Metabolic suppression for ICP control with high dose barbiturates or propofol | 0 == No 1 == Yes |
Records for the Daily TIL whether there was metabolic suppression for ICP control with high dose barbiturates or propofol |
| DailyTIL.TILSedationNeuromuscular | Neuromuscular blockade (paralysis) | 0 == No 1 == Yes |
Records for the Daily TIL whether there was neuromuscular blockade (paralysis) |
| DailyTIL.TILSedationScaleUsed | Was a sedation scale used to adjust sedatives (SAS, RASS, MASS, Ramsay, etc)? | 1 == Yes 0 == No 77 == N/A |
Reflects with regard to sedation management whether a sedation scale (SAS, RASS, MASS, Ramsay, etc) was used to adjust sedatives? |
| DailyTIL.TILSedativesInterrupted | If the patient is receiving infusions of sedatives (opioids), were they interrupted today? | 1 == Yes 0 == No 77 == N/A |
Reflects with regard to sedation management whether infusions of sedatives (opioids) were interrupted during the day if the patient was receiving any. |
| DailyTIL.TILTherapyIntensityNotDone | Daily TIL not done | Marked if Daily TIL was not done for a patient | |
| DailyTIL.TILTime | Time of TIL assessment | Time of Daily TIL records. See also "DailyTIL.TILDate" | |
| DailyTIL.TotalTIL | Daily TIL total | Calculated centrally - 24 hour TILS as the worst sum TILs for each day for the ICU timepoints (day 1-7, 10, 14, 21 and 28) | |
| FollowUp.CTAngulation | CT with or without angulation | 99 == Other 2 == Orbital-meatal line 1 == No angulation (volume scan) |
Reflects the angulation of the Follow up CT. |
| FollowUp.CTAtrophy | Atrophy | 88 == Unknown F == Focal D == Diffuse 0 == No |
CT parameters scored by the investigator: reflects the Atrophy of the Follow up CT. |
| FollowUp.CTHydrocephalus | Hydrocephalus | 1 == Yes 88 == Unknown 0 == No |
CT parameters scored by the investigator: reflects if there was hydrocephalus or not on the Follow up CT. |
| FollowUp.CTManuf | CT scan manufacturer | 99 == Other TOSH == Toshiba SIEM == Siemens PHIL == Philips KONI == Konica Minolta HITA == Hitachi GE == GE CARE == Carestream AGFA == Agfa |
Manufacturer of the CT scanner used |
| FollowUp.CTMidlineShift | CT midline shift assessed by investigator | 0 == No 1 == Yes |
CT parameters scored by the investigator: reflects if there was midline shift on the Follow up CT. |
| FollowUp.CTMidlineShiftMeasure | CT midline shift in mm (assessed by investigator) | CT parameters scored by the investigator: reflects the volume in mm if there was a midline shift on the Follow up CT Check also "FollowUp.CTMidlineShift" | |
| FollowUp.CTMRIDate | Date of follow up imaging captured in CRF | Imaging date captured in the CRF for followup images | |
| FollowUp.CTMRITime | Time of follow up imaging captured in CRF | Imaging time captured in CRF for followup images | |
| FollowUp.CTReason | Reason for Follow up CT | CD == Clinical deterioration LOP == Absence of or slow improvement RFU == Routine follow-up |
Reason for follow up CT could be: Clinical deterioration, Absence of or slow improvement, Routine followup |
| FollowUp.CTScannerType | Type of scanner for follow up CT | 99 == Other 16 == 16-slice 32 == 32-slice 64 == 64-slice 128 == 128-slice 256 == 256-slice 320 == 320-slice |
Type of scanner used for follow up CT |
| FollowUp.CTSubduralHaematomaHygroma | Subdural haematoma / hygroma | B == Bilateral L == Left 88 == Unknown R == Right 0 == No |
CT parameters scored by the investigator: reflects if there was subdural haematoma/hygroma on the Follow up CT and if yes, on which side. |
| FollowUp.CTType | Type of Follow up CT done (PCT, CTA, CCT, NCCT) | PCT == Perfusion CT CTA == CT Angiography CCT == Contrast CT NCCT == Non-contrast CT |
Type of CT scan for followup imaging |
| FollowUp.FUAttendance | In attendance | 0 == No attendance 1 == Subject 2 == Proxy (please specify) 3 == Health care professional taking care of patient 4 == N/A (death) |
Documents who was present at the follow-up assessment. In case of postal Questionnaire, there would be "no attendance" |
| FollowUp.FUAttendanceProxyChild | Attendance by proxy: Child | When a proxy was attending the Follow up visit, specification was needed whether this was: child, parent, partner, sibling or other caretaker. This variable reflects who often the proxy attending the follow up visit was the child of the patient. | |
| FollowUp.FUAttendanceProxyOtherCaretaker | Attendance by proxy: Other caretaker | When a proxy was attending the Follow up visit, specification was needed whether this was: child, parent, partner, sibling or other caretaker. This variable reflects who often the proxy attending the follow up visit was an other caretaker. | |
| FollowUp.FUAttendanceProxyParent | Attendance by proxy: Parent | When a proxy was attending the Follow up visit, specification was needed whether this was: child, parent, partner, sibling or other caretaker. This variable reflects who often the proxy attending the follow up visit was a parent of the patient. | |
| FollowUp.FUAttendanceProxyPartner | Attendance by proxy: Partner | When a proxy was attending the Follow up visit, specification was needed whether this was: child, parent, partner, sibling or other caretaker. This variable reflects who often the proxy attending the follow up visit was the partner of the patient. | |
| FollowUp.FUAttendanceProxySibling | Attendance by proxy: Sibling | When a proxy was attending the Follow up visit, specification was needed whether this was: child, parent, partner, sibling or other caretaker. This variable reflects who often the proxy attending the follow up visit was a sibling of the patient. | |
| FollowUp.FUDisabilityDueToExtracranialInj | Disability due to extracranial injuries | 0 == No 1 == Mild/moderate 2 == Severe (requiring institutional care) |
The variable is only valid when "FollowUp.FUVitStatus" is "alive". It reflects if the patient suffers from any disability due to an extracranial injury |
| FollowUp.FUImagingModality | Follow up lmaging modality | XRay == X-Ray Angiography MRI == MRI CT == CT |
The variables concerning imaging modality, largely overlap with those with the in-hospital phase, however details of recording abnormalities and reasons for performing the imaging studies differ |
| FollowUp.FUIntracranialSurg | Intracranial surgery | 0 == No 1 == Yes 88 == Unknown |
Reflects at the follow up visit if any intracranial surgery was performed after discharge |
| FollowUp.FUIntracranialSurgDate | Date of intracranial surgery | Date of the Intracranial surgery (after discharge) if performed Check also "FollowUp.FUIntracranialSurg". | |
| FollowUp.FUIntracranialSurgOther | Other type of intracranial surgery (please specify) | If any form of intracranial surgery was performed after discharge (re-admission likely), this reflects if the type was other (than hydrocephalus, chronic subdural hematoma or cranioplasty) | |
| FollowUp.FUIntracranialSurgSpecifyType | Type of intracranial surgery | 1 == Hydrocephalus 2 == Chronic subdural hematoma 3 == Cranioplasty 99 == Other |
This variable aims to capture any form of intracranial surgery performed after discharge (re-admission likely) |
| FollowUp.FUIntracranialSurgTime | Time of intracranial surgery | Time of the Intracranial surgery (after discharge) if performed Check also "FollowUp.FUIntracranialSurg" and "FollowUp.FUIntracranialSurgDate" | |
| FollowUp.FUMartlPartnerStatus | Marital status | 1 == Never been married 2 == Married 3 == Living together/common law 4 == Divorced 5 == Separated 6 == Widowed 99 == Other 88 == Unknown |
Only recorded if change in SES; This variable needs to be related to the pre-injury situation: Subject.MartlPartnerStatus |
| FollowUp.FUMedAmantidine | Amantadine | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedAmantidineReason | Reason for amantadine | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedAntibiotics | Antibiotics | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedAntibioticsReason | Reason for antibiotics | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedAntiConv | Anticonvulsants | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedAntiConvReason | Reason for anticonvulsants | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedAntidep | Antidepressants | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedAntidepReason | Reason for antidepressants | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedAntipsycho | Antipsychotic agents | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedAntipsychoReason | Reason for anti-psychotic agents | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedAnxiolytics | Anxiolytics | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedAnxiolyticsReason | Reason for anxiolytics | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedCholinergic | Cholinergic agents | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedCholinergicReason | Reason for cholinergic agents | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedClonidine | Clonidine | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedClonidineReason | Reason for clonidine | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedComplAutonomicInstability | Paroxysmal sympathetic hyperactivity (autonomic instability) | 1 == Yes 0 == No 88 == Unknown |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects whether there has been Paroxysmal sympathetic hyperactivity (autonomic instability). |
| FollowUp.FUMedComplAutonomicInstabilityTreatment | Treatment of paroxysmal sympathetic hyperactivity (autonomic instability) | DRUGS == Drugs BPUMP == Baclofen pump |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects the treatment given in case there has been Paroxysmal sympathetic hyperactivity (autonomic instability.) See also "FollowUp.FUMedComplAutonomicInstability" |
| FollowUp.FUMedComplDVT | DVT | 1 == Yes 0 == No 88 == Unknown |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects whether there has been DVT (Deep venous thrombosis). Intent is to record here only DVT occurring post-discharge. DVT that occurred before/at presentation or during hospital stay is recorded elsewhere: Hospital.HospComplDVT |
| FollowUp.FUMedComplHeteroOss | Heterotopic ossification | 1 == Yes 0 == No 88 == Unknown |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects whether there has been Heterotopic ossification. |
| FollowUp.FUMedComplHeteroOssTreatment | Treatment of heterotopic ossification | PERF == Performed PLAN == Planned |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects the treatment given in case there has been Heterotopic ossification. See also "FollowUp.FUMedComplHeteroOss". |
| FollowUp.FUMedComplPressureSores | Pressure sores | 1 == Yes 0 == No 88 == Unknown |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects whether there has been Pressure sores. |
| FollowUp.FUMedComplPulmonaryEmbolus | Pulmonary embolus | 1 == Yes 0 == No 88 == Unknown |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects whether there has been Pulmonary embolism (PE) post-discharge. PE that occurred before/at presentation or during hospital stay is recorded elsewhere: Hospital.HospComplPumlEmb |
| FollowUp.FUMedComplSeizurePostDischarge | Seizures | 1 == Yes 0 == No 88 == Unknown |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects whether there has been seizures occurring post-discharge. Seizures that occurred before/at presentation or during hospital stay are recorded elsewhere: InjuryHx.EDComplEventSeizures; Vitals.HosComplEventSeizures; Hospital.HospComplSeizures; Vitals.HosComplEventSeizures; Hospital.ICUDisComplSeizure; Outcomes.GOSEEpilepsyFits; Subjective reporting also in: Outcomes.PartQuestACurHltSeiz |
| FollowUp.FUMedComplSpasticity | Spasticity | 1 == Yes 0 == No 88 == Unknown |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects whether there has been spasticity. |
| FollowUp.FUMedComplSpasticityTreatment | Treatment for spasticity | BENZ == Benzodiazepines OBAC == Oral baclofen IBAC == Intrathecal baclofen pump PHYS == Physiotherapy |
On follow-up assessment, information is captured on medical complications and sequelae post-hospitalization. This reflects the treatment given in case there has been spasticity. |
| FollowUp.FUMedication | Medication | 0 == No 1 == Yes 88 == Unknown |
On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. No specific info on agent or dose is captured. |
| FollowUp.FUMedNarc | Narcotics | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedNarcReason | Reason for narcotics | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedOther | Other medication | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedOtherPain | Other pain medication | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedOtherPainReason | Reason for other pain medication | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedOtherReason | Reason for other medication | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. Only applicable if "FollowUp.FUMedication = Yes" and "FollowUp.FUMedOther" marked as valid. |
| FollowUp.FUMedOtherText | Other medication (please specify) | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedPsycho | Psycho-stimulants | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedPsychoReason | Reason for psycho-stimulants | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUMedSteroids | Steroids | Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. | |
| FollowUp.FUMedSteroidsReason | Reason for steroids | 1 == Agitation 2 == Attentional problems 3 == Behavioral disturbance 4 == Depression 5 == Memory difficulties 6 == Disorder of consciousness 7 == Fatigue 8 == Infection 9 == Pain - somatic 10 == Pain - neurogenic 11 == Pain - headache/migraine 12 == Paroxysmal sympathetic hyperactivity (PSH) 13 == Seizure - prophylaxis 14 == Seizure - treatment 15 == Spasticity |
Only applicable if FollowUp.FUMedication = Yes. On Follow-up assessment, general information is captured on classes of medication taken and the reason for taking this. |
| FollowUp.FUPrincipalDeathCause | Principle cause of death | 1 == Head injury/initial injury 2 == Head injury/secondary intracranial damage 3 == Systemic trauma 4 == Medical complications 88 == Unknown 99 == Other |
On Follow-up assessment, information is captured whether the patience is still alive or not. This reflects the (post-hospitalization) death cause if the patient died post-discharge. Only applicable if FollowUp.FUVitStatus = Dead. |
| FollowUp.FUPrincipalDeathCauseOther | Other principal cause of death (please specify) | On Follow-up assessment, information is captured whether the patience is still alive or not. This reflects the (post-hospitalization) death cause if the patient died post-discharge (if the cause was "other" than listed). Only applicable if FollowUp.FUVitStatus = Dead. See also "FollowUp.FUPrincipalDeathCause" | |
| FollowUp.FUPtStillInICU | Is the patient still in ICU? | This variable reflects if the patient was still in ICU at the time of a scheduled follow up visit. | |
| FollowUp.FUReasonNoAttendance | Reason for no attendance | 99 == Other 3 == Refused 1 == Not contactable 2 == Forgotten |
Documents reason if subject did not undergo Follow up assessment. |
| FollowUp.FURehabGenLongTermAcuteCUInPat | Type of in-patient rehabilitation unit: General long term acute care | Reflects the type of in-patient rehab care received: General long term acute care | |
| FollowUp.FURehabGenRehabUnitInPat | Type of in-patient rehabilitation unit: General | Reflects the type of in-patient rehab care received: General | |
| FollowUp.FURehabGeriatricRehabUnitInPat | Type of in-patient rehabilitation unit: Geriatric | Reflects the type of in-patient rehab care received: Geriatric | |
| FollowUp.FURehabInPat | In rehabilitation | Documents that patient received in-patient rehab care at the time of this assessment. | |
| FollowUp.FURehabInPatAdmisDate | Date of admission to in-patient rehabilitation | Date of admission for the in-patient rehab care. | |
| FollowUp.FURehabInPatDischDate | Date of discharge from in-patient rehabilitation | Date of discharge for the in-patient rehab care. | |
| FollowUp.FURehabInPatOngoingRehab | Is in-patient rehabilitation ongoing? | 1 == Yes 0 == No |
Reflects if the in-patient rehab was still ongoing at the time of the follow up assessment. |
| FollowUp.FURehabInPatShortTermInterrup1EndDate | First short-term rehabilitation interruption end date | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup1StartDate | First short-term rehabilitation interruption start date | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup2EndDate | Second short-term rehabilitation interruption end date | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup2StartDate | Second short-term rehabilitation interruption start date | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup3EndDate | Third short-term rehabilitation interruption end date | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup3StartDate | Third short-term rehabilitation interruption start date | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabNo | No rehabilitation | Documents that patient received no rehab at the time of this assessment. | |
| FollowUp.FURehabOutPat | Out-patient rehabilitation | Documents that patient received out-patient rehab care at the time of this assessment. | |
| FollowUp.FURehabOutPatAdmisDate | Date of admission to out-patient rehabilitation | Start Date of the out-patient rehab care. | |
| FollowUp.FURehabOutPatTherpyCog | Cognitive remediation therapy | Reflects the type of out-patient rehab care received: Cognitive remediation | |
| FollowUp.FURehabOutPatTherpyCogFreq | Frequency of cognitive remediation as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of Cognitive remediation received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyCog". |
| FollowUp.FURehabOutPatTherpyCompDayTreatmnt | Comprehensive day treatment as out-patient therapy | Reflects the type of out-patient rehab care received: Comprehensive day treatment | |
| FollowUp.FURehabOutPatTherpyCompDayTreatmntFreq | Frequency of comprehensive day treatment as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of Comprehensive day treatment received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyCompDayTreatmnt" |
| FollowUp.FURehabOutPatTherpyHomeHealth | Home health as out-patient therapy | Reflects the type of out-patient rehab care received: Home health | |
| FollowUp.FURehabOutPatTherpyHomeHealthFreq | Frequency of home-health as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Home health' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyHomeHealth" |
| FollowUp.FURehabOutPatTherpyIndLivngTrainng | Independent living training as out-patient therapy | Reflects the type of out-patient rehab care received: Independent living training | |
| FollowUp.FURehabOutPatTherpyIndLivngTrainngFreq | Frequency of independent living training as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Independent living training' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyIndLivngTrainng" |
| FollowUp.FURehabOutPatTherpyNursServ | Nursing services as out-patient therapy | Reflects the type of out-patient rehab care received: Nursing services | |
| FollowUp.FURehabOutPatTherpyNursServFreq | Frequency of nursing services as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Nursing services' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyNursServ" |
| FollowUp.FURehabOutPatTherpyOcc | Occupational therapy as out-patient therapy | Reflects the type of out-patient rehab care received: Occupational therapy | |
| FollowUp.FURehabOutPatTherpyOccFreq | Frequency of occupational therapy as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Occupational therapy' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyOcc" |
| FollowUp.FURehabOutPatTherpyOther | Other out-patient therapy | Reflects the type of out-patient rehab care received: "Other" than the listed types Check also "FollowUp.FURehabOutPatTherpyOtherText" for the specification on the type of "other". | |
| FollowUp.FURehabOutPatTherpyOtherFreq | Frequency of other out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of "Other" therapy received as out-patient rehab care. |
| FollowUp.FURehabOutPatTherpyOtherText | Other out-patient therapy (please specify) | Specifies the type of "other" out-patient rehab care received. Check also "FollowUp.FURehabOutPatTherpyOther" | |
| FollowUp.FURehabOutPatTherpyPeerMentor | Peer mentoring as out-patient therapy | Reflects the type of out-patient rehab care received: Peer mentoring | |
| FollowUp.FURehabOutPatTherpyPeerMentorFreq | Frequency of peer mentoring as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Peer mentoring' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyPeerMentor" |
| FollowUp.FURehabOutPatTherpyPhysicianInvolved | Rehab physician involved | 1 == Yes 0 == No 88 == Unknown |
Reflects if a Rehab physician was involved, in case the patient received out-patient rehab care. |
| FollowUp.FURehabOutPatTherpyPsychSer | Psychological services as out-patient therapy | Reflects the type of out-patient rehab care received: Psychological services | |
| FollowUp.FURehabOutPatTherpyPsychSerFreq | Frequency of psychological services as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Psychological services' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyPsychSer" |
| FollowUp.FURehabOutPatTherpyPT | Physical therapy as out-patient therapy | Reflects the type of out-patient rehab care received: Physical therapy | |
| FollowUp.FURehabOutPatTherpyPTFreq | Frequency of physical therapy as out-patient therapy | 4 == 4 - Weekly 3 == 3 - < Once a week 2 == 2 - Only follow-up, no active treatment 1 == 1 - None 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Physical therapy' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyPT" |
| FollowUp.FURehabOutPatTherpyRec | Therapeutic recreation as out-patient therapy | Reflects the type of out-patient rehab care received: Therapeutic recreaction | |
| FollowUp.FURehabOutPatTherpyRecFreq | Frequency of therapeutic recreation as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of "Therapeutic recreaction" received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyRec" |
| FollowUp.FURehabOutPatTherpySocWrkCaseMgmt | Social work/case management as out-patient therapy | Reflects the type of out-patient rehab care received: Social work/Case management | |
| FollowUp.FURehabOutPatTherpySocWrkCaseMgmtFreq | Frequency of social work/case management as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Social work/Case management' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpySocWrkCaseMgmt" |
| FollowUp.FURehabOutPatTherpySpeech | Speech therapy as out-patient therapy | Reflects the type of out-patient rehab care received: Speech therapy | |
| FollowUp.FURehabOutPatTherpySpeechFreq | Frequency of speech therapy as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of 'Speech therapy' received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpySpeech" |
| FollowUp.FURehabOutPatTherpyStructure | Structure of out-patient therapy | 1 == Mono-disciplinary (little/nocollaboration between care providers 2 == Multi-disciplinary |
Reflects the structure of the out-patient rehab care received. |
| FollowUp.FURehabOutPatTherpyUnknown | Out-patient rehab care unknown | Reflects if out-patient rehab care was received but the type was "Unknown" | |
| FollowUp.FURehabOutPatTherpyUnknownFreq | Frequency of unknown out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of "Unknown" therapy received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyUnknown" |
| FollowUp.FURehabOutPatTherpyVocServ | Vocational services as out-patient therapy | Reflects the type of out-patient rehab care received: Vocational services | |
| FollowUp.FURehabOutPatTherpyVocServFreq | Frequency of vocational services as out-patient therapy | 1 == 1 - None 2 == 2 - Only follow-up, no active treatment 3 == 3 - < Once a week 4 == 4 - Weekly 5 == 5 - 2-3 times/week 6 == 6 - Daily 7 == 7 - Unknown |
Reflects the frequency of "Vocational services" received as out-patient rehab care. Check also "FollowUp.FURehabOutPatTherpyVocServ" |
| FollowUp.FURehabTBIRehabUnitInPat | Type of in-patient rehabilitation unit: TBI | Reflects the type of in-patient rehab care received: TBI | |
| FollowUp.FURehabTherpyEndDate | Date of discharge from out-patient rehabilitation | End date of the out-patient rehab care. | |
| FollowUp.FURehabTherpyOngoingInd | Is out-patient rehab ongoing? | 0 == No 1 == Yes |
Reflects if the out-patient rehab care was still ongoing at the time of the follow up assessment. |
| FollowUp.FURehabUnknown | Rehab care unknown | Reflects if it was "unknown" whether rehab treatment had occurred at the time of this assessment. | |
| FollowUp.FUResdncType | Living situation/patient's residence | 1 == Living at home independently 2 == Living at home supported by family/carers 11 == Living in shelteed + housing/community care 7 == Rehabilitation centre 10 == Living in nursing home 6 == Living in a long-stay patient ward(hospital) 99 == Other |
Only recorded if change in SES. Reflects the Living situation/patient's residence at the time of follow up assessment, if there was a change in SES. |
| FollowUp.FUResdncTypeOther | Other living situation/patient's residence (please specify) | Only recorded if change in SES Specifies the "Other" Living situation/patient's residence at the time of follow up assessment, if there was a change in SES. | |
| FollowUp.FURtrnToOtherAct | Returned to other activities | 1 == Full return to previous level 2 == Reduced level 0 == No 88 == Unknown |
Prefects if at the time of follow up assessment the patient returned to other activities than work/school and at what level. |
| FollowUp.FURtrnWrkSchlStatus | Returned to work/school | 1 == Returned to previous job / school at same level and hours 8 == Returned to previous job / school at increased levels or hours from pre-injury 2 == Unable to work / go to school 9 == Returned to previous job / school at reduced level or hours 10 == Change of job / different work or school 11 == Special employment / sheltered employment 5 == Looking for work / go to school 7 == Retired NA == N/A 88 == Unknown |
Prefects if at the time of follow up assessment the patient returned to work/school and at what level. |
| FollowUp.FUSESChange | Any change to the socio-economic status from the previous visit? | 0 == No 1 == Yes 88 == Unknown |
This variable aims to document any change in socio-economic status following the TBI |
| FollowUp.FUSESPeopleLivingWith | Number of people living with | Only recorded if change in SES Reflects the "Number of people living with" at the time of follow up assessment, if there was a change in SES. | |
| FollowUp.FUSESPrimAdultAlone | Persons living with: Alone | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Alone | |
| FollowUp.FUSESPrimAdultCarerUnrelated | Persons living with: Carers unrelated to patient | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Carers unrelated to patient | |
| FollowUp.FUSESPrimAdultChildren | Persons living with: Child/children | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Child/children | |
| FollowUp.FUSESPrimAdultOther | Persons living with: Other (incl) correctional facility inmates) | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Other (incl. correctional facility inmates) | |
| FollowUp.FUSESPrimAdultParents | Persons living with: Parents | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Parents | |
| FollowUp.FUSESPrimAdultSiblings | Persons living with: Siblings | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Siblings | |
| FollowUp.FUSESPrimAdultSignOther | Persons living with: Significant other partner | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Significant other partner | |
| FollowUp.FUSESPrimAdultSpousePartner | Persons living with: Spouse (including common law partner) | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Spouse (including common law partner) | |
| FollowUp.FUSESPrimAdultUnknown | Change in Socio-economic Status unknown | Only recorded if change in SES Reflects the "Persons living with" at the time of follow up assessment, if there was a change in SES: Unknown | |
| FollowUp.FUSurgCranioplastyPerformed | Cranioplasty performed | 1 == Yes 2 == No, but scheduled 0 == No |
On Follow-up assessment, general information is captured on Medical and Surgical Therapies. This reflects if Cranioplasty was performed. Only applicable in case a decompressive craniectomy was performed during the in-hospital period |
| FollowUp.FUSurgExtracranialSurg | Extracranial surgery | 88 == Unknown 0 == No 1 == Yes |
On Follow-up assessment, general information is captured on Medical and Surgical Therapies. This variable aims to capture any form of extracranial surgery performed after discharge |
| FollowUp.FUSurgExtracranialSurgDate | Date of extracranial surgery | On Follow-up assessment, general information is captured on Medical and Surgical Therapies. This variable reflects the date, in case any form of extracranial surgery was performed. | |
| FollowUp.FUSurgExtracranialSurgSpecify | Type of extracranial surgery (please specify) | On Follow-up assessment, general information is captured on Medical and Surgical Therapies. This variable specifies the type, in case any form of extracranial surgery was performed. | |
| FollowUp.FUSurgExtracranialSurgTime | Time of extracranial surgery | On Follow-up assessment, general information is captured on Medical and Surgical Therapies. This variable reflects the date, in case any form of extracranial surgery was performed. | |
| FollowUp.FUVisitDate | Date of follow-up assessment | Date of follow up visit | |
| FollowUp.FUVisitTime | Time of follow-up assessment | Time of follow up visit. Check also "FollowUp.FUVisitDate" for the date. | |
| FollowUp.FUVisitType | Follow up visit type (scheduled or unscheduled) | UNSCHED == Unscheduled follow-up SCHED == Scheduled study follow-up |
All Follow-up assessments used questionnaire assessments, and at selected pre-specified time points, neuropsychological testing was done during out-patient follow-up. The schedule for assessments was differentiated by stratum. Cross-sectional assessments, including questionnaires and neuropsych, was performed at 6 mnths post injury. Further Questionnaire assessments were schduled as follows: ER stratum: 2-3 weeks and 3 months; Adm stratum: 3 mnths and 12 mnths; ICU stratum: 3 months and 12 months. |
| FollowUp.FUVitStatus | Is the patient dead or alive? | 0 == Dead 1 == Alive 88 == Unknown |
This variable reflects the status of the patient at the time of a scheduled follow up visit. The status could be Dead, Alive, Unknown |
| FollowUp.IcometrixImageId | Icometrix image ID for follow up imaging | Identifier generated for an imaging experiment when images are uploaded from site It's recommended to use: Imaging.CRFIcometrixImageId | |
| FollowUp.IcometrixPassedQA | Follow up images passed QA of icometrix | 1 == Yes 0 == No |
Reflects if images uploaded from site passed QA of icometix. It's recommended to use: Imaging.CRFIcometrixPassedQA |
| FollowUp.IcometrixQADateTime | Date and time of QA icometrix for follow up images | Date and time when central QA was done for followup images It's recommended to use: Imaging.CRFIcometrixQADateTime | |
| FollowUp.IcometrixUploadDateTime | Date and time of upload to icometrix for follow up images | Date/Time of image upload to Icometrix | |
| FollowUp.InitialDataIcometrix | Imaging data in CRF loaded from icometrix (not by study nurse) | Reflects if the imaging data was not entered by the site in the e-CRF but directly from the images at icometrix (if not, it means the data in the e-CRF was entered manually by the study nurse) It's recommended to use "Imaging.CRFInitialDataIcometrix" | |
| FollowUp.MRIManuf | MRI scan manufacturer for follow up MRI | 99 == Other TOSH == Toshiba GE == GE PHIL == Philips SIEM == Siemens |
This variable reflects the manufacturer of the follow up MRI scanner used. It's recommended to use "Imaging.CRFMRIManuf" |
| FollowUp.MRIReason | Reason of MRI for follow up MRI | SP == Study protocol 88 == Unknown 99 == Other CD == Clinical deterioration LOP == Lack of improvement SBL == Suspicious brainstem lesions ISC == Ischemia CR == Clinical routine |
This variable contains the main reason why an MRI at follow up was performed. It's recommended to use Imaging.CRFMRIReason |
| FollowUp.MRIReasonOther | Other Reason of MRI for follow up MRI | Specifies the type of "other" reason for MRI at follow up It's recommended to use Imaging.CRFMRIReasonOther | |
| FollowUp.MRIResultPreExistAbnorm | Pre-existing abnormalities on follow up MRI | 88 == Unknown 0 == No 1 == Yes |
Scored by investigator Reflects if there are pre-existing abnormalities on the follow up MRI. It’s recommended to use Imaging.CRFMRIResultPreExistAbnorm |
| FollowUp.MRIResultTraumaticAbnorm | Traumatic abnormalities on follow up MRI | 88 == Unknown 1 == Yes 0 == No |
Scored by investigator Reflects if there are Traumatic abnormalities on the follow up MRI. It’s recommended to use Imaging.CRFMRIResultTraumaticAbnorm |
| FollowUp.MRIScannerStrength | MRI scanner strength for follow up MRI | This variable describes the follow up MRI scanner strength. This is a text field. It’s recommended to use Imaging.CRFMRIScannerStrength | |
| FollowUp.MRISequences | MRI sequences for follow MRI | 99 == Other PWI == PWI MRSI == MRSI SWI == SWI DTI == DTI GRE == GRE FLAIR == FLAIR DWI == DWI T2 == T2 T1 == T1 |
This variable describes the follow up MRI sequence. Options are: T1, T2, FLAIR, DWI, GRE, SWI, DTI, MRSI, PWI, Other. Multiple options can be selected. It’s recommended to use Imaging.CRFMRISequences |
| FollowUp.MRITraumAbnormASDH | ASDH present on follow up MRI | 88 == Unknown 1 == Yes 0 == No |
This variable describes whether or not there is an acute subdural hematoma present on follow up MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormASDH |
| FollowUp.MRITraumAbnormContusion | Contusion present on follow up MRI | 88 == Unknown 1 == Yes 0 == No |
This variable describes whether or not there is a contusion present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormContusion |
| FollowUp.MRITraumAbnormDAI | DAI present on follow up MRI | 0 == No 1 == Yes 88 == Unknown |
This variable describes whether or not there is DAI (diffuse axonal injury) present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAI |
| FollowUp.MRITraumAbnormDAILesionLocBrainstem | Brain stem lesion present on follow up MRI | 1 == Yes 88 == Unknown 0 == No |
This variable describes whether or not there is a brain stem lesion present on follow up MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAILesionLocBrainstem |
| FollowUp.MRITraumAbnormDAILesionLocCorpusCallosum | Corpus callosum lesion present on follow up MRI | 88 == Unknown 0 == No 1 == Yes |
This variable describes whether or not there is a corpus callosum lesion present on follow up MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAILesionLocCorpusCallosum |
| FollowUp.MRITraumAbnormDAILesionLocDiffuseWhiteMatter | Lesion in diffuse white matter present on follow up MRI | 88 == Unknown 1 == Yes 0 == No |
This variable describes whether or not there is a lesion in diffuse white matter present on follow up MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAILesionLocDiffuseWhiteMatter |
| FollowUp.MRITraumAbnormDAINumLesions | Number of DAI lesions present on follow up MRI | 1 == 1 2 == 2 3 == 3 4 == 4 5 == >= 5 |
This variable describes how many DAI lesions are present on follow up MRI scan (1,2,3,4,>=5). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormDAINumLesions |
| FollowUp.MRITraumAbnormEDH | Epidural hematoma present on follow up MRI | 1 == Yes 88 == Unknown 0 == No |
This variable describes whether or not there is an epidural hematoma present on follow up MRI scan (yes, no, unknown). Assessment by investigator and/or physician. It’s recommended to use Imaging.CRFMRITraumAbnormEDH |
| FollowUp.MRIType | Type of MRI done (MRI, MRA) for follow up MRI | MRA == MRA MRI == MRI |
This variable describes the type of follow up MRI scan that has been made. Options are: MRI, MRA It’s recommended to use Imaging.CRFMRIType |
| FollowUp.TimePoint | Follow-up assessment timepoint | 3mo == 3 months 2wk == 2 weeks 6mo == 6 months 12mo == 12 months 24mo == 24 months |
Follow up timepoints are 2-3 weeks, 3 months, 6 months, 12 months and 24 months. Depending on the stratum and sub-studies of a patient, follow up was performed at some of these time points or at all timepoints. For an overview, please check the SOP Manual. |
| Genetics.CollectionDate | Collection time of the Genetic sample | Collection Date and Time of the Genetic sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Genetics.CollectionTime | Collection date of the Genetic sample | Collection Date and Time of the Genetic sample. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Genetics.FreezerMinusEightyDate | Date the Genetic sample was stored in a -80 freezer | The 4.9ml whole blood sample for genetic assays should be stored at -80°C with a needle to freezer time preferably within 6 hours. This variable reflects the date and time that the sample was stored in a minus 80 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Genetics.FreezerMinusEightyTime | Time the Genetic sample was stored in a -80 freezer | The 4.9ml whole blood sample for genetic assays should be stored at -80°C with a needle to freezer time preferably within 6 hours. This variable reflects the date and time that the sample was stored in a minus 80 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Genetics.FreezerMinusTwentyDate | Date the Genetic sample was stored in a -20 freezer | The 4.9ml whole blood sample for genetic assays should be stored at -80°C with a needle to freezer time preferably within 6 hours. However, if a -80°C freezer was not immediately accessible, samples could be temporarely (max 48 hours) stored in a minus 20°C non-frost-free freezer. This variable reflects the date and time that the sample was stored in a minus 20 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Genetics.FreezerMinusTwentyTime | Time the Genetic sample was stored in a -20 freezer | The 4.9ml whole blood sample for genetic assays should be stored at -80°C with a needle to freezer time preferably within 6 hours. However, if a -80°C freezer was not immediately accessible, samples could be temporarely (max 48 hours) stored in a minus 20°C non-frost-free freezer. This variable reflects the date and time that the sample was stored in a minus 20 freezer. These date/time values were provided by the sites on the “sample collection and processing forms” enclosed to the samples. | |
| Genetics.SampleId | Sample identifier for the Genetic sample | Per patient 1x 4.9 ml blood samples was collected into 1x 4.9 ml potassium EDTA tubes for genetic assays. | |
| Hospital.AdditionalStudiesCoag | Are coagulation studies performed? | 0 == No 1 == Yes |
Intended to provide documentation if the patient was enrolled in the Coagulation sub-study or not. |
| Hospital.AdditionalStudiesECoG | Is Electrocorticography (ECoG) performed? | 0 == No 1 == Yes |
Intended to provide documentation if the patient was enrolled in the ECoG sub-study or not. |
| Hospital.AdditionalStudiesEEG | Is continuous EEG performed? | 0 == No 1 == Yes |
Intended to provide documentation if the patient was enrolled in the EEG sub-study or not. |
| Hospital.AdditionalStudiesTEGRotem | Are TEG/ROTEM studies performed? | 0 == No 1 == Yes |
Intended to provide documentation if the patient was enrolled in the TEG/ROTEM sub-study or not. |
| Hospital.BrainDeathDate | Date of brain death | Reflects the date of Brain death in case of Withdrawal of life-sustaining measures | |
| Hospital.BrainDeathTime | Time of brain death | Reflects the Time of Brain death in case of Withdrawal of life-sustaining measures Check also "Hospital.BrainDeathDate" for the date. | |
| Hospital.ComplCRBSIDateDiagnosis | Date of diagnosis of Catheter Related Bloodstream Infection (CRBSI) at ICU discharge | At discharge, complications and adverse events were summarized. This variable reflects the date of diagnosis of CRBSI in case of systemic complication. | |
| Hospital.DeadAge | Withdraw of life sustaining measures: For reason of age | 0 == No 1 == Yes 88 == Unknown |
Reflects if the reason for Withdrawal of life-sustaining measures was age. |
| Hospital.DeadCoMorbidities | Withdraw of life sustaining measures: For reason of co-morbidities | 0 == No 1 == Yes 88 == Unknown |
Reflects if the reason for Withdrawal of life-sustaining measures was co-morbidities. |
| Hospital.DeadDeterminationOfBrainDeath | Withdraw of life sustaining measures: Determination of brain death (according to national law) | 0 == No 1 == Yes 88 == Unknown |
Reflects if the reason for Withdrawal of life-sustaining measures was Determination of brain death (according to national law). |
| Hospital.DeadOrganDonation | Is determination of brain death followed by organ donation? | 0 == No 1 == Yes 88 == Unknown |
Reflects if Withdrawal of life-sustaining measures was followed by organ donation. |
| Hospital.DeadPatWill | Withdraw of life sustaining measures: Following living will of patient | 0 == No 1 == Yes 88 == Unknown |
Reflects if the reason for Withdrawal of life-sustaining measures was Following living will of patient. |
| Hospital.DeadRequestRelatives | Withdraw of life sustaining measures: On request of relatives | 0 == No 1 == Yes 88 == Unknown |
Reflects if the reason for Withdrawal of life-sustaining measures was On request of relatives. |
| Hospital.DeadSeverityofTBI | Withdraw of life sustaining measures: For severity of TBI | 0 == No 1 == Yes 88 == Unknown |
Reflects if the reason for Withdrawal of life-sustaining measures was Severity of TBI. |
| Hospital.DeathAutopsy | Was autopsy performed? | 0 == No 1 == Yes, forensic 2 == Yes, clinical 88 == Unknown |
Reflects if an autopsy was performed after the death of the patient. |
| Hospital.DeathCause | Principal cause of death | 4 == Medical complications 3 == Systemic trauma 2 == Head injury/secondary intracranial damage 1 == Head injury/initial injury 99 == Other |
Reflects the principal cause of death of a patient in-hospital. |
| Hospital.DeathCauseOther | Other principal cause of death (please specify) | Reflects if the cause of in-hospital death was "other" than the listed causes. | |
| Hospital.DischargeStatus | Is patient alive or dead at ward discharge? | 1 == Alive 0 == Dead 88 == Unknown |
Assessment by investigator Reflects if the patient was dead or alive at discharge. |
| Hospital.DispHosp | Destination from Hospital | 3 == Nursing home 2 == Rehab unit 1 == Other hospital 99 == Other 5 == Home 88 == Unknown |
Documents destination upon hospital discharge |
| Hospital.DispHospOther | Other destination from Hospital (please specify) | Specifies if the reason for hospital discharge was "other" than the listed discharge reasons. | |
| Hospital.GCSHospDischargeEyes | Eye opening (E) response at Hospital discharge | O == Untestable (other) 4 == 4-Spontaneously S == Untestable (swollen) 2 == 2-To pain 1 == 1-None 3 == 3-To speech UN == Unknown |
Eye opening score for GCS at hospital discharge. |
| Hospital.GCSHospDischargeMotor | Motor (M) response at Hospital discharge | P == Untestable (Deep sedation/paralyzed) 6 == 6-Obeys command 4 == 4-Normal flexion/withdrawal 5 == 5-Localizes to pain 3 == 3-Abnormal flexion 2 == 2-Abnormal extension 1 == 1-None O == Untestable (Other) UN == Unknown |
Motor score for GCS at hospital discharge. |
| Hospital.GCSHospDischargeScore | GCS score at Hospital discharge | GCS score at hospital discharge. | |
| Hospital.GCSHospDischargeVerbal | Verbal (V) response at Hospital discharge | O == Untestable (Other) T == Untestable (tracheotomy/endotracheal tube) 5 == 5-Oriented 4 == 4-Confused 1 == 1-None 3 == 3-Inappropriate words 2 == 2-Incomprehensible sound UN == Unknown |
Verbal score for GCS at hospital discharge. |
| Hospital.HospComplCardio | Cardiovascular complication at Hospital discharge | 1 == Yes 0 == No |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Cardiovascular as systemic complications. |
| Hospital.HospComplCRBSI | Catheter Related Bloodstream Infection (CRBSI) at Hospital discharge | 0 == No 1 == Yes |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of CRBSI (catheter related blood stream infection) as systemic complications. |
| Hospital.HospComplDelayedHaema | Delayed haematoma at Hospital discharge | 1 == Yes 0 == No |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Delayed haematoma as Intracranial complications (requiring treatment). |
| Hospital.HospComplDVT | Deep Vein Thrombosis (DVT) at Hospital discharge | 1 == Yes 0 == No |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of DVT (deep venous thrombosis) as systemic complications. |
| Hospital.HospComplIntraCranOther | Other Intracranial complication at Hospital discharge | 0 == No 1 == Yes |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of "Other" Intracranial complications (requiring treatment) than listed. |
| Hospital.HospComplIntraCranOtherTxt | Other Intracranial complication at Hospital discharge (please specify) | At discharge, complications and adverse events were summarized. This variable reflects the type of "Other" Intracranial complications (requiring treatment). | |
| Hospital.HospComplMeningitis | Meningitis/Ventriculitis at Hospital discharge | 1 == Yes 0 == No |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Meningitis/Ventriculitis as Intracranial complications (requiring treatment). |
| Hospital.HospComplMetabolic | Metabolic complication at Hospital discharge | 0 == No 1 == Yes |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Metabolic as systemic complications. |
| Hospital.HospComplPressureSore | Pressures sores (decubitus) at Hospital discharge | 0 == No 1 == Yes |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Pressures sores (decubitus) as systemic complications. |
| Hospital.HospComplPumlEmb | Pulmonary embolus at Hospital discharge | 1 == Yes 0 == No |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Pulmonary embolus as systemic complications. |
| Hospital.HospComplRasiedICP | Raised/increased ICP at Hospital discharge | 0 == No 1 == Yes |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Raised ICP as Intracranial complications (requiring treatment). |
| Hospital.HospComplResp | Respiratory complication at Hospital discharge | 1 == Yes 0 == No |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Respiratory as systemic complications. |
| Hospital.HospComplSeizures | Seizures at Hospital discharge | 1 == Yes 0 == No |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Seizures as Intracranial complications (requiring treatment). |
| Hospital.HospComplSystemOther | Other Systemic complication at Hospital discharge | 0 == No 1 == Yes |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of "Other" systemic complications than listed. |
| Hospital.HospComplSystemOtherTxt | Other Systemic complication at Hospital discharge (please specify) | At discharge, complications and adverse events were summarized. This variable reflects the type of "Other" systemic complications. | |
| Hospital.HospComplUTI | Urinary tract infection at Hospital discharge | 1 == Yes 0 == No |
At discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Urinary tract infection as systemic complications. |
| Hospital.HospDischargeBodyWeightkg | Body weight reported at Hospital discharge | Body weight on discharge in Kgs | |
| Hospital.HospDischargeBodyWeightlbs | Body weight on discharge in Lbs | Body weight on discharge in Lbs | |
| Hospital.HospDischargeBodyWeightMeasure | Reliability of body weight reported at Hospital discharge | 1 == Estimated 2 == Measured |
Reflects if Body weight was measured at discharge |
| Hospital.HospDischargeBodyWeightUnit | Unit used for body weight at discharge (kg or lbs) | 1 == kgs 2 == lbs |
Reflects the unit used for body weight at discharge (kgs or lbs). |
| Hospital.HospDischargeCTProgression | CT progression | 0 == No 1 == Yes |
Pre-defined early endpoints recorded at ICU or hospital discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, number of CTs performed and CT progression. |
| Hospital.HospDischargeCTProgressionYes | CT progression (please specify) | 1 == Increase in initial lesion 2 == Development of new lesion |
Pre-defined early endpoints recorded at ICU discharge or hospital discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, number of CTs performed and CT progression. If CT progression was "yes", this reflects if there was Increase in initial lesion or Development of new lesion. |
| Hospital.HospDischargeNumberCT | Number of CT's performed | 0 == No 1 == Yes |
Pre-defined early endpoints recorded at ICU or hospital discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, number of CTs performed and CT progression. |
| Hospital.HospDischargeReason | Reason for Hospital discharge | 0 == No institutional care necessary 3 == Waiting list for rehab 2 == Clinical rehab required but not approved 1 == No institutional care in trauma center necessary 99 == Other 4 == Clinical rehab required and approved 5 == No benefit of clinical rehab anticipated |
WHY question: documents reason for choice of (hospital) discharge destination. |
| Hospital.HospDischargeReasonOther | Other reason for Hospital discharge (please specify) | Specifies if the reason for (hospital) discharge destination was "other". | |
| Hospital.HospDischargeTimeToObeyCommands | Time to obey commands | Pre-defined early endpoints recorded at ICU or hospital discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, number of CTs performed and CT progression. | |
| Hospital.HospDischargeTimeToObeyCommandsNotApplic | No improvement in obeying commands at discharge | Intended for use in patients who did not improve to obeying commands at the time of discharge. However, some sites may have used this to mark also patients who never had a depression of consciousness, to the extend that they did not obey commands. | |
| Hospital.HospDischDate | Date of Hospital discharge | Hospital discharge:this variable was included also in the ICU form, in particular to record discharge dates for patients discharged directly from the ICU either dead or alive. | |
| Hospital.HospDischPTADays | PTA on discharge | This variable aims to facilitate collection of more information on PTA for subjects who were still in PTA at the time of admission to hospital. For study-broad interpretation of PTA,, the PTA as recorded on discharge from ER should also be taken into consideration: InjuryHx.LOCPTADuration | |
| Hospital.HospDischPTADaysNA | Patient had no PTA or did not recover from PTA at discharge | This variable could have been interpreted as either patients never having had PTA or alternatively, a patient who did not recover out of PTA by the time of discharge. | |
| Hospital.HospDischPTAOngoing | PTA ongoing at hospital discharge | Intended to designate patients who are still in PTA at the moment of discharge of hospital | |
| Hospital.HospDischTime | Time of Hospital discharge | Hospital discharge:this variable was included also in the ICU form, in particular to record discharge dates for patients discharged directly from the ICU either dead or alive. | |
| Hospital.HospNeuroworseEpisode | Any episode of Neuroworsening until Hospital discharge | 0 == No 1 == Yes |
Pre-defined early endpoints recorded at ICU or hospital discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, number of CTs performed and CT progression. |
| Hospital.ICDCode1 | (1) ICD code at Hospital discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode10 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode11 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode12 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode13 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode14 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode15 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode16 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode2 | (2) ICD code at Hospital discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode3 | (3) ICD code at Hospital discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode4 | (4) ICD code at Hospital discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode5 | (5) ICD code at Hospital discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode6 | (6) ICD code at Hospital discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode7 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode8 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode9 | Up to 16 fields to enter ICD codes (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCodeVersion | Version of ICD code used at Hospital discharge | 9 == ICD-9 10 == ICD-10 |
This variable reflects if the ICD code version 9 or version 10 was used. Up to 16 fields are available to enter diagnosis as recorded by hospital administration according to ICD codes. |
| Hospital.ICPDevice | Type of ICP monitor | 1 == Ventricular 2 == Ventricular +inbuilt sensor 3 == Parenchymal 99 == Other |
Type of ICP monitoring device used. |
| Hospital.ICPDeviceOther | Other type of ICP monitor (please specify) | Free text field with description of which ICP monitoring device was used, in case the device was not listed in the pre-specified list of the CRF. Some patients have had more than one ICP monitoring device, which are listed here. | |
| Hospital.ICPInsDate | Date ICP monitoring started | Start date of ICP monitoring. | |
| Hospital.ICPInsTime | Time ICP monitoring started | Start time of ICP monitoring Check also "Hospital.ICPInsDate" for the start date. | |
| Hospital.ICPMonitorNo | ICP not monitored | Indicates if a patient does not have intracranial pressure (ICP) monitoring. If Hospital.ICPMonitorNo=1, see Hospital.ICUReasonNoICP. | |
| Hospital.ICPMonitorStop | ICP monitoring stopped | 1 == Yes 0 == No |
If ICP monitoring has stopped or not. Time and date is found in Hospital.ICPRemTime and Hospital.ICPRemDate. Reason for stopping ICP monitoring is found in Hospital.ICPStopReason. |
| Hospital.ICPMonitorStopReasonOther | Other reason for stopping ICP monitoring (please specify) | Specifies the "other" reason if the reason for stopping ICP was not on the pre-defined list. Check also "Hospital.ICPStopReason" | |
| Hospital.ICPMonitorYes | ICP monitored | 0 == No 1 == Yes |
Indicates if a patient has intracranial pressure (ICP) monitoring. If yes, see Hospital.ICUReasonICP and Hospital.ICPDevice. |
| Hospital.ICPMontDuration | Duration of ICP monitoring | The duration of ICP monitoring. Calculated variable: Hospital.ICPRemDateTime-Hospital.ICPInsDateTime. | |
| Hospital.ICPRemDate | Date ICP monitoring stopped | Date for stopping ICP monitoring. | |
| Hospital.ICPRemTime | Time ICP monitoring stopped | Time of stopping ICP monitoring. | |
| Hospital.ICPStopReason | Reason for stopping ICP monitoring | 1 == Clinically improved 2 == ICP stable and < 20 mmHg 3 == Monitor/catheter failure 4 == Patient considered unsalvagable 5 == Patient died 99 == Other |
Reason for stopping ICP. Also check Hospital.ICPMonitorStop. |
| Hospital.ICPUnit | Origin of patient when transfered to ICU | 1 == ER 2 == OR 3 == Ward 4 == High dependency unit 99 == Other hospital |
The type of department the patient was transferred from to the ICU. |
| Hospital.ICUAdmDate | Date of admission to ICU | Date of Admission to the ICU. In principle the date of injury; date of enrollment and Date of Admission to ICU will match, but in some cases there can be a difference of 1 or 2 days. For example when a patient was injured late at night, it is possible that the consent was only obtained in the morning, hence the date of Study Enrollment will be 1 day later than the date of injury. Or in some hospitals a patient is kept for 24 hours in observation at the ER in a specific unit before being transferred to ICU or Ward. Hence the Date of Admission to ICU or Ward can be 1 or 2 days later. Or if there is no bed available on ICU or Ward for a patient being injured late at night, there can be a delay in admitting the patient. | |
| Hospital.ICUAdmisStatusHaemoStable | Was patient Haemodynamically stable at ICU arrival? | 0 == No 1 == Yes 88 == Unknown |
Reflects the status of the patient on admission to the ICU: Haemodynamically stable |
| Hospital.ICUAdmisStatusIntubated | Was patient intubated at ICU arrival? | 0 == No 1 == Yes 88 == Unknown |
Reflects the status of the patient on admission to the ICU: Intubated |
| Hospital.ICUAdmisStatusMechVent | Was patient mechanically ventilated at ICU arrival? | 0 == No 1 == Yes 88 == Unknown |
Reflects the status of the patient on admission to the ICU: Mechanically ventilated |
| Hospital.ICUAdmReason | Reason for admission to ICU | 6 == Clinical deterioration 5 == Neurological operation 4 == Extracranial injuries 3 == Haemodynamic invasive monitoring 2 == Frequent neurological observations 1 == Mechanical ventilation 99 == Other |
Main reason for admission to ICU |
| Hospital.ICUAdmReasonOther | Other reason for admission to ICU | Specifies the "other" if the main reason for admission to the ICU was other than the pre-defined list. | |
| Hospital.ICUAdmTime | Time of admission to ICU | Time of admission to the ICU. Check also "Hospital.ICUAdmDate" for the date of admission. | |
| Hospital.ICUCardiacOutput | Cardiac output | 0 == No 1 == Yes |
Reflects the type, in case of systemic monitoring on ICU: Cardiac output |
| Hospital.ICUCatheterICP | ICP catheter revised | 0 == No 1 == Yes |
Reflects if the ICP catheter has been revised in case of ICP monitoring |
| Hospital.ICUCatheterICPDate | Date of revision of ICP catheter | Reflects the date on which ICP catheter has been revised in case of ICP monitoring Check also "Hospital.ICUCatheterICP" | |
| Hospital.ICUCatheterICPTime | Time of revision of ICP catheter | Reflects the time on which ICP catheter has been revised in case of ICP monitoring Check also "Hospital.ICUCatheterICP" and "Hospital.ICUCatheterICPDate" | |
| Hospital.ICUCentralVenousPress | Central venous pressure | 0 == No 1 == Yes |
Reflects the type, in case of systemic monitoring on ICU: Central venous pressure |
| Hospital.ICUComplUTI | Urinary tract infection (UTI) at ICU discharge | 0 == No 1 == Yes |
At discharge, complications and adverse events were summarized. This variable reflects the date of diagnosis of Urinary tract infection in case of systemic complication. |
| Hospital.ICUDisAdditionalStudiesCoag | Are coagulation studies performed? | 0 == No 1 == Yes |
Intended to provide documentation if the patient was enrolled in the Coagulation sub-study or not. |
| Hospital.ICUDisAdditionalStudiesTEGRotem | Are TEG/ROTEM studies performed? | 0 == No 1 == Yes |
Intended to provide documentation if the patient was enrolled in the TEG/ROTEM sub-study or not. |
| Hospital.ICUDischargeICDCode1 | (1) ICD code at ICU discharge | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode10 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode11 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode12 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode13 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode14 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode15 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode16 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode2 | (2) ICD code at ICU discharge | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode3 | (3) ICD code at ICU discharge | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode4 | (4) ICD code at ICU discharge | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode5 | (5) ICD code at ICU discharge | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode6 | (6) ICD code at ICU discharge | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode7 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode8 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode9 | Up to 16 fields to enter ICD codes at ICU discharge (of hospital administration) | The intent here is to register ICD code as recorded in hospital administrative files for patients directly discharged from the ICU. Up to 16 codes can be entered, ICD codes are further captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCodeVersion | Version of ICD code used at ICU discharge | 9 == 9 10 == 10 |
This variable reflects if the ICD code version 9 or version 10 was used. Up to 16 fields are available to enter diagnosis as recorded by hospital administration according to ICD codes. |
| Hospital.ICUDischargeStatus | Is the patient alive or dead at ICU discharge? | 1 == Alive 2 == Dead 88 == Unknown |
Reflects if patient was alive or dead on discharge from ICU |
| Hospital.ICUDischargeTo | Destination from ICU discharge | 1 == General ward 2 == Other ICU 3 == Other hospital 4 == Rehab unit 5 == Home 6 == Nursing home 7 == Step down/high care unit 99 == Other 88 == Unknown |
Reflects location to which the patient was discharged from ICU |
| Hospital.ICUDischargeToOther | Other destination from ICU discharge (please specify) | Specifies the "other" location to which the patient was discharged from ICU Check also "Hospital.ICUDischargeTo" | |
| Hospital.ICUDischDate | Date of ICU discharge | Reflects the ICU Discharge Date | |
| Hospital.ICUDischPTADays | PTA on discharge | Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. | |
| Hospital.ICUDischPTADaysNA | PTA on discharge Not applicable | Reflects if PTA was not applicable. Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. | |
| Hospital.ICUDischPTAOngoing | PTA ongoing at ICU discharge | Reflects of PTA was ongoing on ICU discharge. Pre-defined early endpoints recorded at ICU or hospital discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, number of CTs performed and CT progression. | |
| Hospital.ICUDischTime | Time of ICU discharge | ICU Discharge Time Check also "Hospital.ICUDischDate" for the ICU discharge Date | |
| Hospital.ICUDisComplCardiacArrest | Cardiovascular complication at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Cardiovascular systemic complication. |
| Hospital.ICUDisComplCRBSI | Catheter Related Bloodstream Infection (CRBSI) | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of CRBSI (catheter-related bloodstream infection) as systemic complication. |
| Hospital.ICUDisComplDVT | Deep Vein Thrombosis (DVT) at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of DVT (Deep venous thrombosis) as systemic complication. |
| Hospital.ICUDisComplIntraCranOther | Other intracranial complication at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of "Other" Intracranial complication (requiring treatment). |
| Hospital.ICUDisComplIntraCranOtherTxt | Other Intracranial complication at ICU discharge (please specify) | At ICU discharge, complications and adverse events were summarized. This variable specifies the type of "Other" Intracranial complication (requiring treatment). | |
| Hospital.ICUDisComplMeningitis | Meningitis/Ventriculitis at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of "Meningitis/Ventriculitis" as Intracranial complication (requiring treatment). |
| Hospital.ICUDisComplMetabolic | Metabolic complication at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Metabolic systemic complication. |
| Hospital.ICUDisComplPE | Pulmonary embolus at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Pulmonary embolus as systemic complication. |
| Hospital.ICUDisComplPressureSores | Pressures sores (decubitus) at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Pressures sores (decubitus) as systemic complication. |
| Hospital.ICUDisComplRaisedICP | Raised or increased ICP at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of "Raised ICP" as Intracranial complication (requiring treatment). |
| Hospital.ICUDisComplRespiratoryFailure | Respiratory complication at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of Respiratory systemic complication. |
| Hospital.ICUDisComplSeizure | Seizures at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of "Seizures" Intracranial complication (requiring treatment). |
| Hospital.ICUDisComplSeromaHematoma | Delayed haematoma at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of "Delayed haematoma" Intracranial complication (requiring treatment). |
| Hospital.ICUDisComplSystemOther | Other systemic complication at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of "Other" systemic complication. |
| Hospital.ICUDisComplSystemOtherTxt | Other systemic complication at ICU discharge (please specify) | At ICU discharge, complications and adverse events were summarized. This variable specifies the type of "Other" systemic complication. | |
| Hospital.ICUDisComplVAP | Ventilator Associated Pneumonia (VAP) at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. This variable reflects the presence or absence of VAP (Ventilator associated pneumonia) as systemic complication. |
| Hospital.ICUDisCTProg | CT progression | 0 == No 1 == Yes |
Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. |
| Hospital.ICUDisCTProgYes | CT progression (please specify) | 1 == Increase in initial lesion 2 == Development of new lesion |
Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. If CT progression was "yes", this reflects if there was Increase in initial lesion or Development of new lesion. |
| Hospital.ICUDishDurVent | Duration ventilation | Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. | |
| Hospital.ICUDishDurVentNA | Duration of ventilation on discharge Not applicable | Reflects if Duration of ventilation was not applicable. Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. | |
| Hospital.ICUDisNeuroworseEpisode | Any episode of Neuroworsening until ICU dischage | 0 == No 1 == Yes |
Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. |
| Hospital.ICUDisNososcomialPneumNum | Nosocomial pneumonia number | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This variable reflects the Nosocomial pneumonia number. | |
| Hospital.ICUDisNumCT | Number of CT's performed | Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. | |
| Hospital.ICUDisPatDeadAtICU | Has patient died in the ICU? | 0 == No 1 == Yes |
Reflects if the patient was declared dead on the ICU. Intended as an introductory question for the details on withdrawal of treatment, brain death and organ donation |
| Hospital.ICUDisPneumAntibiotic1StartDate | Date of the beginning of first Antibiotic treatment | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the start date of antibiotic treatment if given. | |
| Hospital.ICUDisPneumAntibiotic2StartDate | Date of the beginning second Antibiotic treatment | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the start date of antibiotic treatment if given. | |
| Hospital.ICUDisPneumAntibiotic3StartDate | Date of the beginning third Antibiotic treatment | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the start date of antibiotic treatment if given. | |
| Hospital.ICUDisPneumAntibiotic4StartDate | Date of the beginning fourth Antibiotic treatment | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the start date of antibiotic treatment if given. | |
| Hospital.ICUDisPneumAntibioticTreat | Antibiotic treatment started at ICU discharge | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the antibiotic treatment was given for VAP. |
| Hospital.ICUDisPneumBacteriaSmpl | Bacteriological sample | 1 == BAL 2 == Tracheal suction 3 == PDP 4 == Brush |
At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the type of Bacteriological sample taken. |
| Hospital.ICUDisPneumBloodFiO2pc | FiO2 at ICU discharge | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects the details of blood gas. | |
| Hospital.ICUDisPneumBloodPaCO2mmHg | PaCO2 at ICU discharge | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the details on blood gas. | |
| Hospital.ICUDisPneumBloodPaO2mmHg | PaO2 at ICU discharge | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the details on blood gas. | |
| Hospital.ICUDisPneumBloodPEPcmH2O | Positive End-Expiratory Pressure (PEEP) at ICU discharge | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the details on blood gas. | |
| Hospital.ICUDisPneumBloodPF | PaO2/FiO2 at ICU discharge | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects if the details on blood gas. | |
| Hospital.ICUDisPneumChestX | Chest X-ray | 1 == New pneumonia 2 == Modification of an old one 3 == No infiltrate 4 == Diffuse (or patchy) infiltrate 5 == Localized infiltrate |
At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects the details on the Chest X-ray. |
| Hospital.ICUDisPneumClinical | Clinical | 1 == Fever >=38degC or hypothermia <=36degC 2 == Purulent trachea aspirations 3 == Leukocytes >=12000/ml or <=4000/ml |
At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects the clinical details on VAP. |
| Hospital.ICUDisPneumDate | Date of occurrence of Ventilator Associated Pneumonia (VAP) | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects the date of occurrence of the VAP. | |
| Hospital.ICUDisPneumPathogen1 | (1) Name of pathogen | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects details on the responsible pathogens for the VAP. | |
| Hospital.ICUDisPneumPathogen1QuantUCFml | (1) Quantity of pathogen | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects details on the responsible pathogens for the VAP. | |
| Hospital.ICUDisPneumPathogen2 | (2) Name of pathogen | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects details on the responsible pathogens for the VAP. | |
| Hospital.ICUDisPneumPathogen2QuantUCFml | (2) Quantity of pathogen | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects details on the responsible pathogens for the VAP. | |
| Hospital.ICUDisPneumPathogen3 | (3) Name of pathogen | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects details on the responsible pathogens for the VAP. | |
| Hospital.ICUDisPneumPathogen3QuantUCFml | (3) Quantity of pathogen | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects details on the responsible pathogens for the VAP. | |
| Hospital.ICUDisPneumPathogen4 | (4) Name of pathogen | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects details on the responsible pathogens for the VAP. | |
| Hospital.ICUDisPneumPathogen4QuantUCFml | (4) Quantity of pathogen | At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes, details on the VAP were recorded. This reflects details on the responsible pathogens for the VAP. | |
| Hospital.ICUDisPneumSepsis | Sepsis or septic shock associated | 0 == No 1 == Yes |
At ICU discharge, complications and adverse events were summarized. Presence or absence of VAP (Ventilator associated pneumonia) as systemic complication was recorded. In case presence of VAP was "yes", details on the VAP were recorded. This reflects details on the sepsis or if septic chock associated. |
| Hospital.ICUDisSixMonthOutcomeDate | Date of prognostic estimate of 6 month outcome | At ICU discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ICU". This reflects the date of the prognostic estimate. | |
| Hospital.ICUDisSixMonthOutcomeGOS | Expected GOS (Glasgow Outcome Scale) at 6 months | D == Death V == Vegetative state SD == Severe Disability MD == Moderate Disability GR == Good Recovery |
At ICU discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ICU". This reflects the Expected outcome (GOS). |
| Hospital.ICUDisSixMonthOutcomeQualification | Qualification of the physician estimating the six month outcome | 1 == Resident 2 == Junior staff (< 5 years) 3 == Senior staff ( >5 years) 4 == Head of department |
At ICU discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ICU". This reflects the qualification of the physician who provided prognostic estimate on discharge from ICU |
| Hospital.ICUDisSixMonthOutcomeType | Type of the physician estimating the six month outcome | 99 == Other 1 == ER physician 2 == Intensive care physician 3 == Neurology 4 == Neurosurgery 5 == Traumatology 88 == Unknown |
At ICU discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ICU". The reflects the specialty of the physician who provided prognostic estimate on discharge from ICU |
| Hospital.ICUDisSixMonthOutcomeUnfavourable | Expected risk of unfavourable outcome (D, VS, SD) at 6 months | At ICU discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ICU". This reflects the risk of unfavorable outcome (D,VS,SD) in % | |
| Hospital.ICUDisSupportWithdrawnDate | Date of withdrawal of support | This variable documents date and time at which life prolonging therapy was withdrawn (together with "Hospital.ICUDisSupportWithdrawnTime") | |
| Hospital.ICUDisSupportWithdrawnTime | Time of withdrawal of support | This variable documents date and time at which life prolonging therapy was withdrawn (together with "Hospital.ICUDisSupportWithdrawnDate") | |
| Hospital.ICUDisTimeToObeyCommands | Time to obey commands | Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. | |
| Hospital.ICUDisTimeToObeyCommandsNA | Time to obey commands at discharge Not applicable | Pre-defined early endpoints recorded at ICU discharge include: neuroworsening (any episode), time to obeying commands, duration of PTA, duration of ventilation, number of CTs performed and CT progression. This reflects if 'Time to obey commands' was Not applicable. | |
| Hospital.ICUDisWithdrawalTreatmentDecisionDate | Date of decision to withdraw active treatment | Investigators were requested to record the details of Withdrawal of Treatment or Life support if applicable. | |
| Hospital.ICUDisWithdrawalTreatmentDecisionTime | Time of decision to withdraw active treatment | Investigators were requested to record the details of Withdrawal of Treatment or Life support if applicable. | |
| Hospital.ICUDisWithdrawlTreatmentDecision | Decision to withdraw active treatment | 1 == Multi disciplinary 2 == By a single physician 3 == With relatives |
Investigators were requested to record the details of Withdrawal of Treatment or Life support if applicable. |
| Hospital.ICUEndTidalCO2 | End Tidal CO2 | 0 == No 1 == Yes |
Reflects the type, in case of systemic monitoring on ICU: End Tidal CO2 |
| Hospital.ICUGCSDischargeEyes | Eye opening (E) response at ICU discharge | 1 == 1-None 2 == 2-To pain 3 == 3-To speech S == Untestable (swollen) 88 == Unknown 4 == 4-Spontaneously O == Untestable (other) |
Eye opening score for GCS at ICU discharge. |
| Hospital.ICUGCSDischargeMotor | Motor (M) response at ICU discharge | O == Untestable (Other) 1 == 1-None 2 == 2-Abnormal extension 3 == 3-Abnormal flexion 4 == 4-Normal flexion/withdrawal 5 == 5-Localizes to pain P == Untestable (Deep sedation/paralyzed) 6 == 6-Obeys command UN == Unknown |
Motor score for GCS at ICU discharge. |
| Hospital.ICUGCSDischargeScore | GCS score at ICU discharge | GCS score at ICU discharge. | |
| Hospital.ICUGCSDischargeVerbal | Verbal (V) response at ICU discharge | 5 == 5-Oriented 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused T == Untestable (tracheotomy/endotracheal tube) P == Untestable (tracheotomy/endotracheal tube) O == Untestable (Other) UN == Unknown |
Verbal score for GCS at ICU discharge. |
| Hospital.ICUInvasiveBP | Invasive BP monitoring | 0 == No 1 == Yes |
Reflects the type, in case of systemic monitoring on ICU: Invasive BP monitoring |
| Hospital.ICUProblemsICP | Any there any problems in ICP monitoring? | 0 == No 1 == Yes |
In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable reflects Problems in ICP monitoring. |
| Hospital.ICUProblemsICPYes | Explain ICP problems | 1 == Accidental catheter removal 2 == Catheter obstruction/failure 3 == Suspicion of inaccurate measurement |
In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable explains the Problems in ICP monitoring if applicable. |
| Hospital.ICUPulseOximetry | Pulse oximetry | 0 == No 1 == Yes |
Reflects the type, in case of systemic monitoring on ICU: Pulse oximetry |
| Hospital.ICURaisedICP | Raised ICP (sustained) | 0 == No 1 == Yes, controlled 2 == Yes, refractory |
In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable reflects if there was Raised ICP (sustained). |
| Hospital.ICUReasonForTypeICPMont | Reason for the choice of ventricular/ventricular and sensor monitoring | 1 == Routine in our department 2 == Not routine, but enlarged ventricles 3 == No parenchymal device available 99 == Other |
In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable reflects WHY Question: reason for choosing ventricular monitor |
| Hospital.ICUReasonForTypeICPMontPare | Reason for choice of parenchymal sensor | 1 == Routine in our department 2 == Not routine, but small ventricles 3 == Mainly motivated by time of day 4 == No OR available for placement ventr. catheter 5 == Failed implantation ventricular catheter 99 == Other |
In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable reflects WHY Question: reason for choosing parenchymal monitor. |
| Hospital.ICUReasonForTypeICUMontOther | Other reason for the choice of ventricular/ventricular sensor monitoring (please specify) | In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable reflects "Other Reason of choice for ventricular/ventricular+sensor monitoring" | |
| Hospital.ICUReasonForTypeICUMontParOther | Other reason for the choice of parenchymal sensor (please specify) | In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable reflects 'Other Reason of choice for parenchymal sensor'. | |
| Hospital.ICUReasonICP | Reasons for monitoring ICP | 1 == Guideline criteria 2 == Radiological signs raised ICP 3 == Clinical suspicion raised ICP 4 == Anaesthesia or mechanical ventilation required for extracranial injuries 5 == To inform surgical indication for mass lesion 99 == Other |
In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable reflects WHY Question: documents reason for monitoring ICP in patient admitted to ICU |
| Hospital.ICUReasonICPOther | Other reason for ICP monitoring (please specify) | In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable is a free text field for description of why the patient has ICP monitoring if there is another reason than pre-specified in Hospital.ICUReasonICP. | |
| Hospital.ICUReasonNoICP | Reason for NOT monitoring ICP | 1 == GCS >8 2 == No radiological signs of raised ICP 3 == Risk of raised ICP considered low 4 == Patient considered unsalvageable 5 == Coagulopathy 6 == Use of anticoagulants or platelet aggregation inhibitors 7 == No device available 8 == Not local policy to monitor ICP 9 == Too costly 99 == Other |
In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable reflects WHY Question: documents reason for not monitoring ICP in patient admitted to ICU |
| Hospital.ICUReasonNoICPOther | Other reason for NOT monitoring ICP (please specify) | In case of brain specific monitoring in the ICU, all details on the ICP monitoring were recorded. This variable is a free text field for description of the reason why ICP has not been monitored in ICU patient if there is another reason than pre-specified in Hospital.ICUReasonNoICP. | |
| Hospital.MonContEGG | Continuous EEG | 0 == No 1 == Yes |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects if there was continuous EEG monitoring. |
| Hospital.MonContEGGDuration | Duration of Continuous EEG | Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects the duration if there was continuous EEG monitoring. | |
| Hospital.MonECoG | ECoG (Electrocorticography) | 0 == No 1 == Yes |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects if there was continuous ECoG monitoring. |
| Hospital.MonECoGDuration | Duration of ECoG (Electrocorticography) | Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects the duration if there was continuous EEG monitoring. | |
| Hospital.MonJugularDesatEpisodes | Jugular desaturation episodes (<50%) | 0 == No 1 == Yes 77 == N/A |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects if there were Jugular desaturation episodes (<50%). |
| Hospital.MonJugularSatDuration | Duration of Jugular oximetry | Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects the duration if there was Jugular oximetry. | |
| Hospital.MonJugularSatStopReason | Reason for stopping Jugular oximetry | 4 == Clinically no longer required 3 == Patient died 2 == Patient considered unsalvageable 1 == Monitor/catheter failure |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects the reason for stopping if there was Jugular oximetry. |
| Hospital.MonJugularSatUsed | Jugular oximetry | 1 == Yes 0 == No |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects if there was Jugular oximetry. |
| Hospital.MonLicoxDuration | Duration of Brain tissue PO2 | Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects the duration if there was Brain tissue PO2 monitoring. | |
| Hospital.MonLicoxPO2 | Brain tissue PO2 < 15 mmHg | 0 == No 1 == Yes 77 == N/A |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects if there was Brain tissue PO2 <15mmHg monitoring. |
| Hospital.MonLicoxStopReason | Reason for stopping Brain tissue PO2 | 4 == Clinically no longer required 3 == Patient died 2 == Patient considered unsalvageable 1 == Monitor/catheter failure |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects the reason for stopping if there was Brain tissue PO2 monitoring. |
| Hospital.MonLicoxUsed | Brain tissue PO2 | 0 == No 1 == Yes |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects if there was Brain tissue PO2 monitoring. |
| Hospital.MonMicrodialysisDuration | Duration of Microdialysis | Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects the duration if there was Microdialysis. | |
| Hospital.MonMicrodialysisStopReason | Reason for stopping Microdialysis | 1 == Monitor/catheter failure 2 == Patient considered unsalvageable 3 == Patient died 4 == Clinically no longer required |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects the reason for stopping if there was Microdialysis. |
| Hospital.MonMicrodialysisUsed | Microdialysis | 0 == No 1 == Yes |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects if there was Microdialysis. |
| Hospital.MonTranscranDoppler | Transcranial Doppler | 0 == No 1 == Yes |
Beside brain specific ICP monitoring in the ICU, details were recorded on other types of monitoring in the ICU. This variable reflects if there was Transcranial Doppler monitoring. |
| Hospital.OrganDonationDate | Date of organ donation | Reflects the date of organ donation in case of Withdrawal of life-sustaining measures, if applicable. | |
| Hospital.OrganDonationTime | Time of organ donation | Reflects the time of organ donation in case of Withdrawal of life-sustaining measures, if applicable. | |
| Hospital.SixMonthOutcomeDate | Date of prognostic estimate of 6 month outcome | At hospital discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge from hospital". This same information was also recorded for discharge specifically from ICU. This reflects the Date of prognostic estimate. | |
| Hospital.SixMonthOutcomeGOS | Expected GOS (Glasgow Outcome Scale) at 6 months | D == Death V == Vegetative state SD == Severe Disability MD == Moderate Disability GR == Good Recovery |
At hospital discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge from hospital". This same information was also recorded for discharge specifically from ICU. This reflects the Expected outcome (GOS). |
| Hospital.SixMonthOutcomeQualification | Qualification of the physician estimating the six month outcome | 1 == Resident 2 == Junior staff (< 5 years) 3 == Senior staff ( >5 years) 4 == Head of department |
At hospital discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge from hospital". This same information was also recorded for discharge specifically from ICU. This reflects the qualification of the physician who provided prognostic estimate on hospital discharge |
| Hospital.SixMonthOutcomeType | Type of the physician estimating the six month outcome | 1 == ER physician 2 == Intensive care physician 3 == Neurology 4 == Neurosurgery 5 == Traumatology 88 == Unknown 99 == Other |
At hospital discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge from hospital". This same information was also recorded for discharge specifically from ICU. This reflects the type of the physician who provided prognostic estimate on hospital discharge. |
| Hospital.SixMonthOutcomeUnfavourable | Expected risk of unfavourable outcome (D, VS, SD) at 6 months | At hospital discharge, physician estimate of six month outcome was recorded: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge from hospital". This same information was also recorded for discharge specifically from ICU. This reflects the Risk of unfavorable outcome (D,VS,SD) in % | |
| Hospital.SupportWithdrawnDate | Date of withdrawal of support | Investigators were requested to record the details of Withdrawal of Treatment or Life support if applicable. | |
| Hospital.SupportWithdrawnTime | Time of withdrawal of support | Investigators were requested to record the details of Withdrawal of Treatment or Life support if applicable. | |
| Hospital.TimeSinceICUAdmisDeath | Time between admission in the ICU and death | Investigators were requested to record the details of Withdrawal of Treatment or Life support if applicable. This reflects the time between admission in the ICU and death | |
| Hospital.WardAdmDate | Date of admission to Ward | Date of admission to the ward In principle the date of injury; date of enrollment and Date of Admission to Ward will match, but in some cases there can be a difference of 1 or 2 days. For example when a patient was injured late at night, it is possible that the consent was only obtained in the morning, hence the date of Study Enrollment will be 1 day later than the date of injury. Or in some hospitals a patient is kept for 24 hours in observation at the ER in a specific unit before being transferred to ICU or Ward. Hence the Date of Admission to ICU or Ward can be 1 or 2 days later. Or if there is no bed available on ICU or Ward for a patient being injured late at night, there can be a delay in admitting the patient. | |
| Hospital.WardAdmReason | Reason for admission to Ward | 10 == Could be discharged home, but no adequate supervision 9 == No ICU bed available 8 == Clinical observation for TBI 4 == Extracranial injuries 7 == CT abnormalities 99 == Other |
WHY question: documents main reason for admission to ward (and not to ICU or discharge home) |
| Hospital.WardAdmReasonOther | Other reason for admission to Ward | If the variable WardAdmReason was set to Other the reason for admission to the ward is filled in here. | |
| Hospital.WardAdmTime | Time of admission to Ward | Time of admission to the ward | |
| Hospital.WithdrawalTreatmentDecision | Decision to withdraw active treatment | 1 == Multi disciplinary 2 == By a single physician 3 == With relatives |
Intended only to be scored if a medical decision was made to withdraw active treatment because of anticipated poor prognosis. However, some investigators may have scored this when patients had recovered to an extent that active treatment was no longer necessary. |
| Hospital.WithdrawalTreatmentDecisionDate | Date of decision to withdraw active treatment | Investigators were requested to record the details of Withdrawal of Treatment or Life support if applicable. Intended only to be scored if a medical decision was made to withdraw active treatment because of anticipated poor prognosis. However, some investigators may have scored this when patients had recovered to an extent that active treatment was no longer necessary. | |
| Hospital.WithdrawalTreatmentDecisionTime | Time of decision to withdraw active treatment | Investigators were requested to record the details of Withdrawal of Treatment or Life support if applicable. Intended only to be scored if a medical decision was made to withdraw active treatment because of anticipated poor prognosis. However, some investigators may have scored this when patients had recovered to an extent that active treatment was no longer necessary. | |
| HourlyMeasurements.DaySinceInjury | Calculated day since injury for hourly measurements | Calculated from HourlyValues.HVDate and Subject.DateInj | |
| HourlyMeasurements.HVCPP | Normalized datay for HVCPP2, HVCPP4, ect (calculated) | Normalized data for HVCPP2, HVCPP 4 etc. Calculated from MAP-ICP (HVSBP+2*HVDBP)/3-HVICP. | |
| HourlyMeasurements.HVDateTime | Calulated date and time for hourly value measurements | The date and time manually entered for the measurements in HourlyValues at time 2,4,6... are combined into this variable to match the entries in the HourlyMeasurements variables for HVSBP, HVDBP, HVICP. | |
| HourlyMeasurements.HVDBP | All diastolic blood pressures combined | All diastolic blood pressures combined into one variable, measured twice hourly. To get intended measurement time, see HourlyMeasurements.HVMeasurementDateTime. | |
| HourlyMeasurements.HVICP | All intracranial pressures combined | All intracranial pressures combined into one variable, measured twice hourly. To get intended measurement time, see HourlyMeasurements.HVMeasurementDateTime. | |
| HourlyMeasurements.HVMeasurementDateTime | Derived intended date and time for all hourly values measurements | The intended date and time for all hourly values measurements (HVSBP, HVDBP, HVICP, HVCPP) derived from HVDate+HVTimeX where HVTimeX is HVTime2->02.00, HVTime4->04.00,..., HVTime24->23.59. | |
| HourlyMeasurements.HVSBP | All systolic blood pressures combined | All systolic blood pressures combined into one variable, measured twice hourly. To get intended measurement time, see HourlyMeasurements.HVMeasurementDateTime. | |
| HourlyMeasurements.HVTIL | Combination of all hourly TIL values in a long format | Investigators were requested to document any change in TIL at 4 hour intervals (6 times per day), in a way that corresponds with the documentation of hourly values (04:00-08:00-12:00-16:00-20:00-24:00). This variable combines the hourly TIL values and represents in a long format these hourly measurements. See also HourlyValues.HVTIL4, HourlyValues.HVTIL8, HourlyValues.HVTIL12, HourlyValues.HVTIL16, HourlyValues.HVTIL20, HourlyValues.HVTIL24 | |
| HourlyValues.HourlyValueAccurate | Are measured values for ICP over this day considered accurate? | 0 == No 2 == Doubtful 1 == Yes |
Are the measured values for ICP over this day considered to be accurate? An explanation can be found in HourlyValues.HourlyValueNotAccurateProblems. Associated with the date in HourlyValues.HVDate. |
| HourlyValues.HourlyValueICPDiscontinued | Was active ICP treatment discontinued (poor prognosis)? | 0 == No 1 == Yes |
Answer to the question: "Was active ICP treatment discontinued (due to poor prognosis)?" |
| HourlyValues.HourlyValueLevelABP | Level for zeroing ABP | 1 == Right atrium 2 == Level of arterial catheter 99 == Other |
Differences in level of zeroing the arterial blood pressure transducer may affect calculations of CPP and comparisons between centres. |
| HourlyValues.HourlyValueLevelABPOther | Other level for zeroing ABP (please specify) | A free text description of the level of ABP transducer if HourlyValues.HourlyValueLevelABP is "other". | |
| HourlyValues.HourlyValueLevelICP | Level for zeroing ICP | 1 == Foramen of Monro 2 == Same level as ABP 3 == Meatus externus (ear) |
Only applicable in case ICP monitored; Differences in level of zeroing ICP may affect calculation of CPP and comparisons between centres. |
| HourlyValues.HourlyValueNotAccurateProblems | Why the measured values for ICP over this day are not considered accurate? | Explanation in free text of the variable HourlyValues.HourlyValueAccurate. Associated with the date in HourlyValues.HVDate. | |
| HourlyValues.HVCPP10 | CPP associated with the Hourly value DateTime10 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime10. Calculated by the equation HVCPP10 = (HVSBP10+ 2*HVDBP10)/3-HVICP10. It is set to NA if any of the values in the equation is missing or HVICP10 is 0. | |
| HourlyValues.HVCPP12 | CPP associated with the Hourly value DateTime12 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime12. Calculated by the equation HVCPP12 = (HVSBP12+ 2*HVDBP12)/3-HVICP12. It is set to NA if any of the values in the equation is missing or HVICP12 is 0. | |
| HourlyValues.HVCPP14 | CPP associated with the Hourly value DateTime14 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime14. Calculated by the equation HVCPP14 = (HVSBP14+ 2*HVDBP14)/3-HVICP14. It is set to NA if any of the values in the equation is missing or HVICP14 is 0. | |
| HourlyValues.HVCPP16 | CPP associated with the Hourly value DateTime16 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime16. Calculated by the equation HVCPP16 = (HVSBP16+ 2*HVDBP16)/3-HVICP16. It is set to NA if any of the values in the equation is missing or HVICP16 is 0. | |
| HourlyValues.HVCPP18 | CPP associated with the Hourly value DateTime18 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime18. Calculated by the equation HVCPP18 = (HVSBP18+ 2*HVDBP18)/3-HVICP18. It is set to NA if any of the values in the equation is missing or HVICP18 is 0. | |
| HourlyValues.HVCPP2 | CPP associated with the Hourly value DateTime2 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime2. This variable is calculated by HVCPP2 = (HVSBP2+2*HVDBP2)/3 - HVICP2. It is set to NA if any of the values in the equation is missing or HVICP2 is 0. | |
| HourlyValues.HVCPP20 | CPP associated with the Hourly value DateTime20 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime20. Calculated by the equation HVCPP20 = (HVSBP20+ 2*HVDBP20)/3-HVICP20. It is set to NA if any of the values in the equation is missing or HVICP20 is 0. | |
| HourlyValues.HVCPP22 | CPP associated with the Hourly value DateTime22 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime22. Calculated by the equation HVCPP22 = (HVSBP22+ 2*HVDBP22)/3-HVICP22. It is set to NA if any of the values in the equation is missing or HVICP22 is 0. | |
| HourlyValues.HVCPP24 | CPP associated with the Hourly value DateTime24 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime24. Calculated by the equation HVCPP24 = (HVSBP24+ 2*HVDBP24)/3-HVICP24. It is set to NA if any of the values in the equation is missing or HVICP24 is 0. | |
| HourlyValues.HVCPP4 | CPP associated with the Hourly value DateTime4 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime4. This variable is calculated by the equation HVCPP4 = (HVSBP4+ 2*HVDBP4)/3-HVICP4. It is set to NA if any of the values in the equation is missing or HVICP2 is 0. | |
| HourlyValues.HVCPP6 | CPP associated with the Hourly value DateTime6 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime6. Calculated by the equation HVCPP6 = (HVSBP6+ 2*HVDBP6)/3-HVICP6. It is set to NA if any of the values in the equation is missing or HVICP6 is 0. | |
| HourlyValues.HVCPP8 | CPP associated with the Hourly value DateTime8 | The cerebral perfusion pressure, CPP, associated with the HourlyValues.HVDateTime8. Calculated by the equation HVCPP8 = (HVSBP8+ 2*HVDBP8)/3-HVICP8. It is set to NA if any of the values in the equation is missing or HVICP8 is 0. | |
| HourlyValues.HVDate | Date value is recorded | The date the hourly values are measured. | |
| HourlyValues.HVDBP10 | Diastolic BP associated with the Hourly value DateTime10 | The diastolic blood pressure associated with HourlyValues.HVDateTime10. | |
| HourlyValues.HVDBP12 | Diastolic BP associated with the Hourly value DateTime12 | The diastolic blood pressure associated with HourlyValues.HVDateTime12. | |
| HourlyValues.HVDBP14 | Diastolic BP associated with the Hourly value DateTime14 | The diastolic blood pressure associated with HourlyValues.HVDateTime14. | |
| HourlyValues.HVDBP16 | Diastolic BP associated with the Hourly value DateTime16 | The diastolic blood pressure associated with HourlyValues.HVDateTime16. | |
| HourlyValues.HVDBP18 | Diastolic BP associated with the Hourly value DateTime18 | The diastolic blood pressure associated with HourlyValues.HVDateTime18. | |
| HourlyValues.HVDBP2 | Diastolic BP associated with the Hourly value DateTime2 | The diastolic blood pressure associated with HourlyValues.HVDateTime2. | |
| HourlyValues.HVDBP20 | Diastolic BP associated with the Hourly value DateTime20 | The diastolic blood pressure associated with HourlyValues.HVDateTime20. | |
| HourlyValues.HVDBP22 | Diastolic BP associated with the Hourly value DateTime22 | The diastolic blood pressure associated with HourlyValues.HVDateTime22. | |
| HourlyValues.HVDBP24 | Diastolic BP associated with the Hourly value DateTime24 | The diastolic blood pressure associated with HourlyValues.HVDateTime24. | |
| HourlyValues.HVDBP4 | Diastolic BP associated with the Hourly value DateTime4 | The diastolic blood pressure associated with HourlyValues.HVDateTime4. | |
| HourlyValues.HVDBP6 | Diastolic BP associated with the Hourly value DateTime6 | The diastolic blood pressure associated with HourlyValues.HVDateTime6. | |
| HourlyValues.HVDBP8 | Diastolic BP associated with the Hourly value DateTime8 | The diastolic blood pressure associated with HourlyValues.HVDateTime8. | |
| HourlyValues.HVICP10 | ICP associated with the Hourly value DateTime10 | The intracranial pressure associated with HourlyValues.HVDateTime10. | |
| HourlyValues.HVICP12 | ICP associated with the Hourly value DateTime12 | The intracranial pressure associated with HourlyValues.HVDateTime12. | |
| HourlyValues.HVICP14 | ICP associated with the Hourly value DateTime14 | The intracranial pressure associated with HourlyValues.HVDateTime14. | |
| HourlyValues.HVICP16 | ICP associated with the Hourly value DateTime16 | The intracranial pressure associated with HourlyValues.HVDateTime16. | |
| HourlyValues.HVICP18 | ICP associated with the Hourly value DateTime18 | The intracranial pressure associated with HourlyValues.HVDateTime18. | |
| HourlyValues.HVICP2 | ICP associated with the Hourly value DateTime2 | The intracranial pressure associated with HourlyValues.HVDateTime2. | |
| HourlyValues.HVICP20 | ICP associated with the Hourly value DateTime20 | The intracranial pressure associated with HourlyValues.HVDateTime20. | |
| HourlyValues.HVICP22 | ICP associated with the Hourly value DateTime22 | The intracranial pressure associated with HourlyValues.HVDateTime22. | |
| HourlyValues.HVICP24 | ICP associated with the Hourly value DateTime24 | The intracranial pressure associated with HourlyValues.HVDateTime24. | |
| HourlyValues.HVICP4 | ICP associated with the Hourly value DateTime4 | The intracranial pressure associated with HourlyValues.HVDateTime4. | |
| HourlyValues.HVICP6 | ICP associated with the Hourly value DateTime6 | The intracranial pressure associated with HourlyValues.HVDateTime6. | |
| HourlyValues.HVICP8 | ICP associated with the Hourly value DateTime8 | The intracranial pressure associated with HourlyValues.HVDateTime8. | |
| HourlyValues.HVSBP10 | Systolic BP associated with the Hourly value DateTime10 | The systolic blood pressure associated with HourlyValues.HVDateTime10. | |
| HourlyValues.HVSBP12 | Systolic BP associated with the Hourly value DateTime12 | The systolic blood pressure associated with HourlyValues.HVDateTime12. | |
| HourlyValues.HVSBP14 | Systolic BP associated with the Hourly value DateTime14 | The systolic blood pressure associated with HourlyValues.HVDateTime14. | |
| HourlyValues.HVSBP16 | Systolic BP associated with the Hourly value DateTime16 | The systolic blood pressure associated with HourlyValues.HVDateTime16. | |
| HourlyValues.HVSBP18 | Systolic BP associated with the Hourly value DateTime18 | The systolic blood pressure associated with HourlyValues.HVDateTime18. | |
| HourlyValues.HVSBP2 | Systolic BP associated with the Hourly value DateTime2 | The systolic blood pressure associated with HourlyValues.HVDateTime2. | |
| HourlyValues.HVSBP20 | Systolic BP associated with the Hourly value DateTime20 | The systolic blood pressure associated with HourlyValues.HVDateTime20. | |
| HourlyValues.HVSBP22 | Systolic BP associated with the Hourly value DateTime22 | The systolic blood pressure associated with HourlyValues.HVDateTime22. | |
| HourlyValues.HVSBP24 | Systolic BP associated with the Hourly value DateTime24 | The systolic blood pressure associated with HourlyValues.HVDateTime24. | |
| HourlyValues.HVSBP4 | Systolic BP associated with the Hourly value DateTime4 | The systolic blood pressure associated with HourlyValues.HVDateTime4. | |
| HourlyValues.HVSBP6 | Systolic BP associated with the Hourly value DateTime6 | The systolic blood pressure associated with HourlyValues.HVDateTime6. | |
| HourlyValues.HVSBP8 | Systolic BP associated with the Hourly value DateTime8 | The systolic blood pressure associated with HourlyValues.HVDateTime8. | |
| HourlyValues.HVTIL12 | Change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 0 == No change 1 == Increasing intensity 2 == Decreasing intensity |
Investigators were requested to document any change in TIL at 4 hour intervals (6 times per day), in a way that corresponds with the documentation of hourly values (04:00-08:00-12:00-16:00-20:00-24:00) |
| HourlyValues.HVTIL16 | Change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 0 == No change 1 == Increasing intensity 2 == Decreasing intensity |
Investigators were requested to document any change in TIL at 4 hour intervals (6 times per day), in a way that corresponds with the documentation of hourly values (04:00-08:00-12:00-16:00-20:00-24:00) |
| HourlyValues.HVTIL20 | Change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 0 == No change 1 == Increasing intensity 2 == Decreasing intensity |
Investigators were requested to document any change in TIL at 4 hour intervals (6 times per day), in a way that corresponds with the documentation of hourly values (04:00-08:00-12:00-16:00-20:00-24:00) |
| HourlyValues.HVTIL24 | Change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 0 == No change 1 == Increasing intensity 2 == Decreasing intensity |
Investigators were requested to document any change in TIL at 4 hour intervals (6 times per day), in a way that corresponds with the documentation of hourly values (04:00-08:00-12:00-16:00-20:00-24:00) |
| HourlyValues.HVTIL4 | Change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 0 == No change 1 == Increasing intensity 2 == Decreasing intensity |
Investigators were requested to document any change in TIL at 4 hour intervals (6 times per day), in a way that corresponds with the documentation of hourly values (04:00-08:00-12:00-16:00-20:00-24:00) |
| HourlyValues.HVTIL8 | Change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 0 == No change 1 == Increasing intensity 2 == Decreasing intensity |
Investigators were requested to document any change in TIL at 4 hour intervals (6 times per day), in a way that corresponds with the documentation of hourly values (04:00-08:00-12:00-16:00-20:00-24:00) |
| HourlyValues.HVTILChangeReason12 | Reason for change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 1 == Intensified: Clinical deterioration 2 == Intensified: Suspicion of increased of ICP (not measured) 3 == Intensified: Increased ICP (documented) 4 == Intensified:Clinical decision to target other mechanism 5 == Intensified:Change of doctor (different shift) 6 == Decreasing:Clinical improvement 7 == Decreasing:Adequate control over ICP 8 == Decreasing:Upper treatment limit reached/past 9 == Decreasing: Further treatment considered futile 10 == Decreasing: Change of doctor (different shift) |
WHY question: Differentiated for: - Intensified: Clinical deterioration - Intensified: Suspicion of increased of ICP - Intensified: increased ICP (documented) - Intensified:Clinical decision to target other mechanism - Intensified:Change of doctor (different shift) - Decreasing:Clinical improvement - Decreasing:Adequate control over ICP - Decreasing:Upper treatment limit reached/past - Decreasing: Further treatment considered futile - Decreasing: Change of doctor (different shift). The hours at which the reasons for change are documented should correspond to the hours for documentation of any change in TIL; documentation of reason is only required in case of a change in TIL |
| HourlyValues.HVTILChangeReason16 | Reason for change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 1 == Intensified: Clinical deterioration 2 == Intensified: Suspicion of increased of ICP (not measured) 3 == Intensified: Increased ICP (documented) 4 == Intensified:Clinical decision to target other mechanism 5 == Intensified:Change of doctor (different shift) 6 == Decreasing:Clinical improvement 7 == Decreasing:Adequate control over ICP 8 == Decreasing:Upper treatment limit reached/past 9 == Decreasing: Further treatment considered futile 10 == Decreasing: Change of doctor (different shift) |
WHY question: Differentiated for: - Intensified: Clinical deterioration - Intensified: Suspicion of increased of ICP - Intensified: increased ICP (documented) - Intensified:Clinical decision to target other mechanism - Intensified:Change of doctor (different shift) - Decreasing:Clinical improvement - Decreasing:Adequate control over ICP - Decreasing:Upper treatment limit reached/past - Decreasing: Further treatment considered futile - Decreasing: Change of doctor (different shift). The hours at which the reasons for change are documented should correspond to the hours for documentation of any change in TIL; documentation of reason is only required in case of a change in TIL |
| HourlyValues.HVTILChangeReason20 | Reason for change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 1 == Intensified: Clinical deterioration 2 == Intensified: Suspicion of increased of ICP (not measured) 3 == Intensified: Increased ICP (documented) 4 == Intensified:Clinical decision to target other mechanism 5 == Intensified:Change of doctor (different shift) 6 == Decreasing:Clinical improvement 7 == Decreasing:Adequate control over ICP 8 == Decreasing:Upper treatment limit reached/past 9 == Decreasing: Further treatment considered futile 10 == Decreasing: Change of doctor (different shift) |
WHY question: Differentiated for: - Intensified: Clinical deterioration - Intensified: Suspicion of increased of ICP - Intensified: increased ICP (documented) - Intensified:Clinical decision to target other mechanism - Intensified:Change of doctor (different shift) - Decreasing:Clinical improvement - Decreasing:Adequate control over ICP - Decreasing:Upper treatment limit reached/past - Decreasing: Further treatment considered futile - Decreasing: Change of doctor (different shift). The hours at which the reasons for change are documented should correspond to the hours for documentation of any change in TIL; documentation of reason is only required in case of a change in TIL |
| HourlyValues.HVTILChangeReason24 | Reason for change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 1 == Intensified: Clinical deterioration 2 == Intensified: Suspicion of increased of ICP (not measured) 3 == Intensified: Increased ICP (documented) 4 == Intensified:Clinical decision to target other mechanism 5 == Intensified:Change of doctor (different shift) 6 == Decreasing:Clinical improvement 7 == Decreasing:Adequate control over ICP 8 == Decreasing:Upper treatment limit reached/past 9 == Decreasing: Further treatment considered futile 10 == Decreasing: Change of doctor (different shift) |
WHY question: Differentiated for: - Intensified: Clinical deterioration - Intensified: Suspicion of increased of ICP - Intensified: increased ICP (documented) - Intensified:Clinical decision to target other mechanism - Intensified:Change of doctor (different shift) - Decreasing:Clinical improvement - Decreasing:Adequate control over ICP - Decreasing:Upper treatment limit reached/past - Decreasing: Further treatment considered futile - Decreasing: Change of doctor (different shift). The hours at which the reasons for change are documented should correspond to the hours for documentation of any change in TIL; documentation of reason is only required in case of a change in TIL |
| HourlyValues.HVTILChangeReason4 | Reason for change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 1 == Intensified: Clinical deterioration 2 == Intensified: Suspicion of increased of ICP (not measured) 3 == Intensified: Increased ICP (documented) 4 == Intensified:Clinical decision to target other mechanism 5 == Intensified:Change of doctor (different shift) 6 == Decreasing:Clinical improvement 7 == Decreasing:Adequate control over ICP 8 == Decreasing:Upper treatment limit reached/past 9 == Decreasing: Further treatment considered futile 10 == Decreasing: Change of doctor (different shift) |
WHY question: Differentiated for: - Intensified: Clinical deterioration - Intensified: Suspicion of increased of ICP - Intensified: increased ICP (documented) - Intensified:Clinical decision to target other mechanism - Intensified:Change of doctor (different shift) - Decreasing:Clinical improvement - Decreasing:Adequate control over ICP - Decreasing:Upper treatment limit reached/past - Decreasing: Further treatment considered futile - Decreasing: Change of doctor (different shift). The hours at which the reasons for change are documented should correspond to the hours for documentation of any change in TIL; documentation of reason is only required in case of a change in TIL |
| HourlyValues.HVTILChangeReason8 | Reason for change in TIL at 4 hours interval (4, 8, 12 ,16, 20, 24) | 1 == Intensified: Clinical deterioration 2 == Intensified: Suspicion of increased of ICP (not measured) 3 == Intensified: Increased ICP (documented) 4 == Intensified:Clinical decision to target other mechanism 5 == Intensified:Change of doctor (different shift) 6 == Decreasing:Clinical improvement 7 == Decreasing:Adequate control over ICP 8 == Decreasing:Upper treatment limit reached/past 9 == Decreasing: Further treatment considered futile 10 == Decreasing: Change of doctor (different shift) |
WHY question: Differentiated for: - Intensified: Clinical deterioration - Intensified: Suspicion of increased of ICP - Intensified: increased ICP (documented) - Intensified:Clinical decision to target other mechanism - Intensified:Change of doctor (different shift) - Decreasing:Clinical improvement - Decreasing:Adequate control over ICP - Decreasing:Upper treatment limit reached/past - Decreasing: Further treatment considered futile - Decreasing: Change of doctor (different shift). The hours at which the reasons for change are documented should correspond to the hours for documentation of any change in TIL; documentation of reason is only required in case of a change in TIL |
| HourlyValues.HVTime10 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime12 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime14 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime16 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime18 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime2 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators were allowed to enter another timepoint in this field. | |
| HourlyValues.HVTime20 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime22 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime24 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime4 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime6 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| HourlyValues.HVTime8 | Hourly values at 2h interval 12 times a day (2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24) | Investigators were requested to document hourly values every 2 hours (12 times per day) for all patients receiving ICP monitoring. The timeperiods were pre-specified (02:00-24:00); however, investigators may have entered values at different times and have then entered the time of obtaining hourly values; a possible confusion may exist if investigators entered the time of documenting the hourly values rather than the time at which they were obtained. | |
| Imaging.AcquisitionDate | Date of acquisition | Acquisition date and time for each scan of an entire session - retrieved from the DICOM header | |
| Imaging.AcquisitionTime | Time of acquisition | Acquisition date and time for each scan of an entire session - retrieved from the DICOM header | |
| Imaging.AnyIntracranTraumaticAbnormality | Any intracranial traumatic abnormality? | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether any of the 12 following CDEs is present (Mass lesion, ExtraaxialHematoma, EpiduralHematoma, SubduralHematomaAcute, SubduralHematomaSubacuteChronic, SubduralCollectionMixedDensity, Contusion, TAI, traumaticSubarachnoidHemorrhage, IntraventricularHemorrhage, MidlineShift or CisternalCompression. | |
| Imaging.BvalURL | Bval file path structure | This variable contains the file name of the generated Bval file. These files can be shared upon request. To request access please contact the CENTER-TBI office. | |
| Imaging.BvecURL | Bvec file path structure | This variable contains the file path structure of the generated Bvec file. These files can be shared upon request. To request access please contact the CENTER-TBI office. | |
| Imaging.CisternalCompression | Cisternal Compression | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether there is compression of one or more the basal cisterns (i.e. suprasellar, quadrigeminal, prepontine, ambient, cisterna magna). More descriptive information (location, compression vs. absence) can be found in the JSON files. | |
| Imaging.Contusion | Contusion (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether one or more contusions are present. More descriptive information (location, volume, number) and advanced information (e.g. hemorrhagic, non-hemorrhagic, intracerebral hemorrhage, etc.) can be found in the JSON files. Volume was estimated using the AxBxC/2 method. Edema was included in the measurements. | |
| Imaging.CRFCTAngulation | CT Angulation | This variable describes if a CT scan is performed with or without angulation. There are three options: no angulation (volume scan), orbital-meatal line and other. There is a risk of different interpretation, since there was no definition. | |
| Imaging.CRFCTManuf | CT scanner manufacturer | This variable describes the CT scans manufacturer. | |
| Imaging.CRFCTMidlineShift | Midline shift | CT parameters scored by the investigator: reflects if there was midline shift on the CT. | |
| Imaging.CRFCTMidlineShiftMeasure | Midline shift (please specify) | CT parameters scored by the investigator: reflects the volume in mm if there was a midline shift on the CT Check also "Imaging.CRFCTMidlineShift" | |
| Imaging.CRFCTMRIDate | Date of imaging captured in CRF | Date of Imaging captured in CRF | |
| Imaging.CRFCTMRITime | Time of imaging captured in CRF | Time of imaging captured in CRF | |
| Imaging.CRFCTReason | Reason for CT scan | This variable contains the main reason why a CT-scan, during hospital stay, was performed. One of following options: standard follow-up, post-operative control, clinical deterioration, (suspicion of) increasing ICP, lack of improvement, unknown, other (specified in CTMRI.CTReasonOther) The reason for making an early CT-scan/ER scan can be found in: CTMRI.CTERReason | |
| Imaging.CRFCTScannerType | Type of CT scanner | This variable specifies the type of CT-scanner by the number of slices. | |
| Imaging.CRFCTType | CT type | This variable describes the type of CT scan that has been made. Multiple options can be selected from: Non-contrast CT, Contrast CT, CT Angiography, Perfusion CT. | |
| Imaging.CRFForm | CRF used at the time of scan | Acute or follow up form in the e-CRF. | |
| Imaging.CRFIcometrixImageId | Icometrix image ID | This variable combines data from CTMRI.IcometrixImageId and FollowUp.IcometrixImageId. Identifier generated for an imaging experiment when images are uploaded from site. | |
| Imaging.CRFIcometrixPassedQA | Images passed QA of icometrix | Reflects if images uploaded from site passed QA of icometix. This variable combines data from CTMRI.IcometrixPassedQA and FollowUp.IcometrixPassedQA. | |
| Imaging.CRFInitialDataIcometrix | Imaging data in CRF loaded from icometrix (not by study nurse) | Reflects if the imaging data was initially loaded from Icometrix into the e-CRF (if not, it means the data in the e-CRF was entered manually by the study nurse) This variable combines data from CTMRI.InitialDataIcometrix and FollowUp.InitialDataIcometrix. | |
| Imaging.CRFMRIManuf | MRI scanner manufacturer | This variable describes the MRI-scan manufacturer. This variable combines data from CTMRI.MRIManuf and FollowUp.MRIManuf | |
| Imaging.CRFMRIReason | Reason for MRI scan | This variable contains the main reason why an MRI was performed. This variable combines data from CTMRI.MRIReason and FollowUp.MRIReason | |
| Imaging.CRFMRIReasonOther | Other reason for MRI scan (please specify) | This variable contains the main reason why an MRI was performed, when in the variable "MRIReason", the option "other" was chosen. This is a text field. This variable combines data from CTMRI.MRIReasonOther and FollowUp.MRIReasonOther | |
| Imaging.CRFMRIResultPreExistAbnorm | MRI scan results: Pre-existing abnormalities | This variable describes whether or not there are pre-existing abnormalities present on MRI scan (yes, no, unknown). Assessment by investigator and or physician. This variable combines data from CTMRI.MRIResultPreExistAbnorm and FollowUp.MRIResultPreExistAbnorm | |
| Imaging.CRFMRIResultTraumaticAbnorm | MRI scan results: Traumatic abnormalities | This variable describes whether or not there are traumatic abnormalities present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRIResultTraumaticAbnorm and FollowUp.MRIResultTraumaticAbnorm | |
| Imaging.CRFMRIScannerStrength | MRI scanner strength | This variable describes the MRI scanner strength. This is a text field. This variable combines data from CTMRI.MRIScannerStrength and FollowUp.MRIScannerStrength | |
| Imaging.CRFMRISequences | MRI sequence(s) | This variable describes the MRI sequence. Options are: T1, T2, FLAIR, DWI, GRE, SWI, DTI, MRSI, PWI, Other. Multiple options can be selected. This variable combines data from CTMRI.MRISequences and FollowUp.MRISequences | |
| Imaging.CRFMRITraumAbnormASDH | Location: ASDH | This variable describes whether or not there is an acute subdural hematoma present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRITraumAbnormASDH and FollowUp.MRITraumAbnormASDH | |
| Imaging.CRFMRITraumAbnormContusion | Location: Contusions | This variable describes whether or not there is a contusion present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRITraumAbnormContusion and FollowUp.MRITraumAbnormContusion | |
| Imaging.CRFMRITraumAbnormDAI | MRI scan results: DAI | This variable describes whether or not there is DAI (diffuse axonal injury) present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRITraumAbnormDAI and FollowUp.MRITraumAbnormDAI | |
| Imaging.CRFMRITraumAbnormDAILesionLocBrainstem | Location: Brainstem | This variable describes whether or not there is a brain stem lesion present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRITraumAbnormDAILesionLocBrainstem and FollowUp.MRITraumAbnormDAILesionLocBrainstem | |
| Imaging.CRFMRITraumAbnormDAILesionLocCorpusCallosum | Location: Corpus Callosum | This variable describes whether or not there is a corpus callosum lesion present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRITraumAbnormDAILesionLocCorpusCallosum and FollowUp.MRITraumAbnormDAILesionLocCorpusCallosum | |
| Imaging.CRFMRITraumAbnormDAILesionLocDiffuseWhiteMatter | Location: Diffuse white matter | This variable describes whether or not there is a lesion in diffuse white matter present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRITraumAbnormDAILesionLocDiffuseWhiteMatter and FollowUp.MRITraumAbnormDAILesionLocDiffuseWhiteMatter | |
| Imaging.CRFMRITraumAbnormDAINumLesions | Number of lesions | This variable describes how many DAI lesions are present on MRI scan (1,2,3,4,>=5). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRITraumAbnormDAINumLesions and FollowUp.MRITraumAbnormDAINumLesions | |
| Imaging.CRFMRITraumAbnormEDH | Location: EDH | This variable describes whether or not there is an epidural hematoma present on MRI scan (yes, no, unknown). Assessment by investigator and/or physician. This variable combines data from CTMRI.MRITraumAbnormEDH and FollowUp.MRITraumAbnormEDH | |
| Imaging.CRFMRIType | MRI type | This variable describes the type of MRI scan that has been made. Options are: MRI, MRA This variable combines data from CTMRI.MRIType and FollowUp.MRIType | |
| Imaging.CRFTimePoint | Imaging timepoint | Imaging.CRFTimepoint = CTMRI.Timepoint + FollowUp.Timepoint Imaging related data from CTMRI table and Followup is combined under Imaging table so that all data is available in a single place. We only combine the ones with a valid IcometrixImageId | |
| Imaging.DicomHeaderURL | DICOM header file name | DICOM header can add more information to the Nifti image files. The DICOM header is the meta-data part of a DICOM file and is organized as a constant and standardized series of tags. This variable contains the file name of the header file. These files can be shared upon request. To request access please contact the CENTER-TBI office. | |
| Imaging.EpiduralHematoma | Epipidural hematoma (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether an epidural hematoma or multiple epidural hematomas are present. More descriptive information (location, volume, number) and advanced information (e.g. arterial versus venous) can be found in the JSON files. Note: Volume was estimated using the AxBxC/2 method. In the JSON files, "descriptive_volume" is the estimated volume of the lesion and can be used for analysis, "descriptive_length", "descriptive_width", "descriptive_max_thickness" are measurements that should not be used in any analysis. | |
| Imaging.ExperimentDate | Date of Imaging experiment | Experiment Date and time for the entire scan session - retrieved from the DICOM header | |
| Imaging.ExperimentId | Scanning Experiment ID | S: Experiment id which is generated by the imaging repository (XNAT). B: Is a unique identifier. XNAT is the imaging platform used to collect the data. A: Format of this identifier looks like CTBI_E00000. R: ExperimentId is equal to all the scans within the same experiment: projects/PROJECT_ID/subjects/SUBJECT_ID/experiments/EXPT_ID/scans/SCAN_ID/files/file1.img | |
| Imaging.ExperimentLabel | Experiment label | S: Experiment label created by the imaging repository. B: Usually looks like: "GUPI_CTx" or "GUPI_MRx" with x specifying the rank of the upload. This label is not a unique identifier. A: Label of the experiment. R: Users are allowed to edit. Label is only unique within one center. | |
| Imaging.ExperimentTime | Time of Imaging experiment | Experiment Date and time for the entire scan session - retrieved from the DICOM header | |
| Imaging.ExtraaxialHematoma | Extraaxial Hematoma | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether an extra-axial hematoma or multiple extra-axial hematomas are present. This term was mostly used for bleedings that were difficult to classify or for bleedings that were evacuated (i.e. after craniectomy). More descriptive information (location, volume, number) and advanced information (e.g. arterial versus venous) can be found in the JSON files. Note: Volume was estimated using the AxBxC/2 method. In the JSON files, "descriptive_volume" is the estimated volume of the lesion and can be used for analysis, "descriptive_length", "descriptive_width", "descriptive_max_thickness" are measurements that should not be used in any analysis. | |
| Imaging.FisherClassification | Modified Fisher scale | S: A CT grading scale for traumatic Subarachnoid Hemorrhage B: Useful in predicting the occurrence and severity of cerebral vasospasm. Ranges from 1-4 (No tSAH, no IVH (1), no IVH, trace or moderate tSAH (can be in multiple locations) (2), No IVH, full tSAH (3), IVH (4) R: Only available for CT scans. For each patient, the FisherClassification can be found in the Imaging.LesionData variable. For CENTER-TBI, only the older version of Fisher was scored, not the newer "modified" version. | |
| Imaging.Frames | Frames | B: Scan are acquired in dicom format. A: Number of dicom files that compose the scan. | |
| Imaging.GreenCTGrade | Computed tomogrophy grade | A CT grading scale for traumatic Subarachnoid Hemorrhage (tSAH). Useful for outcome prediction. Ranges from 1-4, with a subdivision of 3 into "31", "32" and 4 into "41" and "42". (thin tSAH (1), thick tSAH (2), thin tSAH with mass lesion and no MLS (31), thin tSAH with mass lesion and MLS (32), thick tSAH with mass lesion and no MLS (41), thick tSAH with mass lesion and MLS (42). Only available for CT scans. For each patient, the GreenCTgrade can be found in the Imaging.LesionData variable. Could only be filled out when tSAH was present. | |
| Imaging.HelsinkiCTScore | Helsinki CT score | S: A general CT grading scale B: Useful for outcome prediction. Ranges from -3 to 14. Scoring is done as follows: subdural (+2), intracerebral hematoma (+2), epidural hematoma (-3), mass lesion size >25 cc (+2), IVH (+3), compressed cisterns (+1), obliterated cisterns (+5) R: Only available for CT scans. For each patient, the HelsinkiCTscore can be found in the Imaging.LesionData variable. Empty values for the HelsinkiCTscore stand for a normal CT scan! A score of 0 does not necessarily mean the patient had a normal CT. (e.g. epidural hematoma -3, + IVH = 3 = 0). | |
| Imaging.IntraventricularHemorrhage | Intraventricular Hemorrhage (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether intraventricular blood is present. More descriptive information (location) can be found in the JSON files. | |
| Imaging.LesionData | Information on lesion(s) as per icometrix (JSON format) | This variable contains ALL lesion information as assessed by central review. There are 23 CDEs that have been evaluated for each patient and 6 classifications that have been filled out. For 13 CDEs and all 6 classifications separate variables have been made available. (see "imaging." variables: SkullFracture, Mass lesion, ExtraaxialHematoma, EpiduralHematoma, SubduralHematomaAcute, SubduralHematomaSubacuteChronic, SubduralCollectionMixedDensity, Contusion, TAI, traumaticSubarachnoidHemorrhage, IntraventricularHemorrhage, MidlineShift, CisternalCompression. A derived variable was also created with AnyIntracranTraumaticAbnormality). These 13 CDEs only contain basic information (i.e. lesion is present, absent, indeterminate, uninterpretable, not interpreted). | |
| Imaging.Manufacturer | Imaging manufacturer | S: Imaging scanner manufacturer. R: Tag (0008,0070) from dicom header available in Imaging.DicomHeaderURL | |
| Imaging.MarshallCTClassification | Marshall CT classification | A general CT grading scale. Useful for outcome prediction. Ranges from 1 to 6 in our dataset. (No visible pathology on CT (1), Cisterns present, MLS < 5 mm (2), Cisterns compressed or absent, MLS < 5 mm (3), MLS > 5 mm, no mass lesion > 25 cc (4), Evacuated mass lesion (5), Non-evacuated mass lesion (6)) Only available for CT scans. For each patient, the MarshallCTClassification can be found in a Imaging.LesionData variable. For the Marshall CT classification the admission scan was scored. (which is not necessarily the "worst"). | |
| Imaging.MassLesion | Mass lesion (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether a mass lesion is present. "Mass Lesion" in this case was defined as a total brain lesion volume > 25 cc. Note that this can mean that there is at least one large lesion or multiple co-existing lesions (contusions, subdural hematomas, etc.) that add up to > 25 cc. More information can be found in the JSON files. | |
| Imaging.MidlineShift | Midline shift (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether a midline shift of > 5 mm is present. More descriptive information (direction) can be found in the JSON files. | |
| Imaging.MorrisMarshallClassification | Morris-Marshall classification | S: A CT grading scale for traumatic Subarachnoid Hemorrhage (tSAH) B: Useful for outcome prediction. Ranges from 0-4. (no tSAH (0), trace or moderate tSAH in one location (basal, cortical or tentorial) (1), one location full, or 2 not full (2), two locations full (3), 3 locations or more (4)) R: Only available for CT scans. For each patient, the MorrisMarshallClassification can be found in a Imaging.LesionData variable. | |
| Imaging.NiftiURL | NIFTI URL | S: nifti files are converted from original dicom files. B: nifti is an imaging format (Neuroimaging Informatics Technology Initiative file format). A: This variable is an URL towards the scan session that contains the generated nifti file. R: Open-source tool to convert DICOM to nifti https://github.com/icometrix/dicom2nifti | |
| Imaging.QCResultsURL | QC results file name | S: A json file containing MR quality measures. B: All different quality measures that have been applied are being collected in one json file. These comprises at least a protocol check, snr, cnr, head coverage, GM/WM, FA/MD, tensor residuals, ... A: These json files can be shared upon request. To request access please contact the CENTER-TBI office. | |
| Imaging.ReportStatus | Report status | S: Visual inspection remark B: All MR images have been visually inspected and labeled as approved, rejected or approved with remark. The remark can be found in Imaging.ReportStatusComments R: Imaging.QCResultsURL is being used during this visual inspection. This is the prefered status of the quality of the images. | |
| Imaging.ReportStatusComments | Report status (comments, if any) | S: Comment on the report status B: All MR images have been visually inspected and labeled as approved, rejected or approved with remark. This variable contains the motivation if the status is rejected or approved with remark. | |
| Imaging.RotterdamCTScore | Rotterdam CT score | S: A general CT grading scale B: Useful for outcome prediction. Ranges from 1 to 6 in our dataset. Scoring was as follows: IVH or tSAH (+1), Epidural Mass not present (+1), MLS > 5 mm (+1), cisterns compressed (+1), cisterns absent (+1), SUM SCORE = +1 R: Only available for CT scans. For each patient, the RotterdamCTscore can be found in the Imaging.LesionData variable. | |
| Imaging.ScanDetection | Detection quality | S: Triaging variable for the usablity of a CT scan B: Since all clinical CT scans (head, neck, spine, ...) are uploaded, it is not always clear which scans are usable an which not. In order to know what scans are usable, a variable is defined. This variable gives as an output: UNUSABLE SCANS / USABLE SCANS / DOUBTFULL. R: This triaging is done by computer algorithms and is not 100% water tight. | |
| Imaging.ScanLabel | Scan label | S: Scan label is a specific identifier for a scan. A: Scan label contains 3 parts: Imaging.ExperimentID Imaging.ExperimentLabel (0020,0011) Series Number (from dicom header) Format: Imaging.ExperimentID_Imaging.ExperimentLabel_SeriesNumber " | |
| Imaging.Scanner | Imaging type of scanner used | Imaging scanner This information is available from the Imaging.DicomHeaderURL | |
| Imaging.ScanNotes | Notes | S: Free text remarks from dcm2nii conversion B: This free text variable is used for internal purpose A: R: opensource dcm2nii converter available https://github.com/icometrix/dicom2nifti | |
| Imaging.ScanQuality | Scan quality | S: This variable is specified by the one who uploaded the images to the imaging repository B: Possible values are usable, questionable, unusable A: Quality of the scan R: Might be very arbitrary and therefor preferable use Imaging.QCResultsURL data and Imaging.ReportStatus as quality reference. | |
| Imaging.ScanType | Scan type | S: MR Mapping for series description B: Since all centers use different series description, a mapping for T2, T1, FLAIR, T2*, DTI and rs-fMRI is provided. R: For CT, ScanType and Series Description should be the same. | |
| Imaging.SeriesDescription | Series description | S: Scan Series description retrieved from DICOM header A: Serie Name Given by the image acquisition center. R: DICOM Tag (0008,103E) Series Description | |
| Imaging.SkullFracture | Skull fracture (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether a skull fracture or multiple skull fractures are present. More descriptive information (location, number) and advanced information (morphology: e.g. depressed, compound, etc.) can be found in the JSON files. | |
| Imaging.SnapshotURL | Imaging mid-slice snapshot in 3 planes | S: Mid-slice snapshot from three planes: axial, sagittal, and coronal. B: In order to have a quick view of the data, a snapshot of the mid-slice in 3 planes is provided. A: Snapshot files of generated nifti images can be accessed through XNAT under the specified scan session. R: Screenshots are defaced. | |
| Imaging.SubduralCollectionMixedDensity | Subdural Collection Mixed Density (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether one or multiple subdural collections/mixed density hematomas are present. More descriptive information (location, volume, number) and advanced information (e.g. isodensity, hypodensity, acute on chronic, chronic recurrent etc.) can be found in the JSON files. Volume was estimated using the AxBxC/2 method. Note: cfr. epidural and subdural hematoms regarding volumes. Note: In the JSON files length, width and depth of lesions can not be used as metrics in any analysis! Only "descriptive volume" is a valid metric (in cc) | |
| Imaging.SubduralHematomaAcute | Subdural Hematoma Acute (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether an acute subdural hematoma or multiple acute subdural hematomas are present. More descriptive information (location, volume, number) and advanced information (homogeneous versus heterogeneous) can be found in the JSON files.Volume was estimated using the AxBxC/2 method, however, small traces of acute subdural blood on the tentorium or interhemispheric were not measured. Note: cfr. epidural: only "descriptive_volume" can be used for analysis. Note: In the JSON files length, width and depth of lesions can not be used as metrics in any analysis! Only "descriptive volume" is a valid metric (in cc) | |
| Imaging.SubduralHematomaSubacuteChronic | Subdural Hematoma subacute chronic (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether one or multiple subacute/chronic subdural hematoma(s) are present. More descriptive information (location, volume, number) can be found in the JSON files.Note: Volume was estimated using the AxBxC/2 method. Note: this variable is best considered together with the "SubduralCollectionMixedDensity" variable, as the central reviewer did not have information to time of injury. Many subacute/chronic subdurals were therefore categorised as "mixed density". Note: cfr. epidural and acute subdural hematoma regarding volumes. Note: In the JSON files length, width and depth of lesions can not be used as metrics in any analysis! Only "descriptive volume" is a valid metric (in cc) | |
| Imaging.SubjectGroup | Subject stratum (ER, ADM, ICU) | S: Subject stratum B: Possible options are: ER, ADMISSION, ICU | |
| Imaging.TAI | TAI (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether axonal injury is present. More descriptive information (location, TAI versus DAI) can be found in the JSON files. Note: be aware of the modality you are interested in (i.e. CT or MRI). | |
| Imaging.ThumbnailURL | Thumbnail storage location | S: Screenshots are automatically generated. B: Thumbnails are reduced-size versions of pictures. A: Thumbnails of generated nifti images can be accessed through XNAT under the specified scan session. R: You can find higher-resolution images using the provided snapshots through the XNAT portal. Screenshots are defaced. | |
| Imaging.Timepoint | Timepoint (Imaging) | S: Timepoint of the scan acquisition B: For CT scans, possible options are: CT Early, CT Followup, CT Post-op For MR scans, possible options are: MR Early, MR 2 weeks, MR 3 months, MR 6 months, MR 12 months, MR 24 months A: Timepoint of the scan acquisition. R: Date and Time of the experiment is available in Imaging.ExperimentDateTime In order to have the intitial CT reports, download this variable in Neurobot, together with Subject.GUPI, Imaging.ExperimentId and your variables of interest. See steps Imaging.ExperimentId variable. | |
| Imaging.TraumaticSubarachnoidHemorrhage | Traumatic Subarachnoid Hemorrhage (present/absent) | This variable was assessed by a central review panel, according the TBI-Common Data Elements. This variable indicates whether traumatic subarachnoid blood is present. More descriptive information (location and amount (e.g. trace, moderate, severe)) can be found in the JSON files. * Location can be: cortical, basal, interhemispheric or tentorial. | |
| Imaging.WindowDetectionComment | Window detection (comments, if any) | Available in case Imaging.WindowDetectionQuality = Window Uncertainty. Imaging.WindowDetection specify if the images are Bone Window, Brain Window or if there is Window Uncertainty. Only available for CT scans. | |
| Imaging.WindowDetectionQuality | Window detection quality | S: Automated Detection for bone versus brain. B: Possible options: Bone Window, Brain Window, Window Uncertainty R: Only available for CT scans. No brain window scans should be classified as bone window. | |
| Imaging.XsiType | Xsi type | S: Type of imaging (CT/MR) A: Assess if the scan is CT or MR R: Possible values 'xnat:mrSessionData' and 'xnat:ctSessionData' | |
| InjuryHx.AbdomenPelvicContentsAIS | Abdomen/Pelvic Contents AIS | AIS score for the Abdomen/Pelvic Contents In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.AbdomenPelvicContentsDesc | Abdomen/Pelvic Contents injury description | 99 == Other 5 == Retroperitoneal hematoma 4 == Kidney contusion 3 == Perforating abdominal injury 2 == Liver rupture 1 == Spleen rupture |
Injury description related to the AIS/ISS score for the Abdomen/Pelvic Contents |
| InjuryHx.AbdomenPelvicContentsISS | ISS score for the abdomen/pelvic content | ISS score for the Abdomen/Pelvic Contents | |
| InjuryHx.AbdomenPelvicLumbarRegionAIS | AIS score for the abdomen/pelvic lumbar region | AIS score for the Abdomen/Pelvic Lumbar region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.ACEFocalNeuroDeficit | Focal neurological deficit (e.g. paresis or dysphasia) | 0 == No 1 == Yes 88 == Unknown |
On the neurological assessment at presentation overall rating was recorded on Focal neurological deficit (eg paresis or dysphasia) |
| InjuryHx.ACEFocalNeuroDeficitDysphasia | Dysphasia | 88 == Unknown 1 == Yes 0 == No |
On the neurological assessment at presentation overall rating was recorded on Focal neurological deficit (eg paresis or dysphasia). If this was rate as "yes", details were recorded on whether it was paresis or dysphasia. |
| InjuryHx.ACEFocalNeuroDeficitOther | Other focal neurological deficit | On the neurological assessment at presentation overall rating was recorded on Focal neurological deficit (eg paresis or dysphasia) If this was rate as "yes", details were recorded on whether it was paresis or dysphasia or other. | |
| InjuryHx.ACEFocalNeuroDeficitOtherTxt | Other focal neurological deficit (please specify) | On the neurological assessment at presentation overall rating was recorded on Focal neurological deficit (eg paresis or dysphasia) If this was rate as "yes", details were recorded on whether it was paresis or dysphasia or other, and for other it was specified which one. | |
| InjuryHx.ACEFocalNeuroDeficitParesis | Paresis | 88 == Unknown 1 == Yes 0 == No |
On the neurological assessment at presentation overall rating was recorded on Focal neurological deficit (eg paresis or dysphasia) If this was rate as "yes", details were recorded on whether it was paresis or dysphasia. |
| InjuryHx.ACEOverallRating | How different is the person acting compared to his/her usual self? | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
On the neurological assessment at presentation overall rating was recorded on "How different the person is acting compared to his/her usual self" The rating was on a scale from 1 (normal) to 6 (very different). |
| InjuryHx.ACEOverallRatingUnknown | Overall rating of neurological assessment unknown | On the neurological assessment at presentation overall rating was recorded on "How different the person is acting compared to his/her usual self" This variable reflects if the rating was "unknown". | |
| InjuryHx.ACERatedBy | Rating performed by | 1 == Proxy 2 == Subject 3 == Both proxy and subject 4 == Not done |
On the neurological assessment at presentation overall rating was recorded on "How different the person is acting compared to his/her usual self" This variable reflects by whom the rating was performed. |
| InjuryHx.AlcPriorUseInd | Past use: Alcoholic beverages (beer, wine, spirits) (>2/day) | 0 == No 1 == Yes 88 == Unknown |
On presentation the behavioral history of the patient was recorded. This reflects his past use of alcoholic beverages (beer, wine, spirits). |
| InjuryHx.AlcUseDur | Past use: No. of years of use of alcoholic beverages (beer, wine, spirits) (>2/day) | On presentation the behavioral history of the patient was recorded. This reflects the number of years of alcohol use, if past use of alcoholic beverages (beer, wine, spirits) was 'yes'. | |
| InjuryHx.AlcUseLstMoDaysDrankNum | Use in the past three months: Alcoholic beverages (beer, wine, spirits> (>2/day) | 88 == Unknown 0 == No 1 == Yes |
On presentation the behavioral history of the patient was recorded. This reflects his use in the past three months of alcoholic beverages (beer, wine, spirits) (>2/day) |
| InjuryHx.AUDITCAlcDrnkTypclDayNumScore | Average number of alcoholic drinks on a drinking day | 1 == 1-2 2 == 3-4 3 == 5-6 4 == 7-9 5 == 10 or more 88 == Unknown |
On presentation the behavioral history of the patient was recorded. In case of past use of alcoholic beverages (beer, wine, spirits), this reflects the alcohol frequency: average number of drinks on a "drinking" day |
| InjuryHx.AUDITCDrnkContainAlcFreqScore | Frequency of having a drink containing alcohol | 0 == Never 1 == Monthly or less 2 == 2-4 times a month 3 == 2-3 times a week 4 == 4 or more times a week 88 == Unknown |
Detailed questions on the use of alcohol are derived from the first 3 questions of the "AUDIT" questionnaire, a screening tool developed by the World Health Organization (WHO) to assess alcohol consumption, drinking behaviors, and alcohol-related problems. The same questions are asked post-injury during full follow-up assessments (including cognitive testing.) This reflects the frequency of having a drink containing alcohol. |
| InjuryHx.AUDITCMoreThan6AlcDrnkFreqScore | Frequency of having six or more alcoholic drinks on one occasion | 7 == Weekly 5 == Less than monthly 6 == Monthly 8 == Daily or almost daily 0 == Never 1 == Monthly or less (incorrect please correct) 2 == 2-4 times a month (incorrect please correct) 3 == 2-3 times a week (incorrect please correct) 4 == 4 or more times a week (incorrect please correct) 88 == Unknown |
Detailed questions on the use of alcohol are derived from the first 3 questions of the "AUDIT" questionnaire, a screening tool developed by the World Health Organization (WHO) to assess alcohol consumption, drinking behaviors, and alcohol-related problems. The same questions are asked post-injury during full follow-up assessments (including cognitive testing.) This reflects the frequency of having six or more drinks on one occasion. |
| InjuryHx.BaselineGCSMostReliableAssessmentCondition | Conditions of baseline risk assessment | 1 == Under sedation 3 == After stopping sedation 0 == No sedation/paralysis 4 == After pharmacological reversal |
A baseline risk assessment was performed at the hospital (ER). This reflects the Conditions of assessment for the Most reliable Motor Score for risk assessment. |
| InjuryHx.BaselineGCSMostReliableAssessmentTime | Time of baseline risk assessment | 1 == Admission 2 == Post-stabilization 3 == First hospital 4 == Scene of accident 5 == Other |
A baseline risk assessment was performed at the hospital (ER). This reflects the Time of assessment for the Most reliable Motor Score for risk assessment. |
| InjuryHx.BaselineGCSMostReliableMotorScore | Most reliable Motor score for baseline risk assessment | A baseline risk assessment was performed at the hospital (ER). This reflects the Most reliable baseline Motor score of the GCS as given by sites - for use in prognostic models. | |
| InjuryHx.BaselineGOS6MoDateOfPrognosticEstimate | Date of prognostic estimate of 6 month outcome | At ER discharge, physician estimate of six month outcome was recorded as a baseline risk assessment: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ER or admission to hospital/ICU". This reflects the Date of prognostic estimate | |
| InjuryHx.BaselineGOS6MoExpectedDeathRisk | Expected risk of death at 6 months | At ER discharge, physician estimate of six month outcome was recorded as a baseline risk assessment: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ER or admission to hospital/ICU". This reflects the Risk of death in % | |
| InjuryHx.BaselineGOS6MoExpectedOutcome | Expected GOS (Glasgow Outcome Scale) at 6 months | D == D - Death V == V - Vegetative State SD == SD - Severe Disability MD == MD - Moderate Disability GR == GR - Good Recovery |
At ER discharge, physician estimate of six month outcome was recorded as a baseline risk assessment: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ER or admission to hospital/ICU". This reflects the Expected outcome (GOS) |
| InjuryHx.BaselineGOS6MoUnfavourableOutcomeRisk | Expected risk of unfavourable outcome (D, VS, SD) at 6 months | At ER discharge, physician estimate of six month outcome was recorded as a baseline risk assessment: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ER or admission to hospital/ICU". This reflects the Risk of unfavorable outcome (D, VS, SD) in % | |
| InjuryHx.BaselinePhysEstOf6MoOutcomePhysicianQual | Qualification of the physician estimating the 6 month outcome | 1 == Resident 2 == Junior staff (< 5 years) 3 == Senior staff (>= 5 years) 4 == Head of department |
At ER discharge, physician estimate of six month outcome was recorded as a baseline risk assessment: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ER or admission to hospital/ICU". This reflects the qualification of the physician who provided prognostic estimate on ER discharge/admission to hospital/ICU |
| InjuryHx.BaselinePhysEstOf6MoOutcomePhysicianType | Type of the physician estimating the 6 month outcome | 1 == ER Physician 2 == Intensive Care 3 == Neurology 4 == Neurosurgery 5 == Traumatology 88 == Unknown |
At ER discharge, physician estimate of six month outcome was recorded as a baseline risk assessment: "Given all current available information, what is, in your subjective opinion, the most likely 6-month outcome of this patient? To be based upon information on discharge ER or admission to hospital/ICU". This reflects the type of the physician who provided prognostic estimate on ER discharge/admission to hospital/ICU |
| InjuryHx.BestOfAbdomenPelvicLumbarISS | Abdomen/Pelvic contents, Lumbar Spine ISS | AbdomenPelvicLumbar region (Highest AIS of the region)^2 compare AbdomenPelvicContentsAIS, LumbarSpineAIS. This score is taken forward for ISS calculation | |
| InjuryHx.BestOfChestSpineISS | Thorax/chest, Thoracic Spine ISS | (highest AIS of the region)^2 Compare ThoraxChestAIS, ThoracicSpineAIS and select the highest for ISS calculation | |
| InjuryHx.BestOfExternaISS | Externa (Skin) ISS | External region (ExternaAIS)^2 select the highest external AIS severity code for ISS calculation. | |
| InjuryHx.BestOfExtremitiesISS | Extremities and Pelvic Girdle ISS | Extremities region (Highest AIS of the region)^2 compare UpperExtremitiesAIS, LowerExtremitiesAIS, PelvicGirdleAIS select the highest for ISS calculation | |
| InjuryHx.BestOfFaceISS | Face ISS | Face region (FaceAIS)^2 select the highest facial injury for ISS calculation | |
| InjuryHx.BestOfHeadBrainCervicalISS | Head and Neck, Brain and Cervical spine ISS | HeadBrainCervical region (Highest AIS of the region)^2 Compare HeadNeckAIS, InjuryHx.BrainInjuryAIS, CervicalSpineAIS select the highest scoring injury in any of these 3 areas for ISS calculation | |
| InjuryHx.BrainInjuryAIS | Brain injury AIS | AIS score for the Brain Injury In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.BrainInjuryDesc | Brain injury description | 5 == ASDH 99 == Other 4 == Diffuse Injury 3 == EDH 2 == Contusions 1 == Concussion |
Injury description related to the AIS/ISS score for the Brain Injury. Injury description is coded by drop-down menus for each body region |
| InjuryHx.CannabisCurrentUse | Use in the past three month: Cannabis (marijuana, pot, grass, hash, etc.) | 0 == No 1 == Yes 88 == Unknown |
On presentation the behavioral history of the patient was recorded. This reflects the use in the past three months of Cannabis (marijuana, pot, grass, hash, etc.) |
| InjuryHx.CannabisPriorUse | Past use: Cannabis (marijuana, pot, grass, hash, etc.) | 0 == No 1 == Yes 88 == Unknown |
On presentation the behavioral history of the patient was recorded. This reflects his past use of Cannabis (marijuana, pot, grass, hash, etc.) |
| InjuryHx.CannabisPriorUseDuration | Past use: No. of years of use of cannabis (marijuana, pot, grass, hash, etc.) | On presentation the behavioral history of the patient was recorded. This reflects the number of years of past use of Cannabis if applicable. | |
| InjuryHx.CervicalSpineAIS | Cervical Spine AIS | AIS score for Cervical Spine region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.CervicalSpineDesc | Cervical Spine injury description | 99 == Other 2 == Dislocation 1 == Fracture |
Injury description related to the AIS/ISS score for the Cervical Spine region. |
| InjuryHx.DispER | Destination from ER | 1 == Discharge home 2 == Discharge other facility 3 == Hospital admission--Ward 5 == Hospital admission--ICU 6 == Hospital admission--OR for immediate surgical procedure 7 == Death 8 == Hospital admission--Other (e.g. observation unit) 88 == Unknown 4 == Hospital admission--Intermediate/high care unit |
Destination of the patient at ER discharge. |
| InjuryHx.DrgSubIllctCurntUseInd | Use in the past three months: Other recreational drugs | 0 == No 1 == Yes 88 == Unknown |
On presentation the behavioral history of the patient was recorded. This reflects the use in the past three months of Other recreational drugs (than Cannabis) |
| InjuryHx.DrgSubIllctUseCatOther | Past use: Other recreational drugs (please specify) | On presentation the behavioral history of the patient was recorded. This reflects his past use of which type of drugs. | |
| InjuryHx.DrgSubIllctUseDur | Past use: No. of years of use of other recreational drugs | On presentation the behavioral history of the patient was recorded. This reflects the number of years of his past use of recreational drugs, if applicable. | |
| InjuryHx.DrgSubPriorIllctUseInd | Past use: Other recreational drugs | 0 == No 1 == Yes 88 == Unknown |
On presentation the behavioral history of the patient was recorded. This reflects his past use of Other recreational drugs (other than Cannabis) |
| InjuryHx.DrugIllicitCurrentUseOther | Use in the past three month: Other recreational drugs (please specify) | On presentation the behavioral history of the patient was recorded. This reflects the use in the past three months of which type of drugs | |
| InjuryHx.EDAirway | Airway status at ER discharge | 1 == No specific treatment 2 == Supplemental oxygen (via nasal tube or mask) 3 == Adjunctive airway (eg. Mayo tube) 4 == Temporary support with bag, valve, mask (eg.ambubag) 5 == Intubation 6 == Mechanical ventilation 88 == Unknown |
Records treatment performed in the ER/on admission with regard to Airways. Pre-hospital inteventions are documented at: InjuryHx.PresEmergencyCare |
| InjuryHx.EDArrDBP | Diastolic at ER arrival (first value) | Reflects the vital signs at ER arrival: BP (mmHg) --> Diastolic | |
| InjuryHx.EDArrHR | Heart Rate at ER arrival (first value) | Reflects the vital signs at ER arrival: Heart rate --> Beats per min. | |
| InjuryHx.EDArrivalAirway | Airway status at ER arrival | 1 == Clear 2 == Obstructed 3 == Adjunctive Airway 4 == Intubated 88 == Unknown |
The ABC status on arrival documents the status of Airway, Breathing and Circulation upon arrival to Study Hospital (ER); In addition, administration of supplemental oxygen and spinal immobilization is documented. |
| InjuryHx.EDArrivalArtpCO2kPa | Arterial pCO2 at ER arrival in kPa | Reflects the vital signs at ER arrival: Arterial pCO2 --> kPa | |
| InjuryHx.EDArrivalArtpCO2mmhg | Arterial pCO2 at ER arrival (first value) | Reflects the vital signs at ER arrival: Arterial pCO2 --> mmHg | |
| InjuryHx.EDArrivalArtpCO2unit | Unit used for Arterial pCO2 at ER arrival (kPa or mmHg) | 1 == kPa 2 == mmHg |
Reflects the vital signs at ER arrival: Unit used for Arterial pCO2 |
| InjuryHx.EDArrivalArtpCO2Unknown | Arterial pCO2 at ER arrival unknown | Reflects the vital signs at ER arrival: Arterial pCO2 --> Unknown | |
| InjuryHx.EDArrivalArtpO2kPa | Arterial pO2 at ER arrival in kPa | Reflects the vital signs at ER arrival: Arterial pO2 --> kPa | |
| InjuryHx.EDArrivalArtpO2mmhg | Arterial pO2 at ER arrival (first value) | Reflects the vital signs at ER arrival: Arterial pO2 --> mmHg | |
| InjuryHx.EDArrivalArtpO2unit | Unit used for Arterial pO2 at ER arrival (kPa or mmHg) | 1 == kPa 2 == mmHg |
Reflects the vital signs at ER arrival: Unit used for Arterial pO2 |
| InjuryHx.EDArrivalArtpO2Unknown | Arterial pO2 at ER arrival unknown | Reflects the vital signs at ER arrival: Arterial pO2 --> Unknown | |
| InjuryHx.EDArrivalBaseExcess | Base Excess at ER arrival (first value) | Reflects the vital signs at ER arrival: Base excess --> mEq/l | |
| InjuryHx.EDArrivalBaseExcessUnit | Unit used for Base excess at ER arrival (mEq/l or other) | 99 == Other 1 == mEq/l |
Reflects the vital signs at ER arrival: the unit used for Base excess |
| InjuryHx.EDArrivalBaseExcessUnitSpecify | Which other (than standard) unit used for Base excess at ER arrival | Reflects the vital signs at ER arrival: specifies if another unit was used than the standard unit for Base excess | |
| InjuryHx.EDArrivalBaseExcessUnknown | Base excess at ER arrival unknown | Reflects the vital signs at ER arrival: Base excess --> Unknown | |
| InjuryHx.EDArrivalBloodGasDone | First arterial blood gas done at ER arrival | 0 == No 1 == Yes |
Reflects the vital signs at ER arrival: reflects if First arterial blood gas was done Arterial blood gas analysis is not required for all subjects. Performed on clinical indication; will generally be restricted to subjects with more severe injuries |
| InjuryHx.EDArrivalBloodPressureUnknown | Blood Pressure at ER arrival unknown | 88 == Unknown | Reflects the vital signs at ER arrival: BP (mmHg) --> Unknown |
| InjuryHx.EDArrivalBMI | BMI at ER arrival (based on inches and pounds) | BMI using height in inches (EDArrivalHeightInches) and weight in pounds (EDArrivalBodyWeightLbs) BMI=((weight/(height*height)) * 704.5469 | |
| InjuryHx.EDArrivalBMIKgCm | BMI (Body Mass Index) at ER arrival | BMI using height in cm (EDArrivalHeightCm) and weight (EDArrivalBodyWeightKg) BMI= (Weight/(Height*Height))) * 10000 | |
| InjuryHx.EDArrivalBodyWeightKg | Body weight at ER arrival | Body weight in KG at ER arrival | |
| InjuryHx.EDArrivalBodyWeightLbs | Body weight at ER arrival in Lbs | Body weight in LBS at ER arrival | |
| InjuryHx.EDArrivalBodyWeightMeasured | Reliability of the body weight reported at ER arrival | 1 == Estimated 2 == Self reported 3 == Measured 4 == Proxy reported 88 == Unknown |
Provides an indication of accuracy of reported body weight at ER arrival |
| InjuryHx.EDArrivalBodyWeightUnit | Unit used for body weight at ER arrival (kg or lbs) | 1 == kg 2 == lbs |
Unit used for Body weight at ER arrival |
| InjuryHx.EDArrivalBreathing | Breathing status at ER arrival | 1 == Spontaneous, adequate 2 == Spontaneous, insufficient 3 == Manual support with bag, valve, mask 4 == Mechanical ventilation 88 == Unknown |
The ABC status on arrival documents the status of Airway, Breathing and Circulation upon arrival to Study Hospital (ER); In addition, administration of supplemental oxygen and spinal immobilization is documented. |
| InjuryHx.EDArrivalCirculation | Circulation status at ER arrival | 0 == No specific therapy 1 == IV Fluids 2 == Vasopressors 3 == CPR 88 == Unknown |
The ABC status on arrival documents the status of Airway, Breathing and Circulation upon arrival to Study Hospital (ER); In addition, administration of supplemental oxygen and spinal immobilization is documented. |
| InjuryHx.EDArrivalFiO2 | FiO2 at ER arrival (first value) | Reflects the vital signs at ER arrival: FiO2 (in %) Information on FiO2 (Fraction of Inspired oxygen) at time of arterial blood gas sampling is requested in order to be able to calculate PaO2/FiO2 as measure of severity of hypoxaemia; dependent on altitude; at sea-level, normal values are > 500 mmHg | |
| InjuryHx.EDArrivalFiO2Unknown | FiO2 at ER arrival | Reflects the vital signs at ER arrival: FiO2 (in %) = unknown | |
| InjuryHx.EDArrivalHeartRateUnknown | Heart rate at ER arrival Unknown | Reflects the vital signs at ER arrival: Heart rate --> Unknown | |
| InjuryHx.EDArrivalHeightCm | Height | Reflects Height in cm at ER arrival | |
| InjuryHx.EDArrivalHeightInches | Height in inches at ER arrival | Reflects Height in inches at ER arrival | |
| InjuryHx.EDArrivalHeightMeasured | Reliability of height reported | 1 == Estimated 2 == Self reported 3 == Measured 4 == Proxy reported 88 == Unknown |
Provides an indication of accuracy of reported height at ER arrival |
| InjuryHx.EDArrivalHeightUnit | Unit used for height at ER arrival (cm or inches) | 1 == cm 2 == inch |
Reflects unit used for Height at arrival |
| InjuryHx.EDArrivalLactate | Lactate at ER arrival (first value) | Reflects the vital signs at ER arrival: Lactate --> mEq/l | |
| InjuryHx.EDArrivalLactateUnit | Unit used for lactate at ER arrival (if not standard unit) | 99 == Other 1 == mEq/l |
Reflects if for "lactate" as vital signs at ER arrival another unit was used than the standard. |
| InjuryHx.EDArrivalLactateUnitSpecify | Which other unit used for lactate at ER arrival (if not standard unit) | Reflects the vital signs at ER arrival: Specifies for Lactate the unit used if another unit than the standard was used | |
| InjuryHx.EDArrivalLactateUnknown | Lactate at ER arrival Unknown | Reflects the vital signs at ER arrival: Lactate --> Unknown | |
| InjuryHx.EDArrivalOxygenSatUnknown | Oxygen saturation at ER arrival Unknown | Reflects the vital signs at ER arrival: Oxygen saturation --> Unknown | |
| InjuryHx.EDArrivalpH | pH at ER arrival (first value) | Reflects the vital signs at ER arrival: pH | |
| InjuryHx.EDArrivalpHUnknown | pH at ER arrival Unknown | Reflects the vital signs at ER arrival: pH --> Unknown | |
| InjuryHx.EDArrivalRespRateUnknown | Respiratory rate at ER arrival Onknown | 1 == Spontaneous 2 == Ventilated 88 == Unknown |
Reflects the vital signs at ER arrival: Respiratory rate --> Unknown |
| InjuryHx.EDArrivalSpinalImmob | Spinal Immobilization at ER arrival | 0 == No 1 == Yes 88 == Unknown |
The ABC status on arrival documents the status of Airway, Breathing and Circulation upon arrival to Study Hospital (ER); In addition, administration of supplemental oxygen and spinal immobilization is documented. |
| InjuryHx.EDArrivalSupplementalOxygen | Supplemental Oxygen at ER arrival | 0 == No 1 == Yes 88 == Unknown |
The ABC status on arrival documents the status of Airway, Breathing and Circulation upon arrival to Study Hospital (ER); In addition, administration of supplemental oxygen and spinal immobilization is documented. |
| InjuryHx.EDArrivalTemperatureUnknown | Temperature at ER arrival Unknown | The ABC status on arrival documents the status of Airway, Breathing and Circulation upon arrival to Study Hospital (ER); In addition, administration of supplemental oxygen and spinal immobilization is documented. | |
| InjuryHx.EDArrPupilLftEyeMeasr | Left eye pupil size at ER arrival | 1 == 1 10 == 10 9 == 9 8 == 8 7 == 7 6 == 6 5 == 5 4 == 4 3 == 3 2 == 2 |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the size of the left eye pupil for the assessment at Arrival to ER of the study hospital. |
| InjuryHx.EDArrPupilLftEyeMeasrUnkUnt | Left pupil at ER arrival Untestable/Unknown | 88 == Unknown 66 == Untestable |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects if GCS was Untestable/Unknown for the assessment at Arrival to ER of the study hospital. |
| InjuryHx.EDArrPupilReactivityLghtLftEyeReslt | Left eye pupil reactivity at ER arrival | 3 == - (Negative) 2 == + (Sluggish) 1 == + (Brisk) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the reactivity of the left eye pupil for the assessment at Arrival to ER of the study hospital. |
| InjuryHx.EDArrPupilReactivityLghtRtEyeReslt | Right eye pupil reactivity at ER arrival | 3 == - (Negative) 2 == + (Sluggish) 1 == + (Brisk) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the reactivity of the right eye pupil for the assessment at Arrival to ER of the study hospital. |
| InjuryHx.EDArrPupilRtEyeMeasr | Right eye pupil size at ER arrival | 3 == 3 2 == 2 1 == 1 10 == 10 9 == 9 8 == 8 7 == 7 6 == 6 5 == 5 4 == 4 |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the size of the right eye pupil for the assessment at Arrival to ER of the study hospital. |
| InjuryHx.EDArrPupilRtEyeMeasrUnkUnt | Right pupil at ER arrival Untestable/Unknown | 88 == Unknown 66 == Untestable |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects if GCS was Untestable/Unknown for the assessment at Arrival to ER of the study hospital. |
| InjuryHx.EDArrPupilSymmetry | Pupil symmetry at ER arrival | 3 == Unequal L>R 2 == Unequal R>L 1 == Equal 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the Pupil symmetry for the assessment at Arrival to ER of the study hospital. |
| InjuryHx.EDArrRespRate | Respiratory Rate at ER arrival (first value) | Reflects the vital signs at ER arrival: Respiratory rate --> cycles per min | |
| InjuryHx.EDArrSBP | Systolic at ER arrival (first value) | Reflects the vital signs at ER arrival: BP (mmHg) --> Systolic | |
| InjuryHx.EDArrSpO2 | Oxygen saturation at ER arrival (first value) | Reflects the vital signs at ER arrival: Oxygen saturation (in %) | |
| InjuryHx.EDArrTempCelsius | Body temperature at ER arrival (first value) | Reflects the vital signs at ER arrival: Temperature --> Celcius | |
| InjuryHx.EDArrTempFahrenheit | Temperature at ER arrival in Fahrenheit | Reflects the vital signs at ER arrival: Temperature --> Fahrenheit | |
| InjuryHx.EDArrTempUnit | Unit used for temperature at ER arrival (C° or F) | 1 == C 2 == F |
Reflects the unit used for temperature measurement as vital signs at ER arrival |
| InjuryHx.EDBloodGasConditions | Conditions of ABG (Arterial Blood Gas) test at ER arrival | 1 == Pre-intubation, room air 2 == Pre-intubation, +O2 3 == Post-intubation, not ventilated 4 == Post-intubation, ventilated |
Reflects the vital signs at ER arrival: Conditions for First arterial blood gas done (if applicable) |
| InjuryHx.EDBloodGasDate | Date of first ABG (Arterial Blood Gas) test at ER arrival | Reflects the vital signs at ER arrival: date for First arterial blood gas done (if applicable) | |
| InjuryHx.EDBloodGasTime | Time of first ABG (Arterial Blood Gas) test at ER arrival | Reflects the vital signs at ER arrival: time for First arterial blood gas done (if applicable) | |
| InjuryHx.EDBloodTrans | Blood transfusion | 1 == Yes 0 == No 88 == Unknown |
Reflects of blood transfusion was done in the ER of the study hospital |
| InjuryHx.EDCircCPR | Circulation: CPR | Records treatment performed in the ER/on admission with regard to Circulation: CPR. Pre-hospital inteventions are documented at: InjuryHx.PresEmergencyCare | |
| InjuryHx.EDCircIV | Circulation: IV fluids | Records treatment performed in the ER/on admission with regard to Circulation: IV fluids. Pre-hospital inteventions are documented at: InjuryHx.PresEmergencyCare | |
| InjuryHx.EDCircNone | Circulation: No specific treatment | Records treatment performed in the ER/on admission with regard to Circulation: no specific treatment Pre-hospital inteventions are documented at: InjuryHx.PresCirculationTreatmentNone | |
| InjuryHx.EDCircUnknown | Circulation treatment at ER arrival Unknown | Records treatment performed in the ER/on admission with regard to Circulation: unknown. Pre-hospital inteventions are documented at: InjuryHx.PresEmergencyCare | |
| InjuryHx.EDCircVaso | Circulation: Vasopressors | Records treatment performed in the ER/on admission with regard to Circulation: vasopressors. Pre-hospital inteventions are documented at: InjuryHx.PresEmergencyCare | |
| InjuryHx.EDCoagulopathyType1 | (1) Type of coagulopathy | 15 == Vitamin K (Konakion) 1 == Packed red blood cell concentrates (pRBCs) 2 == Fresh whole blood 3 == Fresh frozen plasma (FFP) 4 == Freeze dried plasma / lypholized plasma 5 == Platelet concentrates 6 == PCC (prothrombin complex concentrates) 7 == Fibrinogen concentrate 8 == Albumin 9 == Recombinant factor FVIIa 10 == Tranexamic acid (TXA) 11 == Cryoprecipitate 12 == Desmopression (DDAVP) 13 == Factor XIII 14 == Calcium |
Reflects the type of transfusion or coagulopathy treatment given in the ER of the study hospital (if applicable) |
| InjuryHx.EDCoagulopathyType2 | (2) Type of coagulopathy | 15 == Vitamin K (Konakion) 1 == Packed red blood cell concentrates (pRBCs) 2 == Fresh whole blood 3 == Fresh frozen plasma (FFP) 4 == Freeze dried plasma / lypholized plasma 5 == Platelet concentrates 6 == PCC (prothrombin complex concentrates) 7 == Fibrinogen concentrate 8 == Albumin 9 == Recombinant factor FVIIa 10 == Tranexamic acid (TXA) 11 == Cryoprecipitate 12 == Desmopression (DDAVP) 13 == Factor XIII 14 == Calcium |
Reflects the type of transfusion or coagulopathy treatment given in the ER of the study hospital (if applicable) |
| InjuryHx.EDCoagulopathyType3 | (3) Type of coagulopathy | 15 == Vitamin K (Konakion) 1 == Packed red blood cell concentrates (pRBCs) 2 == Fresh whole blood 3 == Fresh frozen plasma (FFP) 4 == Freeze dried plasma / lypholized plasma 5 == Platelet concentrates 6 == PCC (prothrombin complex concentrates) 7 == Fibrinogen concentrate 8 == Albumin 9 == Recombinant factor FVIIa 10 == Tranexamic acid (TXA) 11 == Cryoprecipitate 12 == Desmopression (DDAVP) 13 == Factor XIII 14 == Calcium |
Reflects the type of transfusion or coagulopathy treatment given in the ER of the study hospital (if applicable) |
| InjuryHx.EDCoagulopathyType4 | (4) Type of coagulopathy | 15 == Vitamin K (Konakion) 1 == Packed red blood cell concentrates (pRBCs) 2 == Fresh whole blood 3 == Fresh frozen plasma (FFP) 4 == Freeze dried plasma / lypholized plasma 5 == Platelet concentrates 6 == PCC (prothrombin complex concentrates) 7 == Fibrinogen concentrate 8 == Albumin 9 == Recombinant factor FVIIa 10 == Tranexamic acid (TXA) 11 == Cryoprecipitate 12 == Desmopression (DDAVP) 13 == Factor XIII 14 == Calcium |
Reflects the type of transfusion or coagulopathy treatment given in the ER of the study hospital (if applicable) |
| InjuryHx.EDCoagulopathyVolume1 | (1) Volume | Reflects the volume of transfusion or coagulopathy treatment given in the ER of the study hospital (if applicable) | |
| InjuryHx.EDCoagulopathyVolume2 | (2) Volume | Reflects the volume of transfusion or coagulopathy treatment given in the ER of the study hospital (if applicable) | |
| InjuryHx.EDCoagulopathyVolume3 | (3) Volume | Reflects the volume of transfusion or coagulopathy treatment given in the ER of the study hospital (if applicable) | |
| InjuryHx.EDCoagulopathyVolume4 | (4) Volume | Reflects the volume of transfusion or coagulopathy treatment given in the ER of the study hospital (if applicable) | |
| InjuryHx.EDCompEventHypothermia | Hypothermia (core temp < 35 degree Celsius) | 88 == Unknown 0 == No 1 == Definite 2 == Suspect |
Second Insults reported here relate to the pre-hospital and ER phase. Hypothermia is defined as a documented core temperature of < 35 C. |
| InjuryHx.EDComplEventCardArr | Cardiac Arrest | 0 == No 1 == Yes |
Second Insults reported here relate to the pre-hospital and ER phase: Cardiac Arrest |
| InjuryHx.EDComplEventHypotension | Hypotensive Episode (Systolic BP < 90 mmHg in adults) | 0 == No 2 == Suspect 1 == Definite 88 == Unknown |
Second Insults reported here relate to the pre-hospital and ER phase. Definite hypotension is defined as a documented systolic BP < 90 mm Hg (adults); "Suspected" was scored if the patient did not have a documented blood pressure, but was reported to be in shock or have an absent brachial pulse (not related to injury of the extremity) |
| InjuryHx.EDComplEventHypoxia | Hypoxic Episode (PaO2 < 8 kPa (60 mmHg)/SaO2 < 90%) | 0 == No 2 == Suspect 1 == Definite 88 == Unknown |
Second Insults reported here relate to the pre-hospital and ER phase. Definite hypoxia is defined as a documented PaO2 <8 kPa (60 mm Hg) and/or SaO2<90%; "Suspected" was scored if the patient did not have documented hypoxia by PaO2 or SaO2, but there was a clinical suspicion , as evidenced by for example cyanosis, apnoea or respiratory distress |
| InjuryHx.EDComplEventSeizures | Seizures | 0 == No 1 == Partial/Focal 2 == Generalized 3 == Status epilepticus 88 == Unknown |
Second Insults reported here relate to the pre-hospital and ER phase: seizures |
| InjuryHx.EDCorrCoagulopathy | Transfusions and treatment of coagulopathy | 1 == Yes 0 == No 88 == Unknown |
Documents blood transfusions and treatment of coagulopathy in the acute phase at presentation. |
| InjuryHx.EDDischDate | Date of ER discharge | Documents the date of discharge from the ER/admission to Ward/ICU | |
| InjuryHx.EDDischPupilLftEyeMeasr | Left eye pupil size poststabilization | 5 == 5 4 == 4 3 == 3 2 == 2 1 == 1 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the size of the left eye pupil for the assessment POST-STABILIZATION. |
| InjuryHx.EDDischPupilLftEyeMeasrUnkUnt | Left pupil at ER discharge Untestable/Unknown | 88 == Unknown 66 == Untestable |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects is left eye pupil was Untestable/Unknown for the assessment POST-STABILIZATION. |
| InjuryHx.EDDischPupilReactivityLghtLftEyeReslt | Left eye pupil reactivity poststabilization | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the reactivity of the left eye pupil for the assessment POST-STABILIZATION. |
| InjuryHx.EDDischPupilReactivityLghtRtEyeReslt | Right eye pupil reactivity poststabilization | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the reactivity of the right eye pupil for the assessment POST-STABILIZATION. |
| InjuryHx.EDDischPupilRtEyeMeasr | Right eye pupil size poststabilization | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the size of the right eye pupil for the assessment POST-STABILIZATION. |
| InjuryHx.EDDischPupilRtEyeMeasrUnkUnt | Right pupil at ER discharge Untestable/Unknown | 88 == Unknown 66 == Untestable |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects if right eye pupil was Untestable/Unknown for the assessment POST-STABILIZATION. |
| InjuryHx.EDDischPupilSymmetry | Pupil symmetry post-stabilization | 3 == Unequal L>R 2 == Unequal R>L 1 == Equal 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects pupil symmetry for the assessment POST-STABILIZATION. |
| InjuryHx.EDDischTime | Time of ER discharge | Documents the time of discharge from the ER/admission to Ward/ICU | |
| InjuryHx.EDICPMonitoring | ICP monitoring scheduled at ER discharge | 0 == No 1 == Yes 88 == Unknown |
Scheduled for ICP monitoring; e.g. may not accurately reflect if ICP monitoring was indeed performed |
| InjuryHx.EDIVAlbumin | IV fluids specifics: Albumin | Records treatment performed in the ER/on admission with regard to Circulation: IV fluids --> Albumin | |
| InjuryHx.EDIVBlood | IV fluids specifics: Blood | Records treatment performed in the ER/on admission with regard to Circulation: IV fluids --> Blood | |
| InjuryHx.EDIVColloids | IV fluids specifics: Colloids | Records treatment performed in the ER/on admission with regard to Circulation: IV fluids --> Colloids | |
| InjuryHx.EDIVCrystalloids | IV fluids specifics: Crystalloids | Records treatment performed in the ER/on admission with regard to Circulation: IV fluids --> Crystalloids | |
| InjuryHx.EDIVMannitol | IV fluids specifics: Mannitol | Records treatment performed in the ER/on admission with regard to Circulation: IV fluids --> Mannitol | |
| InjuryHx.EDIVSaline | IV fluids specifics: Hypertonic saline | Records treatment performed in the ER/on admission with regard to Circulation: IV fluids --> Hypertonic saline | |
| InjuryHx.EDSecondInsultsNeuroWorse | Neuroworsening | 0 == No 1 == Yes 88 == Unknown |
The importance of Neuroworsening was first described by Morris and Marshall. The occurrence of neuroworsening is related to poorer outcome in subjects with moderate to severe TBI. Neuroworsening is defined as 1) a decrease in GCS motor score of 2 or more points; 2) a new loss of pupillary reactivity or development of pupillary assymmetry >= 2mm; 3) deterioration in neurological or CT status sufficient to warrant immediate medical or surgical intervention |
| InjuryHx.EDSecondInsultsNeuroWorseYes | Neuroworsening (please describe) | 1 == Decrease in motor score >= 2 points 2 == Development of pupillary abnormalities 3 == Other neurological and/or CT deterioration |
This variable provides a specification of the type of neuroworsening if it occurs. |
| InjuryHx.EDSecondInsultsPreAdmisCourse | Pre-admission course | 0 == Deterioration 1 == Stable 2 == Improving 88 == Unknown |
The pre-admission course should only be considered an intracranial second insult in case of Deterioration. The nature of deterioration will in most cases be further detailed under the variable "Neuroworsening". |
| InjuryHx.EDSpinalImmob | Spinal immobilization at ER discharge | 0 == No 1 == Yes 88 == Unknown |
Records treatment performed in the ER/on admission with regard to Spinal immobilization. Pre-hospital inteventions are documented at: InjuryHx.PresEmergencyCare |
| InjuryHx.EmergSurgInterventionsExtraCran | Emergency extracranial surgical intervention scheduled at ER discharge | 0 == No 1 == Yes 88 == Unknown |
Documents emergency extracranial surgery performed in study hospital. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERextracranialSurg |
| InjuryHx.EmergSurgInterventionsExtraCranYes | Emergency extracranial surgical intervention scheduled at ER discharge (please specify) | 3 == Extraperitoneal pelvic packing 4 == External fixation limb 2 == Damage control laparotomy 1 == Damage control thoracotomy 5 == Cranio-maxillo-facial reconstruction 99 == Other |
Documents emergency extracranial surgery performed in study hospital. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERextracranialSurg |
| InjuryHx.EmergSurgInterventionsExtraCranYesOther | Other emergency extracranial surgical intervention scheduled at ER discharge (please specify) | Documents emergency extracranial surgery performed in study hospital. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERextracranialSurg | |
| InjuryHx.EmergSurgInterventionsIntraCran | Emergency intracranial surgical intervention scheduled at ER discharge | 0 == No 1 == Yes 88 == Unknown |
Documents emergency intracranial surgery performed in study hospital. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERIntracranialSurg |
| InjuryHx.EmergSurgInterventionsIntraCranYes | Emergency intracranial surgical intervention scheduled at ER discharge (please specify) | 1 == Craniotomy for haematoma/contusion 2 == Decompressive Craniectomy 3 == Depressed skull fracture 99 == Other intracranial procedure |
Documents emergency intracranial surgery performed in study hospital. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERIntracranialSurg |
| InjuryHx.EmerSurgIntraCranSurviveNoSurg | Emergency intracranial surgical interventions scheduled at ER discharge: The short term survival chances of the patients if I DO NOT operate will be | "InjuryHx.EmerSurgIntraCranSurviveNoSurg" and "InjuryHx.EmerSurgIntraCranSurviveYesSurg" These 2 variables aim to capture information on the surgeon's expectations, eg if the surgeon considers a realistic expectation of benefit, or performs the surgery as a "last resort" in a likely hopeless case. 'The short term survival chances of the patients if I DO NOT operate will be (in %)' | |
| InjuryHx.EmerSurgIntraCranSurviveYesSurg | Emergency intracranial surgical interventions scheduled at ER discharge: The short term survival chances of the patients if I DO operate will be | "InjuryHx.EmerSurgIntraCranSurviveNoSurg" and "InjuryHx.EmerSurgIntraCranSurviveYesSurg" These 2 variables aim to capture information on the surgeon's expectations, eg if the surgeon considers a realistic expectation of benefit, or performs the surgery as a "last resort" in a likely hopeless case. 'The short term survival chances of the patients if I DO operate will be (in %)' | |
| InjuryHx.ERDestICDCodes1 | (1) ICD code at ER discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes10 | Up to 16 fields to enter ICD codes at ER discharge (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes11 | Up to 16 fields to enter ICD codes at ER discharge (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes12 | Up to 16 fields to enter ICD codes at ER discharge (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes13 | Up to 16 fields to enter ICD codes at ER discharge (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes14 | Up to 16 fields to enter ICD codes at ER discharge (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes15 | Up to 16 fields to enter ICD codes at ER discharge (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes16 | Up to 16 fields to enter ICD codes at ER discharge (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes2 | (2) ICD code at ER discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes3 | (3) ICD code at ER discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes4 | (4) ICD code at ER discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes5 | (5) ICD code at ER discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes6 | (6) ICD code at ER discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes7 | (7) ICD code at ER discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes8 | (8) ICD code at ER discharge | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodes9 | Up to 16 fields to enter ICD codes at ER discharge (of hospital administration) | Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 | |
| InjuryHx.ERDestICDCodesVersion | ICD code version at ER discharge | 9 == ICD-9 10 == ICD-10 |
Reflects the version used: ICD-9 or ICD-10. Up to 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients discharged directly from the ER. For patients admitted to hospital or ICU, ICD codes are documented in: Hospital.ICDCode1 and Hospital.ICUDischargeICDCode1 |
| InjuryHx.ERDischHomeSchedApptOutpatient | Any out-patient visit scheduled following ER discharge | 0 == No 1 == Yes 88 == Unknown |
Reflects the scheduled appointments for patients discharged from ER to home or to another facility. The scheduled appointments gives details on Outpatient visit, Referred to general practitioner, study protocol follow up and MR study planned. |
| InjuryHx.ERDischHomeSchedApptOutpatientDate | Date of the out-patient visit following ER discharge | Reflects the scheduled appointments for patients discharged from ER to home or to another facility. The scheduled appointments gives details on Outpatient visit, Referred to general practitioner, study protocol follow up and MR study planned. | |
| InjuryHx.ERDischHomeSchedApptReferToGP | Referred to general practitioner | 0 == No 1 == Yes 88 == Unknown |
Reflects the scheduled appointments for patients discharged from ER to home or to another facility. The scheduled appointments gives details on Outpatient visit, Referred to general practitioner, study protocol follow up and MR study planned. |
| InjuryHx.ERDischHomeSchedApptStudyProtoFU | Study protocol follow-up | 0 == No 1 == Yes 88 == Unknown |
Reflects the scheduled appointments for patients discharged from ER to home or to another facility. The scheduled appointments gives details on Outpatient visit, Referred to general practitioner, study protocol follow up and MR study planned. |
| InjuryHx.ERDischHomeTypeOfCarePlanned | Type of care planned following ER discharge | 0 == None 1 == Symptomatic treatment or/and advice for the next 24/48h 2 == Systematic follow-up visit by GP 3 == Systematic follow-up visit by specialist practitioner 4 == Oral information on TBI, its possible late consequences, and where to consult in case of difficulties 5 == Written information on TBI, its possible late consequences, and where to consult in case of difficulties |
Reflects the type of care planned for patients discharged from ER to home or to another facility. |
| InjuryHx.ERDischMotivForDestChoice | Motivation for the choice of destination from ER | 1 == Normal CT 2 == Medical necessity 3 == Social circumstances 4 == No (ICU-) beds available 5 == Requiring specialized facilities 88 == Unknown 99 == Other |
WHY Question: documents main reason for choice of destination at ER discharge. |
| InjuryHx.ERDischMotivForDestChoiceOther | Other destination from ER (please specify) | WHY Question: documents main reason for choice of destination after ER discharge --> Other | |
| InjuryHx.ExternaAIS | Externa (skin) AIS | AIS score for the Externa (skin) region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.ExternaDesc | Externa (skin) injury description | 1 == No values yet | Injury description related to the AIS/ISS score for the Externa (skin) region. |
| InjuryHx.FaceAIS | Face AIS | AIS score for the Face (incl.maxillofacial) region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.FaceDesc | Face injury description | 99 == Other 5 == Zygomatic arch fracture 4 == Orbital fracture 2 == Maxillo-facial fracture le Fort II 3 == Maxillo-facial fracture le Fort III 1 == Maxillo-facial fracture le Fort I |
Injury description related to the AIS/ISS score for the Face (incl.maxillofacial) region |
| InjuryHx.FirstHospAssmtCondition | GCS assessment conditions at First Hospital | 0 == No sedation or paralysis 2 == Paralyzed 1 == Sedated 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This Describes the condition under which the GCS was assessed at First Hospital. |
| InjuryHx.GcsEDArrAssmtCond | GCS assessment conditions at ER arrival | 99 == Other 0 == No sedation or paralysis 2 == Paralyzed 1 == Sedated 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the condition under which the GCS was assessed at Arrival to ER of the study hospital. |
| InjuryHx.GCSEDArrEyes | Eye opening (E) response at ER arrival | 4 == 4-Spontaneously 3 == 3-To speech 2 == 2-To pain 1 == 1-None S == Untestable (swollen) UN == Unknown O == Untestable (other) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the GCS Eye opening at Arrival to ER of study hospital. |
| InjuryHx.GCSEDArrMotor | Motor (M) response at ER arrival | 6 == 6-Obeys command 5 == 5-Localizes to pain 4 == 4-Normal flexion/withdrawal 3 == 3-Abnormal flexion 2 == 2-Abnormal extension 1 == 1-None P == Untestable (Deep sedation/paralyzed) O == Untestable (Other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the GCS Motor score at Arrival to ER of study hospital. |
| InjuryHx.GcsEDArrNotDone | GCS at arrival of study hospital Not done | 77 == Not done / Results not available | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This indicates that GCS at Arrival to Study hospital was not done. |
| InjuryHx.GCSEDArrScore | GCS score at ER arrival | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This is a Calculated score for Arrival at ER of study hospital: GCSEDArrEyes + GCSEDArrMotor + GCSEDArrVerbal. If one or more of these is Untestable or unknown then = "No Sum" | |
| InjuryHx.GcsEDArrScoreDate | Date of GCS assessment at ER arrival | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the date of assessment at Arrival to ER of the study hospital. | |
| InjuryHx.GcsEDArrScoreTime | Time of GCS assessment at ER arrival | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the time of assessment at Arrival to ER of the study hospital. | |
| InjuryHx.GCSEDArrVerbal | Verbal (V) response at ER arrival | 5 == 5-Oriented 4 == 4-Confused 3 == 3-Inappropriate words 2 == 2-Incomprehensible sound 1 == 1-None T == Untestable (Tracheotomy/endotracheal tube) O == Untestable (Other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects GCS Verbal score at Arrival to ER of study hospital |
| InjuryHx.GcsEDDischAssmtCond | GCS assessment conditions poststabilization | 99 == Other 0 == No Sedation or Paralysis 2 == Paralyzed 1 == Sedated 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the condition under which the GCS was assessed POST-STABILIZATION. |
| InjuryHx.GCSEDDischEyes | Eye opening (E) response poststabilization | 4 == 4-Spontaneously 3 == 3-To speech 2 == 2-To pain 1 == 1-None O == Untestable (other) UN == Unknown S == Untestable (swollen) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects GCS eye opening for the assessment POST-STABILIZATION. |
| InjuryHx.GCSEDDischMotor | Motor (M) response poststabilization | 6 == 6-Obeys command 5 == 5-Localizes to pain 4 == 4-Normal flexion/withdrawal 3 == 3-Abnormal flexion 2 == 2-Abnormal extension 1 == 1-None P == Untestable (Deep sedation/paralyzed) UN == Unknown O == Untestable (Other) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects GCS Motor score for the assessment POST-STABILIZATION. |
| InjuryHx.GcsEDDischNotDone | GCS at ER discharge Not done | 77 == Not done / Results not available | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This indicates that GCS at Post-stabilization was not done. |
| InjuryHx.GCSEDDischScore | GCS score poststabilization | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This is the Calculated score for the POST-STABILIZATION assessment: GCSEDDischEyes + GCSEDDischMotor + GCSEDDischVerbal. If one or more of these is Untestable or unknown then = "No Sum" | |
| InjuryHx.GcsEDDischScoreDate | Date of GCS assessment poststabilization | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects Date for the assessment POST-STABILIZATION. | |
| InjuryHx.GcsEDDischScoreTime | Time of GCS assessment poststabilization | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the Time for the assessment POST-STABILIZATION. | |
| InjuryHx.GCSEDDischVerbal | Verbal (V) response poststabilization | 5 == 5-Oriented 4 == 4-Confused 3 == 3-Inappropriate words 2 == 2-Incomprehensible sound 1 == 1-None T == Untestable (Tracheotomy/endotracheal tube) O == Untestable (Other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects GCS Verbal score for the assessment POST-STABILIZATION. |
| InjuryHx.GCSFirstHospEyes | Eye opening (E) response at First Hospital | 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously S == Untestable (swollen) O == Untestable (other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects GCS eye opening for the assessment at First Hospital. |
| InjuryHx.GCSFirstHospMotor | Motor (M) response at First Hospital | 1 == 1-None O == Untestable (Other) 2 == 2-Abnormal extension 3 == 3-Abnormal flexion 4 == 4-Normal flexion/withdrawal 5 == 5-Localizes to pain 6 == 6-Obeys command P == Untestable (Deep sedation/paralyzed) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects GCS Motor score for the assessment at First Hospital. |
| InjuryHx.GCSFirstHospNotDone | GCS at arrival of first hospital Not done | 77 == Not done / Results not available | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This indicates that GCS at for the assessment at First hospital was not done. |
| InjuryHx.GCSFirstHospPupilLftEyeMeasure | Left eye pupil size at First Hospital | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects Left Pupil Size for the assessment at First Hospital. | |
| InjuryHx.GCSFirstHospPupilLftEyeMeasureUnkUnt | Left pupil at first hospital Untestable/Unknown | 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This indicates that Left Pupil size was untestable/unknown for the assessment at First Hospital. |
| InjuryHx.GCSFirstHospPupilReactivityLightLftEyeReslt | Left eye pupil reactivity at First Hospital | 3 == - (Negative) 1 == + (Sluggish) 2 == + (Brisk) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the reactivity of the Left Pupil for the assessment at First Hospital. |
| InjuryHx.GCSFirstHospPupilReactivityLightRghtEyeReslt | Right eye pupil reactivity at First Hospital | 3 == - (Negative) 1 == + (Sluggish) 2 == + (Brisk) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the reactivity of the Right Pupil for the assessment at First Hospital. |
| InjuryHx.GCSFirstHospPupilRightEyeMeasure | Right eye pupil size at First Hospital | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects Right Pupil Size for the assessment at First Hospital. | |
| InjuryHx.GCSFirstHospPupilRightEyeMeasureUnkUnt | Right pupil at first hospital Untestable/Unknown | 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects that the Right Pupil size was Untestable/Unknown for the assessment at First Hospital. |
| InjuryHx.GCSFirstHospPupilSymmetry | Pupil symmetry at First Hospital | 3 == Unequal L>R 1 == Equal 2 == Unequal R>L 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the pupil symmetry for the assessment at First Hospital. |
| InjuryHx.GCSFirstHospReportedTotalScore | GCS sum score at first hospital | 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 11 == 11 12 == 12 13 == 13 14 == 14 15 == 15 |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects Score by investigators in case component scores not available, but GCS sum score available for the assessment at First Hospital. |
| InjuryHx.GCSFirstHospScore | GCS score at First Hospital | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This is the Calculated Score for the assessment at First Hospital: GCSFirstHospEyes + GCSFirstHospMotor + GCSFirstHospVerbal. If one or more of these is Untestable or unknown then = "No Sum" Sum Score may be recorded with no components | |
| InjuryHx.GCSFirstHospScoreDate | Date of GCS assessment at First Hospital | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the Date for the assessment at First Hospital. | |
| InjuryHx.GCSFirstHospScoreTime | Time of GCS assessment at First Hospital | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the Time for the assessment at First Hospital. | |
| InjuryHx.GCSFirstHospVerbal | Verbal (V) response at First Hospital | 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented T == Untestable (tracheotomy/endotracheal tube) O == Untestable (Other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects the GCS Verbal score for the assessment at First Hospital. |
| InjuryHx.GCSMotorBaselineDerived | IMPACT Motor response | This is a derived variable calculated centrally. It represents the GCS motor score for baseline risk adjustment with missing values imputed using IMPACT methodology - take Poststabilisation value and if absent work back in time towards prehospital values until non-missing value found. RECOMMENDED FOR BASELINE RISK ADJUSTMENT. | |
| InjuryHx.GCSOtherAssmtConditions | GCS assessment conditions at other stage | 0 == No Sedation or Paralysis 2 == Paralyzed 1 == Sedated 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes the condition under which the GCS was assessed for the assessment "Other". |
| InjuryHx.GCSOtherDate | Date of GCS assessment at other stage | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes the Date for the assessment "Other". | |
| InjuryHx.GCSOtherEyes | Eye opening (E) response at other stage | O == Untestable (other) UN == Unknown 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously S == Untestable (swollen) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes the GCS Eye opening for the assessment "Other". |
| InjuryHx.GCSOtherMotor | Motor (M) response at other stage | 1 == 1-None 2 == 2-Abnormal extension 3 == 3-Abnormal flexion 4 == 4-Normal flexion/withdrawal 5 == 5-Localizes to pain 6 == 6-Obeys command P == Untestable (Deep sedation/paralyzed) O == Untestable (Other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes GCS Motor score for the assessment "Other". |
| InjuryHx.GCSOtherNotDone | GCS at other than prespecified assessments Not Done | 77 == Not done / Results not available | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This indicates that GCS was not done for the assessment "Other". |
| InjuryHx.GCSOtherPupilLftEyeMeasure | Left eye pupil size at other stage | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes Left Pupil Size for the assessment "Other". | |
| InjuryHx.GCSOtherPupilLftEyeMeasureUnkUnt | Left pupil at other than prespecified assessments Untestable/Unknown | 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This reflects when the Left Pupil Size was Untestable/Unknown for the assessment "Other". |
| InjuryHx.GCSOtherPupilReactivityLightLftEyeReslt | Left eye pupil reactivity at other stage | 3 == - (Negative) 1 == + (Sluggish) 2 == + (Brisk) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes the reactivity of the LEFT pupil for the assessment "Other". |
| InjuryHx.GCSOtherPupilRightEyeMeasure | Right eye pupil size at other stage | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes the Right pupil size for the assessment "Other". | |
| InjuryHx.GCSOtherPupilSymmetry | Pupil symmetry at other stage | 3 == Unequal L>R 2 == Unequal R>L 1 == Equal 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes the pupil symmetry for the assessment "Other". |
| InjuryHx.GCSOtherReactivityLightRghtEyeReslt | Right eye pupil reactivity at other stage | 3 == - (Negative) 1 == + (Sluggish) 2 == + (Brisk) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes the reactivity of the Right Pupil for the assessment "Other". |
| InjuryHx.GCSOtherRightEyeMeasureUnkUnt | Right pupil at other than prespecified assessments Untestable/Unknown | 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This reflects if the Right pupil was Untestable/Unknown for the assessment "Other". |
| InjuryHx.GCSOtherScore | GCS score at other stage | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This is the Calculated Score for the assessment "Other": GCSOtherEyes + GCSOtherMotor + GCSOtherVerbal. If one or more of these is Untestable or unknown then = "No Sum" Sum score may be reported when components not available | |
| InjuryHx.GCSOtherTime | Time of GCS assessment at other stage | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This reflects the Time for the assessment "Other". | |
| InjuryHx.GCSOtherVerbal | Verbal (V) response at other stage | 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented T == Untestable (tracheotomy/endotracheal tube) O == Untestable (Other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. There was also an additional option "Other" assessment. This describes the GCS Verbal score for the assessment "Other". |
| InjuryHx.GcsPreHospBestDate | Date of GCS assessment at accident scene | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the Date for the assessment at Scene Of Accident. | |
| InjuryHx.GCSPreHospBestEyes | Eye opening (E) response at accident scene | 3 == 3-To speech 2 == 2-To pain 1 == 1-None 4 == 4-Spontaneously S == Untestable (swollen) O == Untestable (Other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the GCS Eye opening for the assessment at Scene Of Accident. |
| InjuryHx.GCSPreHospBestMotor | Motor (M) response at accident scene | 5 == 5-Localizes to pain 4 == 4-Normal flexion/withdrawal 3 == 3-Abnormal flexion 2 == 2-Abnormal extension 1 == 1-None 6 == 6-Obeys command P == Untestable (Deep sedation/paralyzed) O == Untestable (Other) UN == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the GCS Motor score for the assessment at Scene Of Accident. |
| InjuryHx.GCSPreHospBestReportedTotalScore | GCS sum score at scene of accident | 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 11 == 11 12 == 12 13 == 13 14 == 14 15 == 15 |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. Score by investigators in case the component scores are not available, but GCS sum score available for the assessment at Scene Of Accident. |
| InjuryHx.GCSPreHospBestScore | GCS score at accident scene | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This is the Calculated Score for the assessment at Scene Of Accident: GCSPreHospBestEyes + GCSPreHospBestMotor + GCSPreHospBestVerbal. If one or more of these is Untestable or unknown then = "No Sum" GCS sum score may be recorded when components not available - check "InjuryHx.GCSPreHospBestReportedTotalScore" | |
| InjuryHx.GcsPreHospBestTime | Time of GCS assessment at accident scene | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the Time for the assessment at Scene Of Accident. | |
| InjuryHx.GCSPreHospBestVerbal | Verbal (V) response at accident scene | 5 == 5-Oriented 2 == 2-Incomprehensible sound 1 == 1-None 4 == 4-Confused 3 == 3-Inappropriate words T == Untestable (Tracheotomy/endotracheal tube) UN == Unknown O == Untestable (Other) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the GCS Verbal score for the assessment at Scene Of Accident. |
| InjuryHx.GcsPreHospLftEyeMeasr | Left eye pupil size at accident scene | 6 == 6 5 == 5 4 == 4 3 == 3 2 == 2 1 == 1 7 == 7 8 == 8 9 == 9 |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the Left Pupil Size for the assessment at Scene Of Accident. |
| InjuryHx.GcsPreHospNotDone | GCS at scene of accident Not done | 77 == Not Done / Results not available | Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. Indication that GCS for the assessment at Scene of accident was not done. |
| InjuryHx.GCSPreHospPupilLftEyeMeasureUnkUnt | Left pupil at scene of accident Untestable/Unknown | 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes if the Left Pupil was Untestable/Unknown for the assessment at Scene Of Accident. |
| InjuryHx.GCSPreHospPupilReactivityLghtLftEyeResult | Left eye pupil reactivity at accident scene | 1 == + (Sluggish) 3 == - (Negative) 2 == + (Brisk) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the reactivity of the Left pupil for the assessment at Scene Of Accident. |
| InjuryHx.GCSPreHospPupilReactivityLghtRghtEyeResult | Right eye pupil reactivity at accident scene | 1 == + (Sluggish) 3 == - (Negative) 2 == + (Brisk) |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the reactivity of the Right pupil for the assessment at Scene Of Accident. |
| InjuryHx.GCSPreHospPupilRightEyeMeasureUnkUnt | Right pupil at scene of accident Untestable/Unknown | 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This reflects if the Right Pupil was Untestable/Unknown for the assessment at Scene Of Accident. |
| InjuryHx.GCSPreHospPupilSymmetry | Pupil symmetry at accident scene | 1 == Equal 3 == Unequal L>R 2 == Unequal R>L 66 == Untestable 88 == Unknown |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the Pupil symmetry for the assessment at Scene Of Accident. |
| InjuryHx.GcsPreHospRghtEyeMeasr | Right eye pupil size at accident scene | 9 == 9 6 == 6 5 == 5 4 == 4 3 == 3 2 == 2 1 == 1 7 == 7 8 == 8 |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the Right Pupil Size for the assessment at Scene Of Accident. |
| InjuryHx.GCSScoreBaselineDerived | IMPACT GCS score | This is a derived variable calculated centrally. It represents the total GCS (single timepoint) for baseline risk adjustment with missing values imputed using IMPACT methodology - take Poststabilisation value and if absent work back in time towards prehospital values until non-missing value found. Intubated / untestable V score treated as unknown. RECOMMENDED FOR BASELINE RISK ADJUSTMENT. | |
| InjuryHx.HeadNeckAIS | Head and Neck AIS | 0 == 0 5 == 5 6 == 6 4 == 4 2 == 2 3 == 3 1 == 1 |
AIS score for the Head and Neck region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| InjuryHx.HeadNeckDesc | Head and Neck injury description | Injury description for the Head and Neck AIS. | |
| InjuryHx.HighestGCSMotorDerived | Highest Motor response | This is a derived variable calculated centrally. It represents the GCS motor score for baseline risk adjustment with missing values imputed using ‘highest’ value (best neurology) methodology- take best neurology of any of prehospital to Poststabilisation time points. DEPRECATED: we recommend using GCSMotorBaselineDerived for baseline risk adjustment instead (higher pseudo-R-squared in proportional odds model). | |
| InjuryHx.HighestGCSTotalDerived | Highest GCS score | This is a derived variable calculated centrally. Total GCS (single timepoint) for baseline risk adjustment with missing values imputed using ‘highest’ value (best neurology) methodology - take best neurology of any of prehospital to Poststabilisation time points. Intubated / untestable V score treated as unknown. DEPRECATED: we recommend using GCSScoreBaselineDerived for baseline risk adjustment instead (higher pseudo-R-squared in proportional odds model). | |
| InjuryHx.HighestPupilsDerived | Highest unreactive pupils | This is a derived variable calculated centrally. Number of unreactive pupils for baseline risk adjustment with missing values imputed using ‘highest’ value (best neurology) methodology- take best neurology of any of prehospital to Poststabilisation time points. Untestable pupil ignored: I.e. 1 reactive + 1 untestable = 1 reactive (this assumption applies only to a small proportion of the data). DEPRECATED: we recommend using PupilsBaselineDerived for baseline risk adjustment instead (higher pseudo-R-squared in proportional odds model). | |
| InjuryHx.InjArea | Area of injury | 88 == Unknown 2 == Rural 1 == Urban (city) |
Reflects the area where the injury took place (urban or rural). |
| InjuryHx.InjCause | Cause of injury | 1 == Road traffic incident 2 == Incidental fall 3 == Other non-intentional injury 4 == Violence/assault 5 == Act of mass violence 6 == Suicide attempt 99 == Other 88 == Unknown |
Reflects the cause of injury. |
| InjuryHx.InjCauseOther | Other cause of injury (please specify) | Reflects if the cause of injury was "other" than the pre-listed causes. See also InjuryHx.InjCause | |
| InjuryHx.InjIndContactSportType | Sports injury: Individual contact sports | 1 == Boxing 2 == Martial Arts 99 == Other |
Reflects the kind of contact sport involved as cause of injury - Only applicable for sports/recreational injuries |
| InjuryHx.InjIndSportTypeOther | Sports injury: Other individual contact sports (please specify) | Reflects if the kind of contact sport involved as cause of injury was "other" than the pre-defined list - Only applicable for sports/recreational injuries. See also InjuryHx.InjIndContactSportType | |
| InjuryHx.InjIntention | Intention | 3 == Undetermined 1 == Intentional 2 == Unintentional |
Reflects if the cause on injury was intentional or unintentional. |
| InjuryHx.InjMech | Mechanism of injury | 1 == High velocity trauma (acceleration/deceleration) 2 == Direct impact: blow to head 3 == Direct impact: head against object 6 == Ground level fall 7 == Fall from height > 1 meter/5 stairs 99 == Other closed head injury |
Reflects the mechanism of injury - only applicable for Closed TBI |
| InjuryHx.InjMechOther | Mechanism of injury: Other closed head injury (please specify) | Reflects if the mechanism of injury was "other" than the pre-defined list - only applicable for Closed TBI. See also InjuryHx.InjMech | |
| InjuryHx.InjOtherPartyInvolved | Was other party involved? | 77 == N/A | Reflects that "another party involved in the cause of injury = N/A". |
| InjuryHx.InjOtherPartySleepingPills | Was other party under the influence of sedatives or sleeping pills? | 0 == No 1 == Suspect 2 == Definite 88 == Unknown |
Reflects if sedatives or sleeping pills were involved in the cause of injury. |
| InjuryHx.InjPenetratingType | Mechanism of penetrating injury | 1 == Gunshot wound 2 == Fragment (incl. shell/shrapnel) 99 == Other penetrating brain injury |
Reflects the mechanism of injury - only applicable if Penetrating brain injury |
| InjuryHx.InjPenetratingTypeOther | Other mechanism of penetrating injury (please specify) | Reflects if the mechanism of injury was other than the pre-defined list - only applicable if Penetrating brain injury. See also InjuryHx.InjPenetratingType | |
| InjuryHx.InjPlace | Place of injury | 99 == Other 3 == Work/school 88 == Unknown 5 == Military deployment 4 == Sport/Recreational 1 == Street/highway 2 == Home/domestic 6 == Public location (eg. bar, station, nightclub) |
Reflects the place where the TBI injury occurred. |
| InjuryHx.InjPlaceOther | Other place of injury (please specify) | Reflects if the place where the TBI injury occurred was "other" than the pre-defined list. See also InjuryHx.InjPlace | |
| InjuryHx.InjRecSportType | Sports injury: Other sports and recreational activities | 1 == Rollerblading/Skateboarding/Scootering 2 == Skiing 3 == Snowboarding 4 == Hiking/Climbing 5 == Horseriding 6 == Golf 7 == Cycling 8 == Off-road vehicular sports 9 == Water sports 10 == Playground activity 99 == Other 88 == Unknown |
Reflects of the cause of injury was "Other Sport & Recreational Activities" - Only applicable for sports/recreational injuries |
| InjuryHx.InjRecSportTypeOther | Sports injury: Any other sports and recreational activities (please specify) | Describes which was the cause of injury if "Other Sport & Recreational Activities" - Only applicable for sports/recreational injuries | |
| InjuryHx.InjRoadAccEjectedFromVehicle | Road traffic accident injury: Ejected from vehicle | 0 == No 1 == Yes 88 == Unknown |
Reflects if the subject was ejected from the vehicle - Only applicable if subject was motor vehicle occupant |
| InjuryHx.InjRoadAccOtherParty | Road traffic accident injury: Victim | 1 == Motor vehicle 2 == Pedestrian 3 == Cyclist 4 == Moped/Scooter 5 == Tram/Bus 6 == Train/Metro 7 == Obstacle 10 == Motor Bike 88 == Unknown 99 == Other 11 == Lorry (camion) |
Reflects if another party was involved in the Cause of Injury in case of a Road Traffic accident |
| InjuryHx.InjRoadAccOtherPartyInvolved | Road traffic accident injury: Other party involved | 0 == No 1 == Yes 88 == Unknown |
Describes if another party than the pre-defined list was involved in the Cause of Injury in case of a Road Traffic accident |
| InjuryHx.InjRoadAccOtherPartyOther | Road traffic accident injury: Other victim (please specify) | Describes which other party than the pre-defined list was involved in the Cause of Injury in case of a Road Traffic accident | |
| InjuryHx.InjRoadAccVictim | Road traffic accident injury: Victim | 1 == Motor vehicle occupant 2 == Pedestrian 3 == Cyclist 4 == Moped/Scooter 5 == Motor Bike 99 == Other |
Describes the type of victim in case of a Road traffic accident. |
| InjuryHx.InjRoadAccVictimOther | Road traffic accident injury: Other victim (please specify) | Reflects if the type of victim was "other" than the predefined list in case of a Road traffic accident. | |
| InjuryHx.InjRoadAccVictimVehiclePlace | Road traffic accident injury: Occupant's placement in vehicle | 1 == Driver 2 == Front seat passenger 3 == Back seat passenger |
Reflects the occupant placement of the victim in the vehicle in case of a Road Traffic Accident |
| InjuryHx.InjSafetyAirbag | Airbag deployed | 88 == Unknown 77 == Not Applicable 0 == No 1 == Yes |
Perfects if the airbag was deployed - Only applicable if subject was motor vehicle occupant |
| InjuryHx.InjSafetyHelmet | Helmet used | 88 == Unknown 77 == Not Applicable 0 == No 1 == Yes |
Reflects if the victim was wearing a safety helmet. Only applicable in case of cyclist, scooter, motorbike incident. However, may also have been scored for various sports injuries. |
| InjuryHx.InjSafetySeatbelt | Seatbelt used | 88 == Unknown 77 == Not Applicable 0 == No 1 == Yes |
Reflects if the victim was wearing a seat-belt. Only applicable if subject was motor vehicle occupant |
| InjuryHx.InjTeamSportType | Sports injury: Team sports | 1 == Football (soccer) 2 == Rugby 3 == Field Hockey 4 == Ice Hockey 5 == Lacrosse 99 == Other |
Reflects the type of team sport that was the cause of the injury - Only applicable for sports/recreational injuries |
| InjuryHx.InjTeamSportTypeOther | Sports injury: Other team sports (please specify) | Reflects if the type of team sport that was the cause of the injury was "other" than the predefined list- Only applicable for sports/recreational injuries | |
| InjuryHx.InjType | Type of injury | 1 == Closed 88 == Unknown 3 == Crush 2 == Blast 5 == Penetrating 6 == Penetrating-perforating 7 == Penetrating-tangential 8 == Closed with open depressed skull fracture |
Details of Injury are captured in 4 different variables: Type of Injury, Place of Injury, Cause of Injury and Mechanism of injury. This reflects the type of injury. |
| InjuryHx.InjVictimAlcoholTestType | Test used to determine whether the victim was under the influence of alcohol | Blood == Blood Test Breath == Breath Test |
Reflects type of alcohol test used (breath test or blood test) for the victim |
| InjuryHx.InjVictimBloodAlcoholmgdL | Alcohol level in victim's blood | Reflects the level of mg/dL alcohol recorded in the victim during the alcohol test in case alcohol was related to the cause of injury. | |
| InjuryHx.InjVictimBloodAlcoholpermil | Alcohol level in victim's blood | Reflects the level of alcohol per mil (0/00) recorded in the victim during the alcohol test in case alcohol was related to the cause of injury. | |
| InjuryHx.InjVictimBloodAlcoholUnit | Unit used for alcohol level of victim (if applicable) | 1 == mg/dL 2 == per mil (0/00) |
Reflects the value used for alcohol level recorded during the alcohol test of the victim in case alcohol was related to the cause of injury. |
| InjuryHx.InjVictimDrugsTypeOther | If the victim was under the influence of other drugs (please specify) | Describes which other drugs where involved for the victim in the cause of injury. | |
| InjuryHx.InjVictimSleepingPills | Was victim under the influence of sedatives or sleeping pills? | 0 == No 1 == Suspect 2 == Definite 88 == Unknown |
Reflects if for the victim use of sedatives of sleeping pills were involved in the cause of injury. |
| InjuryHx.InjVictimTypeDrugs | Was victim under the influence of drugs? | 88 == Unknown 1 == Cannabis 2 == Cocaine 3 == Methamphetamine's 4 == Opioids 5 == XTC 99 == Other |
Rf elects which kind of drugs were involved in the cause of injury at the victims site. |
| InjuryHx.InjViolence | Type of violence injury | 1 == Robbery 2 == Interpersonal violence (fight) 3 == Domestic assault 4 == Child abuse 5 == Gang violence 6 == Military deployment 99 == Other 88 == Unknown |
Reflects the type of violence used as cause of injury - Only applicable if violence was the cause of injury |
| InjuryHx.InjViolenceOther | Other type of violence injury (please specify) | Reflects the "other" type of violence than the predefined list used as cause of injury - Only applicable if violence was the cause of injury | |
| InjuryHx.InjViolenceOtherPartyAlcohol | Substance abuse: Other party under the influence of Alcohol | 1 == Definite 2 == Suspect 0 == No 88 == Unknown |
Information on drug and alcohol abuse of possible influence on the incident is different for victim versus "other party" (if involved) This reflects if alcohol was involved in the cause of injury for the other party involved |
| InjuryHx.InjViolenceOtherPartyDrugs | Substance abuse: Other party under the influence of Drugs | 0 == No 2 == Suspect 1 == Definite 88 == Unknown |
Information on drug and alcohol abuse of possible influence on the incident is different for victim versus "other party" (if involved). This reflects if drugs was involved as cause of injury for the other party involved |
| InjuryHx.InjViolenceVictimAlcohol | Substance abuse: Victim under the influence of Alcohol | 0 == No 2 == Suspect 1 == Definite 88 == Unknown |
Information on drug and alcohol abuse of possible influence on the incident is different for victim versus "other party" (if involved) This reflects alcohol involvement for the victim. |
| InjuryHx.InjViolenceVictimDrugs | Substance abuse: Victim under the influence of Drugs | 0 == No 2 == Suspect 1 == Definite 88 == Unknown |
Information on drug and alcohol abuse of possible influence on the incident is different for victim versus "other party" (if involved) This reflects drugs involvement for the victim. |
| InjuryHx.InterventRadiology | Interventional radiology scheduled at ER discharge | 0 == No 1 == Yes 88 == Unknown |
Reflects if at time of discharge from the ER some Interventional Radiology was scheduled |
| InjuryHx.LOCAOC | AOC (Alteration of Consciousness) | 88 == Unknown 3 == Suspected 1 == Yes, immediate 0 == No 2 == Not tested due to LOC 4 == Yes, delayed onset |
TBI may be present in the absence of LOC or PTA. Alteration of Consciousness (AOC) is then the main presenting symptom and considered diagnostic of TBI. Details of symptoms are captured in the Rivermead Questionnaire. |
| InjuryHx.LOCAOCDelayedHrs | AOC: Number of hours after injury that alteration of consciousness occurred | TBI may be present in the absence of LOC or PTA. Alteration of Consciousness (AOC) is then the main presenting symptom and considered diagnostic of TBI. This reflects the Number of hours after injury that alteration of consciousness occurred - Only in case of delayed onset. Details of symptoms are captured in the Rivermead Questionnaire. | |
| InjuryHx.LOCAOCDelayedHrsUnk | Number of hours after injury that AOC occured Unknown | TBI may be present in the absence of LOC or PTA. Alteration of Consciousness (AOC) is then the main presenting symptom and considered diagnostic of TBI. This reflects if the Number of hours after injury that alteration of consciousness occurred = Unknown. Details of symptoms are captured in the Rivermead Questionnaire. | |
| InjuryHx.LOCAOCDuration | AOC: Duration of LOC | 88 == Unknown 7 == >7 days 6 == 1-7 days 5 == 1-24 hours 4 == 30-59 minutes 3 == 1-29 minutes 2 == <1 minute 0 == None |
TBI may be present in the absence of LOC or PTA. Alteration of Consciousness (AOC) is then the main presenting symptom and considered diagnostic of TBI. This reflects the Duration of alteration of consciousness. Details of symptoms are captured in the Rivermead Questionnaire. |
| InjuryHx.LOCAOCReportedBy | AOC: Source of verification | 4 == Medical chart 3 == Clinical interview 2 == Witness 1 == Patient 5 == Not available |
TBI may be present in the absence of LOC or PTA. Alteration of Consciousness (AOC) is then the main presenting symptom and considered diagnostic of TBI. This reflects by whom the alteration of consciousness was reported. Details of symptoms are captured in the Rivermead Questionnaire. |
| InjuryHx.LOCDuration | LOC: Duration of LOC | 6 == 1-7 days 5 == 1-24 hours 3 == 1-29 minutes 4 == 30-59 minutes 2 == <1 minute 0 == No return of consciousness 7 == >7 days 88 == Unknown |
LOC and PTA are reported as part of the neurological assessment. This reflects the duration of Loss of Consciousness (LOC). Note: for patients admitted to hospital, the time to obeying commands is documented on hospital discharge: Hospital.HospDischargeTimeToObeyCommands |
| InjuryHx.LOCGCSSumDet | GCS sum score deterioration within one hour after presentation | 88 == Unknown 2 == 2 or more points 1 == 1 point 0 == None |
LOC and PTA are reported as part of the neurological assessment. This reflects for the Loss of Consciousness (LOC) the GCS sum score deterioration within one hour after presentation. |
| InjuryHx.LOCLossOfConsciousness | LOC (Loss Of Consciousness) | 88 == Unknown 1 == Yes 3 == Suspected 0 == No |
LOC and PTA are reported as part of the neurological assessment. Loss of Consciousness (LOC) is a definite sign of TBI. However, TBI may be present without any LOC. Presence and duration is captured. |
| InjuryHx.LOCLucidInterval | LOC: Lucid Interval | 1 == Yes 0 == No 88 == Unknown |
LOC and PTA are reported as part of the neurological assessment. Lucid Interval is defined as a temporary improvement in a patient's condition after a traumatic brain injury, after which the condition deteriorates. A lucid interval is especially indicative of an epidural hematoma. An estimated 20 to 50% of patients with epidural hematoma experience such a lucid interval. |
| InjuryHx.LOCLucidIntervalHrs | LOC: Number of hours after injury that secondary deterioration occurred | Lucid Interval is defined as a temporary improvement in a patient's condition after a traumatic brain injury, after which the condition deteriorates. This reflects the Number of hours after injury that secondary deterioration occurred (in case Lucid Interval = Yes) | |
| InjuryHx.LOCLucidIntervalHrsUnk | Number of hours after injury that secondary deterioration occured Unknown | Lucid Interval is defined as a temporary improvement in a patient's condition after a traumatic brain injury, after which the condition deteriorates. This reflects if the Number of hours after injury that secondary deterioration occurred is Unknown (in case Lucid Interval = Yes). | |
| InjuryHx.LOCPTA | PTA (Post Traumatic Amnesia) | 3 == Suspected 1 == Yes, ongoing 88 == Unknown 0 == No 2 == Yes, resolved |
LOC and PTA are reported as part of the neurological assessment. Post-traumatic amnesia (PTA) is the period after the injury that the patient cannot remember. In contrast to retrograde amnesia, the duration of PTA remains constant over time. To document presence/absence of PTA on discharge from the ER, the GOAT questionnaire is requested: Outcomes.GOATDate |
| InjuryHx.LOCPTADuration | PTA: Duration of LOC | 28 == >28 6 == 1-7 days 5 == 1-24 hours 2 == <1 hour 88 == Unknown 77 == N/A (e.g. death) 0 == None 8 == 1-2 hours 9 == 2-4 hours 10 == 4-24 hours 11 == >1 day 7 == 7-28 days |
LOC and PTA are reported as part of the neurological assessment. This variable is recorded only Only if PTA is yes. The duration of PTA reflects the severity of TBI. In patients with more sever TBI, the duration of PTA cannot be determined on presentation. For patients admitted to hospital, the duration of TBI in days is also captured on hospital discharge:.Hospital.HospDischPTADays |
| InjuryHx.LOCPTAReportedBy | PTA: Source of verification | 1 == Patient 2 == Witness 3 == Retrospective assessment/ clinical interview 4 == Medical chart 5 == Not available 6 == Prospective assessment with PTA scale |
LOC and PTA are reported as part of the neurological assessment. This reflects by whom PTA is reported. |
| InjuryHx.LOCPTAScale | PTA: Scale used | 1 == GOAT 2 == Westmead 3 == O-Log 4 == Nijmegen PTA scale 99 == Other |
LOC and PTA are reported as part of the neurological assessment. In some centres, prospective assessment of amnesia (PTA) after TBI is performed using a dedicated scale. This variable documents the scale used. |
| InjuryHx.LOCReportedBy | LOC: Source of verification | 2 == Witness 1 == Self report 3 == Clinical interview 4 == Medical chart 5 == Not available |
LOC and PTA are reported as part of the neurological assessment. This variable reflects by whom LOC was reported. |
| InjuryHx.LOCRGA | Retrograde Amnesia | 1 == Yes 88 == Unknown 0 == No |
This reflects presence or absence of retrograde amnesia during neurological assessment. Amnesia after injury is a sign of TBI. Retrograde amnesia is the period before the injury that the patient cannot remember. The duration of retrograde amnesia becomes shorter as the injury is longer ago. The duration of retrograde amnesia is therefore dependent on time after injury at which it was assessed. |
| InjuryHx.LOCRGADur | Retrograde Amnesia: Duration | 88 == Unknown 2 == >= 30 minutes 1 == <30 0 == None |
This reflects the duration of retrograde amnesia is present during neurological assessment. |
| InjuryHx.LOCRGAReportBy | Retrograde Amnesia: Source of verification | 4 == Medical chart 5 == Not available 3 == Clinical interview 2 == Witness 1 == Self report |
This reflects by whom Retrograde amnesia was reported if present during neurological assessment. |
| InjuryHx.LowerExtremitiesAIS | Lower Extremities AIS | AIS score for Lower extremities as subdomain of Extremities and pelvic girdle. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.LowerExtremitiesDesc | Lower Extremities injury description | 2 == Tibia plateau fracture 3 == Tibia fracture 4 == Ankle fracture 5 == Calcaneus fracture 6 == Metatarsal/tarsal fracture (toe fracture) 7 == Fibula fracture 1 == Femoral fracture |
Injury Description for the AIS score for Lower extremities as subdomain of Extremities and pelvic girdle. |
| InjuryHx.LumbarSpineAIS | Lumbar Spine AIS | AIS score for Lumbar spine as subdomain of Abdomen/Pelvic contents. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.LumbarSpineDesc | Lumbar Spine injury description | 1 == Fracture 2 == Dislocation 3 == Sacral fracture 99 == Other |
Injury description for AIS score for Lumbar spine as subdomain of Abdomen/Pelvic contents. |
| InjuryHx.NeuroAssmtsAVPU | AVPU score at ER arrival | 88 == Unknown P == The patient responds to painful stimulation V == Patient responds to verbal stimulation A == Patient is awake U == The patient is completely unresponsive |
AVPU is scored as part of the neurological assessment on arrival to the ER. The AVPU scale (an acronym from "alert, voice, pain, unresponsive") is a system by which a health care professional can measure and record a patient's responsiveness, indicating their level of consciousness. |
| InjuryHx.PainScale | Pain rating (0 = No pain; 100 = Unbearable pain) | During neurological assessment at arrival to ER an overall rating was recorded for pain intensity going from 0 (zero pain) to 100 (unbearable pain). | |
| InjuryHx.PainScaleUnk | Pain intensity at ER arrival Untestable/Unknown | 88 == Unknown 77 == Untestable |
During neurological assessment at arrival to ER an overall rating was recorded for pain intensity going from 0 (zero pain) to 100 (unbearable pain). This variable reflects if the pain intensity was Untestable of Unknown. |
| InjuryHx.PelvicGirdleAIS | Pelvic Girdle AIS | AIS score for Pelvic Girdle as subdomain of Extremities and pelvic girdle. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.PelvicGirdleDesc | Pelvic Girdle injury description | 3 == Hip dislocation 2 == Hip fracture 1 == Pelvic fracture |
Injury description for AIS score for Pelvic Girdle as subdomain of Extremities and pelvic girdle. |
| InjuryHx.PreHospAssmtConditions | GCS assessment conditions at accident scene | 0 == No sedation or paralysis 1 == Sedated 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other 2 == Paralyzed |
Neurological assessment (GCS and pupils) was recorded for the scene of accident, the first hospital (if applicable), the Arrival to ER of the study hospital and post-stabilization. This describes the condition under which the GCS was assessed for the assessment at Scene Of Accident. |
| InjuryHx.PresArrivalMethod | Mode of transport from accident scene | 99 == Other 4 == Walk in or drop off 1 == Ambulance 2 == Helicopter 3 == Medical mobile team |
Reflects the mode of transportation used to transport the subject from the scene of accident to the hospital. |
| InjuryHx.PresCirculationTreatmentCPR | Circulation: CPR | The status of Airway, Breathing and Circulation on scene are documented. This records Emergency care treatment on scene performed with regard to Circulation: CPR (Cardio-pulmonary resuscitation) ER arrival status is documented at: InjuryHX.EDArrivalCirculation | |
| InjuryHx.PresCirculationTreatmentIVFluids | Circulation: IV Fluids | The status of Airway, Breathing and Circulation on scene are documented. This records Emergency care treatment on scene performed with regard to Circulation: IV Fluids ER arrival status is documented at: InjuryHX.EDArrivalCirculation | |
| InjuryHx.PresCirculationTreatmentNone | Circulation: No treatment | The status of Airway, Breathing and Circulation on scene are documented. This records Emergency care treatment on scene performed with regard to Circulation: None ER arrival status is documented at: InjuryHX.EDArrivalCirculation | |
| InjuryHx.PresCirculationTreatmentUnknown | Circulation treatment at on scenen Emergency care treatment Unknown | The status of Airway, Breathing and Circulation on scene are documented. This records Emergency care treatment on scene performed with regard to Circulation: Unknown ER arrival status is documented at: InjuryHX.EDArrivalCirculation | |
| InjuryHx.PresCTBrain | CT scan at First Hospital | 88 == Unknown 0 == No 1 == Yes |
In case of a Secondary referral (see InjuryHx.PresTBIref), details of procedures performed at the first hospital (not study hospital) were recorded. This reflects if a CT Brain was performed in the first hospital (not study hospital). |
| InjuryHx.PresEmergencyCare | Emergency medical care at accident scene | 0 == None 1 == Untrained person (by stander) 2 == Trainer/coach 3 == Military, non-medic 4 == Paramedic 5 == Nurse 6 == Physician 7 == Medical rescue team 99 == Other |
Reflects if and by whom emergency medical care was given at the scene of accident (highest level of assistance) |
| InjuryHx.PresEmergencyCareIntubation | Emergency care on scene: Intubation | 0 == No 1 == Yes 88 == Unknown |
Reflects if intubation was performed on scene. |
| InjuryHx.PresEmergencyCareSuppOxygen | Emergency care on scene: Supplemental oxygen | 0 == No 1 == Yes 88 == Unknown |
Reflects if supplemental oxygen was given on scene. |
| InjuryHx.PresEmergencyCareVentilation | Emergency care on scene: Mechanical ventilation | 0 == No 1 == Yes 88 == Unknown |
Reflects if Mechanical Ventilation was done on scene. |
| InjuryHx.PresEmergencyServiceAmbuBasic | Emergency service involved at accident scene: Ambulance (basic: EMT-B) | Reflects type of Emergency service involved at accident scene --> Ambulance (basic EMTB) | |
| InjuryHx.PresEmergencyServiceAmbuSpec | Emergency service involved at accident scene: Ambulance specialized (EMT-P) | Reflects type of Emergency service involved at accident scene --> Ambulance specialized (EMTP) | |
| InjuryHx.PresEmergencyServiceFirefighter | Emergency service involved at accident scene: Firefighter | Reflects type of Emergency service involved at accident scene --> Firefighter | |
| InjuryHx.PresEmergencyServiceHelicopter | Emergency service involved at accident scene: Helicopter | Reflects type of Emergency service involved at accident scene --> Helicopter | |
| InjuryHx.PresEmergencyServiceNone | Emergency service involved at accident scene: None | Reflects type of mergency service involved at accident scene --> None | |
| InjuryHx.PresEmergencyServicePolice | Emergency service involved at accident scene: Police | Reflects type of Emergency service involved at accident scene --> Police | |
| InjuryHx.PresERExtracranialSurg | Emergency Extracranial surgery at First Hospital | 1 == Yes 0 == No 88 == Unknown |
In case of a Secondary referral (see InjuryHx.PresTBIref), details of procedures performed at the first hospital (not study hospital) were recorded. This reflects if Emergency intracranial surgery was performed in the first hospital (not study hospital). |
| InjuryHx.PresERIntracranialSurg | Emergency Intracranial surgery at First Hospital | 88 == Unknown 0 == No 1 == Yes |
In case of a Secondary referral (see InjuryHx.PresTBIref), details of procedures performed at the first hospital (not study hospital) were recorded. This reflects if Emergency extracranial surgery was performed in the first hospital (not study hospital). Surgical procedures decided on to perform directly on arrival to the Study hospital are recorded within InjuryHx.EmergSurgInterventionsIntraCran. |
| InjuryHx.PresFHospDate | Date of arrival at the First Hospital | In case of a Secondary referral (see InjuryHx.PresTBIref), details of procedures performed at the first hospital (not study hospital) were recorded. First hospital is defined as the initial hospital to which the patient was brought before being transferred to Study hospital. This reflects Date of arrival to first hospital. | |
| InjuryHx.PresFHospTime | Time of arrival at the First Hospital | In case of a Secondary referral (see InjuryHx.PresTBIref), details of procedures performed at the first hospital (not study hospital) were recorded. First hospital is defined as the initial hospital to which the patient was brought before being transferred to Study hospital. This reflects Time of arrival to first hospital. | |
| InjuryHx.PresFirstOnSceneDate | Time of arrival of emergency service at accident scene | Reflects Times at accident scene --> First on scene --> Date | |
| InjuryHx.PresFirstOnSceneDepartUnknownTime | Departure time of EMS at accident scene N/A or Unknown | 88 == Unknown 77 == N/A if emergency service=none |
Reflects Times at accident scene --> Departure time -->N/A (if emergency service=none) or when Unknown |
| InjuryHx.PresFirstOnSceneDepartureDate | Date of departure of emergency service from accident scene | Reflects Times at accident scene --> Departure time --> Date | |
| InjuryHx.PresFirstOnSceneDepartureTime | Time of departure of emergency service from accident scene | Reflects Times at accident scene --> Departure time --> Time | |
| InjuryHx.PresFirstOnSceneTime | Time of arrival of emergency service at accident scene | Reflects Times at accident scene --> First on scene --> Time | |
| InjuryHx.PresFirstOnSceneUnknownTime | Arrival time of EMS at accident scene N/A or Unknown | 88 == Unknown 77 == N/A if emergency service=none |
Reflects if Time of arrival of EMS to incident scene = unknown or N/A (f.e. if no EMS involved) |
| InjuryHx.PresIntubation | Intubated at First Hospital | 88 == Unknown 0 == No 1 == Yes |
In case of a Secondary referral (see InjuryHx.PresTBIref), details of procedures performed at the first hospital (not study hospital) were recorded. This reflects if the subject was intubated at first hospital (not study hospital). |
| InjuryHx.PresSTHospDate | Date of arrival at the Study Hospital | Reflects the Date of arrival to study hospital | |
| InjuryHx.PresSTHospTime | Time of arrival at the Study Hospital | Reflects Time of arrival to study hospital | |
| InjuryHx.PresTBIRef | Referral | 2 == Secondary 1 == Primary |
Reflects if the subject was transported from the scene of accident immediately to the study hospital (primary referral) or if secondary referral occurred from a first hospital to the Study hospital. |
| InjuryHx.PupilsBaselineDerived | IMPACT unreactive pupils | This is a derived variable calculated centrally. Number of unreactive pupils for baseline risk adjustment with missing values imputed using IMPACT methodology- take Poststabilisation value and if absent work back in time towards prehospital values until non-missing value found. Untestable pupil ignored: I.e. 1 reactive + 1 untestable = 1 reactive (this assumption applies only to a small proportion of the data). RECOMMENDED FOR BASELINE RISK ADJUSTMENT. | |
| InjuryHx.PupilsNonSymmetric | Non-symmetric pupils | Pupil symmetry derived variable calculated from (GCSFirstHospPupilSymmetry,EDArrPupilSymmetry,GCSPreHospPupilSymmetry,EDDischPupilSymmetry,PupilsNonSymmetric) | |
| InjuryHx.SedativeCurrentUse | Use in the past three months: Sedatives or sleeping pills | 0 == No 1 == Yes 88 == Unknown |
On presentation the behavioral history of the patient was recorded. This reflects if in the past three months the subjects used sedatives or sleeping pills. |
| InjuryHx.SedativePriorUse | Past use: Sedatives or sleeping pills | 0 == No 1 == Yes 88 == Unknown |
On presentation the behavioral history of the patient was recorded. This reflects his past use of Sedatives or sleeping pill. |
| InjuryHx.SedativePriorUseDuration | Past use: No. of years of use of sedatives or sleeping pills | On presentation the behavioral history of the patient was recorded. This reflects the number sof years of his past use sedatives (if applicable). | |
| InjuryHx.SympSkullFract | Clinical signs of skull base fracture (e.g. raccoon eyes, battle sign, hemotympanun, CSF otorrhea, CRF rhinorrhea, bleeding from ear) | 88 == Unknown 0 == No 1 == Yes |
During neurological assessment at arrival in the ER, Clinical signs of skull base fracture (e.g. raccoon eyes, battle sign, hemotympanun, CSF otorrhea, CRF rhinorrhea, bleeding from ear) were recorded. |
| InjuryHx.SympVomiting | Vomiting | 0 == No 1 == Once 2 == More than once 88 == Unknown |
During neurological assessment at arrival in the ER, Vomiting was recorded. |
| InjuryHx.ThoracicSpineAIS | Thoracic Spine AIS | AIS score for the Thoracic Spine as subdomain of Thorax/Chest. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.ThoracicSpineDesc | Thorax Spine injury description | 1 == Fracture 2 == Dislocation |
Injury description for the AIS of Thoracic spine as subdomain of Thorax/Chest |
| InjuryHx.ThoraxChestAIS | Thorax/Chest AIS | AIS score for the Thorax/Chest region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.ThoraxChestDesc | Thorax/Chest injury description | 99 == Other 6 == Hemato-thorax 4 == Aorta dissection 5 == Pneumo-thorax 3 == Cardiac contusion 1 == Rib fracture 2 == Lung contusion |
Injury description for the AIS of the Thorax/Chest region. |
| InjuryHx.TobcoCurntUseInd | Use in the past three months: Tobacco products (cigarettes, cigars, pipe, chewing tobacco, etc.) | 0 == No 1 == Yes 88 == Unknown |
On presentation the behavioral history of the patient was recorded. This reflects his use in the past three months of Tobacco products (cigarettes, cigars, pipe, chewing tobacco, etc.) |
| InjuryHx.TobcoPriorUseInd | Past use: Tobacco products (cigarettes, cigars, pipe, chewing tobacco, etc.) | 0 == No 1 == Yes 88 == Unknown |
The form "Behavioral History" captures information on past and current use of alcohol, tobacco, sedatives/sleeping pills, cannabis and other recreational drugs. Use is differentiated as "Past user" (eg stopped) versus "use in the past 3 months. Note: These variables do not reflect use of these substances at the time of injury. |
| InjuryHx.TobcoUseDur | Past use: No. of years of use of tobacco (cigarettes, cigars, pipe, chewing tobacco, etc.) | On presentation the behavioral history of the patient was recorded. This reflects the number of years of his past use of Tobacco (if applicable). | |
| InjuryHx.TotalISS | Total ISS | The Injury Severity Score is calculated as the sum of the squares of the the 3 body regions with the highest AIS score. The max score for the ISS = 75. If any body region AIS is assigned a score of "6", the ISS is automatically set to 75 (highest score). In the calculation of the ISS, only the 6 main body regions are taken into consideration. | |
| InjuryHx.UpperExtremitiesAIS | Upper Extremities AIS | AIS score of the Upper extremities as subdomain of Extremities and pelvic girdle. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| InjuryHx.UpperExtremitiesDesc | Upper Extremities injury description | 5 == Finger 3 == Dislocation 4 == Hand 2 == Radial and/or ulnar fracture 1 == Humerus fracture |
Injury description for the AIS score of the Upper extremities as subdomain of Extremities and pelvic girdle. |
| Labs.DLA10Extem | A10 (Amplitude/clot firmness at 10 minutes) measured from EXTEM test | Only applicable to sites doing ROTEM studies. ROTEM --> A10 --> EXTEM | |
| Labs.DLA10Fibtem | A10 (Amplitude/clot firmness at 10 minutes) measured from FIBTEM test | Only applicable to sites doing ROTEM studies. ROTEM --> A10 --> FIBTEM | |
| Labs.DLA10NotDone | ROTEM A10 labs Not Done | Only applicable to sites doing ROTEM studies. ROTEM --> A10 --> Not Done | |
| Labs.DLA5Extem | A5 (Amplitude/clot firmness at 5 minutes) measured from EXTEM test | Only applicable to sites doing ROTEM studies. ROTEM --> A5 --> EXTEM | |
| Labs.DLA5Fibtem | A5 (Amplitude/clot firmness at 5 minutes) measured from FIBTEM test | Only applicable to sites doing ROTEM studies ROTEM --> A5 --> FIBTEM | |
| Labs.DLA5NotDone | ROTEM A5 labs Not Done | Only applicable to sites doing ROTEM studies. ROTEM --> A5 --> Not Done | |
| Labs.DLaAngleExtem | alpha-angle measured from EXTEM test | Only applicable to sites doing ROTEM studies. ROTEM --> α-angle --> EXTEM | |
| Labs.DLaAngleFibtem | alpha-angle measured from FIBTEM test | Only applicable to sites doing ROTEM studies. ROTEM --> α-angle --> FIBTEM | |
| Labs.DLaAngleNotDone | ROTEM α-angle labs Not Done | Only applicable to sites doing ROTEM studies. ROTEM --> α-angle --> Not Done | |
| Labs.DLACT | ACT (Activated Clotting Time) | Only applicable to sites doing ROTEM/TEG studies. TEG --> ACT (rapid TEG only) | |
| Labs.DLACTNotDone | TEG ACT labs Not Done | Only applicable to sites doing ROTEM/TEG studies. TEG --> ACT --> Not Done | |
| Labs.DLADPAggreg | Aggregation measured from ADP (Adenosine diphosphate) test | Only applicable to sites doing multiplate studies. MULTIPLATE TEST --> ADP Test --> Aggregation | |
| Labs.DLADPAUC | AUC measured from ADP (Adenosine diphosphate) test | Only applicable to sites doing multiplate studies. MULTIPLATE TEST --> ADP Test --> AUC (AU*min) | |
| Labs.DLADPAUCU | Multiplate ADP test AUC in U | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> ADP Test --> AUC (U) | |
| Labs.DLADPVelocity | Velocity measured from ADP (Adenosine diphosphate) test | Only applicable to sites doing multiplate studies. MULTIPLATE TEST --> ADP Test --> Velocity | |
| Labs.DLAlatSgptNotDone | Blood chemistry ALAT/SGPT Not Done | BLOOD CHEMISTRY --> ALAT/SGPT ( Alanine Aminotrasferase) --> Not done | |
| Labs.DLAlatSgptOther | Result in other unit for blood chemistry ALAT/SGPT | Preferred unit for ALAT/SGPT was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAlatSgptOtherUnit | Other unit (than standard) used for blood chemistry ALAT/SGPT Not Done | Preferred unit for ALAT/SGPT was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAlatSgptUL | ALAT/SGPT (Alanine Aminotrasferase) level | BLOOD CHEMISTRY --> ALAT/SGPT Recorded in "preferred" units (U/L) | |
| Labs.DLAlbumingL | Albumin level | BLOOD CHEMISTRY --> Albumin Recorded in "preferred" units (g/dL) | |
| Labs.DLAlbuminNotDone | Blood chemistry Albumin Not Done | BLOOD CHEMISTRY --> Albumin --> Not done | |
| Labs.DLAlbuminOther | Result in other unit for blood chemistry Albumin | Preferred unit for Albumin was g/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAlbuminOtherUnit | Other unit (than standard) used for blood chemistry Albumin | Preferred unit for Albumin was g/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAlkalinePhosphataseNotDone | Blood chemistry Alkaline Phosphatase Not Done | BLOOD CHEMISTRY --> Alkaline Phosphatase --> Not done | |
| Labs.DLAlkalinePhosphataseOther | Result in other unit for blood chemistry Alkaline Phosphatase | Preferred unit for Alkaline Phosphatase was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAlkalinePhosphataseOtherUnit | Other unit (than standard) used for blood chemistry Alkaline Phosphatase | Preferred unit for Alkaline Phosphatase was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAlkalinePhosphataseUL | Alkaline Phosphatase level | BLOOD CHEMISTRY --> Alkaline Phosphatase Recorded in "preferred" units (U/L) | |
| Labs.DLAmylaseNotDone | Blood chemistry Amylase Not Done | BLOOD CHEMISTRY --> Amylase --> Not done | |
| Labs.DLAmylaseOther | Result in other unit for blood chemistry Amylase | Preferred unit for Amylase was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAmylaseOtherUnit | Other unit (than standard) used for blood chemistry Amylase | Preferred unit for Amylase was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAmylaseUL | Amylase level | BLOOD CHEMISTRY --> Amylase Recorded in "preferred" units (U/L) | |
| Labs.DLaPttNotDone | Haematology aPTT Not Done | HAEMATOLOGY --> Activated thromboplastine time (aPTT) --> Not done | |
| Labs.DLaPttOther | Result in other unit for Haematology aPTT | Preferred unit for aPTT was sec. When sites used another unit, the value was recorded here. | |
| Labs.DLaPttOtherUnit | Other unit (than standard) used for Haematology aPTT | Preferred unit for aPTT was sec. When sites used another unit, the other unit was recorded here. | |
| Labs.DLaPttsec | aPTT (Activated Thromboplastine Time) level | HAEMATOLOGY --> Activated thromboplastine time (aPTT) Recorded in "preferred" units (sec.) | |
| Labs.DLAsatSgotNotDone | Blood chemistry ASAT/SGOT Not Done | BLOOD CHEMISTRY --> ASAT/SGOT --> Not done | |
| Labs.DLAsatSgotOther | Result in other unit for blood chemistry ASAT/SGOT | Preferred unit for ASAT/SGOT was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAsatSgotOtherUnit | Other unit (than standard) used for blood chemistry ASAT/SGOT | Preferred unit for ASAT/SGOT was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAsatSgotUL | ASAT/SGOT (Aspartate Aminotrasferase) level | BLOOD CHEMISTRY --> ASAT/SGOT Recorded in "preferred" units (U/L) | |
| Labs.DLASPIAggreg | Aggregation measured from ASPI test | Only applicable to sites doing multiplate studies. MULTIPLATE TEST --> ASPI Test --> Aggregation | |
| Labs.DLASPIAUC | AUC measured from ASPI test | Only applicable to sites doing multiplate studies | |
| Labs.DLASPIAUCU | Multiplate ASPI test AUC in U | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> ASPI Test --> AUC (U) | |
| Labs.DLASPIVelocity | Velocity measured from ASPI test | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> ASPI Test --> Velocity (AU*min) | |
| Labs.DLBloodChemDone | Blood Chemistry Done | Reflects if Blood chemistry was done. | |
| Labs.DLCalciummmolL | Calcium level | BLOOD CHEMISTRY --> Calcium Recorded in "preferred" units (mmol/L) | |
| Labs.DLCalciumNotDone | Blood chemistry Calcium Not Done | BLOOD CHEMISTRY --> Calcium --> Not done | |
| Labs.DLCalciumOther | Result in other unit for blood chemistry Calcium | Preferred unit for Calcium was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLCalciumOtherUnit | Other unit (than standard) used for blood chemistry Calcium | Preferred unit for Calcium was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLCFTExtem | CFT (Clot Formation Time) measured from EXTEM test | Only applicable to sites doing ROTEM studies. ROTEM --> CFT --> EXTEM | |
| Labs.DLCFTFibtem | CFT (Clot Formation Time) measured from FIBTEM test | Only applicable to sites doing ROTEM studies. ROTEM --> CFT --> FIBTEM | |
| Labs.DLCFTNotDone | ROTEM CFT labs Not Done | Only applicable to sites doing ROTEM studies. ROTEM --> CFT --> Not Done | |
| Labs.DLCL30 | CL30 (Clot Lysis at 30 minutes) | Only applicable to sites doing ROTEM/TEG studies. TEG --> CL30 | |
| Labs.DLCL30NotDone | TEG CL30 labs Not Done | Only applicable to sites doing ROTEM/TEG studies. TEG --> CL30 --> Not Done | |
| Labs.DLCL60 | CL60 (Clot Lysis at 60 minutes) | Only applicable to sites doing ROTEM/TEG studies. TEG --> CL60 | |
| Labs.DLCL60NotDone | TEG CL60 labs Not Done | Only applicable to sites doing ROTEM/TEG studies. TEG --> CL60 --> Not Done | |
| Labs.DLCLTExtem | CLT (Clot Lysis Time) measured from EXTEM test | Only applicable to sites doing ROTEM studies ROTEM --> CLT --> EXTEM | |
| Labs.DLCLTFibtem | CLT (Clot Lysis Time) measured from FIBTEM test | Only applicable to sites doing ROTEM studies ROTEM --> CLT --> FIBTEM | |
| Labs.DLCLTNotDone | ROTEM CLT labs Not Done | Only applicable to sites doing ROTEM studies ROTEM --> CLT --> Not Done | |
| Labs.DLCOLAggreg | Aggregation measured from COL (Collagen) test | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> COL Test --> Aggregation | |
| Labs.DLCOLAUC | AUC measured from COL (Collagen) test | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> COL Test --> AUC (AU*min) | |
| Labs.DLCOLAUCU | Multiplate COL test AUC in U | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> COL Test --> AUC (U) | |
| Labs.DLCOLVelocity | Velocity measured from COL (Collagen) test | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> COL Test --> Velocity (AU*min) | |
| Labs.DLCreatinineNotDone | Blood chemistry Creatinine Not Done | BLOOD CHEMISTRY --> Creatinine --> Not done | |
| Labs.DLCreatinineOther | Result in other unit for blood chemistry Creatinine | Preferred unit for Creatinine was µmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLCreatinineOtherUnit | Other unit (than standard) used for blood chemistry Creatinine | Preferred unit for Creatinine was µmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLCreatinineumolL | Creatinine level | BLOOD CHEMISTRY --> Creatinine Recorded in "preferred" units (µmol/L) | |
| Labs.DLCRPmgL | CRP (C-reactive Protein) level | HAEMATOLOGY --> C-reactive protein (CRP) Recorded in "preferred" units (mg/L) | |
| Labs.DLCRPNotDone | Haematology CRP Not Done | HAEMATOLOGY --> C-reactive protein (CRP) --> Not done | |
| Labs.DLCRPOther | Result in other unit for Haematology CRP | Preferred unit for CRP was mg/L. When sites used another unit, the value was recorded here. | |
| Labs.DLCRPOtherUnit | Other unit (than standard) used for Haematology CRP | Preferred unit for CRP was mg/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLCTExtem | CT (Clotting Time) measured from EXTEM test | Only applicable to sites doing ROTEM studies ROTEM --> CT --> EXTEM | |
| Labs.DLCTFibtem | CT (Clotting Time) measured from FIBTEM test | Only applicable to sites doing ROTEM studies ROTEM --> CT --> FIBTEM | |
| Labs.DLCTNotDone | ROTEM CT labs Not Done | Only applicable to sites doing ROTEM studies ROTEM --> CT --> Not Done | |
| Labs.DLDate | Date of lab testing | Date of labs | |
| Labs.DLDdimersNotDone | Haematology D-dimers Not Done | HAEMATOLOGY --> D-dimers --> Not done | |
| Labs.DLDdimersOther | Result in other unit for Haematology D-dimers | Preferred unit for D-dimers was µg/L. When sites used another unit, the value was recorded here. | |
| Labs.DLDdimersOtherUnit | Other unit (than standard) used for Haematology D-dimers | Preferred unit for D-dimers was µg/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLDdimersugL | D-dimers level | HAEMATOLOGY --> D-dimers Recorded in "preferred" units ( µg/L) | |
| Labs.DLEosinophilsNotDone | Haematology Eosinophils Not Done | HAEMATOLOGY --> Eosinophils --> Not done | |
| Labs.DLEosinophilsOther | Result in other unit for Haematology Eosinophils | Preferred unit for Eosinophils was %. When sites used another unit, the value was recorded here. | |
| Labs.DLEosinophilsOtherUnit | Other unit (than standard) used for Haematology Eosinophils | Preferred unit for Eosinophils was %. When sites used another unit, the other unit was recorded here. | |
| Labs.DLEosinophilspct | Eosinophils level | HAEMATOLOGY --> Eosinophils Recorded in "preferred" units (%) | |
| Labs.DLEPL | EPL (Estimated Percent Lysis) | Only applicable to sites doing TEG/ROTEM studies TEG --> EPL | |
| Labs.DLEPLNotDone | TEG EPL Labs Not Done | Only applicable to sites doing TEG/ROTEM studies TEG --> EPL--> Not Done | |
| Labs.DLFibrinogenmgdL | Fibrinogen level | HAEMATOLOGY --> Fibrinogen Recorded in "preferred" units (mg/dL) | |
| Labs.DLFibrinogenNotDone | Haematology Fibrinogen Not Done | HAEMATOLOGY --> Fibrinogen --> Not done | |
| Labs.DLFibrinogenOther | Result in other unit for Haematology Fibrinogen | Preferred unit for Fibrinogen was mg/dL. When sites used another unit, the value was recorded here. | |
| Labs.DLFibrinogenOtherUnit | Other unit (than standard) used for Haematology Fibrinogen | Preferred unit for Fibrinogen was mg/dL. When sites used another unit, the other unit was recorded here. | |
| Labs.DLGlucosemmolL | Glucose level | BLOOD CHEMISTRY --> Glucose Recorded in "preferred" units (mmol/L) | |
| Labs.DLGlucoseNotDone | Blood chemistry Glucose Not Done | BLOOD CHEMISTRY --> Glucose --> Not done | |
| Labs.DLGlucoseOther | Result in other unit for blood chemistry Glucose | Preferred unit for Glucose was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLGlucoseOtherUnit | Other unit (than standard) used for blood chemistry Glucose | Preferred unit for Glucose was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLHaematologyDone | Haematology labs done | Reflects if Haematology labs was done | |
| Labs.DLHematocritNotDone | Haematology Hematocrit Not Done | HAEMATOLOGY --> Hematocrit --> Not done | |
| Labs.DLHematocritOther | Result in other unit for Haematology Hematocrit | Preferred unit for Hematocrit was %. When sites used another unit, the value was recorded here. | |
| Labs.DLHematocritOtherUnit | Other unit (than standard) used for Haematology Hematocrit | Preferred unit for Hematocrit was %. When sites used another unit, the other unit was recorded here. | |
| Labs.DLHematocritpct | Hematocrit level | HAEMATOLOGY --> Hematocrit Recorded in "preferred" units (%) | |
| Labs.DLHemoglobingdL | Haemoglobin level | HAEMATOLOGY --> Hemoglobin Recorded in "preferred" units (g/dL) | |
| Labs.DLHemoglobinNotDone | Haematology Hemoglobin Not Done | HAEMATOLOGY --> Hemoglobin --> Not done | |
| Labs.DLHemoglobinOther | Result in other unit for Haematology Hemoglobin | Preferred unit for Hemoglobin was g/dL. When sites used another unit, the value was recorded here. | |
| Labs.DLHemoglobinOtherUnit | Other unit (than standard) used for Haematology Hemoglobin | Preferred unit for Hemoglobin was g/dL. When sites used another unit, the other unit was recorded here. | |
| Labs.DLInr | INR (International Normalized Ratio) level | HAEMATOLOGY --> INR | |
| Labs.DLInrNotDone | Haematology INR Not Done | HAEMATOLOGY --> INR --> Not done | |
| Labs.DLInrOther | Result in other unit for Haematology INR | INR results if other units used than standard | |
| Labs.DLInrOtherUnit | Other unit (than standard) used for Haematology INR | INR results if other units used than standard | |
| Labs.DLK | K value | Only applicable to sites doing TEG/ROTEM studies TEG --> K | |
| Labs.DLKNotDone | TEG K-value not done | Only applicable to sites doing TEG/ROTEM studies TEG --> K--> Not Done | |
| Labs.DLLabsNotDone | Hospital labs not done | Reflects when hospital labs were not done | |
| Labs.DLLabsNotDoneOther | Reason why hospital labs not done | Specifies the reason why hospital labs were not done | |
| Labs.DLLdhNotDone | Blood chemistry LDH (Lactate Dehydrogenase) Not Done | BLOOD CHEMISTRY --> LDH (Lactate Dehydrogenase) --> Not done | |
| Labs.DLLdhOther | Result in other unit for Blood chemistry LDH (Lactate Dehydrogenase) | Preferred unit for LDH was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLLdhOtherUnit | Other unit (than standard) used for Blood chemistry LDH (Lactate Dehydrogenase) | Preferred unit for LDH was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLLdhUL | LDH (Lactate Dehydrogenase) level | BLOOD CHEMISTRY --> LDH (Lactate Dehydrogenase) Recorded in "preferred" units (U/L) | |
| Labs.DLLY30Extem | LI30 (Lysis Index after 30 minutes) measured from EXTEM test | Only applicable to sites doing ROTEM studies ROTEM --> LY30 --> EXTEM | |
| Labs.DLLY30Fibtem | LI30 (Lysis Index after 30 minutes) measured from FIBTEM test | Only applicable to sites doing ROTEM studies ROTEM --> LY30 --> FIBTEM | |
| Labs.DLLY30NotDone | ROTEM LY30 Not Done | Only applicable to sites doing ROTEM studies ROTEM --> LY30 --> Not Done | |
| Labs.DLLY60Extem | LI60 (Lysis Index after 60 minutes) measured from EXTEM test | Only applicable to sites doing ROTEM studies ROTEM --> LY60 --> EXTEM | |
| Labs.DLLY60Fibtem | LI60 (Lysis Index after 60 minutes) measured from FIBTEM test | Only applicable to sites doing ROTEM studies ROTEM --> LY60 --> FIBTEM | |
| Labs.DLLY60NotDone | ROTEM LY60 Not Done | Only applicable to sites doing ROTEM studies ROTEM --> LY60 --> Not Done | |
| Labs.DLLymphocytesNotDone | Haematology Lymphocytes Not Done | HAEMATOLOGY --> Lymphocytes --> Not done | |
| Labs.DLLymphocytesOther | Result in other unit for Haematology Lymphocytes | Preferred unit for Lymphocytes was %. When sites used another unit, the value was recorded here. | |
| Labs.DLLymphocytesOtherUnit | Other unit (than standard) used for Haematology Lymphocytes | Preferred unit for Lymphocytes was %. When sites used another unit, the other unit was recorded here. | |
| Labs.DLLymphocytespct | Lymphocytes level | HAEMATOLOGY --> Lymphocytes Recorded in "preferred" units (%) | |
| Labs.DLMA | MA (Maximum Amplitude) | Only applicable to sites doing TEG/ROTEM studies TEG --> MA | |
| Labs.DLMagnesiummmolL | Magnesium level | BLOOD CHEMISTRY --> Magnesium Recorded in "preferred" units (mmol/L) | |
| Labs.DLMagnesiumNotDone | Blood chemistry Magnesium Not Done | BLOOD CHEMISTRY --> Magnesium --> Not done | |
| Labs.DLMagnesiumOther | Result in other unit for blood chemistry Magnesium | Preferred unit for Magnesium was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLMagnesiumOtherUnit | Other unit (than standard) used for blood chemistry Magnesium | Preferred unit for Magnesium was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLMANotDone | TEG MA Not Done | Only applicable to sites doing TEG/ROTEM studies TEG --> MA --> Not Done | |
| Labs.DLMCFExtem | MCF (Maximum Clot Firmness) measured from EXTEM test | Only applicable to sites doing ROTEM studies ROTEM --> MCF --> EXTEM | |
| Labs.DLMCFFibtem | MCF (Maximum Clot Firmness) measured from FIBTEM test | Only applicable to sites doing ROTEM studies ROTEM --> MCF --> FIBTEM | |
| Labs.DLMCFNotDone | ROTEM MCF Not Done | Only applicable to sites doing ROTEM studies ROTEM --> MCF --> Not Done | |
| Labs.DLMCFtExtem | MCF-t (Time to Maximum Clot Firmness) measured from EXTEM test | Only applicable to sites doing ROTEM studies ROTEM --> MCF-t --> EXTEM | |
| Labs.DLMCFtFibtem | MCF-t (Time to Maximum Clot Firmness) measured from FIBTEM test | Only applicable to sites doing ROTEM studies ROTEM --> MCF-t --> FIBTEM | |
| Labs.DLMCFtNotDone | ROTEM MCF-t Not Done | Only applicable to sites doing ROTEM studies ROTEM --> MCF-t --> Not Done | |
| Labs.DLMLExtem | ML (Maximum Lysis) measured from EXTEM test | Only applicable to sites doing ROTEM studies ROTEM --> ML --> EXTEM | |
| Labs.DLMLFibtem | ML (Maximum Lysis) measured from FIBTEM test | Only applicable to sites doing ROTEM studies ROTEM --> ML --> FIBTEM | |
| Labs.DLMLNotDone | ROTEM ML Not Done | Only applicable to sites doing ROTEM studies ROTEM --> ML --> Not Done | |
| Labs.DLMultiplateDone | Multiplate Labs Not Done | Reflects if Multiplate was done - Only in selected sites | |
| Labs.DLNeutrophilsNotDone | Haematology Neutrophils Not Done | HAEMATOLOGY --> Neutrophils --> Not done | |
| Labs.DLNeutrophilsOther | Result in other unit for Haematology Neutrophils | Preferred unit for Neutrophils was %. When sites used another unit, the value was recorded here. | |
| Labs.DLNeutrophilsOtherUnit | Other unit (than standard) used for Haematology Neutrophils | Preferred unit for Neutrophils was %. When sites used another unit, the other unit was recorded here. | |
| Labs.DLNeutrophilspct | Neutrophils level | HAEMATOLOGY --> Neutrophils Recorded in "preferred" units (%) | |
| Labs.DLPlatelet10_5L | Platelet count | HAEMATOLOGY --> Platelet Recorded in "preferred" units (X10^9/L or X10^3/µL) | |
| Labs.DLPlateletNotDone | Haematology Platelet Not Done | HAEMATOLOGY --> Platelet --> Not done | |
| Labs.DLPlateletOther | Result in other unit for Haematology Platelet | Preferred unit for Platelet was X10^9/L or X10^3/μL. When sites used another unit, the value was recorded here. | |
| Labs.DLPlateletOtherUnit | Other unit (than standard) used for Haematology Platelet | Preferred unit for Platelet was X10^9/L or X10^3/μL. When sites used another unit, the other unit was recorded here. | |
| Labs.DLPotassiummmolL | Potassium level | BLOOD CHEMISTRY --> Potassium Recorded in "preferred" units (mmol/L) | |
| Labs.DLPotassiumNotDone | Blood chemistry Potassium Not Done | BLOOD CHEMISTRY --> Potassium --> Not done | |
| Labs.DLPotassiumOther | Result in other unit for Blood chemistry Potassium | Preferred unit for Potassium was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLPotassiumOtherUnit | Other unit (than standard) used for Blood chemistry Potassium | Preferred unit for Potassium was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLProthrombineTimeNotDone | Haematology Prothrombine Time Not Done | HAEMATOLOGY --> Prothrombine Time --> Not done | |
| Labs.DLProthrombineTimeOther | Result in other unit for Haematology Prothrombine Time | Preferred unit for Prothrombine Time was sec. When sites used another unit, the value was recorded here. | |
| Labs.DLProthrombineTimeOtherUnit | Other unit (than standard) used for Haematology Prothrombine Time | Preferred unit for Prothrombine Time was sec. When sites used another unit, the other unit was recorded here. | |
| Labs.DLProthrombineTimeSec | PT (Prothrombine Time) level | HAEMATOLOGY --> Prothrombine Time Recorded in "preferred" units (sec.) | |
| Labs.DLR | R value (Reaction time) | Only applicable to sites doing TEG/ROTEM studies TEG --> R | |
| Labs.DLRISTOAggreg | Aggregation measured from RISTO (Ristocetin) test | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> RISTO Test --> Aggregation | |
| Labs.DLRISTOAUC | AUC measured from RISTO (Ristocetin) test | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> RISTO Test --> AUC (AU*min) | |
| Labs.DLRISTOAUCU | Multiplate RISTO test AUC in U | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> RISTO Test --> AUC (U) | |
| Labs.DLRISTOVelocity | Velocity measured from RISTO (Ristocetin) test | Only applicable to sites doing multiplate studies MULTIPLATE TEST --> RISTO Test --> Velocity (AU*min) | |
| Labs.DLRNotDone | TEG R Labs Not Done | Only applicable to sites doing TEG studies TEG --> R --> Not Done | |
| Labs.DLROTEMDone | ROTEM labs Done | Reflects if ROTEM was done - Only applicable to sites doing ROTEM tests | |
| Labs.DLS100BNotDone | Blood chemistry S100B Not Done | BLOOD CHEMISTRY --> S100B --> Not done | |
| Labs.DLS100BOther | Result in other unit for Blood chemistry S100B | Preferred unit for S100B was µg/L. When sites used another unit, the value was recorded here. | |
| Labs.DLS100BOtherUnit | Other unit (than standard) used for Blood chemistry S100B | Preferred unit for S100B was µg/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLS100BugL | S100B level | BLOOD CHEMISTRY --> S100B Recorded in "preferred" units (µg/L) | |
| Labs.DLSodiummmolL | Sodium level | BLOOD CHEMISTRY --> Sodium Recorded in "preferred" units (mmol/L) | |
| Labs.DLSodiumNotDone | Blood chemistry Sodium Not Done | BLOOD CHEMISTRY --> Sodium --> Not done | |
| Labs.DLSodiumOther | Result in other unit for Blood chemistry Sodium | Preferred unit for Sodium mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLSodiumOtherUnit | Other unit (than standard) used for Blood chemistry Sodium | Preferred unit for Sodium mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLTEGA10 | A10 (Amplitude/clot firmness at 10 minutes) | Only applicable for sites doing TEG TEG --> A10 | |
| Labs.DLTEGA10NotDone | TEG A10 Labs not Done | Only applicable for sites doing TEG TEG --> A10 --> Not Done | |
| Labs.DLTEGA5 | A5 (Amplitude/clot firmness at 5 minutes) | Only applicable for sites doing TEG TEG --> A5 | |
| Labs.DLTEGA5NotDone | TEG A5 Labs not Done | Only applicable for sites doing TEG TEG --> A5 --> Not Done | |
| Labs.DLTEGaAngle | alpha-angle | Only applicable for sites doing TEG TEG --> α-angle | |
| Labs.DLTEGaAngleNotDone | TEG α-angle labs Not Done | Only applicable for sites doing TEG TEG --> α-angle --> Not Done | |
| Labs.DLTEGDone | TEG Labs Done | Reflects if TEG was done - Only applicable for selected sites doing TEG | |
| Labs.DLTEGType | TEG (Thromboelastography) type | Reflects type of TEG done - Only applicable for selected sites doing TEG | |
| Labs.DLTime | Time of lab testing | Time of labs | |
| Labs.DLTMA | TMA (Time to Maximum Amplitude) | Only applicable for sites doing TEG TEG --> TMA | |
| Labs.DLTMANotDone | TEG TMA labs Not Done | Only applicable for sites doing TEG TEG --> TMA --> Not Done | |
| Labs.DLTotalBilirubinNotDone | Blood chemistry Total Bilirubin Not Done | BLOOD CHEMISTRY --> Total Bilirubin --> Not done | |
| Labs.DLTotalBilirubinOther | Result in other unit for Blood chemistry Total Bilirubin | Preferred unit for Total Bilirubin was µmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLTotalBilirubinOtherUnit | Other unit (than standard) used for Blood chemistry Total Bilirubin | Preferred unit for Total Bilirubin was µmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLTotalBilirubinumolL | Total Bilirubin level | BLOOD CHEMISTRY --> Total Bilirubin Recorded in "preferred" units (µmol/L) | |
| Labs.DLToxScreen | Result of toxic drug screen test | Toxic Drug Screen Result Only if performed as part of clinical routine | |
| Labs.DLToxScreenDone | Toxic drug screen done | Reflects if Toxic Drug Screen was done. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosAmphet | Positive for Amphetamines | Reflects if Toxic Drug Screen was positive for Amphetamines. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosBarb | Positive for Barbiturates | Reflects if Toxic Drug Screen was positive for Barbiturates. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosBenzo | Positive for Benzodiazepines | Reflects if Toxic Drug Screen was positive for Benzodiazepines. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosCannabis | Positive for Cannabinoids | Reflects if Toxic Drug Screen was positive for Cannabinoids. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosCocaine | Positive for Cocaine | Reflects if Toxic Drug Screen was positive for Cocaine. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosMeth | Positive for Methadone | Reflects if Toxic Drug Screen was positive for Methadone. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosMethaqual | Positive for Methaqualone | Reflects if Toxic Drug Screen was positive for Methaqualone. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosOpiate | Positive for Opiates | Reflects if Toxic Drug Screen was positive for Opiates. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosOther | Positive for other drugs | Reflects if Toxic Drug Screen was positive for Other drugs than the predefined list. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosOtherTxt | Positive for other drugs (please specify) | Specifies for which drugs, if Toxic Drug Screen was positive for Other drugs than the predefined list. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenPosPhency | Positive for Phencyclidine | Reflects if Toxic Drug Screen was positive for Phencyclidine. Only if performed as part of clinical routine. | |
| Labs.DLToxScreenType | Type of sample used in toxic drug screen test | Specifies the type of sample, Urine or Serum, if Toxic Drug Screen was performed. Only if performed as part of clinical routine. | |
| Labs.DLTRAPAggreg | Aggregation measured from TRAP (Thrombin Receptor Activating Peptide) test | Only applicable to sites doing multiplate studies. MULTIPLATE TEST --> TRAP Test --> Aggregation | |
| Labs.DLTRAPAUC | AUC measured from TRAP (Thrombin Receptor Activating Peptide) test | Only applicable to sites doing multiplate studies. MULTIPLATE TEST --> TRAP Test --> AUC (AU*min) | |
| Labs.DLTRAPAUCU | Multiplate TRAP test AUC in U | Only applicable to sites doing multiplate studies. MULTIPLATE TEST --> TRAP Test --> AUC (U) | |
| Labs.DLTRAPVelocity | Velocity measured from TRAP (Thrombin Receptor Activating Peptide) test | Only applicable to sites doing multiplate studies. MULTIPLATE TEST --> TRAP Test --> Velocity (AU*min) | |
| Labs.DLTTL | TTL (Time To Lysis) | Only applicable to sites doing TEG studies TEG --> TTL | |
| Labs.DLTTLNotDone | TEG TTL Labs not Done | Only applicable to sites doing TEG studies TEG --> TTL --> Not Done | |
| Labs.DLUreammolL | Urea level | BLOOD CHEMISTRY --> Urea Recorded in "preferred" units (mmol/L) | |
| Labs.DLUreaNotDone | Blood chemistry Urea Not Done | BLOOD CHEMISTRY --> Urea --> Not done | |
| Labs.DLUreaOther | Result in other unit for Blood chemistry Urea | Preferred unit for Urea was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLUreaOtherUnit | Other unit (than standard) used for Blood chemistry Urea | Preferred unit for Urea was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLWhiteBloodCellNotDone | Blood chemistry White Blood cell Not Done | HAEMATOLOGY --> White blood cell --> Not done | |
| Labs.DLWhiteBloodCellOther | Result in other unit for Blood White Blood cell | Preferred unit for White Blood Cell was X10^9/L or X10^3/μL. When sites used another unit, the value was recorded here. | |
| Labs.DLWhiteBloodCellOtherUnit | Other unit (than standard) used for Blood White Blood cell | Preferred unit for White Blood Cell was X10^9/L or X10^3/μL. When sites used another unit, the other unit was recorded here. | |
| Labs.DLWhiteBloodCellpct | WBC (White Blood Cell) count | HAEMATOLOGY --> White blood cell Recorded in "preferred" units (X10^9/L or X10^3/μL) | |
| LabSampling.LSBiomarkersCollctnDate | Date of collection of blood samples for biomarkers status | This reflects the biomarker sampling collection date. Protein biomarker sampling was planned in all subjects. 1 x 9ml blood sample was collected in a serum separator tube. After 45 minutes (±15) of coagulation at room temperature, it is centrifuged at 1500g for 10 minutes, 8 x 0.5ml of serum is then aliquoted into barcoded 1.8 ml blue capped cryovials. Note: not available for all subjects - Blood sampling required specific informed consent, but this was not provided by all subjects, and in others biomarker collection was not possible for logistic reasons. | |
| LabSampling.LSBiomarkersCollctnTime | Time of collection of blood samples for biomarkers status | This reflects the biomarker sampling collection time. Protein biomarker sampling was planned in all subjects. 1 x 9ml blood sample was collected in a serum separator tube. After 45 minutes (±15) of coagulation at room temperature, it is centrifuged at 1500g for 10 minutes, 8 x 0.5ml of serum is then aliquoted into barcoded 1.8 ml blue capped cryovials. Note: not available for all subjects - Blood sampling required specific informed consent, but this was not provided by all subjects, and in others biomarker collection was not possible for logistic reasons. | |
| LabSampling.LSBiomarkersFreezerCollctnDate | Date blood samples are stored in the freezer for biomarkers status | This reflects the biomarker freezer date. Protein biomarker sampling was planned in all subjects. 1 x 9ml blood sample was collected in a serum separator tube. After 45 minutes (±15) of coagulation at room temperature, it is centrifuged at 1500g for 10 minutes, 8 x 0.5ml of serum is then aliquoted into barcoded 1.8 ml blue capped cryovials. Note: not available for all subjects - Blood sampling required specific informed consent, but this was not provided by all subjects, and in others biomarker collection was not possible for logistic reasons. | |
| LabSampling.LSBiomarkersFreezerCollctnTime | Time blood samples are stored in the freezer for biomarkers status | This reflects the biomarker freezer time. Protein biomarker sampling was planned in all subjects. 1 x 9ml blood sample was collected in a serum separator tube. After 45 minutes (±15) of coagulation at room temperature, it is centrifuged at 1500g for 10 minutes, 8 x 0.5ml of serum is then aliquoted into barcoded 1.8 ml blue capped cryovials. Note: not available for all subjects - Blood sampling required specific informed consent, but this was not provided by all subjects, and in others biomarker collection was not possible for logistic reasons. | |
| LabSampling.LSBiomarkersNotCollReason | Reason for not collecting blood samples for biomarkers status | 1 == No informed consent 2 == Blood draw not successful 3 == Logistic reasons |
This specifies the reason why biomarker sampling was not obtained. |
| LabSampling.LSBloodTransBfSampl | Did the patient receive blood transfusion before sampling? | 0 == No 1 == Yes 99 == Unknown |
Reflects if the patient received a blood transfusion before blood sampling |
| LabSampling.LSCoagulationCollctnDate | Date of collection of blood samples for coagulation status | This reflects the Coagulation sampling collection date. Central haemostasis investigations were complementary to routine tests performed by local laboratories at participating sites and were performed only in selected centers. This involved the collection of blood into: 1 x 2.7 ml potassium EDTA tube and 1 x 10 ml and 1 x 5 ml sodium-citrate tubes at the enrollment time points for a limited number of subjects from the Admission and ICU stratum. Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU subjects (at this sampling point no potassium EDTA tubes/samples were requested). | |
| LabSampling.LSCoagulationCollctnTime | Time of collection of blood samples for coagulation status | This reflects the Coagulation sampling collection time. Central haemostasis investigations were complementary to routine tests performed by local laboratories at participating sites and were performed only in selected centers. This involved the collection of blood into: 1 x 2.7 ml potassium EDTA tube and 1 x 10 ml and 1 x 5 ml sodium-citrate tubes at the enrollment time points for a limited number of subjects from the Admission and ICU stratum. Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU subjects (at this sampling point no potassium EDTA tubes/samples were requested). | |
| LabSampling.LSCoagulationFreezerDate | Date blood samples are stored in the freezer for coagulation status | This reflects the Coagulation sampling freezer date. Central haemostasis investigations were complementary to routine tests performed by local laboratories at participating sites and were performed only in selected centers. This involved the collection of blood into: 1 x 2.7 ml potassium EDTA tube and 1 x 10 ml and 1 x 5 ml sodium-citrate tubes at the enrollment time points for a limited number of subjects from the Admission and ICU stratum. Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU subjects (at this sampling point no potassium EDTA tubes/samples were requested). | |
| LabSampling.LSCoagulationFreezerTime | Time blood samples are stored in the freezer for coagulation status | This reflects the Coagulation sampling freezer time. Central haemostasis investigations were complementary to routine tests performed by local laboratories at participating sites and were performed only in selected centers. This involved the collection of blood into: 1 x 2.7 ml potassium EDTA tube and 1 x 10 ml and 1 x 5 ml sodium-citrate tubes at the enrollment time points for a limited number of subjects from the Admission and ICU stratum. Post-op samples and Day 2 samples were also obtained in the same two sodium citrate tubes from a limited number of ICU subjects (at this sampling point no potassium EDTA tubes/samples were requested). | |
| LabSampling.LSGeneticCollctnDate | Date of collection of blood samples for genetic analyses | This reflects the Genetic sampling collection date. Two genetic samples should be obtained in all CENTER-TBI participants. It is recognized by the CENTER-TBI coordinators that obtaining genetic samples post transfusion could result in “chimerism” in the genotype and that this could persists for long periods after trauma. However, the coordinators have taken a pragmatic view that samples should be taken at baseline when taking biomarker samples (+/- coagulation samples for those sites in the sub-study). This pragmatic approach has numerous advantages; it limits the complexity of the sampling regimen, reduces the need for repeat venepunctures and minimises the risk of missed samples if the participant is lost to follow-up. Accurate documentation of the participant’s transfusion status is essential for future analysis. In some cases, blood sampling for genetic analysis were obtained later. | |
| LabSampling.LSGeneticCollctnTime | Time of collection of blood samples for genetic analyses | This reflects the Genetic sampling collection time. Two genetic samples should be obtained in all CENTER-TBI participants. It is recognized by the CENTER-TBI coordinators that obtaining genetic samples post transfusion could result in “chimerism” in the genotype and that this could persists for long periods after trauma. However, the coordinators have taken a pragmatic view that samples should be taken at baseline when taking biomarker samples (+/- coagulation samples for those sites in the sub-study). This pragmatic approach has numerous advantages; it limits the complexity of the sampling regimen, reduces the need for repeat venepunctures and minimises the risk of missed samples if the participant is lost to follow-up. Accurate documentation of the participant’s transfusion status is essential for future analysis. In some cases, blood sampling for genetic analysis were obtained later. | |
| LabSampling.LSGeneticFreezerDate | Date blood samples are stored in the freezer for genetic analyses | This reflects the Genetic sampling freezer date. Two genetic samples should be obtained in all CENTER-TBI participants. It is recognized by the CENTER-TBI coordinators that obtaining genetic samples post transfusion could result in “chimerism” in the genotype and that this could persists for long periods after trauma. However, the coordinators have taken a pragmatic view that samples should be taken at baseline when taking biomarker samples (+/- coagulation samples for those sites in the sub-study). This pragmatic approach has numerous advantages; it limits the complexity of the sampling regimen, reduces the need for repeat venepunctures and minimises the risk of missed samples if the participant is lost to follow-up. Accurate documentation of the participant’s transfusion status is essential for future analysis. In some cases, blood sampling for genetic analysis were obtained later. | |
| LabSampling.LSGeneticFreezerTime | Time blood samples are stored in the freezer for genetic analyses | This reflects the Genetic sampling freezer time. Two genetic samples should be obtained in all CENTER-TBI participants. It is recognized by the CENTER-TBI coordinators that obtaining genetic samples post transfusion could result in “chimerism” in the genotype and that this could persists for long periods after trauma. However, the coordinators have taken a pragmatic view that samples should be taken at baseline when taking biomarker samples (+/- coagulation samples for those sites in the sub-study). This pragmatic approach has numerous advantages; it limits the complexity of the sampling regimen, reduces the need for repeat venepunctures and minimises the risk of missed samples if the participant is lost to follow-up. Accurate documentation of the participant’s transfusion status is essential for future analysis. In some cases, blood sampling for genetic analysis were obtained later. | |
| LabSampling.LSGeneticNotCollReason | Reason for not collecting blood samples for genetic analyses | 1 == No informed consent 2 == Blood draw not successful 3 == Logistic reasons |
This reflects the reason why Genetic sampling was not obtained. |
| LabSampling.LSHospitalCollctnDate | Date of collection of blood samples for hospital lab | This reflects the blood sampling collection date for routine hospital labs. Sites were requested to document results of all routinely performed lab assessments at baseline, including where possible/applicable point-of-care testing. For patients with multiple labs at different times during the day, a new Lab form was created for each collection | |
| LabSampling.LSHospitalCollctnTime | Time of collection of blood samples for hospital lab | This reflects the blood sampling collection time for routine hospital labs. Sites were requested to document results of all routinely performed lab assessments at baseline, including where possible/applicable point-of-care testing. For patients with multiple labs at different times during the day, a new Lab form was created for each collection | |
| LabSampling.LSPointOfCareCollctnDate | Date of collection of blood samples for point of care testing | Reflects the date for Point of care testing. | |
| LabSampling.LSPointOfCareCollctnTime | Time of collection of blood samples for point of care testing | Reflects the time for Point of care testing | |
| LabSampling.LSTissueCollctnDate | Date of collection of blood samples for tissue | Reflects the date for Tissue collection. | |
| LabSampling.LSTissueCollctnTime | Time of collection of blood samples for tissue | Reflects the time for Tissue collection. | |
| MedHx.AnticoagAntiThrombinProtein | Anticoagulants: Antithrombin protein therapeutics (Atryn) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of antithrombin protein therapeutics (Atryn). | |
| MedHx.AnticoagCoumarin | Anticoagulants: Coumarin derivative (Coumadin, Warfarin) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of Coumarin derivative (Coumadin, Warfarin). | |
| MedHx.AnticoagDirectThrombinInhib | Anticoagulants: Direct thrombin inhibitor (eg. dabigatran, argatroban, melagatran) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of direct thrombin inhibitors (eg. dabigatran, argatroban, melagatran). | |
| MedHx.AnticoagFactorXaInhib | Anticoagulants: Inhibitor of factor Xa (eg. Rivaroxaban) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of inhibitor of factor Xa (eg. rivaroxaban). | |
| MedHx.AnticoagHeparin | Anticoagulants: Heparin | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of heparin. | |
| MedHx.AnticoagLowMolHeparin | Anticoagulants: Low-molecular weight heparin | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of low molecular weight heparin | |
| MedHx.AnticoagulantOther | Anticoagulants: Other | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of another type of anticoagulant or platelet aggregation inhibitor, not specified elsewhere. | |
| MedHx.AnticoagulantOtherTxt | Anticoagulants: Other (please specify) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of another type of anticoagulant or platelet aggregation inhibitor, not specified elsewhere. Text field. | |
| MedHx.AnticoagulantReasonCardiac | Were cardiac problems a reason for taking anticoagulant medication or platelet aggregation inhibitors? | 0 == No 1 == Yes |
Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiac. |
| MedHx.AnticoagulantReasonCardiacCABG | Cardiac: CABG | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiac, specifically CABG. | |
| MedHx.AnticoagulantReasonCardiacFibrill | Cardiac: Atrial Fibrillation/Flutter | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiac, specifically atrial fibrillation/flutter. | |
| MedHx.AnticoagulantReasonCardiacStent | Cardiac: Cardiac stent | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiac, specifically a cardiac stent. | |
| MedHx.AnticoagulantReasonCardiacValve | Cardiac: Valve prosthesis | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiac, specifically a valve prosthesis. | |
| MedHx.AnticoagulantReasonCardiovas | Were cadiovascular problems a reason for taking anticoagulant medication or platelet aggregation inhibitors? | 0 == N0 1 == Yes |
Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiovascular. |
| MedHx.AnticoagulantReasonCardiovasCarotidStent | Cardiovascular: Carotid or cerebral stent | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiovascular, specifically a carotid or cerebral stent. | |
| MedHx.AnticoagulantReasonCardiovasLimbIsch | Cardiovascular: Limb ischaemia | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiovascular, specifically limb ischaemia. | |
| MedHx.AnticoagulantReasonCardiovasOtherStent | Cardiovascular: Other stent | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiovascular, specifically a stent not specified elsewhere. | |
| MedHx.AnticoagulantReasonCardiovasStenosis | Cardiovascular: Cardiovascular stenosis | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiovascular, specifically a cardiovascular stenosis | |
| MedHx.AnticoagulantReasonCardiovasTIS | Cardiovascular: Transient Ischaemic Attack (TIA)/stroke | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is cardiovascular, specifically a transient ischaemic attack/stroke | |
| MedHx.AnticoagulantReasonOther | Other reason for taking anticoagulant medication or platelet aggregation inhibitors | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is not specified elsewhere. | |
| MedHx.AnticoagulantReasonOtherTxt | Other reason for taking anticoagulant medication or platelet aggregation inhibitors (please specify) | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is not specified elsewhere (text field). | |
| MedHx.AnticoagulantReasonThrombo | Was Thromboembolism a reason for taking anticoagulant medication or platelet aggregation inhibitors | 0 == No 1 == Yes |
Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is thromboembolic. |
| MedHx.AnticoagulantReasonThromboDVTLess6 | Thromboembolism: Single episode of DVT or PE < 6 months | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is thromboembolic, specifically a single episode of DVT (deep venous thrombosis) or PE (pulmonary embolism) <6 months. | |
| MedHx.AnticoagulantReasonThromboDVTMore6 | Thromboembolism: Single episode of DVT or PE > 6 months | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is thromboembolic, specifically a single episode of DVT (deep venous thrombosis) or PE (pulmonary embolism) >6 months. | |
| MedHx.AnticoagulantReasonThromboMultipleEpisode | Thromboembolism: Two or more episodes of DVT or PE | Medical history. This variable is populated when the reason for using anticoagulants or platelet aggregation inhibitors by the patient is thromboembolic, specifically two or more episodes of DVT (deep venous thrombosis) or PE (pulmonary embolism). | |
| MedHx.AnticoagXarelto | Anticoagulants: Xarelto | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of Xarelto | |
| MedHx.BetaBlocker | Does patient take blockers? | 0 == No 1 == Yes 88 == Unknown |
A specific question on the use of beta-blockers is included as some reports indicate better outcome with the use of beta blockers (Research interest Rotterdam). If yes, specification is requested and differentiated into: Non-selective blockers/Selective beta-1 blockers/alpha-1 and beta blockers. |
| MedHx.BetaBlockerAlphaBucundolol | Alpha-1 and beta blockers: Bucundolol | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of a beta blocker, specifically Bucindolol. | |
| MedHx.BetaBlockerAlphaCarvedilol | Alpha-1 and beta blockers:Carvedilol (Eucardic) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of a beta blocker, specifically Carvedilol (Eucardic). | |
| MedHx.BetaBlockerAlphaLabetolol | Alpha-1 and beta blockers: Labetolol (Trandate) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of a beta blocker, specifically Labetalol (Trandate). | |
| MedHx.BetaBlockerAlphaOther | Alpha-1 and beta blockers: Other | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of an alpha 1 and beta-blocker, not specified elsewhere. | |
| MedHx.BetaBlockerAlphaOtherTxt | Alpha-1 and beta blockers: Other (please specify) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of an alpha 1 and beta-blocker, not specified elsewhere (text field). | |
| MedHx.BetaBlockerNonSelectCarteolol | Carteolol as Non-selective blockers | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, specifically Carteolol. | |
| MedHx.BetaBlockerNonSelectNadolol | Nadolol as Non-selective blockers | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, specifically Nadolol | |
| MedHx.BetaBlockerNonSelectOther | Other non-selective blockers (please specify) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, nonselective, not specified elsewhere. | |
| MedHx.BetaBlockerNonSelectOtherTxt | Other non-selective blockers (please specify) | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, nonselective, not specified elsewhere (textfield). | |
| MedHx.BetaBlockerNonSelectPenbutolol | Penbutolol as Non-selective blockers | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, specifically Penbutolo. | |
| MedHx.BetaBlockerNonSelectPindolol | Pindolol as Non-selective blockers | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, specifically Pindolol (Viskeen) | |
| MedHx.BetaBlockerNonSelectPropranolol | Propranol as Non-selective blockers | Medical history. This variable describes the use of beta blockers, specifically Propranolol | |
| MedHx.BetaBlockerNonSelectSotalol | Sotacor (Sotalol) as non-selective blockers | Medical history. This variable describes the use of beta blockers, specifically Sotalol (Sotacor) | |
| MedHx.BetaBlockerSelectAcebutolol | Acebutolol (Sectral) as Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically Acebutolol (Sectral) | |
| MedHx.BetaBlockerSelectAtenolol | Atenolol (Tenormin) as Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically Atenolol (Tenormin) | |
| MedHx.BetaBlockerSelectBetaxolol | Betaxolol (Kerlon) as Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically Betaxolol (Kerlon) | |
| MedHx.BetaBlockerSelectBisoprolol | Bisoprolol (Emcor) as Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically Bisoprolol (Emcor) | |
| MedHx.BetaBlockerSelectCeliprolol | Celiprolol (Dilanorm) as Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically Celiprolol (Dilanorm) | |
| MedHx.BetaBlockerSelectEsmolol | Esmolol (Brevibloc) as Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically Esmolol (Brevibloc) | |
| MedHx.BetaBlockerSelectMetoprolol | Metoprolol (Selokeen) as Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically Metoprolol (Selokeen). | |
| MedHx.BetaBlockerSelectNebivolol | Nebivolol (Nebilet) as Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically Nebivolol (Nebilet) | |
| MedHx.BetaBlockerSelectOther | Other Selective beta1-blockers | Medical history. This variable describes the use of beta blockers, specifically selective beta1blockers not specified elsewhere. | |
| MedHx.BetaBlockerSelectOtherTxt | Other Selective beta1-blockers (please specify) | Medical history. This variable describes the use of beta blockers, specifically selective beta1blockers not specified elsewhere (text field). | |
| MedHx.MedHxAnticoagulantsOrPlatelet | Does patient take either anticoagulants or platelet aggregation inhibitors? | 88 == Unknown 1 == Yes anticoagulants 0 == No 2 == Yes platelet aggregation inhibitors 3 == Yes, both |
Summary question to document if the subject was taking anticoagulants or platelet aggregation inhibitors prior to injury. If yes, details are requested concerning which (groups of) agents were used. This information is of high relevance in relation to the shift of epidemiologic patterns in TBI towards higher age (with more co-morbidities and medication). |
| MedHx.MedHxCardio | 010 Cardiovascular | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history. |
| MedHx.MedHxCardioArrhythmia | 012 Cardiovascular: Arrhythmia | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, specifically arrhythmia. | |
| MedHx.MedHxCardioCongenitalHD | 011 Cardiovascular: Congenital heart disease | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, specifically congenital heart disease. | |
| MedHx.MedHxCardioHTN | 015 Cardiovascular: Hypertension | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, specifically hypertension | |
| MedHx.MedHxCardioIschemicHD | 013 Cardiovascular: Ischemic heart disease | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, specifically Ischemic heart disease | |
| MedHx.MedHxCardioNYHA | Cardiovascular: NYHA classification | I == I II == II III == III IV == IV |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, specifically NYHA, a classification system for severity of cardiac disease - generally used for ischaemia, but used here in broader sense. |
| MedHx.MedHxCardioOther | 018 Cardiovascular: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, not specified elsewhere. | |
| MedHx.MedHxCardioOtherTxt | Cardiovascular: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, not specified elsewhere (textfield) | |
| MedHx.MedHxCardioPeripheralVascular | 017 Cardiovascular: Peripheral vascular disease | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, specifically peripheral vascular disease. | |
| MedHx.MedHxCardioThromboembolic | 016 Cardiovascular: Thromboembolic | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, specifically thromboembolic | |
| MedHx.MedHxCardioValvularHD | 014 Cardiovascular: Valvular heart disease | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting cardiovascular medical history, specifically valvular heart disease | |
| MedHx.MedHxDevelopmental | 150 Developmental | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting developmental diseases. |
| MedHx.MedHxDevelopmentalADDandADHD | 152 Developmental: Attention deficit/hyperactivity disorder | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting developmental diseases, specifically attention deficit/hyperactivity disorder. | |
| MedHx.MedHxDevelopmentalLearningDisability | 151 Developmental: Learning disability | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting developmental diseases, specifically learning disability | |
| MedHx.MedHxDevelopmentalOther | 153 Developmental: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting developmental diseases that are not specified elsewhere. | |
| MedHx.MedHxDevelopmentalOtherTxt | Developmental: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting developmental diseases that are not specified elsewhere (textfield). | |
| MedHx.MedHxEndocrine | 020 Endocrine | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting endocrine diseases |
| MedHx.MedHxEndocrineIDDM | 022 IDDM (Endocrine: Insulin Dependent Diabetes Mellitus) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting endocrine diseases, specifically IDDM (Insulin dependent diabetes mellitus) | |
| MedHx.MedHxEndocrineIDDMControl | Endocrine: How well is IDDM controlled? | 1 == Well controlled 2 == Difficult controlled 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting for endocrine diseases, specifically IDDM (Insulin dependent diabetes mellitus) - how well it is controlled. |
| MedHx.MedHxEndocrineNIDDM | 023 NDDM (Endocrine: Non-insulin Dependent Diabetes Mellitus) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting endocrine diseases, specifically NIDDM (Non-insulin dependent diabetes mellitus) | |
| MedHx.MedHxEndocrineNIDDMControl | Endocrine: How well is NIDDM controlled? | 1 == Well controlled 2 == Difficult controlled 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting for endocrine diseases, specifically NIDDM (Non-insulin dependent diabetes mellitus), how well it is controlled. |
| MedHx.MedHxEndocrineOther | 024 Endocrine: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting endocrine diseases not mentioned elsewhere. | |
| MedHx.MedHxEndocrineOtherTxt | Endocrine: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting endocrine diseases not specified elsewhere (textfield). | |
| MedHx.MedHxEndocrineThyroid | 021 Endocrine: Thyroid | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting endocrine diseases, specifically thyroid disorder. | |
| MedHx.MedHxENT | 030 ENT (Eye, Ear, Nose and Throat) | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting ENT (Eye, Ear, Nose & Throat) disease |
| MedHx.MedHxENTHearing | 033 ENT (Eye, Ear, Nose and Throat): Hearing | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting ENT (Eye, Ear, Nose & Throat) disease, specifically hearing deficits. | |
| MedHx.MedHxENTOther | 034 ENT (Eye, Ear, Nose and Throat): Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting ENT (Eye, Ear, Nose & Throat) diseases not specified elsewhere. | |
| MedHx.MedHxENTOtherTxt | ENT (Eye, Ear, Nose and Throat): Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting ENT (Eye, Ear, Nose & Throat) diseases not specified elsewhere (textfield). | |
| MedHx.MedHxENTSinusitis | 031 ENT (Eye, Ear, Nose and Throat): Sinusitis | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting ENT (Eye, Ear, Nose & Throat) diseases, specifically sinusitis. | |
| MedHx.MedHxENTVisionAbn | 032 ENT (Eye, Ear, Nose and Throat): Vision abnormality | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting ENT (Eye, Ear, Nose & Throat) diseases, specifically vision. | |
| MedHx.MedHxGastro | 040 Gastrointestinal | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting gastrointestinal disease. |
| MedHx.MedHxGastroGERD | 041 Gastrointestinal: GERD (Gastroesophageal Reflux Disease) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting gastrointestinal disease, specifically GERD (Gastroesophageal Reflux Disease). | |
| MedHx.MedHxGastroGIBleed | 042 Gastrointestinal: GI bleed | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting gastrointestinal disease, specifically gastrointestinal bleeding. | |
| MedHx.MedHxGastroIBS | 043 Gastrointestinal: Inflammatory bowel disease | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting gastrointestinal disease, specifically inflammatory bowel disease. | |
| MedHx.MedHxGastroOther | 044 Gastrointestinal: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting gastrointestinal disease not specified elsewhere. | |
| MedHx.MedHxGastroOtherTxt | Gastrointestinal: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting gastrointestinal disease not specified elsewhere (textfield). | |
| MedHx.MedHxHematologic | 050 Hematologic | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hematologic diseases. |
| MedHx.MedHxHematologicAIDS | 053 Hematologic: AIDS | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hematologic diseases, specifically AIDS | |
| MedHx.MedHxHematologicAnemia | 051 Hematologic: Anemia | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hematologic diseases, like anemia. | |
| MedHx.MedHxHematologicHIV | 052 Hematologic: HIV positive | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hematologic diseases, like HIV positive. | |
| MedHx.MedHxHematologicOther | 055 Hematologic: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hematologic diseases, not specified elsewhere. | |
| MedHx.MedHxHematologicOtherTxt | Hematologic: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hematologic diseases, not specified elsewhere (textfield). | |
| MedHx.MedHxHematologicSickleCell | 054 Hematologic: Sickle cell disease | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hematologic diseases, specifically sickle cell disease. | |
| MedHx.MedHxHepatic | 060 Hepatic | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hepatic diseases. |
| MedHx.MedHxHepaticCirrhosis | 064 Hepatic: Cirrhosis | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hepatic diseases, specifically cirrhosis. | |
| MedHx.MedHxHepaticFailure | 062 Hepatic: Failure | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hepatic diseases, specifically hepatic failure | |
| MedHx.MedHxHepaticHepatitis | 063 Hepatic: Hepatitis | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hepatic diseases, specifically hepatitis. | |
| MedHx.MedHxHepaticInsufficiency | 061 Hepatic: Insufficiency | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hepatic diseases, specifically hepatic insufficiency. | |
| MedHx.MedHxHepaticOther | 065 Hepatic: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hepatic diseases not specified elsewhere | |
| MedHx.MedHxHepaticOtherTxt | Hepatic: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting hepatic diseases not specified elsewhere (textfield) | |
| MedHx.MedHxMusculoskeletal | 070 Musculoskeletal | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting musculoskeletal diseases |
| MedHx.MedHxMusculoskeletalArthritis | 071 Musculoskeletal: Arthritis | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting musculoskeletal diseases, specifically arthritis | |
| MedHx.MedHxMusculoskeletalOther | 072 Musculoskeletal: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting musculoskeletal diseases not specified elsewhere. | |
| MedHx.MedHxMusculoskeletalOtherTxt | Musculoskeletal: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting musculoskeletal diseases not specified elsewhere (textfield) | |
| MedHx.MedHxNeuro | 080 Neurologic | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases. |
| MedHx.MedHxNeuroCerebrovascularAccident | 081 Neurologic: Cerebrovascular accident | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically cerebrovascular accidents. | |
| MedHx.MedHxNeuroEpilepsyGeneralized | 085 Neurologic: Epilepsy (generalized) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically epilepsy (generalized). | |
| MedHx.MedHxNeuroEpilepsyOther | 086 Neurologic: Epilepsy (other) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically epilepsy (other). | |
| MedHx.MedHxNeuroEpilepsyPartial | 084 Neurologic: Epilepsy (partial) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically epilepsy (partial). | |
| MedHx.MedHxNeuroFebrileSeizures | 083 Neurologic: Febrile seizures (children) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically febrile seizures (children). | |
| MedHx.MedHxNeuroHeadache | 091 Neurological (Aches): Headache - non migraine | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically headache (non migraine). | |
| MedHx.MedHxNeuroMigraine | 092 Neurological (Aches): Headache - migraines | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically migraines. | |
| MedHx.MedHxNeuroMigraineFamHist | 093 Neurological (Aches): Family history of migraine | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically family history of migraine. | |
| MedHx.MedHxNeuroOther | 086 Neurologic: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases not specified elsewhere. | |
| MedHx.MedHxNeuroOtherTxt | Neurologic: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases not specified elsewhere (textfield) | |
| MedHx.MedHxNeuroPain | 090 Neurological (Aches) | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases not specified elsewhere (textfield) |
| MedHx.MedHxNeuroTIA | 082 Neurologic: Transient ischemic attacks (TIA) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting neurological diseases, specifically transient ischemic attacks | |
| MedHx.MedHxOncologic | 110 Oncologic | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases. |
| MedHx.MedHxOncologicBreast | 113 Oncologic: Breast cancer | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases, like breast cancer. | |
| MedHx.MedHxOncologicGI | 116 Oncologic: GI cancer | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases, specifically gastrointestinal cancer. | |
| MedHx.MedHxOncologicKidney | 117 Oncologic: Kidney cancer | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases, specifically kidney cancer. | |
| MedHx.MedHxOncologicLeukemia | 111 Oncologic: Leukemia | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases, specifically leukemia. | |
| MedHx.MedHxOncologicLung | 115 Oncologic: Lung cancer | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases, specifically lung cancer. | |
| MedHx.MedHxOncologicLymphoma | 112 Oncologic: Lymphoma | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases, specifically lymphoma. | |
| MedHx.MedHxOncologicOther | 118 Oncologic: Other cancer | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases not specified elsewhere | |
| MedHx.MedHxOncologicOtherTxt | Oncologic: Other cancer (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic diseases not specified elsewhere (textfield). | |
| MedHx.MedHxOncologicProstate | 114 Oncologic: Prostrate cancer | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting oncologic, specifically prostate cancer. | |
| MedHx.MedHxOther | 160 Other medical history | 0 == No 1 == Yes |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting other medical history, not specified elsewhere. |
| MedHx.MedHxOtherTxt | Other medical history (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting other medical history, not specified elsewhere (textfield) | |
| MedHx.MedHxPreInjASAPSClass | Pre-injury ASA-PS Classification system | 88 == Unknown 1 == A normal healthy patient 2 == A patient with mild systemic disease 3 == A patient with severe systemic disease 4 == A patient with a severe systemic disease that is a constant threat to life |
Preinjury ASAPS classification. Common classification system used in anaesthesia; denotes overall health |
| MedHx.MedHxPreTBIConcussions | 100 Previous TBI or concussions | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting previous TBI/ concussions |
| MedHx.MedHxPreTBIConcussionsTotal | Total number of TBI or concussions | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting total number of previous TBI/ concussions | |
| MedHx.MedHxPreTBIConcussionsTotalHosAdmit | Number of hospital admissions for TBI or concussions | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting total number of hospital admissions for previous TBI/ concussions | |
| MedHx.MedHxPsychiatric | 130 Psychiatric | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting psychiatric diseases. |
| MedHx.MedHxPsychiatricAnx | 131 Psychiatric: Anxiety | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting psychiatric diseases, specifically anxiety. | |
| MedHx.MedHxPsychiatricDep | 132 Psychiatric: Depression | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting psychiatric diseases, specifically depression. | |
| MedHx.MedHxPsychiatricOther | 135 Psychiatric: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting psychiatric diseases not documented elsewhere. | |
| MedHx.MedHxPsychiatricOtherTxt | Psychiatric: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting psychiatric diseases not documented elsewhere (textfield). | |
| MedHx.MedHxPsychiatricSchiz | 134 Psychiatric: Schizophrenia | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting psychiatric diseases, specifically schizophrenia. | |
| MedHx.MedHxPsychiatricSleep | 133 Psychiatric: Sleep disorders | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting psychiatric diseases, specifically sleep disorders. | |
| MedHx.MedHxPsychiatricSubstanceAbuse | 135 Psychiatric: Substance abuse disorder | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting psychiatric diseases, specifically substance abuse disorders. | |
| MedHx.MedHxPulmonary | 120 Pulmonary | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting pulmonary diseases |
| MedHx.MedHxPulmonaryAsthma | 122 Pulmonary: Asthma | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting pulmonary diseases, specifically asthma. | |
| MedHx.MedHxPulmonaryCOPD | 121 Pulmonary: COPD | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting pulmonary diseases, specifically COPD (Chronic Obstructive Pulmonary Disease) | |
| MedHx.MedHxPulmonaryOther | 125 Pulmonary: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting pulmonary diseases not specified elsewhere. | |
| MedHx.MedHxPulmonaryOtherTxt | Pulmonary: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting pulmonary diseases not specified elsewhere (textfield). | |
| MedHx.MedHxPulmonaryPneumonia | 123 Pulmonary: Pneumonia | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting pulmonary diseases, specifically pneumonia. | |
| MedHx.MedHxPulmonaryTB | 124 Pulmonary: Tuberculosis | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting pulmonary diseases, specifically tuberculosis. | |
| MedHx.MedHxRenal | 140 Renal | 0 == No 1 == Yes 88 == Unknown |
Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting renal diseases. |
| MedHx.MedHxRenalFailure | 143 Renal: Failure | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting renal diseases, specifically renal failure. | |
| MedHx.MedHxRenalInsufficiency | 141 Renal: Insufficiency | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting renal diseases, specifically renal insufficiency. | |
| MedHx.MedHxRenalOther | 144 Renal: Other | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting renal diseases not specified elsewhere. | |
| MedHx.MedHxRenalOtherTxt | Renal: Other (please specify) | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting renal diseases not specified elsewhere (textfield). | |
| MedHx.MedHxRenalUTI | 143 Renal: UTI | Details on Medical History are captured for 15 body regions/disease area's. If overall question for the body region/disease is "yes", more detailed info is requested and captured in the sub-domains. This variable is used for documenting renal diseases, specifically chronic UTI (urinary tract infection). | |
| MedHx.PlateletAggreOther | Platelet aggregation inhibitors: Other | Medical history. Variable documents the use of anticoagulants or platelet aggregation inhibitors. This variable contains the medication of this type not specified elsewhere. | |
| MedHx.PlateletAggreOtherTxt | Platelet aggregation inhibitors: Other (please specify) | Medical history. Variable documents the use of anticoagulants or platelet aggregation inhibitors. This variable contains the medication of this type not specified elsewhere (textfield). | |
| MedHx.PltAggregAdenosineInhib | Platelet aggregation inhibitors: Adenosine re-uptake inhibitor (eg. Persantin, Dipyridamole) | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of an adenosine reuptake inhibitor (eg. Persantin, dipyridamole). | |
| MedHx.PltAggregADPReceptInhib | Platelet aggregation inhibitors: ADP receptor inhibitors | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of ADP receptor inhibitors. | |
| MedHx.PltAggregADPReceptInhibEffient | Platelet aggregation inhibitors: Parasugrel (Effient) | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of Parasugrel (Effient) | |
| MedHx.PltAggregADPReceptInhibOther | Platelet aggregation inhibitors: Other ADP receptor inhibitors | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of ADP receptor inhibitors, not specified elsewhere. | |
| MedHx.PltAggregADPReceptInhibOtherTxt | Platelet aggregation inhibitors: Other ADP receptor inhibitors (please specify) | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of ADP receptor inhibitors, not specified elsewhere (textfield). | |
| MedHx.PltAggregADPReceptInhibPlavix | Platelet aggregation inhibitors: Clopidogrel (Plavix) | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of Clopidogrel (Plavix). | |
| MedHx.PltAggregADPReceptInhibTiclid | Platelet aggregation inhibitors: Ticlopidine (Ticlid) | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of Ticlopidine (Ticlid). | |
| MedHx.PltAggregAspirin | Platelet aggregation inhibitors: Aspirin | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of Aspirin | |
| MedHx.PltAggregGlycoproteinInhib | Platelet aggregation inhibitors: Glycoprotein IIB/IIIA inhibitors (eg. Aggrastat) | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of glycoprotein IIB/IIIA inhibitors (eg. Aggrastat). | |
| Medication.Agent | Agent | 99 == Other, specify in Agent Other: Other 66 == Prokinetics: Metoclopramide (Primperan) 64 == Prokinetics: Domperidon (Motilium) 65 == Prokinetics: Erythromycin 63 == Proton pump inhibitors: Pantoprazole (Pantozol) 62 == Proton pump inhibitors: Esomeprazol (Nexium) 61 == Proton pump inhibitors: Omeprazol (Losec) 60 == H2 receptor antagonist: Ranitidine (Zantac) 59 == H2 receptor antagonist: Cimetidine 58 == Antacids: other 57 == Antacids: Aluminium hydroxide 56 == Steroids: hydrocortisone/cortisone 55 == Steroids: dexametasone 54 == Steroids: bétametasone 53 == Steroids: methylprednisolone 52 == Calcium channel blockers: verapamil 51 == Calcium channel blockers: nicardipine 50 == Calcium channel blockers: nimodipine 49 == Anti- hypertensive: diuretics 48 == Anti- hypertensive: clonidine 47 == Anti- hypertensive: bètablockers (propanolol) 46 == Anti- hypertensive: angiotensininhibitors (cardesartan etc) 45 == Anti- hypertensive: ACE blockers (captopril, perindopril etc) 44 == Antibiotics: other 43 == Antibiotics: sulfonamides (co-trimoxazole, doxycycline) 42 == Antibiotics: quinolones (ciprofloxacine etc) 41 == Antibiotics: amoxycilline/clavulanic acid (augmentin, tyclav etc) 40 == Antibiotics: penicillines (ampicilline, cloxacilline) 39 == Antibiotics: nitrofurones (furoxone, furadantine etc) 38 == Antibiotics: macrolidis (erythromycine etc) 37 == Antibiotics: lincosamides (clindamycine etc) 36 == Antibiotics: glycopeptides (vancomycine) 35 == Antibiotics: cephalosporin 5th gen (ceftasoline etc) 34 == Antibiotics: cephalosporin 4th gen (cefepime, maxipime etc) 33 == Antibiotics: cephalosporin 3rd gen (cefotaxine etc) 32 == Antibiotics: cephalosporin 2nd gen (cefuroxim etc) 31 == Antibiotics: cephalosporin 1st gen (cefalexin etc) 30 == Antibiotics: carbapemens (meronem etc) 29 == Antibiotics: aminoglycoside (amikacine, gentamicine etc) 28 == Anti- epileptic: other 27 == Anti- epileptic: valproate (depakine) 26 == Anti- epileptic: phenytoine (diphantoine) 25 == Anti- epileptic: levetirazetam (keppra) 24 == Anti- epileptic: lamotrigine (lamectal) 23 == Anti- epileptic: carbamazepine (tegretol) 22 == Neuromuscular blockade: other 21 == Neuromuscular blockade: vecuronium (norcuron) 20 == Neuromuscular blockade: rocuronium (zemuron) 19 == Neuromuscular blockad: gallamine (flaxedil) 18 == Neuromuscular blockade: cisatracurium (nimbex) 17 == Neuromuscular blockade: atracurium (tracium) 16 == Neuromuscular blockade: pancuronium (pavulon) 15 == Sedatives/treatment of agitation: other 14 == Sedatives/treatment of agitation: propofol 13 == Sedatives/treatment of agitation: morphine 12 == Sedatives/treatment of agitation: midazolam 11 == Sedatives/treatment of agitation: lorazepam (tenesta, ect) 10 == Sedatives/treatment of agitation: haloperidol (haldol) 9 == Sedatives/treatment of agitation: fentanyl 8 == Sedatives/treatment of agitation: diazepam 7 == Sedatives/treatment of agitation: dexmedetomidine 6 == Sedatives/treatment of agitation: clondine 5 == Sedatives/treatment of agitation: barbiturates (penthothal, ect) 4 == Analgesic: opioids (morphine, ect) 3 == Analgesic: tramadol 2 == Analgesic: NSAIDs 1 == Analgesic: paracetamol 67 == Analgesic: other 68 == Anti- hypertensive: other 69 == Calcium channel blockers: other 70 == Steroids: other 71 == H2 receptor antagonist: other 72 == Proton pump inhibitors: other 73 == Prokinetics:other |
Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes the Agent. Agents commonly used for treatment of raised ICP are listed in the TIL section, but not included in the medication lists here. |
| Medication.AgentOther | Other agent (please specify) | Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes if the Agent was "other" than the predefined list. | |
| Medication.Class | Class | 99 == Other, specify in Agent Other 1 == Analgesic 6 == Anti- hypertensive 5 == Antibiotics 4 == Anti- epileptic 3 == Neuromuscular blockade 2 == Sedatives/treatment of agitation 11 == Proton pump inhibitors 12 == Prokinetics 10 == H2 receptor antagonist 8 == Steroids 9 == Antacids 7 == Calcium channel blockers |
Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes the Classes. Classes: analgesic, sedatives, neuromuscular blocking agents, anti-epileptic drugs, antibiotiucs, anti-hypertensive, calcium channel blockers, steroids, antacids, H2 receptor antagonists, proton pump inhibitors and prokinetics. Agents commonly used for treatment of raised ICP are listed in the TIL section, but not included in the medication lists here. |
| Medication.HighestDailyDose | Highest daily dose | Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes the Highest Daily Dose. These details should be entered for each agent. | |
| Medication.Ongoing | Is medication ongoing? | Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes if medication was still ongoing on discharge. These details should be entered for each agent. | |
| Medication.Reason | Reason for taking medication | 99 == Other, specify in Agent Other: Other 46 == Prokinetics: Other 45 == Proton pump inhibitors: Other 44 == H2 receptor antagonist: Other 43 == Antacids: Other 42 == Steroids: Other 41 == Calcium channel blockers: Other 40 == Anti- hypertensive: Other 39 == Antibiotics: Other 37 == Sedatives/treatment of agitation: Other 38 == Anti- epileptic: Other 36 == Neuromuscular blockade: other 35 == Analgesic: other 33 == Prokinetics: routine care 32 == Prokinetics: constipation 31 == Prokinetics: vomiting 30 == Prokinetics: gastric retention 29 == Proton pump inhibitors: treatment of ulcer 28 == Proton pump inhibitors: gastric protection 27 == H2 receptor antagonist: treatment of ulcer 26 == H2 receptor antagonist: gastric protection 25 == Antacids: reflux 24 == Antacids: gastric protection 23 == Steroids: sepsis 22 == Steroids: hypopituitarism 21 == Steroids: ARDS 20 == Steroids: traumatic brain injury 19 == Calcium channel blockers: cardiac indication 17 == Calcium channel blockers: treatment of vasospasm 18 == Calcium channel blockers: anti- hypertensive 16 == Calcium channel blockers: prevention of vasospasm 15 == Anti- hypertensive: treatment agitation 14 == Anti- hypertensive: to lower blood pressure 12 == Antibiotics: periprocedural prophylaxis 13 == Antibiotics: meningitis 11 == Antibiotics: intracranial abces/empyeme 10 == Antibiotics: catheter related bloodstream infection 9 == Antibiotics: urinary tract infection 7 == Antibiotics: fever, no clear focus 8 == Antibiotics: pneumonia 6 == Anti- epileptic: treatment of (silent) seizure activity 4 == Anti- epileptic: treatment of overt seizure 3 == Anti- epileptic: prophylaxis 2 == Sedatives/treatment of agitation: metabolic suppression 1 == Sedatives/treatment of agitation: mechanical ventilation |
Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes the Reason for medication. These details should be entered for each agent. |
| Medication.ReasonOther | Other reason for taking medication (please specify) | Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes the Reason for medication if this was "other than the predefined ones. These details should be entered for each agent. | |
| Medication.Route | Route | Sc == Subcutaneous To == Topical Pv == Vaginal PO == Oral Im == Intramuscular Re == Rectal Ih == Inhaled IvInt == Intermittent IV IvCont == Continuous IV ED == Epidural |
Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes the Route. These details should be entered for each agent. |
| Medication.StartDate | Date medication was started | Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes the Start date for medication. These details should be entered for each agent. | |
| Medication.StopDate | Date medication was stopped | Details on medication captured information on Class, Agent, Reason, Highest daily dose, Route, start and stop date and whether or not medication has been ongoing after discharge. This variable describes the Stop date for medication. These details should be entered for each agent. | |
| Meds.DVTMechOngoing | Is mechanical treatment ongoing? | These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes if Mechanical DVT was still ongoing after discharge. | |
| Meds.DVTPharmOngoing | Is pharmacological treatment ongoing? | These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes if Pharmacologic DVT was still ongoing after discharge. | |
| Meds.DVTPharmType | Type of pharmacological prophylaxis | 8 == Tinzaparin 7 == Reviparin 4 == Enoxaparin 3 == Dalteparin (Fragmin) 1 == Heparin 6 == Parnaparin 5 == Nadroparin (Fraxiparine, Fraxodil) 2 == Low molecular weight Heparin |
These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes the Type of prophylaxis in case of Pharmacologic DVT. |
| Meds.DVTProphylaxisMech | Mechanical treatment | 1 == Yes 0 == No |
These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes presence or absence of Mechanical DVT . |
| Meds.DVTProphylaxisMechStartDate | Date mechanical treatment is started | These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes Start date of Mechanical DVT. | |
| Meds.DVTProphylaxisMechStopDate | Date mechanical treatment is stopped | These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes Stop Date of Mechanical DVT. | |
| Meds.DVTProphylaxisMechType | Type of mechanical prophylaxis | These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes the Type of prophylaxis in case of Mechanical DVT. | |
| Meds.DVTProphylaxisPharm | Pharmacological treatment | 0 == No 1 == Yes |
These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes presence or absence of Pharmacologic DVT. |
| Meds.DVTProphylaxisStartDate | Date pharmacological treatment is started | These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes Start date of Pharmacologic DVT. | |
| Meds.DVTProphylaxisStopDate | Date pharmacological treatment is stopped | These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. This variable describes Stop date of Pharmacologic DVT. | |
| Meds.EnteralNutrition | Enteral Nutrition | 0 == No 1 == Yes |
These variables aim to document specific information on nutritional support, provided by parenteral and/or enteral routes. This variable describes the absence or presence of Enteral Nutrition. |
| Meds.EnteralNutritionRoute | Route of enteral administration | 3 == Gastrostomy 2 == Transpyloric tube 1 == Nasogastric tube |
These variables aim to document specific information on nutritional support, provided by parenteral and/or enteral routes. This variable describes the route of administration for Enteral Nutrition. |
| Meds.EnteralNutritionStartDate | Date enteral nutrition is started | These variables aim to document specific information on nutritional support, provided by parenteral and/or enteral routes. This variable describes the Start Date of Enteral Nutrition. | |
| Meds.EnteralNutritionStopDate | Date enteral nutrition is stopped | These variables aim to document specific information on nutritional support, provided by parenteral and/or enteral routes. This variable describes the Stop Date of Enteral Nutrition. | |
| Meds.Intubation | Intubation | 0 == No 1 == Yes |
This variable describes the absence or presence of Intubation as Ventilation Management (only for ICU patients). |
| Meds.IntubationStartDate | Date intubation is started | This variable describes the Start Date in case of Intubation as Ventilation Management (only for ICU patients). | |
| Meds.IntubationStartTime | Time intubation is started | This variable describes the Start Time in case of Intubation as Ventilation Management (only for ICU patients). | |
| Meds.IntubationStop | Extubation | 0 == No 1 == Yes |
This variable describes the absence or presence of Extubation in case of Ventilation Management (only for ICU patients). |
| Meds.IntubationStopDate | Date extubation is started | This variable describes the Stop Date of Extubation in case of Ventilation Management (only for ICU patients). | |
| Meds.IntubationStopReason | Reason for intubation | 3 == Withdrawal of care 2 == Accidental 1 == Respiratory stable |
This variable describes the Stop Reason of Extubation in case of Ventilation Management (only for ICU patients). |
| Meds.IntubationStopTime | Time extubation is started | This variable describes the Stop Time of Extubation in case of Ventilation Management (only for ICU patients). | |
| Meds.MechVentilation | Mechanical ventilation (any respiratory mode except for CPAP) | 0 == No 1 == Yes |
This variable describes the absence or presence of Mechanical Ventilation (any respiratory mode except for CPAP). |
| Meds.MechVentilationStartDate | Date mechanical ventilation is started | This variable describes the Start Date of Mechanical Ventilation (any respiratory mode except for CPAP). | |
| Meds.MechVentilationStartTime | Time mechanical ventilation is started | This variable describes the Start Time of Mechanical Ventilation (any respiratory mode except for CPAP). | |
| Meds.MechVentilationStopDate | Date mechanical ventilation is stopped | This variable describes the Stop Date of Mechanical Ventilation (any respiratory mode except for CPAP). | |
| Meds.MechVentilationStopTime | Time mechanical ventilation is stopped | This variable describes the Stop Time of Mechanical Ventilation (any respiratory mode except for CPAP). | |
| Meds.Nasogastric | Nasogastric tube | 0 == No 1 == Yes |
Reflects absence or presence of a Nasogastric feeding tube. |
| Meds.NasogastricOngoing | Is nasogastric tube feeding ongoing? | Reflects if a Nasogastric feeding tube remained ongoing. | |
| Meds.NasogastricStartDate | Date nasogastric tube is inserted | Reflects Start Date of a Nasogastric feeding tube. | |
| Meds.NasogastricStopDate | Date nasogastric tube is removed | Reflects Stop Date of a Nasogastric feeding tube. | |
| Meds.OxygenAdm | Oxygen administration | 88 == Unknown 1 == Yes 0 == No |
Reflects presence or absence of Oxygen Administration. |
| Meds.OxygenAdmOngoing | Is oxygen administration ongoing? | Reflects if Oxygen Administration remained ongoing. | |
| Meds.OxygenAdmStartDate | Date oxygen administration is started | Reflects Start Date of Oxygen Administration. | |
| Meds.OxygenAdmStopDate | Date oxygen administration is stopped | Reflects Stop Date of Oxygen Administration. | |
| Meds.ParenteralNutrition | Parenteral Nutrition | 0 == No 1 == Yes |
These variables aim to document specific information on nutritional support, provided by parenteral and/or enteral routes. This variable describes the absence or presence of Parenteral Nutrition. |
| Meds.ParenteralNutritionStartDate | Date parenteral nutrition is started | These variables aim to document specific information on nutritional support, provided by parenteral and/or enteral routes. This variable describes the Start Date of Parenteral Nutrition. | |
| Meds.ParenteralNutritionStopDate | Date parenteral nutrition is stopped | These variables aim to document specific information on nutritional support, provided by parenteral and/or enteral routes. This variable describes the Stop Date of Parenteral Nutrition. | |
| Meds.PEGTube | PEG tube (gastrostomy) | 0 == No 1 == Yes |
This variable describes the absence or presence of a PEG tube (gastrostomy). |
| Meds.PEGTubeOngoing | Is PEG tube feeding ongoing? | This variable describes if presence of a PEG tube (gastrostomy) remained ongoing. | |
| Meds.PEGTubeStartDate | Date PEG tube (gastrostomy) is inserted | This variable describes the Start Date of a PEG tube (gastrostomy) | |
| Meds.PEGTubeStopDate | Date PEG tube (gastrostomy) is removed | This variable describes the Stop Date of a PEG tube (gastrostomy) | |
| Meds.ReIntubation | Need for re-intubation | 0 == No 1 == Yes |
Reflects if there has been a need for re-intubation. |
| Meds.ReIntubationStartDate | Date reintubation is started | Reflects Start Date in case of need for re-intubation. | |
| Meds.ReIntubationStartTime | Time reintubation is started | Reflects Start Time in case of need for re-intubation. | |
| Meds.ReMechVentilation | Need for re-instituting mechanical ventilation | 0 == No 1 == Yes |
Reflects the need for re-instituting mechanical ventilation. |
| Meds.ReMechVentilationReason | Reason for re-instituting mechanical ventilation | 99 == Other 4 == Sepsis 3 == Spontaneous hyperventilation 2 == Neurologic deterioration 1 == Respiratory failure |
Reflects the reason for the need of re-instituting mechanical ventilation. |
| Meds.ReMechVentilationReasonOther | Other reason for re-instituting mechanical ventilation (please specify) | Reflects the "other" reason for the need of re-instituting mechanical ventilation. | |
| Meds.ReMechVentilationStartDate | Date remechanical ventilation is started | Reflects the Start Date for the need of re-instituting mechanical ventilation. | |
| Meds.ReMechVentilationStartTime | Time remechanical ventilation is started | Reflects the Start Time for the need of re-instituting mechanical ventilation. | |
| Meds.TakenMeds | Has the patient taken any medications? | 1 == Yes 0 == No |
Reflects if the patient has taken any medications. Documentation of concomitant medication largely follows a pre-defined structure: A total of 12 classes of drugs are pre-defined, each with a drop-down menu of 1-15 most commonly used agents. The reason for prescribing, the highest daily dose&units as well as route of administration is documented. For agents not listed in the drop-down menu's, the option "other" permits free text entries. |
| Meds.Tracheostomy | Admission Tracheostomy | 0 == No 1 == Yes |
Describes absence or presence of a Tracheostomy. |
| Meds.TracheostomyOngoing | Is tracheostomy ongoing? | Describes if a Tracheostomy remained ongoing. | |
| Meds.TracheostomyStartDate | Date tracheostomy is started | Describes Start Date of a Tracheostomy. | |
| Meds.TracheostomyStopDate | Date tracheostomy is stopped | Describes Stop Date of a Tracheostomy. | |
| Meds.UrineCath | Urinary catheter | 0 == No 1 == Yes |
Describes absence or presence of an Urinary catheter. |
| Meds.UrineCathOngoing | Is urinary catheterisation ongoing? | Describes if an Urinary catheter remained ongoing. | |
| Meds.UrineCathStartDate | Date urinary catheter is inserted | Describes Start Date of an Urinary catheter. | |
| Meds.UrineCathStopDate | Date urinary catheter is removed | Describes Stop Date of an Urinary catheter. | |
| Meds.VentilationMgmtNA | Ventilation Management not applicable (patient not in ICU) | Describes if Ventilation Management was not applicable because patient was not in ICU. | |
| Outcomes.10mWALKBestTestTime | Best trial time | Describes the best trial time for the 10m Walk outcome test. | |
| Outcomes.10mWALKCompletionCode | 10m Walk outcome test completed or not and the reason if not | 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 3.6 == 3.6 Not attempted - Logistical 3.5 == 3.5 Not attempted - Illness 3.4 == 3.4 Not attempted - Language 2.6 == 2.6 Not completed - Logistical 2.5 == 2.5 Not completed - Illness 2.4 == 2.4 Not completed - Language 2.3 == 2.3 Not completed - Poor effort 3.3 == 3.3 Not attempted - Poor effort 3.2 == 3.2 Not attempted - Non-neuro/phys 3.1 == 3.1 Not attempted - Cognitive/neuro 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full |
Describes if the 10m Walk outcome test was completed or not and the reason if not. |
| Outcomes.10mWALKDate | Date of 10m Walk assessment | Describes the Date of the 10m Walk outcome test. | |
| Outcomes.10mWALKTest1 | Test 1 time | Describes the Test 1 time for the 10m Walk outcome test. | |
| Outcomes.10mWALKTest2 | Test 2 time | Describes the Test 2 time for the 10m Walk outcome test. | |
| Outcomes.10mWALKTest3 | Test 3 time | Describes the Test 3 time for the 10m Walk outcome test. | |
| Outcomes.10mWALKTestAttemptdNotCompOptions | Reason for attempting but not completing 10m Walk | 2.6 == Not completed - Logistical reasons, other reasons 2.5 == Not completed - Illness/fatigue 2.4 == Not completed - Language 2.3 == Not completed - Lack of effort/uncooperative 2.2 == Not completed - Non-neurological/physical reason 2.1 == Not completed - Cognitive/neurological deficits 2.7 == Not completed - Examiner error |
This variable describes why the 10m Walk test was attempted, but not completed. |
| Outcomes.10mWALKTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing 10m Walk assessment | This variable describes the "other" reason why the 10m Walk test was attempted, but not completed. | |
| Outcomes.10mWALKTestCompletedOptions | 10m Walk assessment completion type | 3.2 == Non-standard administration - Other 3.1 == Test completed - Non-standard, results valid 3.0 == Test completed in full - results valid |
Describes the test completeness for the 10m Walk outcome test. |
| Outcomes.10mWALKTestComplNonStandAdminOTHER | Other non-standard administration reason for 10m Walk assessment (please specify) | This variable specifies the "other" reason for the 10m Walk outcome test in case of "Non-standard administration - Other". | |
| Outcomes.10mWALKTestNotDoneOptions | Reason for not attempting 10m Walk assessment | 1.6 == Not attempted - Logistical reasons, other reasons 1.5 == Not attempted - Illness/fatigue 1.4 == Not attempted - Language 1.3 == Not attempted - Lack of effort/uncooperative 1.2 == Not attempted - Non-neurological/physical reasons 1.1 == Not attempted - Cognitive/neurological deficits 1.7 == Not attempted - Examiner error 1.8 == Not attempted - Patient not available |
This variable describes the reason why the 10m Walk test was not done. |
| Outcomes.10mWALKTestNotDoneOptionsOTHER | Other reason for not attempting 10m Walk assessment | This variable specifies the "other" reason for why the 10m Walk test was not done. | |
| Outcomes.10mWALKTUGNeuroPsychCompCode | 10m Walk and TUG completion code | 3.0 == 3.0 Test completed 2.0 == 2.0 Test attempted but not completed 1.0 == 1.0 Test not done |
This variable describes the completion status of the 10m Walk outcome assessment. |
| Outcomes.CANTABAST | CANTAB AST completed or not and the reason if not | 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 3.6 == 3.6 Not attempted - Logistical 3.5 == 3.5 Not attempted - Illness 3.4 == 3.4 Not attempted - Language 3.3 == 3.3 Not attempted - Poor effort 3.2 == 3.2 Not attempted - Non-neuro/phys 3.1 == 3.1 Not attempted - Cognitive/neuro 2.6 == 2.6 Not completed - Logistical 2.5 == 2.5 Not completed - Illness 2.4 == 2.4 Not completed - Language 2.3 == 2.3 Not completed - Poor effort 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full |
Reflects if the CANTAB AST (Attention Switching Task) was completed or not and the reason if not. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABASTCompCode | CANTAB-AST assessment completion code | Reflects if the CANTAB AST (Attention Switching Task) was done or not. Completion codes of CANTAB testings were not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMeanBlock3Correct | Cantab AST: mean for correct trials in block 3 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Mean for correct trials in Block 3. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMeanBlock5Correct | Cantab AST: mean for correct trials in block 5 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Mean for correct trials in Block 5. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMeanBlock7Correct | Cantab AST: mean for correct trials in block 7 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Mean for correct trials in Block 7. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMeanCorrect | Cantab AST: mean for all correct trials | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Mean for all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMedianBlock3Correct | Cantab AST: median for correct trials in block 3 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Median for correct trials in Block 3. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMedianBlock5Correct | Cantab AST: median for correct trials in block 5 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Median for correct trials in Block 5. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMedianBlock7Correct | Cantab AST: median for correct trials in block 7 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Median for correct trials in Block 7. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMedianCorrect | Cantab AST: median for all correct trials | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Median for all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostSDBlock3Correct | Cantab AST: standard deviation for correct trials in block 3 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Standard deviation for correct trials in Block 3. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostSDBlock5Correct | Cantab AST: standard deviation for correct trials in block 5 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Standard deviation for correct trials in Block 5. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostSDBlock7Correct | Cantab AST: standard deviation for correct trials in block 7 | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Standard deviation for correct trials in Block 7. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostSDCorrect | Cantab AST: standard deviation for all correct trials | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Standard deviation for all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatency | Cantab AST: mean response latency on all correct trials | Attention Switching Task (AST): Mean response latency on all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencyCongruent | Cantab AST: mean response latency on correct congruent task trials | Attention Switching Task (AST): Mean response latency on correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencyDirection | Cantab AST: mean response latency on correct direction task trials | Attention Switching Task (AST): Mean response latency on correct direction task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencyIncongruent | Cantab AST: mean response latency on correct incongruent task trials | Attention Switching Task (AST): Mean response latency on correct incongruent task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencyNonSwitched | Cantab AST: mean response latency on correct task non-switched trials | Attention Switching Task (AST): Mean response latency on correct task non-switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencySide | Cantab AST: mean response latency on correct side task trials | Attention Switching Task (AST): Mean response latency on correct side task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencySwitched | Cantab AST: mean response latency on correct task switched trials | Attention Switching Task (AST): Mean response latency on correct task switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatency | Cantab AST: median response latency on all correct trials | Attention Switching Task (AST): Median response latency on all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencyCongruent | Cantab AST: median response latency on correct congruent task trials | Attention Switching Task (AST): Median response latency on correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencyDirection | Cantab AST: median response latency on correct direction task trials | Attention Switching Task (AST): Median response latency on correct direction task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencyIncongruent | Cantab AST: median response latency on correct incongruent task trials | Attention Switching Task (AST): Median response latency on correct incongruent task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencyNonSwitched | Cantab AST: median response latency on correct task non-switched trials | Attention Switching Task (AST): Median response latency on correct task non-switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencySide | Cantab AST: median response latency on correct side task trials | Attention Switching Task (AST): Median response latency on correct side task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencySwitched | Cantab AST: median response latency on correct task switched trials | Attention Switching Task (AST): Median response latency on correct task switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSDCorrectLatency | Cantab AST: standard deviation of response latency on all correct trials | Attention Switching Task (AST): Standard deviation of response latency on all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSDCorrectLatencyCongruent | Cantab AST: standard deviation of response latency on correct congruent task trials | Attention Switching Task (AST): Standard deviation of response latency on correct congruent trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencyDirection | Cantab AST: standard deviation of response latency on correct direction task trials | Attention Switching Task (AST): Standard deviation of response latency on correct direction task trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencyIncongruent | Cantab AST: standard deviation of response latency on correct incongruent task trials | Attention Switching Task (AST): Standard deviation of response latency on correct incongruent task trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencyNonSwitched | Cantab AST: standard deviation of response latency on correct task non-switched trials | Attention Switching Task (AST): Standard deviation of response latency on correct task non-switched trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencySide | Cantab AST: standard deviation of response latency on correct side task trials | Attention Switching Task (AST): Standard deviation of response latency on correct side task trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencySwitched | Cantab AST: standard deviation of response latency on correct task switched trials | Attention Switching Task (AST): Standard deviation of response latency on correct task switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMeanCorrect | Cantab AST: mean for correct trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMeanCorrectCongruent | Cantab AST: mean for congruent task trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Mean for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMeanCorrectIncongruent | Cantab AST: mean for incongruent task trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Mean for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMedianCorrect | Cantab AST: median for correct trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Median for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMedianCorrectCongruent | Cantab AST: median for congruent task trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Median for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMedianCorrectIncongruent | Cantab AST: median for incongruent task trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Median for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostSDCorrect | Cantab AST: standard deviation for correct trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Standard deviation for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostSDCorrectCongruent | Cantab AST: standard deviation for congruent task trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Standard deviation for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostSDCorrectIncongruent | Cantab AST: standard deviation for incongruent task trials with switching rules | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Standard deviation for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestAttemptdNotCompOptions | Reason for attempting but not completing CANTAB-AST assessment | Reason for not completing the CANTAB AST test. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing CANTAB-AST assessment (please specify) | "Other" reason for not completing the CANTAB AST test. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestCompletedOptions | CANTAB-AST assessment completion type | Reflects if the CANTAB AST test was done or not. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestComplNonStandAdminOTHER | Other non-standard administration reason for CANTAB-AST assessment (please specify) | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestNotDoneOptions | Reason for not attempting CANTAB-AST assessment | Reflects the reason why the CANTAB AST test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestNotDoneOptionsOTHER | Other reason for not attempting CANTAB-AST assessment (please specify) | Reflects the "other" reason why the CANTAB AST test was not attempted. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCommissionErrors | Cantab AST: total errors in all blocks | Attention Switching Task (AST): This is the total number of trials for which the trial outcome was a commission error –where the subject responded too soon; either prior to the end of the pre-empt window or prior to the appearance of the stimulus. Total errors in all blocks. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCommissionErrorsBlock3 | Cantab AST: total errors in block 3 | Attention Switching Task (AST): This is the total number of trials for which the trial outcome was a commission error –where the subject responded too soon; either prior to the end of the pre-empt window or prior to the appearance of the stimulus. Total errors in block 3. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCommissionErrorsBlock5 | Cantab AST: total errors in block 5 | Attention Switching Task (AST): This is the total number of trials for which the trial outcome was a commission error –where the subject responded too soon; either prior to the end of the pre-empt window or prior to the appearance of the stimulus. Total errors in block 5. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCommissionErrorsBlock7 | Cantab AST: total errors in block 7 | Attention Switching Task (AST): This is the total number of trials for which the trial outcome was a commission error –where the subject responded too soon; either prior to the end of the pre-empt window or prior to the appearance of the stimulus. Total errors in block 7. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrials | Cantab AST: total correct in all trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct all trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsBlock3 | Cantab AST: total correct in block 3 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct Block 3. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsBlock5 | Cantab AST: total correct in block 5 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct Block 5. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsBlock7 | Cantab AST: total correct in block 7 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct Block 7. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsCongruent | Cantab AST: total correct congruent trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct congruent trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsDirection | Cantab AST: total correct direction trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsIncongruent | Cantab AST: total correct incongruent trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct incongruent trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsLeftDirection | Cantab AST: total correct left direction trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct left direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsLeftSide | Cantab AST: total correct left side trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct left side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsNonSwitched | Cantab AST: total correct non-switched trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct non-switched trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsRightDirection | Cantab AST: total correct right direction trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct right direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsRightSide | Cantab AST: total correct right side trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct right side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsSide | Cantab AST: total correct side trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsSwitched | Cantab AST: total correct switched trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct switched trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrials | Cantab AST: total incorrect in all trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect all trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsBlock3 | Cantab AST: total incorrect in block 3 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect Block 3. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsBlock5 | Cantab AST: total incorrect in block 5 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect Block 5. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsBlock7 | Cantab AST: total incorrect in block 7 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect Block 7. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsCongruent | Cantab AST: total incorrect congruent trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect congruent trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsDirection | Cantab AST: total incorrect direction trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsIncongruent | Cantab AST: total incorrect incongruent trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect incongruent trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsLeftDirection | Cantab AST: total incorrect left direction trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect left direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsLeftSide | Cantab AST: total incorrect left side trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect left side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsNonSwitched | Cantab AST: total incorrect non-switched trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect non-switched trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsRightDirection | Cantab AST: total incorrect right direction trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect right direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsRightSide | Cantab AST: total incorrect right side trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect right side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsSide | Cantab AST: total incorrect side trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsSwitched | Cantab AST: total incorrect switched trials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect switched trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalOmissionErrors | Cantab AST: total omission errors in all trials | Attention Switching Task (AST): This is the total number of trials, for which the trial outcome was an omission error which the trial outcome was an omission error – where the subject responded too late, after end where the subject responded too late, after end of the response window. Total errors all trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalOmissionErrorsBlock3 | Cantab AST: total omission errors in block 3 | Attention Switching Task (AST): This is the total number of This is the total number of trials, for which the trial outcome was an omission error which the trial outcome was an omission error – where the subject responded too late, after end where the subject responded too late, after end of the response window. Total errors Block 3. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalOmissionErrorsBlock5 | Cantab AST: total omission errors in block 5 | Attention Switching Task (AST): This is the total number of This is the total number of trials, for which the trial outcome was an omission error which the trial outcome was an omission error – where the subject responded too late, after end where the subject responded too late, after end of the response window. Total errors Block 5 For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalOmissionErrorsBlock7 | Cantab AST: total omission errors in block 7 | Attention Switching Task (AST): This is the total number of This is the total number of trials, for which the trial outcome was an omission error which the trial outcome was an omission error – where the subject responded too late, after end where the subject responded too late, after end of the response window. Total errors Block 7 For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABBattery | CANTAB battery used | CANTAB Test battery used. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABDaysPost | Duration between patient's injury and CANTAB session | CANTAB test session days post-injury. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPAL | CANTAB PAL completed or not and the reason if not | 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 3.4 == 3.4 Not attempted - Language 3.3 == 3.3 Not attempted - Poor effort 3.2 == 3.2 Not attempted - Non-neuro/phys 3.1 == 3.1 Not attempted - Cognitive/neuro 2.6 == 2.6 Not completed - Logistical 2.5 == 2.5 Not completed - Illness 2.4 == 2.4 Not completed - Language 2.3 == 2.3 Not completed - Poor effort 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full |
Completeness details for the CANTAB PAL (Paired Associate Learning) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABPALCompCode | CANTAB-PAL assessment completion code | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALFirstTrialMemoryScore | Cantab PAL: number of correct box choices on first attempt | Paired Associate Learning (PAL): The number of correct box choices that were made on the first attempt during assessment problems For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALMeanErrorsToSuccess | Cantab PAL: mean number of errors made before stage was successfully completed | Paired Associate Learning (PAL): This measure summarises, for all stages, the mean number of errors made before the stage was successfully completed. It is calculated by summing the total errors for all attempted stages and dividing the result by the number of successfully completed stages. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALMeanTrialsToSuccess | Cantab PAL: mean number of trials before stage was successfully completed | Paired Associate Learning (PAL): This is calculated by calculating the total number of trials required (maximum score=10 trials per stage) to locate all the patterns correctly in all stages attempted, and dividing the result by the number of successfully completed stages. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALNumberOfPatternsReached | Cantab PAL: mean number of trials to locate all patterns correctly | Paired Associate Learning (PAL): This is calculated by calculating the total number of trials required (maximum score=10 trials per stage) to locate all the patterns correctly in all stages attempted, and dividing the result by the number of successfully completed stages. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALStagesCompleted | Cantab PAL: number of stages successfully completed | Paired Associate Learning (PAL): This is a key indicator of the subject’s overall success, recording how many stages were successfully completed. When analysing other outcome measures from PAL it is crucial that analyses are conducted with reference to the number of stages completed. Clearly a subject that fails prior to the successful completion of the 8-pattern stage will have had less opportunity to make errors than a subject who completes the test. Higher is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALStagesCompletedOnFirstTrial | Cantab PAL: number of stages passed on the first trial | Paired Associate Learning (PAL): This is the number of stages passed on the first trial (out of a maximum of 8 stages in the clinical mode). This relates to the PAL first trial memory score. Higher is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestAttemptdNotCompOptions | Reason for attempting but not completing CANTAB-PAL assessment | Reasons for not completing the CANTAB PAL test. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing CANTAB-PAL assessment (please specify) | "Other" reasons for not completing the CANTAB PAL test. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestCompletedOptions | CANTAB-PAL assessment completion type | Info on completion of the CANTAB PAL test. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestComplNonStandAdminOTHER | Other non-standard administration reason for CANTAB-PAL assessment (please specify) | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestNotDoneOptions | Reason for not attempting CANTAB-PAL assessment | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestNotDoneOptionsOTHER | Other reason for not attempting CANTAB-PAL assessment (please specify) | "Other" reason why the CANTAB PAL test was not attempted. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors | Cantab PAL: total number of errors | Paired Associate Learning (PAL): This measure reports the total number of errors across all assessed problems and all stages. Note that subjects failing at any stage of the test have had less opportunity to make errors than subjects who complete the test. The PAL Total errors (adjusted) measure attempts to compensate for this. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors2Shapes | Cantab PAL: total number of errors on 2-pattern trials | Paired Associate Learning (PAL): Total errors on 2-pattern trials For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors2ShapesAdjusted | Cantab PAL: total number of errors on 2-pattern with adjustment | Paired Associate Learning (PAL): This measure reports the total number of errors made at the two 2-pattern stages (when there is a stimulus in two of the 6 boxes), with an adjustment for those who have not reached these stages. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors3Shapes | Cantab PAL: total number of errors on 3-pattern trials | Paired Associate Learning (PAL): Total errors on 3-pattern trials For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors3ShapesAdjusted | Cantab PAL: total number of errors on 3-pattern stages with adjustment | Paired Associate Learning (PAL): This measure reports the total number of errors made at the two 3-pattern stages (when there is a stimulus in three of the 6 boxes), with an adjustment for those who have not reached these stages. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors6Shapes | Cantab PAL: total number of errors on 6-pattern trials | Paired Associate Learning (PAL): Total errors on 6-pattern trials For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors6ShapesAdjusted | Cantab PAL: total number of errors on 6-pattern stages with adjustment | Paired Associate Learning (PAL): This measure reports the total number of errors made at the 6 -pattern stage (when there is a stimulus in each the 6 boxes), with an adjustment for those who have not reached these stage. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors8Shapes | Cantab PAL: total number of errors on 8-pattern trials | Paired Associate Learning (PAL): Total errors on 8-pattern trials For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors8ShapesAdjusted | Cantab PAL: total number of errors on 8-pattern stages with adjustment | Paired Associate Learning (PAL): This measure reports the total number of errors made at the 8-pattern stage (when there is a stimulus in each the 8 boxes), with an adjustment for those who have not reached these stage. | |
| Outcomes.CANTABPALTotalErrorsAdjusted | Cantab PAL: total number of errors with adjustment | Paired Associate Learning (PAL): This measure reports the total number of errors across all assessed problems and all stages, with an adjustment for each stage not attempted due to previous failure. | |
| Outcomes.CANTABPALTotalTrials | Cantab PAL: total number of trials required | Paired Associate Learning (PAL): This measure represents the total number of trials required. | |
| Outcomes.CANTABPALTotalTrials2Shapes | Cantab PAL: total number of trials required at 2-pattern stage | Paired Associate Learning (PAL): This measure represents the number of trials required at the 2-pattern stage. | |
| Outcomes.CANTABPALTotalTrials3Shapes | Cantab PAL: total number of trials required at 3-pattern stage | Paired Associate Learning (PAL): This measure represents the number of trials required at the 3-pattern stage. | |
| Outcomes.CANTABPALTotalTrials6Shapes | Cantab PAL: total number of trials required at 6-pattern stage | Paired Associate Learning (PAL): This measure represents the number of trials required at the 6-pattern stage. | |
| Outcomes.CANTABPALTotalTrials8Shapes | Cantab PAL: total number of trials required at 8-pattern stage | Paired Associate Learning (PAL): This measure represents the number of trials required at the 8-pattern stage. | |
| Outcomes.CANTABPALTotalTrialsAdjusted | Cantab PAL: total number of trials required with adjustment | Paired Associate Learning (PAL): This measure represents the total number of presentations required to locate all the patterns correctly in all stages. When using this measure it is important to analyse the data with reference to the PAL Stages completed score. This is because subjects who fail to complete the test will have had fewer PAL Total trials simply because they had less opportunity to make errors than subjects who completed the test. One possible way of dealing with this is to add the maximum score of 10 trials (or 6, depending on the mode) for each stage not attempted due to an earlier failure and this is what this measure shows. Please note that if this adjustment is made to a dataset in which large numbers of subjects have failed, this will have the effect of markedly reducing variance in later stages. Note that for aborted runs, the adjustment is made based on the subject failing the stage on which the test was aborted, so each of the 10 trials(or 6, depending on the mode) from that stage will count as part of the adjusted score. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTI | CANTAB RTI completed or not and the reason if not | 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 3.6 == 3.6 Not attempted - Logistical 3.5 == 3.5 Not attempted - Illness 3.4 == 3.4 Not attempted - Language 3.3 == 3.3 Not attempted - Poor effort 3.2 == 3.2 Not attempted - Non-neuro/phys 3.1 == 3.1 Not attempted - Cognitive/neuro 2.6 == 2.6 Not completed - Logistical 2.5 == 2.5 Not completed - Illness 2.4 == 2.4 Not completed - Language 2.3 == 2.3 Not completed - Poor effort 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full |
Reflects completeness of the CANTAB RTI (Reaction Time) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRTICompCode | CANTAB-RTI assessment completion code | Reflects if the CANTAB RTI test was done. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScoreAll | Cantab RTI: total number of trials with error (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the total number of trials where the response status is recorded as an error, for assessment trials where the stimuli appear in one of five locations. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScoreInaccurate | Cantab RTI: total number of trials with inaccurate error type (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the total number of trials where the response status is recorded as the specified error type, for assessment trials where the stimuli appear in one of five locations. Error types: inaccurate, incorrect location, premature, or no response settings. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScoreIncorrectLocation | Cantab RTI: total number of trials with incorrect location error type (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the total number of trials where the response status is recorded as the specified error type, for assessment trials where the stimuli appear in one of five locations. Error types: inaccurate, incorrect location, premature, or no response settings. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScoreNoResponse | Cantab RTI: total number of trials with no response error type (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the total number of trials where the response status is recorded as the specified error type, for assessment trials where the stimuli appear in one of five locations. Error types: inaccurate, incorrect location, premature, or no response settings. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScorePremature | Cantab RTI: total number of trials with premature error type (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the total number of trials where the response status is recorded as the specified error type, for assessment trials where the stimuli appear in one of five locations. Error types: inaccurate, incorrect location, premature, or no response settings. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMeanFiveChoiceMovementTime | Cantab RTI: mean movement time (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one of five possible locations. Lower is better. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMeanFiveChoiceReactionTime | Cantab RTI: mean reaction time (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in any one of five locations. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMeanSimpleMovementTime | Cantab RTI: mean movement time (stimuli in 1 location) | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one location. Lower is better. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMeanSimpleReactionTime | Cantab RTI: mean reaction time (stimuli in 1 location) | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in one location. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMedianFiveChoiceMovementTime | Cantab RTI: median movement time (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one of five possible locations. Lower is better. Median for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMedianFiveChoiceReactionTime | Cantab RTI: median reaction time (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in any one of five locations. Median for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMedianSimpleMovementTime | Cantab RTI: median movement time (stimuli in 1 location) | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one location. Lower is better. Median for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMedianSimpleReactionTime | Cantab RTI: median reaction time (stimuli in 1 location) | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in one location. Median for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTISDFiveChoiceMovementTime | Cantab RTI: standard deviation movement time (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one of five possible locations. Lower is better. Standard deviation for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTISDFiveChoiceReactionTime | Cantab RTI: standard deviation reaction time (stimuli in 1 of 5 locations) | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in any one of five locations. Standard deviation for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTISDSimpleMovementTime | Cantab RTI: standard deviation movement time (stimuli in 1 location) | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one location. Lower is better. Standard deviation for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTISDSimpleReactionTime | Cantab RTI: standard deviation reaction time (stimuli in 1 location) | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in one location. Standard deviation for correct congruent trials. Time in msec. | |
| Outcomes.CANTABRTISimpleAccuracyScore | Cantab RTI: total number of trials with correct response (stimuli in 1 location) | Reaction time (RTI): This is the total number of trials where the response is recorded as correct, for assessment trials where the stimuli appear in one location only. Higher is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestAttemptdNotCompOptions | Reason for attempting but not completing CANTAB-RTI assessment | Reasons why the CANTAB RTI test was not completed. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing CANTAB-RTI (please specify) | "Other" reason why the CANTAB RTI test was not completed. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestCompletedOptions | CANTAB-RTI assessment completion type | Info on completeness of the CANTAB RTI test. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestComplNonStandAdminOTHER | Other non-standard administration reason for CANTAB-RTI assessment (please specify) | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestNotDoneOptions | Reason for not attempting CANTAB-RTI assessment | Reasons why the CANTAB RTI test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestNotDoneOptionsOTHER | Other reason for not attempting CANTAB-RTI assessment (please specify) | "Other" reason why the CANTAB RTI test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVP | CANTAB RVP completed or not and the reason if not | 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 3.6 == 3.6 Not attempted - Logistical 3.5 == 3.5 Not attempted - Illness 3.4 == 3.4 Not attempted - Language 3.3 == 3.3 Not attempted - Poor effort 3.2 == 3.2 Not attempted - Non-neuro/phys 3.1 == 3.1 Not attempted - Cognitive/neuro 2.6 == 2.6 Not completed - Logistical 2.5 == 2.5 Not completed - Illness 2.4 == 2.4 Not completed - Language 2.3 == 2.3 Not completed - Poor effort 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full |
Completeness of the CANTAB RVP (Rapid Visual Information Processing) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRVPA | Cantab RVP: A prime signal detection measure | Rapid Visual Information Processing (RVP): A′ (A prime) is the signal detection measure of sensitivity to the target, regardless of response tendency (range 0.00 to 1.00; bad to good). In essence, this measure is a measure of how good the subject is at detectingtarget sequences using p(hit) and p(fa). For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPB | Cantab RVP: B double prime signal detection measure | Rapid Visual Information Processing (RVP): B″ (B double prime) is the signal detection measure of the strength of trace required to elicit a response (range –1.00 to +1.00). Thus, it is the tendency to respond regardless of whether the target sequence is present, and uses the p(hit) and p(fa) results. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPCompCode | CANTAB-RVP assessment completion code | Info on completion of the CANTAB RVP (Rapid Visual Information Processing) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPMeanLatency | Cantab RVP: mean latency time | Rapid Visual Information Processing (RVP): This measure details the mean time taken to respond and is reported in milliseconds. It only includes correct responses made within the response window of 1800 milliseconds. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPMedianLatency | Cantab RVP: median latency time | Rapid Visual Information Processing (RVP): This measure details the median time taken to respond and is reported in milliseconds. It only includes correct responses made within the response window of 1800 milliseconds. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPProbabilityOfFalseAlarm | Cantab RVP: probability of false alarms | Rapid Visual Information Processing (RVP): The probability of a false alarm or p(fa) (the subject responding inappropriately), is equal to total false alarms/(total false alarms + total correct rejections). For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPProbabilityOfHit | Cantab RVP: probability of hits | Rapid Visual Information Processing (RVP): The probability of a ‘hit’ or p(hit), (the subject responding correctly), is calculated from hits/(hits+misses). For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPSDLatency | Cantab RVP: standard deviation latency time | Rapid Visual Information Processing (RVP): This measure details the standard deviation of the time taken to respond and is reported in milliseconds. It only includes correct responses made within the response window of 1800 milliseconds. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestAttemptdNotCompOptions | Reason for attempting but not completing CANTAB-RVP assessment | Reasons why the CANTAB RVP test was not completed. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing CANTAB-RVP assessment (please specify) | "Other" reason why the CANTAB RVP test was not completed. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestCompletedOptions | CANTAB-RVP assessment completion type | Info on completion of the CANTAB RVP test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestComplNonStandAdminOTHER | Other non-standard administration reason for CANTAB-RVP assessment (please specify) | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestNotDoneOptions | Reason for not attempting CANTAB-RVP assessment | Reasons why the CANTAB RVP test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestNotDoneOptionsOTHER | Other reason for not attempting CANTAB-RVP assessment (please specify) | "Other" Reason why the CANTAB RVP test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTotalCorrectRejections | Cantab RVP: number of stimuli correctly rejected | Rapid Visual Information Processing (RVP): This is the number of stimuli that were correctly rejected, i.e., the number of stimuli that were not part of a target sequence and were not responded to. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTotalFalseAlarms | Cantab RVP: total of false alarms | Rapid Visual Information Processing (RVP): This records the number of times the subject responds outside the response window of a target sequence. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTotalHits | Cantab RVP: total of hits | Rapid Visual Information Processing (RVP): This score represents the number of occasions upon which the target sequence is correctly responded to. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTotalMisses | Cantab RVP: total of misses | Rapid Visual Information Processing (RVP): This score reports the number of occasions the subject fails to respond to a target sequence within the response window For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCCompCode | CANTAB-Stockings of Cambridge assessment completion code | Info on completion of the CANTAB SOC (Stockings of Cambridge) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanInitialThinkingTime2Moves | Cantab SOC: mean initial thinking time 2 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanInitialThinkingTime3Moves | Cantab SOC: mean initial thinking time 3 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanInitialThinkingTime4Moves | Cantab SOC: mean initial thinking time 4 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanInitialThinkingTime5Moves | Cantab SOC: mean initial thinking time 5 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanMoves2Moves | Cantab SOC: mean number of moves for 2 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanMoves3Moves | Cantab SOC: mean number of moves for 3 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanMoves4Moves | Cantab SOC: mean number of moves for 4 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanMoves5Moves | Cantab SOC: mean number of moves for 5 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanSubsequentThinkingTime2Moves | Cantab SOC: mean subsequent thinking time 2 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanSubsequentThinkingTime3Moves | Cantab SOC: mean subsequent thinking time 3 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanSubsequentThinkingTime4Moves | Cantab SOC: mean subsequent thinking time 4 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanSubsequentThinkingTime5Moves | Cantab SOC: mean subsequent thinking time 5 moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves | Cantab SOC: minimum number of moves to solve problem | Stockings of Cambridge (SOC): This is a fundamental measure, recording the number of occasions upon which the subject has successfully completed a test problem in the minimum possible number of moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves2Moves | Cantab SOC: minimum number of moves to solve problem for 2 moves | Stockings of Cambridge (SOC): Describes the mean number of moves required by the subject to solve problems where the solution can be reached in a minimum of 2 moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves3Moves | Cantab SOC: minimum number of moves to solve problem for 3 moves | Stockings of Cambridge (SOC): Describes the mean number of moves required by the subject to solve problems where the solution can be reached in a minimum of 3 moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves4Moves | Cantab SOC: minimum number of moves to solve problem for 4 moves | Stockings of Cambridge (SOC): Describes the mean number of moves required by the subject to solve problems where the solution can be reached in a minimum of 4 moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves5Moves | Cantab SOC: minimum number of moves to solve problem for 5 moves | Stockings of Cambridge (SOC): Describes the mean number of moves required by the subject to solve problems where the solution can be reached in a minimum of 5 moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestAttemptdNotCompOptions | Reason for attempting but not completing CANTAB-Stockings of Cambridge assessment | Reasons why the CANTAB SOC (Stockings of Cambridge) test was not completed. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing CANTAB-Stockings of Cambridge assessment (please specify) | "Other" reason why the CANTAB SOC (Stockings of Cambridge) test was not completed. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestCompletedOptions | CANTAB-Stockings of Cambridge assessment completion type | Info on completion of the CANTAB SOC (Stockings of Cambridge) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestComplNonStandAdminOTHER | Other non-standard administration reason for CANTAB-Stockings of Cambridge assessment (please specify) | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestNotDoneOptions | Reason for not attempting CANTAB-Stockings of Cambridge assessment | Reason why the CANTAB SOC test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestNotDoneOptionsOTHER | Other reason for not attempting CANTAB-Stockings of Cambridge assessment (please specify) | "Other" reason why the CANTAB SOC test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABStockingsOfCambridge | CANTAB SOC completed or not and the reason if not | 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 3.6 == 3.6 Not attempted - Logistical 3.5 == 3.5 Not attempted - Illness 3.4 == 3.4 Not attempted - Language 3.3 == 3.3 Not attempted - Poor effort 3.2 == 3.2 Not attempted - Non-neuro/phys 3.1 == 3.1 Not attempted - Cognitive/neuro 2.6 == 2.6 Not completed - Logistical 2.5 == 2.5 Not completed - Illness 2.4 == 2.4 Not completed - Language 2.3 == 2.3 Not completed - Poor effort 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full |
Details on completion of the CANTAB SOC (Stockings Of Cambridge) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSWM | CANTAB SWM completed or not and the reason if not | 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 3.6 == 3.6 Not attempted - Logistical 3.5 == 3.5 Not attempted - Illness 3.4 == 3.4 Not attempted - Language 3.3 == 3.3 Not attempted - Poor effort 3.2 == 3.2 Not attempted - Non-neuro/phys 3.1 == 3.1 Not attempted - Cognitive/neuro 2.6 == 2.6 Not completed - Logistical 2.5 == 2.5 Not completed - Illness 2.4 == 2.4 Not completed - Language 2.3 == 2.3 Not completed - Poor effort 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full |
Details on the completion of the CANTAB SWM (Spatial Working Memory) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSWMBetweenErrors | Cantab SWM: number of between errors | Spatial Working Memory (SWM): Between errors are defined as times the subject revisits a box in which a token has previously been found. This is calculated for all trials of four or more tokens only. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMBetweenErrors4Boxes | Cantab SWM: number of between errors 4 boxes | Spatial Working Memory (SWM): Between errors are defined as times the subject revisits a box in which a token has previously been found. This is calculated for trials of four tokens only. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMBetweenErrors6Boxes | Cantab SWM: number of between errors 6 boxes | Spatial Working Memory (SWM): Between errors are defined as times the subject revisits a box in which a token has previously been found. This is calculated for trials of six tokens only. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMBetweenErrors8Boxes | Cantab SWM: number of between errors 8 boxes | Spatial Working Memory (SWM): Between errors are defined as times the subject revisits a box in which a token has previously been found. This is calculated for trials of eight tokens only. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMCompCode | CANTAB-SWM assessment completion code | Info on completion of the CANTAB SWM (Spatial Working Memory) test. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToFirstResponse | Cantab SWM: mean time to first response | Spatial Working Memory (SWM): This is the mean time between the problem being presented to the subject and the subject first touching the screen to open a box. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToFirstResponse4Boxes | Cantab SWM: mean time to first response 4 boxes | Spatial Working Memory (SWM): This is the mean time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 4 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToFirstResponse6Boxes | Cantab SWM: mean time to first response 6 boxes | Spatial Working Memory (SWM): This is the mean time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 6 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToFirstResponse8Boxes | Cantab SWM: mean time to first response 8 boxes | Spatial Working Memory (SWM): This is the mean time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 8 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToLastResponse | Cantab SWM: mean time to last response | Spatial Working Memory (SWM): This is the mean time for the subject’s last response for a problem. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToLastResponse4Boxes | Cantab SWM: mean time to last response 4 boxes | Spatial Working Memory (SWM): This is the mean time for the subject’s last response for a problem, for problems with 4 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToLastResponse6Boxes | Cantab SWM: mean time to last response 6 boxes | Spatial Working Memory (SWM): This is the mean time for the subject’s last response for a problem, for problems with 6 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToLastResponse8Boxes | Cantab SWM: mean time to last response 8 boxes | Spatial Working Memory (SWM): This is the mean time for the subject’s last response for a problem, for problems with 8 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTokenSearchPreparationTime | Cantab SWM: mean time between token search touches | This is the mean time between token search touches, for problems with the specified number of boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3 and the CANTAB Eclipse Test Administration Guide! | |
| Outcomes.CANTABSWMMeanTokenSearchPreparationTime4Boxes | Cantab SWM: mean time between token search touches with 4 boxes | This is the mean time between token search touches, for problems with 4 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3 and the CANTAB Eclipse Test Administration Guide! | |
| Outcomes.CANTABSWMMeanTokenSearchPreparationTime6Boxes | Cantab SWM: mean time between token search touches with 6 boxes | This is the mean time between token search touches, for problems with 6 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3 and the CANTAB Eclipse Test Administration Guide! | |
| Outcomes.CANTABSWMMeanTokenSearchPreparationTime8Boxes | Cantab SWM: mean time between token search touches with 8 boxes | This is the mean time between token search touches, for problems with 8 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3 and the CANTAB Eclipse Test Administration Guide! | |
| Outcomes.CANTABSWMMedianTimeToFirstResponse | Cantab SWM: median time to first response | Spatial Working Memory (SWM): This is the median time between the problem being presented to the subject and the subject first touching the screen to open a box. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToFirstResponse4Boxes | Cantab SWM: median time to first response 4 boxes | Spatial Working Memory (SWM): This is the median time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 4 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToFirstResponse6Boxes | Cantab SWM: median time to first response 6 boxes | Spatial Working Memory (SWM): This is the median time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 6 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToFirstResponse8Boxes | Cantab SWM: median time to first response 8 boxes | Spatial Working Memory (SWM): This is the median time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 8 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToLastResponse | Cantab SWM: median time to last response | Spatial Working Memory (SWM): This is the median time for the subject’s last response for a problem. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToLastResponse4Boxes | Cantab SWM: median time to last response 4 boxes | Spatial Working Memory (SWM): This is the median time for the subject’s last response for a problem, for problems with 4 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToLastResponse6Boxes | Cantab SWM: median time to last response 6 boxes | Spatial Working Memory (SWM): This is the median time for the subject’s last response for a problem, for problems with 6 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToLastResponse8Boxes | Cantab SWM: median time to last response 8 boxes | Spatial Working Memory (SWM): This is the median time for the subject’s last response for a problem, for problems with 8 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTokenSearchPreparationTime | Cantab SWM: median time between token search touches | This is the median time between token search touches, for problems with the specified number of boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTokenSearchPreparationTime4Boxes | Cantab SWM: median time between token search touches with 4 boxes | This is the median time between token search touches, for problems with 4 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTokenSearchPreparationTime6Boxes | Cantab SWM: median time between token search touches with 6 boxes | This is the median time between token search touches, for problems with 6 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTokenSearchPreparationTime8Boxes | Cantab SWM: median time between token search touches with 8 boxes | This is the median time between token search touches, for problems with 8 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMProblemReached | Cantab SWM: number of the problem reached | This is the number of the problem that the subject reached, but did not necessarily complete, where problems are numbered from 1 in the order defined for the mode. A problem is reached when the boxes are presented on the screen. Higher is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToFirstResponse | Cantab SWM: standard deviation time to first response | Spatial Working Memory (SWM): This is the time between the problem being presented to the subject and the subject first touching the screen to open a box. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToFirstResponse4Boxes | Cantab SWM: standard deviation time to first response 4 boxes | Spatial Working Memory (SWM): This is the time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 4 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToFirstResponse6Boxes | Cantab SWM: standard deviation time to first response 6 boxes | Spatial Working Memory (SWM): This is the time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 6 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToFirstResponse8Boxes | Cantab SWM: standard deviation time to first response 8 boxes | Spatial Working Memory (SWM): This is the time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 8 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToLastResponse | Cantab SWM: standard deviation time to last response | Spatial Working Memory (SWM): This is the time for the subject’s last response for a problem. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToLastResponse4Boxes | Cantab SWM: standard deviation time to last response 4 boxes | Spatial Working Memory (SWM): This is the time for the subject’s last response for a problem, for problems with 4 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToLastResponse6Boxes | Cantab SWM: standard deviation time to last response 6 boxes | Spatial Working Memory (SWM): This is the time for the subject’s last response for a problem, for problems with 6 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToLastResponse8Boxes | Cantab SWM: standard deviation time to last response 8 boxes | Spatial Working Memory (SWM): This is the time for the subject’s last response for a problem, for problems with 8 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTokenSearchPreparationTime | Cantab SWM: standard deviation time between token search touches | This is the actual time between token search touches, for problems with the specified number of boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTokenSearchPreparationTime4Boxes | Cantab SWM: standard deviation time between token search touches with 4 boxes | This is the actual time between token search touches, for problems with 4 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTokenSearchPreparationTime6Boxes | Cantab SWM: standard deviation time between token search touches with 6 boxes | This is the actual time between token search touches, for problems with 6 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTokenSearchPreparationTime8Boxes | Cantab SWM: standard deviation time between token search touches with 8 boxes | This is the actual time between token search touches, for problems with 8 boxes. This is calculated, for the first touch for a problem, from the time between the problem being presented to the subject and the subject first touching the screen to open a box, and for subsequent touches, from the time between a token being placed in the ‘home’ area and the time the next box is touched. The Box option applies to this measure. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMStrategy | Cantab SWM: search strategy for a token within same problem | For assessed problems with six boxes or more, the number of distinct boxes used by the subject to begin a new search for a token, within the same problem. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMStrategy6To8Boxes | Cantab SWM: search strategy for a token within same problem (6 or 8 boxes) | For assessed problems with six boxes or eight boxes, the number of distinct boxes used by the subject to begin a new search for a token, within the same problem. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestAttemptdNotCompOptions | Reason for attempting but not completing CANTAB-SWM assessment | Reason why CANTAB SWM (Spatial Working Memory) test was not completed. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing CANTAB-SWM assessment (please specify) | "Other" reason why CANTAB SWM (Spatial Working Memory) test was not completed. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestCompletedOptions | CANTAB-SWM assessment completion type | Reflects completion of the CANTAB SWM (Spatial Working Memory ) test. Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestComplNonStandAdminOTHER | Other non-standard administration reason for CANTAB-SWM assessment (please specify) | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestNotDoneOptions | Reason for not attempting CANTAB-SWM assessment | Reason why the CANTAB SWM (Spatial Working Memory) test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestNotDoneOptionsOTHER | Other reason for not attempting CANTAB-SWM assessment (please specify) | "Other" reason why the CANTAB SWM (Spatial Working Memory) test was not attempted. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABTestingLanguage | Language of CANTAB session | CANTAB testing language. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.Composite_SF12ScoreMCS | Composite SF-12 MCS score | This SF12 score is a composite score which uses items from the SF-36v2 when the SF-12v2 is not available. The score is based on information in the following order of precedence: (1) Mental Component Summary scored using the SF-12v2 items (2) Mental Component Summary scored using the SF-12v2 items contained in the SF-36v2 | |
| Outcomes.Composite_SF12ScorePCS | Composite SF-12 PCS score | This SF12 score is a composite score which uses items from the SF-36v2 when the SF-12v2 is not available. The score is based on information in the following order of precedence: (1) Physical Component Summary scored using the SF-12v2 items (2) Physical Component Summary scored using the SF-12v2 items contained in the SF-36v2 | |
| Outcomes.DerivedCompositeGOSE | Composite GOSE | This GOSE rating is a derived composite score based on central review. The categories of Vegetative State and Lower Severe Disability are collapsed in the ratings assigned. Available information is used in the following order of precedence for the composite: (1) Central scoring of GOSE interview questionnaires completed by investigators (2) Central scoring based on GOSE postal questionnaires completed by patients and carers (3) Interviewer ratings for survivors, when neither of the GOSE questionnaires have been completed. (4) Deaths recorded in the eCRF where the date of death is on or before the end of the window for follow-up. | |
| Outcomes.DerivedCompositeGOSEDaysPostInjury | Derived composite GOSE days post injury | Days post-injury for composite GOSE assessment calculated from the date recorded for the corresponding interview or self-report questionnaire. A date is only included for ratings in survivors (i.e Outcomes.DerivedCompositeGOSE >1). | |
| Outcomes.Derived_SF12ScoreBP | Derived Bodily Pain (BP) score | SF-12 Bodily Pain score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreBPNBS | Derived SF- 12 Bodily Pain Norm-Based Score | SF-12 Bodily Pain Norm-Based Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreGH | Derived General Health (GH) score | SF-12 General Health score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreGHNBS | Derived SF- 12 General Health Norm-Based Score | SF-12 General Health Norm-Based score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreHMNBS | Derived SF- 12 Mental Health Norm-Based Score | SF-12 Mental Health Norm-Based Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreMCS | Derived Mental Component Summary (MCS) | Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). This is the Mental component score. | |
| Outcomes.Derived_SF12ScoreMH | Derived Mental Health (MH) score | SF-12 Mental health Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScorePCS | Derived Physical Component Summary (PCS) | Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). This is the Physical component score. | |
| Outcomes.Derived_SF12ScorePF | Derived Physical Functioning (PF) score | SF-12 Physical Functioning Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScorePFNBS | Derived SF- 12 Physical Functioning Health Norm-Based Score | SF-12 Physical Functioning Norm-Based Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreRE | Derived Role Emotional (RE) score | SF-12 Role-Emotional Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreRENBS | Derived SF- 12 Role-Emotional Norm-Based Score | SF-12 Role-Emotional Norm-Based Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreRP | Derived Role Physical (RP) score | SF-12 Role-Physical Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreRPNBS | Derived SF- 12 Role-Physical Norm-Based Score | SF-12 Role-Physical Norm-based Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreSF | Derived Social Functioning (SF) score | SF-12 Social Functioning Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreSFNBS | Derived SF- 12 Social Functioning Norm-Based Score | SF-12 Social Functioning Norm-Based Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreVT | Derived Vitality (V) score | SF-12 Vitality Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreVTNBS | Derived SF- 12 Vitality Norm-Based Score | SF-12 Vitality Norm-Based Score. Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.GAD7Afraid | 7) Over the last 2 weeks, how often have you felt afraid, as if something awful might happen? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Reflects for GAD-7: Over the LAST TWO WEEKS, how often have you been bothered by the following problems: Feeling afraid, as if something awful might happen. |
| Outcomes.GAD7Annoyed | 6) Over the last 2 weeks, how often have you been easily annoyed or irritable? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Reflects for GAD-7: Over the LAST TWO WEEKS, how often have you been bothered by the following problems: becoming easily annoyed or irritable |
| Outcomes.GAD7Date | Date of GAD-7 assessment | Date of GAD-7 outcome test. | |
| Outcomes.GAD7Nervous | 1) Over the last 2 weeks, how often have you felt nervous, anxious or on edge? | 2 == 2 - More than half the days 0 == 0 - Not at all 1 == 1 - Several days 3 == 3 - Nearly every day |
Reflects for GAD-7: Over the LAST TWO WEEKS, how often have you been bothered by the following problems: Feeling nervous, anxious or on edge |
| Outcomes.GAD7NonStopWorry | 2) Over the last 2 weeks, how often have you not been able to stop or control worrying? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Reflects for GAD-7: Over the LAST TWO WEEKS, how often have you been bothered by the following problems: Not being able to stop or control worrying |
| Outcomes.GAD7Performed | Is GAD-7 assessment performed? | 0 == Not performed 1 == Performed/Completed |
reflects if GAD-7 test was performed or not. Responses for the GAD-7 relate to how often the subject has been bothered in the last 2 weeks. |
| Outcomes.GAD7QuestionnaireMode | GAD-7 assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
Perfects the mode of questionnaire for the GAD-7 (telephone, postal, web-based or personal interview). Responses for the GAD-7 relate to how often the subject has been bothered in the last 2 weeks. |
| Outcomes.GAD7Restless | 5) Over the last 2 weeks, how often have you you been restless that it is hard to sit still? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Reflects for GAD-7: Over the LAST TWO WEEKS, how often have you been bothered by the following problems: Being so restless that it is hard to sit still |
| Outcomes.GAD7TotalScore | GAD-7 total score | Reflects the total score for the GAD-7 outcome test. Not scored by investigator, but calculated score. | |
| Outcomes.GAD7TrblRelax | 4) Over the last 2 weeks, how often have you had trouble relaxing? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Reflects for GAD-7: Over the LAST TWO WEEKS, how often have you been bothered by the following problems: Having trouble relaxing |
| Outcomes.GAD7WorryTooMuch | 3) Over the last 2 weeks, how often have you been worried too much about different things? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Reflects for GAD-7: Over the LAST TWO WEEKS, how often have you been bothered by the following problems: Worrying too much about different things |
| Outcomes.GOATBrnDate | 1b) When were you born? | 0 == No Error -4 == Error (-4) |
Reflects for the GOAT outcome test on the question "When were you born?" if the subject made an error or not in his reply. |
| Outcomes.GOATBuldngLoc | 2b) What Hospital are you now? | 0 == No Error -5 == Error (-5) |
Reflects for the GOAT outcome test on the question "Where are you now?" if the subject made an error or not in his reply. |
| Outcomes.GOATCityLoc | 2a) What city are you now? | 0 == No Error -5 == Error (-5) |
Reflects for the GOAT outcome test on the question "Where are you now (which city)?" if the subject made an error or not in his reply. |
| Outcomes.GOATCompletionCode | GOAT completed or not and the reason if not | 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 3.6 == 3.6 Not attempted - Logistical 3.5 == 3.5 Not attempted - Illness 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 2.3 == 2.3 Not completed - Poor effort 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full |
Reflects if the GOAT outcome test was completed and if not, why not. Neuropsych testing was scheduled for all scheduled follow-up visits according to study protocol. Subjects were only considered testable if the GOAT was >=65. Neuropsych testing included: GOAT, RAVLT, TMT, CANTAB subtests, 10 m walk, Timed up-and-go, as well as Participant Questionnaire B. "Untestable" patients received the GOAT and JFK-Coma Recovery Scale-revised. |
| Outcomes.GOATCrntTm | 6) What time is it now? | 0 == No Error -1 == Half-hour error (-1) -2 == One hour error (-2) -3 == One and one-half hour error (-3) -4 == Two hour error (-4) -5 == Two and one-half hour + error (-5) |
Reflects for the GOAT outcome test on the question "What time is it now?" if the subject made an error or not in his reply. |
| Outcomes.GOATDate | Date of GOAT assessment | Reflects the Date of the GOAT outcome test. Assessment of the GOAT was requested on discharge from the ER for all subjects who had regained consciousness and were able to undergo the test. A main research interest was to explore if - and how many - patients were still in PTA on discharge home. Patients are considered out of PTA if they have a total score of 78 or more. | |
| Outcomes.GOATDayDate | 7) What day of the week is it? | 0 == No Error -1 == One day error (-1) -2 == Two day error (-2) -3 == Three day error (-3) |
Reflects for the GOAT outcome test on the question "What day of the week is it?" if the subject made an error or not in his reply. |
| Outcomes.GOATDayMnthDate | 8) What day of the month is it? (i.e. the date) | 0 == No Error -1 == One day error (-1) -2 == Two day error (-2) -3 == Three day error (-3) -4 == Four day error (-4) -5 == Five day + error (-5) |
Reflects for the GOAT outcome test on the question "What day of the month is it? (i.e. the date)" if the subject made an error or not in his reply. |
| Outcomes.GOATDtlRslt | 4b) Can you describe in detail the first event you can remember after the injury? | 0 == No Error -5 == Error (-5) |
Reflects for the GOAT outcome test on the question " What is the first event you can remember after the injury?" if the subject made an error or not in his reply. |
| Outcomes.GOATFirEvntRslt | 4a) What is the first event you can remember after the injury? | 0 == No Error -5 == Error (-5) |
Reflects for the GOAT outcome test on the question "What is the first event you can remember after the injury?" if the subject made an error or not in his reply. |
| Outcomes.GOATFirEvntRsltTxt | First event you can remember after the injury (please specify) | Reflects for the GOAT outcome test on the question "What is the first event you can remember after the injury?" the details described by the subject. | |
| Outcomes.GOATHospAdmDate | 3a) On what date were you admitted to the Hospital? | 0 == No Error -5 == Error (-5) |
Reflects for the GOAT outcome test on the question "On what date were you admitted to the hospital?" if the subject made an error or not in his reply. |
| Outcomes.GOATLiveLoc | 1c) Where do you live? | 0 == No Error -4 == Error (-4) |
Reflects for the GOAT outcome test on the question "Where do you live?" if the subject made an error or not in his reply. |
| Outcomes.GOATLstEvntDtlRslt | 5b) Can you describe in detail the last event you can recall before the injury? | 0 == No Error -5 == Error (-5) |
Reflects for the GOAT outcome test on the question "What is the last event you can recall before the injury - Can you describe in detail?" if the subject made an error or not in his reply. |
| Outcomes.GOATLstEvntRslt | 5a) What is the last event you can recall before the injury? | 0 == No Error -5 == Error (-5) |
Reflects for the GOAT outcome test on the question "What is the last event you can recall before the injury?" if the subject made an error or not in his reply. |
| Outcomes.GOATLstEvntRsltTxt | Last event you can recall before the injury (please specify) | Reflects for the GOAT outcome test the reply on the question "What is the last event you can recall before the injury - Can you describe in detail?" | |
| Outcomes.GOATMnthDate | 9) What is the month? | 0 == No Error -5 == One month error (-5) -10 == Two month error (-10) -15 == Three or more month error (-15) |
Reflects for the GOAT outcome test on the question "What is the month?" if the subject made an error or not in his reply. |
| Outcomes.GOATNeuroPsychCompCode | GOAT assessment completion code | 3.0 == 3.0 Test completed 2.0 == 2.0 Test attempted but not completed 1.0 == 1.0 Test not done |
Reflects if GOAT test was done or not. Neuropsych testing was conducted during scheduled follow-up visits to hospital according to study protocol. Cross-sectional assessments across all strata was performed at 6 mnths after injury. For patients included in the MR substudy full testing was conducted for ER patients at: 2-3 weeks, 3 mnths and 6 mnths; Adm and ICU strata: 6 mnths, 12 mnths and 24 mnths Subjects were only considered testable if the GOAT was >=65. Neuropsych testing included: GOAT, RAVLT, TMT, CANTAB subtests, 10 m walk, Timed up-and-go, as well as Participant Questionnaire B.. "Untestable" patients received the GOAT and JFK-Coma Recovery Scale-revised.. |
| Outcomes.GOATNm | 1a) What is your name? | 0 == No Error -2 == Error (-2) |
Reflects for the GOAT outcome test on the question "What is your name?" if the subject made an error or not in his reply. |
| Outcomes.GOATOutcome | GOAT Outcome | The total GOAT score is calculated as 100 - Total error points; Interpretation: 76-100 = Normal / 66-75 = Borderline / <66 = Impaired | |
| Outcomes.GOATTestAttemptdNotCompOptions | Reason for attempting but not completing GOAT assessment | 2.6 == Not completed - Logistical reasons, other reasons 2.5 == Not completed - Illness/fatigue 2.4 == Not completed - Language 2.3 == Not completed - Lack of effort/uncooperative 2.2 == Not completed - Non-neurological/physical reason 2.7 == Not completed - Examiner error 2.1 == Not completed - Cognitive/neurological deficits |
Documents reasons why GOAT was not completed when it was initially attempted (7 categories) |
| Outcomes.GOATTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing GOAT assessment | Documents the "Other" reasons why GOAT was not completed when it was initially attempted | |
| Outcomes.GOATTestCompletedOptions | GOAT assessment completion type | 3.2 == Non-standard administration - Other 3.1 == Test completed - Non-standard, results valid 3.0 == Test completed in full - results valid |
Reflects the completion of the GOAT outcome test (Test completed in full results valid/Test completed Nonstandard, results valid/Nonstandard administration/Other) |
| Outcomes.GOATTestComplNonStandAdminOTHER | Other non-standard administration reason for GOAT assessment (please specify) | ||
| Outcomes.GOATTestNotDoneOptions | Reason for not attempting GOAT assessment | 1.7 == Not attempted- Return to all normal activities 1.8 == Not attempted - Patient not available 1.6 == Not attempted - Logistical reasons, other reasons 1.5 == Not attempted - Illness/fatigue 1.4 == Not attempted - Language 1.3 == Not attempted - Lack of effort/uncooperative 1.2 == Not attempted - Non-neurological/physical reasons 1.1 == Not attempted - Cognitive/neurological deficits |
Documents reasons why GOAT was not attempted (8 categories) |
| Outcomes.GOATTestNotDoneOptionsOTHER | Other reason for not attempting GOAT assessment | Documents the "other" reason why GOAT was not attempted | |
| Outcomes.GOATTime | Time of GOAT outcome test | Reflects Time of GOAT outcome test. See also Outcomes.GOATDate | |
| Outcomes.GOATTotError | GOAT total error | Total error score for the GOAT outcome test. The total error score is calculated automatically. | |
| Outcomes.GOATTotScr | GOAT total score | Total actual score for the GOAT test. The total GOAT score is calculated as 100 - Total error points; Interpretation: 76-100 = Normal / 66-75 = Borderline / <66 = Impaired | |
| Outcomes.GOATTranspTyp | 3b) How did you get to the Hospital? | 0 == No Error -5 == Error (-5) |
Reflects for the GOAT outcome test on the question "How did you get to the hospital?" if the subject made an error or not in his reply. |
| Outcomes.GOATYrDate | 10) What is the year? | 0 == No Error -10 == One year error (-10) -20 == Two year error (-20) -30 == Three or more year error (-30) |
Reflects for the GOAT outcome test on the question "What is the year?" if the subject made an error or not in his reply. |
| Outcomes.GOSEAssistanceNeeded | 2a) Independence at home: Is the assistance of another person at home essential every day for some activities of daily living? | 1 == Yes 0 == No |
Indicator if the participant needs another person at home essentially every day for some activities of daily living as part of Glasgow Outcome Scale Extended (GOS-E). |
| Outcomes.GOSEDate | Date of GOSE assessment | Date when Glasgow Outcome Scale Extended (GOS-E) (1-8) was administered. | |
| Outcomes.GOSEEpilepsyFits | Since the injury has the head injured person had any epileptic fits? | 1 == No 2 == Yes |
These 2 questions on epilepsy do not form part of the GOSE rating, but are included in the questionnaire as very relevant variables. Subjective reporting also in: Outcomes.PartQuestACurHltSeiz. Seizures that occurred before/at presentation or during hospital stay are recorded alsewhere: InjuryHx.EDComplEventSeizures; Vitals.HosComplEventSeizures; Hospital.HospComplSeizures; Vitals.HosComplEventSeizures; Hospital.ICUDisComplSeizure; |
| Outcomes.GOSEEpilepsyRisk | Have they been told that they are currently at risk of developing epilepsy? | 1 == No 2 == Yes |
These 2 questions on epilepsy do not form part of the GOSE rating, but are included in the questionnaire as very relevant variables |
| Outcomes.GOSEFamilyDisrupt | 7a) Family and friendships: Has there been family or friendship disruption due to psychological problems? | 0 == No 1 == Yes |
Indicator if the participant faces any rifts in family relationships or friendships caused by psychological problems for the GOSE structured. |
| Outcomes.GOSEFamilyDisruptChange | 7c) Family and friendships: Were there problems with family or friends before the injury? | 1 == Yes 0 == No |
Indicator if the level of disruption or strain in family and friendships depicts a change in respect to pre-injury situation, as part of the GOSE Structured. |
| Outcomes.GOSEFamilyDisruptExtent | 7b) Family and friendships: What has been the extent of disruption or strain? | 2 == Frequent - once a week or more, but tolerable (Upper MD) 1 == Occasional - less than weekly (Lower GR) 3 == Constant - daily and intolerable (Lower MD) |
Frequency of the extent of the rifts in relationships, including family and friendships, due to psychological problems, as part of the GOSE structured. |
| Outcomes.GOSEIndependentBefore | 2c) Independence at home: Was assistance at home essential before the injury? | 0 == No 1 == Yes |
Indicator if the assistance at home was essential for the patient before the injury, as part of Glasgow Outcome Scale Extended (GOS-E). |
| Outcomes.GOSENeedFreqHelp | 2b) Independence at home: Do they need frequent help of someone to be around at home most of the time? | 0 == No (upper SD) 1 == Yes (lower SD) |
Indicator if the participant is in need of frequent help of someone to be around at home as part of Glasgow Outcome Scale Extended (GOS-E). |
| Outcomes.GOSEOtherCurrentProb | 8a) Return to normal life: Are there any other current problems relating to the injury which affect daily life? | 1 == Yes (lower GR) 0 == No (upper GR) |
Indicator if the participant faces any other current problems currently due to injury, as part of the GOSE structured. |
| Outcomes.GOSEOtherCurrentProbWorse | 8b) Return to normal life: Were similar problems present before the injury? | 1 == Yes 0 == No |
Indicator if the similar problems were present before injury and have these become markedly worse, as part of the GOSE structured. |
| Outcomes.GOSEOutcomeFactor | What is the most important factor in outcome? | 1 == Effects of head injury 2 == Effects of illness or injury to another part of the body 3 == A mixture of these |
Provides an indication how much disability is not due to TBI, a part of the GOSE structured. |
| Outcomes.GOSEPerformed | Is GOSE assessment performed? | 1 == Performed/Completed 0 == Not performed |
Reflects if the GOSE outcome assessment was performed or not. |
| Outcomes.GOSEPostalPerformed | Is GOSE-Postal assessment performed? | 0 == Not performed 1 == Performed |
Reflects if the Postal GOSE was performed or not. |
| Outcomes.GOSEPOSTAssistanceNeededFreq | 2) As a result of your injury do you now need someone to help look after you at home? | 1 == I do not need help or supervision in the home 2 == I need some help in the home, but not every day 3 == I need help in the home every day, but I could look after myself for at least 8 hours if necessary 4 == I could not look after myself for 8 hours during the day 5 == I need help in the home, but not because of the injury |
Reflects for the GOSE Postal outcome test the answer on the question "As a result of your injury do you now need someone to help look after you at home?” |
| Outcomes.GOSEPOSTComments | Are there any other comments that you would like to make? | Reflects for the GOSE Postal outcome test the answer on the question "Are there any other comments that you would like to make?” | |
| Outcomes.GOSEPOSTCompletionCode | GOSE postal completed or not and the reason if not | 5.0 == 5.0 Not attempted - Other 4.0 == 4.0 Not attempted - Examiner error 3.6 == 3.6 Not attempted - Logistical 3.5 == 3.5 Not attempted - Illness 3.4 == 3.4 Not attempted - Language 3.2 == 3.2 Not attempted - Non-neuro/phys 3.1 == 3.1 Not attempted - Cognitive/neuro 2.6 == 2.6 Not completed - Logistical 2.5 == 2.5 Not completed - Illness 2.4 == 2.4 Not completed - Language 2.3 == 2.3 Not completed - Poor effort 2.2 == 2.2 Not completed - Non-neuro/phys 2.1 == 2.1 Not completed - Cognitive/neuro 1.3 == 1.3 Test completed over the phone 1.2 == 1.2 Non-standard adm - other 1.1 == 1.1 Non-standard adm - written 1.0 == 1.0 Test completed in full 3.3 == 3.3 Not attempted - Poor effort |
Reflects if the GOSE Postal assessment was completed or not, and if not, why not. |
| Outcomes.GOSEPOSTDate | Date of GOSE-Postal assessment | Reflects the Date of the GOSE postal assessment | |
| Outcomes.GOSEPOSTFamilyDisruptBefore | 11) Before the injury did you have any problems in getting on with friends or relatives? | 1 == No 2 == Yes |
Reflects for the GOSE Postal outcome test the answer on the question "Before the injury did you have any problems in getting on with friends or relatives?” |
| Outcomes.GOSEPOSTFamilyDisruptChange | 12) As a result of your injury are there now problems in how you get on with friends or relatives? | 1 == Things are still much the same 2 == There are occasional problems (less than once a week) 3 == There are frequent problems (once a week or more) 4 == There are constant problems (problems every day) 5 == There are problems for some other reason, not because of the injury |
Reflects for the GOSE Postal outcome test the answer on the question "As a result of your injury are there now problems in how you get on with friends or relatives?” |
| Outcomes.GOSEPOSTIndependentBefore | 1) Before the injury were you able to look after yourself at home? | 1 == No 2 == Yes |
Reflects for the GOSE Postal outcome test the answer on the question "Before the injury were you able to look after yourself at home?” |
| Outcomes.GOSEPOSTOtherCurrentProbs | 13) Are there any other problems resulting from your injury which have interfered with your daily life over the past week? (Problems sometimes reported after head injury: headaches, dizziness, tiredness, sensitivity to noise or light, slowness, memory failures, and concentration problems.) | 1 == I have no current problems 2 == I have some problems, but these do not interfere with my daily life 3 == I have some problems, and these have affected my daily life 4 == I have some problems for other reasons, not because of the head injury |
Reflects for the GOSE Postal outcome test the answer on the question "Are there any other problems resulting from your injury which have interfered with your daily life over the past week? (Problems sometimes reported after head injury headaches, dizziness, tiredness, sensitivity to noise or light, slowness, memory failures, and concentration problems.)” |
| Outcomes.GOSEPOSTOtherCurrentProbsBefore | 14) Before the injury were similar problems present? | 1 == I had no problems before, I had minor problems 2 == I had similar problems before |
Reflects for the GOSE Postal outcome test the answer on the question "Before the injury were similar problems present?” |
| Outcomes.GOSEPOSTPatientLocn | Location of patient at the time of GOSE-Postal assessment | 1 == Out of hospital 2 == In hospital or residential care |
This variable describes for the GOSE Postal the location of the subject (in or out hospital). |
| Outcomes.GOSEPOSTResponse | GOSE-Postal assessment completed by | 1 == Patient alone 2 == Relative or friend or carer alone 3 == Patient and relative, friend or carer together |
This variable describes for the GOSE Postal outcome test the respondent that completed the questionnaire. |
| Outcomes.GOSEPOSTShopAloneBefore | 3) Before the injury were you able to buy things at shops without help? | 1 == No 2 == Yes |
This variable describes for the GOSE Postal outcome test if a subject is able to buy things at shops without help. |
| Outcomes.GOSEPOSTShopAssistance | 4) As a result of your injury do you now need help to buy things at shops? | 1 == I do not need help to shop 2 == I need some help, but I can go to local shops on my own 3 == I need help to shop even locally, or I cannot shop at all 4 == I need help to shop, but not because of the injury |
This variable describes for the GOSE Postal outcome test if a subject needs help to buy things at shops as a result of the injury. |
| Outcomes.GOSEPOSTSocialActivityBefore | 9) Before the injury did you take part in regular social and leisure activities outside home (at least once a week)? | 1 == No 2 == Yes |
This variable describes for the GOSE Postal outcome test if a subject did take part in regular social and leisure activities outside home (at least once a week) before the injury. |
| Outcomes.GOSEPOSTSocialActivityChange | 10) As a result of your injury has there been a change in your ability to take part in social and leisure activities outside home? | 1 == I take part about as often as before (the activities may be different from before) 2 == I take part a bit less, but at least half as often 3 == I take part much less, less than half as often 4 == I do not take part at all 5 == My ability to take part has changed for some other reason, not because of the injury |
This variable describes for the GOSE Postal outcome test if there has been a change in the subject's ability to take part in social and leisure activities outside home as a result of the injury. |
| Outcomes.GOSEPOSTTravelAloneBefore | 5) Before the injury were you able to travel without help? | 1 == No 2 == Yes |
This variable describes for the GOSE Postal outcome test if a subject was able to travel without help before the injury. |
| Outcomes.GOSEPOSTTravelAssistance | 6) As a result of your injury do you now need help to travel? | 1 == I do not need help to travel 2 == I need some help, but can travel locally on my own (eg. by arranging a taxi) 3 == I need help to travel even locally, or I cannot travel at all 4 == I need help to travel but not because of the injury |
This variable describes for the GOSE Postal outcome test if a subject needs help to travel as a result of the injury. |
| Outcomes.GOSEPOSTWorkBefore | 7) Employment before the injury | 1 == Working 2 == Looking for work 3 == Looking after family 4 == Studying as a student 5 == Retired 6 == None of these (eg. unfit for work) |
This variable describes for the GOSE Postal outcome test the employment before the injury. |
| Outcomes.GOSEPOSTWorkChange | 8) As a result of your injury has there been a change in your ability to work? (or to study if you were a student; or to look after your family) | 1 == I still do the same work 2 == I still do the same work, but have some problems (e.g. tiredness, lack of concentration). 3 == I still work, but at a reduced level (e.g. change from full-time to part-time, or change in level of responsibility) 4 == I am unable to work, or only able to work in sheltered workshop 5 == My ability to work has changed, but not because of the injury |
This variable describes for the GOSE Postal outcome test the change in ability to work as a result of the injury. |
| Outcomes.GOSEQuestionnaireMode | GOSE assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
This questionnaire describes the mode in which the questionnaire for the GOSE Postal outcome test was completed. |
| Outcomes.GOSEResponse | GOSE assessment completed by | 1 == Relative/friend/caretaker alone 0 == Patient alone 2 == Patient plus relative/friend/caretaker |
This variable describes for the GOSE Structured outcome test who completed the questionnaire. |
| Outcomes.GOSEResumeSocialActivity | 6a) Social and leisure activities: Are they able to resume regular social and leisure activities outside home? | 1 == Yes 0 == No |
This variable describes for the GOSE Structured outcome test if a subject is able to resume regular social and leisure activities outside home. |
| Outcomes.GOSEScore | GOSE total score (overall rating is based on the lowest outcome category indicated on the scale) | 6 == 6-Upper Moderate Disability (Upper MD) 5 == 5-Lower Moderate Disability (Lower MD) 4 == 4-Upper Severe Disability (Upper SD) 3 == 3-Lower Severe Disability (Lower SD) 2 == 2-Vegetative State (VS) 1 == 1-Dead 7 == 7-Lower Good Recovery (Lower GR) 8 == 8-Upper Good Recovery (Upper GR) |
This GOSE Structured rating was assigned by the rater/interviewer at the time of the interview and entered in the e-CRF for a particular follow-up time-point, along with responses on the sections of the interview. In addition, a central review score will be allocated. This variable does not include ratings based on postal questionnaires. REMARK for CINTER (India): For the Indian CINTER dataset, no structured interview was performed since this was too time consuming for many patients. The investigator asked some general questions about quality of life and how the patient felt and then completed the GOSE questionnaire in the e-CRF based on their clinical judgement. |
| Outcomes.GOSEShopAlone | 3a) Independence outside home: Are they able to shop without assistance? | 1 == Yes 0 == No (upper SD) |
This variable describes for the GOSE Structured outcome test if a subject is able to shop without assistance. |
| Outcomes.GOSEShopAloneBefore | 3b) Independence outside home: Were they able to shop without assistance before? | 0 == No 1 == Yes |
This variable describes for the GOSE Structured outcome test if a subject was able to shop without assistance before the injury. |
| Outcomes.GOSESimpleCommands | 1) Consciousness: Is the head-injured person able to obey simple commands or say any words? | 1 == Yes 0 == No (VS) |
This variable describes for the GOSE Structured outcome test if the subject is able to obey simple commands or say any words. |
| Outcomes.GOSESocialActivityRestrict | 6b) Social and leisure activities: What is the extent of restriction on their social and leisure activities? | 3 == Unable to participate rarely, if ever, take part (Lower MD) 2 == Participate much less less than half as often (Upper MD) 1 == Participate a bit less at least half as often as before injury (Lower GR) |
This variable describes for the GOSE Structured outcome test the extent of restriction on the social and leisure activities. |
| Outcomes.GOSESocialActivityRestrictChange | 6c) Social and leisure activities: Did they engage in regular social and leisure activities outside home before the injury? | 1 == Yes 0 == No |
This variable describes for the GOSE Structured outcome test the engagement in regular social and leisure activities outside home before the injury. |
| Outcomes.GOSETravelAlone | 4a) Independence outside home: Are they able to travel locally without assistance? | 0 == No (upper SD) 1 == Yes |
This variable describes for the GOSE Structured outcome test if the subject is able to travel locally without assistance. |
| Outcomes.GOSETravelAloneBefore | 4b) Independence outside home: Were they able to travel locally without assistance before the injury? | 0 == No 1 == Yes |
This variable describes for the GOSE Structured outcome test if a subject was able to travel locally without assistance before the injury. |
| Outcomes.GOSEWork | 5a) Work: Are they currently able to work to their previous capacity? | 0 == No 1 == Yes |
This variable describes for the GOSE Structured outcome test if a subject is currently able to work to the previous capacity. |
| Outcomes.GOSEWorkRestrictChange | 5c) Work: Were they either working or seeking employment before the injury (answer 'yes') or were they doing neither (answer 'no')? | 1 == Yes 0 == No |
This variable describes for the GOSE Structured outcome test whether the subject was either working or seeking employment before the injury or was doing neither. |
| Outcomes.GOSEWorkRestriction | 5b) Work: How restricted are they? | 2 == Able to work only in a sheltered workshop or non-competitive job or currently unable to work (Lower MD) 1 == Reduced work capacity (upper MD) |
Work restriction type experienced by the participant as a result of injury as part of the GOSE Structured outcome test |
| Outcomes.JFKCRSRAdtyFuncScaleScore | Auditory function scale | 4 == 4 - Consistent Movement to Command * 3 == 3 - Reproducible Movement to Command * 2 == 2 - Localization to Sound 1 == 1 - Auditory Startle 0 == 0 - None |
Auditory Function Scale Score for JFK/CRS-R outcome |
| Outcomes.JFKCRSRArousalScaleScore | Arousal scale | 3 == 3 - Attention 2 == 2 - Eye Opening w/o Stimulation 1 == 1 - Eye Opening with Stimulation 0 == 0 - Unarousable |
Arousal Scale Score for JFK/CRS-R outcome |
| Outcomes.JFKCRSRBrainStemCornRflx | Brain stem reflex test: Corneal reflex | 1 == Absent 2 == Present Unilateral 3 == Present Bilateral |
Corneal Reflex for the Brain Stem Reflex Test of the JFK/CRS-R outcome |
| Outcomes.JFKCRSRBrainStemNotes | Brain stem reflex test: Additional notes | Additional Notes on the Brain Stem Reflex Test for the JFK/CRS-R outcome test | |
| Outcomes.JFKCRSRBrainStemOculocRflx | Brain stem reflex test: Oculocephalic reflex | 1 == None 2 == Abnormal 3 == Full 4 == Normal |
Oculocephalic Reflex for the Brain Stem Reflex Test for the JFK/CRS-R outcome test |
| Outcomes.JFKCRSRBrainStemPosturalResp | Brain stem reflex test: Postural responses | 1 == Abnormal Extension 2 == Abnormal Flexion |
Postural Responses for the Brain Stem Reflex Test for the JFK/CRS-R outcome test |
| Outcomes.JFKCRSRBrainStemPosturalRespLimb | Brain stem reflex test: Limb (please specify) | Indicates limb for the Brain Stem Reflex Test for the JFK/CRS-R outcome test | |
| Outcomes.JFKCRSRBrainStemPupilLight | Brain stem reflex test: Pupillary light | 1 == Reactive 2 == Equal 3 == Constricted 4 == Dilated 5 == Pinpoint 6 == Accommodation |
Pupillary Light for the Brain Stem Reflex Test for the JFK/CRS-R outcome test |
| Outcomes.JFKCRSRBrainStemSpontEyeMvmt | Brain stem reflex test: Spontaneous eye movements | 1 == None 2 == Skew Deviation 3 == Conjugate Gaze Deviation 4 == Roving 5 == Dysconjugate |
Spontaneous Eye Movements for the Brain Stem Reflex Test for the JFK/CRS-R outcome test |
| Outcomes.JFKCRSRCommScaleScore | Communication scale | 2 == 2 - Functional, Accurate &dagger 1 == 1 - Non-Functional, Intentional * 0 == 0 - None |
Communication Scale Score for the JFK/CRS-R outcome test |
| Outcomes.JFKCRSRContngntBehvrElicitgStim | Assessment of contingent behaviour: Eliciting stimulus | Eliciting Stimulus for the Assessment of Contingent Behaviour for the JFK/CRS-R outcome test Supplementary item | |
| Outcomes.JFKCRSRContngntBehvrNumElicitdOccur | Assessment of contingent behaviour: No) of occurrences of target behaviour within 10 sec of eliciting stimulus | Occurrences of Target Behaviour within 10sec of Eliciting Stimulus for the Assessment of Contingent Behaviour for the JFK/CRS-R outcome test Supplementary item | |
| Outcomes.JFKCRSRContngntBehvrNumSpontOccur | Assessment of contingent behaviour: Spontaneous occurrences of target behaviour | Spontaneous Occurrences of Target Behaviour for the Assessment of Contingent Behaviour for the JFK/CRS-R outcome test Supplementary item | |
| Outcomes.JFKCRSRContngntBehvrTargtBehvr | Assessment of contingent behaviour: Target behaviour | Target Behaviour for the Assessment of Contingent Behaviour for the JFK/CRS-R outcome test Supplementary item | |
| Outcomes.JFKCRSRDate | Date of CRS-R assessment | Date of the JFK/CRS-R outcome test | |
| Outcomes.JFKCRSRMotrFuncScaleScore | Motor function scale | 6 == 6 - Functional Object Use†5 == 5 - Automatic Motor Response * 4 == 4 - Object Manipulation * 3 == 3 - Localization to Noxious Stimulation * 2 == 2 - Flexion Withdrawal 1 == 1 - Abnormal Posturing 0 == 0 - None/Flaccid |
Motor Function Scale Score for the JFK/CRS-R outcome test |
| Outcomes.JFKCRSRNeuroPsychCompCode | CRS-R assessment completion code | 3.0 == 3.0 Test completed 2.0 == 2.0 Test attempted but not completed 1.0 == 1.0 Test not done |
Completion code for the JFK Coma Recovery Scale: only applicable for patients in a minimally conscious/vegetative state |
| Outcomes.JFKCRSROrmtrVerbFuncScaleScore | Oromotor/verbal function scale | 3 == 3 - Intelligible Verbalization * 2 == 2 - Vocalization/Oral Movement 1 == 1 - Oral Reflexive Movement 0 == 0 - None |
Oromotor/Verbal Function Scale Score for the JFK/CRS-R outcome test |
| Outcomes.JFKCRSRTestAttemptdNotCompOptions | Reason for attempting but not completing CRS-R assessment | 2.6 == Not completed - Logistical reasons, other reasons 2.5 == Not completed - Illness/fatigue 2.4 == Not completed - Language 2.3 == Not completed - Lack of effort/uncooperative 2.2 == Not completed - Non-neurological/physical reason 2.1 == Not completed - Cognitive/neurological deficits 2.7 == Not completed - Examiner error |
Reason why the JFK/CRS-R was not completed |
| Outcomes.JFKCRSRTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing CRS-R assessment | "Other" reason why the JFK/CRS-R was not completed | |
| Outcomes.JFKCRSRTestCompletedOptions | CRS-R assessment completion type | 3.2 == Non-standard administration - Other 3.1 == Test completed - Non-standard, results valid 3.0 == Test completed in full - results valid |
Completion of the JFK/CRS-R Test |
| Outcomes.JFKCRSRTestComplNonStandAdminOTHER | Other non-standard administration reason for CRS-R assessment (please specify) | ||
| Outcomes.JFKCRSRTestNotDoneOptions | Reason for not attempting CRS-R assessment | 1.6 == Not attempted - Logistical reasons, other reasons 1.5 == Not attempted - Illness/fatigue 1.4 == Not attempted - Language 1.3 == Not attempted - Lack of effort/uncooperative 1.2 == Not attempted - Non-neurological/physical reasons 1.1 == Not attempted - Cognitive/neurological deficits 1.7 == Not attempted - Examiner error 1.8 == Not attempted - Patient not available |
Reason why JFK/CRS-R Test not attempted |
| Outcomes.JFKCRSRTestNotDoneOptionsOTHER | Other reason for not attempting CRS-R assessment | "Other" reason why JFK/CRS-R Test not attempted | |
| Outcomes.JFKCRSRTotalScore | CRS-R total score | Total score of JFK/CRS-R outcome test | |
| Outcomes.JFKCRSRVislFuncScaleScore | Visual function scale | 5 == 5 - Object Recognition * 4 == 4 - Object Localization, Reaching * 3 == 3 - Visual Pursuit * 2 == 2 - Fixation * 1 == 1 - Visual Startle 0 == 0 - None |
Visual Function Scale Score for the JFK/CRS-R outcome test |
| Outcomes.OneHundred | Score for GOAT was 100 | 100 == 100 | Reflects that score for GOAT was 100. |
| Outcomes.PartQuestACurHltBack | 8.6) Do you currently have back pain? | 1 == Yes 0 == No |
This variable describes if the subject currently has back pain as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltHead | 8.4) Do you currently have Headaches? | 1 == Yes 0 == No |
This variable describes if the subject currently has headaches as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltHear | 8.2) Do you currently have trouble hearing (even with a hearing aid)? | 1 == Yes 0 == No |
This variable describes if the subject currently has trouble hearing as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltMob | 8.8) Do you currently problems with mobility or walking? | 1 == Yes 0 == No |
This variable describes if the subject has problems with mobility/ walking as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltMove | 8.7) Do you currently have problems with movement of hands or arms? | 1 == Yes 0 == No |
This variable describes if the subject has problems with movement of hands or arms as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltNeck | 8.5) Do you currently have Neck pain or restricted neck movement? | 1 == Yes 0 == No |
This variable describes if the subject has neck pain or restricted neck movement as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltOther | 8.11) Do you currently have any other health problems? | 1 == Yes 0 == No |
This variable describes if the subject currently has any other health problems as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltOthertxt | Any other health problems (please specify) | This variable describes any other health problems the subject currently has as part of QoLIBRI-OS. | |
| Outcomes.PartQuestACurHltSeiz | 8.10) Do you currently have problems with seizures (epileptic fits) ? | 1 == Yes 0 == No |
This variable describes if the subject currently has seizures (epileptic fits) as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltSmell | 8.1) Do you currently have trouble with smelling or tasting? | 1 == Yes 0 == No |
This variable describes if the subject has trouble smelling or tasting as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltSpeech | 8.9) Do you currently have problems with speaking or understanding others? | 1 == Yes 0 == No |
This variable describes if the subject currently has problems with speaking or understanding others as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurHltVis | 8.3) Do you currently have trouble with eye sight/vision (even with glasses) ? | 1 == Yes 0 == No |
This variable describes if the subject currently has trouble with eye sight/vision (even with glasses) as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurrSitChange | 4) In general, how do you compare your current situation to that before injury? | 5 == Much worse 4 == Worse 3 == A little worse 2 == About the same 1 == Better |
This variable describes how the subject compares their current situation to that before injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestACurrSitChangeReason | Reason for change of current situation | 1 == Because of the head injury 2 == Because of other injuries received at the same time 3 == Because of illness related to the injury 4 == Some other reason, not the injury |
This variable describes the reason for change in situation to that before the injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestAEmplmtStatus | If your employment status has changed (please specify) | 1 == Return to previous job (increased level or hours from pre-injury) 2 == Return to previous job (reduced level or hours) 3 == Change of job, different work 4 == Special employment/ sheltered employment 5 == Looking for work, unemployed 6 == Unable to work 7 == Retired 8 == Student 9 == Homemaker, keeping house 88 == Unknown |
This variable describes the current employment of a subject in case there was a change because of the injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestAEmplmtStatusChange | 6) Is your employment status same as before injury? | 1 == Yes 0 == No |
This variable describes if the subject's employment status is the same as before the injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestAMaritalStat | If your martial status has changed (please specify) | 1 == Single (never married) 2 == Married 3 == Partnered (other than married) 4 == Separated/Divorced 5 == Widowed |
This variable describes the current marital status in case there was a change because of the injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestAMaritalStatChange | 5) Is your current marital status same as before injury? | 1 == Yes 0 == No |
This variable describes if there is a change in marital status as part of QoLIBRI-OS. |
| Outcomes.PartQuestASatHospInj | 3a) Overall how satisfied are you with the Hospital care you have received at the time of your injury? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied a subject is with the hospital care at the time of the injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestASatHospPostInj | 3b) Overall how satisfied are you with the health service care afterwards (including rehabilitation)? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied a subject is with the health service care afterwards (including rehabilitation) as part of QoLIBRI-OS. |
| Outcomes.PartQuestASatSupport | 2) Overall how satisfied are you with the availability of support from people close to you? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied a subject is with the availability of support from people close to them as part of QoLIBRI-OS. |
| Outcomes.PartQuestASesPrimAdultChange | 7) Are your living arrangements same as before the injury? | 1 == Yes 0 == No |
This variable describes if the living arrangements of a subject are the same as before the injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestASesPrimAdultChangePlace | If your living arrangements have changed (please specify) | 1 == At home- Supported 2 == At home- Not-supported 3 == Rehabilitation centre 4 == Nursing Home 5 == Hospital 99 == Other |
This variable describes the current living arrangement of a subject, in case the living arrangements are not the same as before the injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestASupHelp | 12) Please indicate any professional help in specific areas that you have been given because of your injury. | 1 == Information from the hospital concerning the effects of head injury 2 == Help for problems with speaking or making yourself understood (e.g. speech therapy) 3 == Help for problems with memory, attention etc (e.g. cognitive rehabilitation) 4 == Help for problems with movement (e.g. physiotherapy) 5 == Help for problems with looking after yourself in daily life (washing, cooking, toileting, mobility) (e.g. occupational therapy) 6 == Help for emotional difficulties, such as anxiety, depression, or stress 7 == Help for problems with behaviour, such as anger 8 == Help for problems with fatigue 9 == Help for managing money 10 == Help returning to work (e.g. vocational rehabilitation or employment services) |
This variable describes any professional help in specific areas being given because of the injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestASupPeopleQty | 9) How many people do you have near that you can readily count on for real help in times of trouble or difficulty, such as watch over children or pets, give rides to Hospital or store, or help if you are sick? | 0 == None 1 == 1 2 == 2-5 6 == 6-9 10 == 10 or more |
This variable describes how many people a subject has near them they can readily count on for real help in times of trouble or difficulty, such as watch over children or pets, give rides to hospital or store, or help if they are sick as part of QoLIBRI-OS. |
| Outcomes.PartQuestASupRehab | 11) Have you received rehabilitation as a result of your head injury? | 1 == In-patient / residential rehabilitation 2 == Out-patient/ community rehabilitation 0 == No rehabilitation |
This variable denotes the patient perspective as part of QoLIBRI-OS. Objective documentation is recorded at variable: FollowUp.FURehabNo; FollowUp.FURehabInPat; FollowUp.FURehabOutPat |
| Outcomes.PartQuestASupRehabNow | If you have received rehabilitation, is this still ongoing? | 1 == Yes 0 == No |
This variable describes if received rehabilitation is still ongoing as part of QoLIBRI-OS. |
| Outcomes.PartQuestASupRehabTime | If you have received rehabilitation, when did this begin? | 1 == Within 1 month of injury 2 == Between 1 and 3 months of injury 3 == Later than 3 months after injury |
This variable describes when rehabilition as a result of head injury began as part of QoLIBRI-OS. |
| Outcomes.PartQuestASupServices | 10) Please indicate the services that you feel have given you support because of your injury. | 1 == Hospital services 2 == Community health services 3 == Private practice 4 == Social services (e.g. social work, housing) 5 == Legal services 6 == Charity services (e.g. head injury support group) 99 == Other |
Questions relate to support you can get or have received - indicates the services that you feel have given you support because of your injury as part of QoLIBRI-OS. |
| Outcomes.PartQuestBAUDITCAlcDrnkTypclDayNumScore | 15) How many drinks containing alcohol do you have on a typical day when you are drinking? | 1 == 1-2 2 == 3-4 3 == 5-6 4 == 7-9 5 == 10 or more |
This variable describes the amount of drinks containing alcohol consumed on a typical day. |
| Outcomes.PartQuestBAUDITCDrnkContainAlcFreqScore | 14) How often do you have a drink containing alcohol? | 0 == Never 1 == Monthly or less 2 == 2-4 times a month 3 == 2-3 times a week 4 == 4 or more times a week |
Detailed questions on the use of alcohol are derived from the first 3 questions of the "AUDIT" questionnaire,a screening tool developed by the World Health Organization (WHO) to assess alcohol consumption, drinking behaviors, and alcohol-related problems. The same questions are asked on in the forms on Behavioral history: InjuryHx.AUDITCDrnkContainAlcFreqScore. This aims to facilitate comparison between post- and pre-injury use. |
| Outcomes.PartQuestBAUDITCMoreThan6AlcDrnkFreqScore | 16) How often do you have six or more drinks on one occasion? | 0 == Never 1 == Less than monthly 2 == Monthly 3 == Weekly 4 == Daily or almost daily |
This variable describes how often the subject has six or more drinks on one occasion. |
| Outcomes.PartQuestBBeforeInjAdmitHosPsy | 13.12) Before the injury have you been admitted to Hospital for psychiatric reasons? | 0 == No 1 == Yes |
This variable describes if the subject has been admitted to hospital for psychiatric reasons before the injury. |
| Outcomes.PartQuestBBeforeInjEmoDis | 13.10) Before the injury, did you ever seek treatment for emotional disorders (e.g. depression or anxiety) ? | 0 == No 1 == Yes |
This variable describes if the subject ever sought treatment for emotional disorders (e.g. depression or anxiety) before the injury. |
| Outcomes.PartQuestBBeforeInjFamMigraine | 13.6) Do your parents and/or any of your brothers/sisters suffer from migraine? | 0 == No 1 == Yes |
This variable describes if the subject's parents and/or any brothers/sisters suffer from migraine. |
| Outcomes.PartQuestBBeforeInjLearnDis | 13.8) Have you had any learning disabilities/ attended special classes? | 0 == No 1 == Yes |
This variable describes if the subject ever had any learning disabilities or attended special classes. |
| Outcomes.PartQuestBBeforeInjMentalHlt | 13.11) Before the injury have you ever sought treatment for any other mental health problem? | 0 == No 1 == Yes |
This variable describes if the subject ever sought treatment for any other mental or health problem before the injury. |
| Outcomes.PartQuestBBeforeInjMob | 13.1) Did you have mobility problems before the injury? | 2 == No 1 == Yes |
This variable describes if the subject had mobility problems before the injury. |
| Outcomes.PartQuestBBeforeInjNeuro | 13.7) Have you ever had a brain or neurological illness before the injury (e.g. epilepsy, tumour, stroke)? | 0 == No 1 == Yes |
This variable describes if the subject ever had a brain or neurological illness before the injury (e.g. epilepsy, tumour, stroke). |
| Outcomes.PartQuestBBeforeInjPhysLim | 13.2) Did you have any other physical limitations before injury? | 0 == No 1 == Yes |
This variable describes if the subject had any other physical limitations before injury. |
| Outcomes.PartQuestBBeforeInjPrevConcus | 13.3) Did you ever have a concussion or brain injury before this injury? | 0 == No 1 == Yes |
This variable describes if the subject ever had a concussion or brain injury before the injury. |
| Outcomes.PartQuestBBeforeInjPrevConcusSport | 13.4) Have you ever previously had a concussion or brain injury as a result of sports or recreational activities? | 0 == No 1 == Yes |
This variable describes if the subject previously ever had a concussion or brain injury as a result of sports or recreational activities. |
| Outcomes.PartQuestBBeforeInjPrevConcusSportFreq | How often have you had a concussion or brain injury as a result of sports or recreational activities? | This variable describes Medical History before head injury: Have you ever previously had a concussion or brain injury as a result of sports or recreational activities? If so, how often? | |
| Outcomes.PartQuestBBeforeInjPrevConcusSportType | What type of sports/recreational activity caused concussion or brain injury? | This variable describes the Medical History before head injury: Have you ever previously had a concussion or brain injury as a result of sports or recreational activities? What type of sports/recreational activity? | |
| Outcomes.PartQuestBBeforeInjSubTrt | 13.9) Before the injury have you ever sought treatment for problems related to use of alcohol or drugs? | 0 == No 1 == Yes |
This variable describes if the subject has ever sought treatment for problems related to use of alcohol or drugs before the injury. |
| Outcomes.PartQuestBBeforeInjTreatMig | 13.5) Before the injury have you ever sought treatment for migraine? | 0 == No 1 == Yes |
This variable describes if a subject ever sought treatment for migraine before the injury. |
| Outcomes.PartQuestBPerformed | Is QoLIBRI-OS (part B) assessment performed? | 1 == Performed/Completed 0 == Not performed |
This variable describes if the questionnaire assessment has been performed. |
| Outcomes.PartQuestBQuestionnaireMode | QoLIBRI-OS (Part B) assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
This variable describes the mode in which the questionnaire was completed. |
| Outcomes.PCL5AngryOutburstInd | 15) In the past month, how much were you bothered by irritable behaviour, angry outbursts, or acting aggressively? | This variable describes how much the subject was bothered by irritable behavior, angry outbursts, or acting aggressively, as part of PCL-5. | |
| Outcomes.PCL5AnswersRefTBIExp | When you responded to the questions in this questionnaire were your answers in reference to the stressful experience which caused your tramatic brain injury? | 0 == No 1 == Yes |
This variable describes how much a subject is bothered when they responded to the questions in this questionnaire were the answers in reference to the stressful experience which caused the tramatic brain injury, as part of PCL-5. |
| Outcomes.PCL5AvoidHavingFeelingInd | 6) In the past month, how much were you bothered by avoiding memories, thoughts, or feelings related to the stressful experience? | This variable describes how much the subject was bothered by avoiding memories, thoughts, or feelings related to the stressful experience, as part of PCL-5. | |
| Outcomes.PCL5AvoidSituationInd | 7) In the past month, how much were you bothered by avoiding external reminders of the stressful experience (for example, people, places, conversations, activities, objects, or situations) ? | This variable describes how much a subject is bothered by avoiding external reminders of the stressful experience (for example, people, places, conversations, activities, objects, or situations), as part of PCL-5. | |
| Outcomes.PCL5Blame | 10) In the past month, how much were you bothered by blaming yourself or someone else strongly for the stressful experience or what happened after it? | This variable describes how much a subject is bothered by blaming themself or someone else strongly for the stressful experience or what happened after it, as part of PCL-5. | |
| Outcomes.PCL5Date | Date of PCL-5 assessment | Reflects the Date of PCL-5 outcome test. | |
| Outcomes.PCL5DifficultyConcentratingInd | 19) In the past month, how much were you bothered by having difficulty concentrating? | This variable describes how much a subject is bothered by having difficulty concentrating, as part of PCL-5. | |
| Outcomes.PCL5DreamsInd | 2) In the past month, how much were you bothered by repeated, disturbing dreams of the stressful experience? | 0 == 0-Not at all 1 == 1-A little bit 2 == 2-Moderately 3 == 3-Quite a bit 4 == 4-Extremely |
This variable describes how much a subject is bothered by repeated, disturbing dreams of the stressful experience, as part of PCL-5. |
| Outcomes.PCL5EmotionallyNumbInd | 14) In the past month, how much were you bothered by trouble experiencing positive feelings (for example, being unable to feel happiness or have loving feelings for people close to you)? | This variable describes how much a subject is bothered by trouble experiencing positive feelings (for example, being unable to feel happiness or have loving feelings for people close to them), as part of PCL-5. | |
| Outcomes.PCL5FallStayAsleepInd | 20) In the past month, how much were you bothered by trouble falling or staying asleep? | This variable describes how much a subject was bothered by trouble falling or staying asleep, as part of PCL-5. | |
| Outcomes.PCL5FeelDistantInd | 13) In the past month, how much were you bothered by feeling distant or cut off from other people? | This variable describes how much the subject if bothered by feeling distant or cut off from other people, as part of PCL-5. | |
| Outcomes.PCL5HappenAgainInd | 3) In the past month, how much were you bothered by suddenly feeling or acting as if the stressful experience were actually happening again (as if you were actually back there reliving it) ? | THis variable describes how much a subject is bothered by suddenly feeling or acting as if the stressful experience was actually happening again, as part of PCL-5. | |
| Outcomes.PCL5JumpyInd | 18) In the past month, how much were you bothered by feeling jumpy or easily startled? | This variable describes how much the subject was bothered by feeling jumpy or easily startled, as part of PCL-5. | |
| Outcomes.PCL5LossInterestInd | 12) In the past month, how much were you bothered by loss of interest in activities that you used to enjoy? | This variable described how much the subject was bothered by loss of interest in activities that they used to enjoy, as part of PCL-5. | |
| Outcomes.PCL5MemoriesInd | 1) In the past month, how much were you bothered by repeated, disturbing, and unwanted memories of the stressful experience? | 0 == 0-Not at all 1 == 1-A little bit 2 == 2-Moderately 3 == 3-Quite a bit 4 == 4-Extremely |
This variable describes how much a subject is bothered by repeated, disturbing, and unwanted memories of the stressful experience, as part of PCL-5. |
| Outcomes.PCL5NegBeliefsOfSelfOthersWorld | 9) In the past month, how much were you bothered by having strong negative beliefs about yourself, other people, or the world (example, having thoughts such as: I am bad, there is something seriously wrong with me, no one can be trusted, the world is completely dangerous) ? | This variable describes how much a subject is bothered by having strong negative beliefs about themself, other people, or the world, as part of PCL-5. | |
| Outcomes.PCL5NegFeelingsFearAngerGuiltShame | 11) In the past month, how much were you bothered by having strong negative feelings such as fear, horror, anger, guilt, or shame? | This variable described how much the subject was bothered by having strong negative feelings such as fear, horror, anger, guilt, or shame, as part of PCL-5. | |
| Outcomes.PCL5Performed | Is PCL-5 assessment performed? | 1 == Performed/Completed 0 == Not performed |
This variable describes if the questionnaire is completed for the PCL-5. |
| Outcomes.PCL5PhysicalReactionsInd | 5) In the past month, how much were you bothered by having strong physical reactions when something reminded you of the stressful experience (example, heart pounding, trouble breathing, sweating)? | This variable desribes how much the subject was bothered by having strong physical reactions when something reminded them of a stressful experience (for example, heart pounding, trouble breathing, sweating), as part of PCL-5. | |
| Outcomes.PCL5QuestionnaireMode | PCL-5 assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
This variable describes in which mode the questionnaire was completed for the PCL-5. |
| Outcomes.PCL5RememberImportantInd | 8) In the past month, how much were you bothered by trouble remembering important parts of the stressful experience? | This variable describes how much a subject is bothered by trouble remembering important parts of the stressful experience, as part of PCL-5. | |
| Outcomes.PCL5Risk | 16) In the past month, how much were you bothered by taking too many risks or doing things that cause you harm? | This variable describes how much a subject is bothered by taking too many risks or doing things that cause them harm, as part of PCL-5. | |
| Outcomes.PCL5SuperAlertInd | 17) In the past month, how much were you bothered by being super-alert or watchful or on guard? | This variable describes how much a subject is bothered by being "super-alert", watchful or on guard, as part of PCL-5. | |
| Outcomes.PCL5TotalScore | PCL-5 total score | PCL-5 Total score. Calculated centrally. | |
| Outcomes.PCL5VeryUpsetInd | 4) In the past month, how much were you bothered by feeling very upset when something reminded you of the stressful experience? | THis variable describes how much a subject is feeling very upset when something reminded them of the stressful experience, as part of PCL-5. | |
| Outcomes.PHQ9AppteIssueScre | 5) Over the last 2 weeks, how often have you been bothered by poor appetite or overeating? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been bothered by abnormal diet/appetite in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9ConcntrtnProbScre | 7) Over the last 2 weeks, how often have you been bothered by having trouble concentrating on things, such as reading the newspaper or watching television? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been bothered with troubling concentrating in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9Date | Date of PHQ-9 assessment | Date of PHQ-9 Depression test. | |
| Outcomes.PHQ9DthHrtThghtScre | 9) Over the last 2 weeks, how often have you been bothered by little interest or pleasure in doing things? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been suffering with the thoughts of that he/she would be better off dead to hurt, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9DwnDeprssnHopelssScre | 2) Over the last 2 weeks, how often have you been bothered by feeling down, depressed, or hopeless? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been feeling down and depressed in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9IntrstPleasrActScre | 1) Over the last 2 weeks, how often have you been bothered by having little interest or pleasure in doing things? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been bothered by having little interest or pleasure in doing things in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9LowSlfEstmScre | 6) Over the last 2 weeks, how often have you been bothered by feeling bad about yourself - or that you are a failure or have let yourself or your family down? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been feeling bad for himself/herself in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9Performed | Is PHQ-9 assessment performed? | 1 == Performed/Completed 0 == Not performed |
Responses for the PHQ-9 relate to how oftent the subject has been bothered in the last 2 weeks |
| Outcomes.PHQ9ProbsEffectOnDailyAct | If you checked off any problems, how difficult have these problems made it for you to do your work, take care of things at home, or get along with other people? | 0 == Not difficult at all 1 == Somewhat difficult 2 == Very difficult 3 == Extremely difficult |
Only applicable if any of the 9 problem areas checked. The scale related to how difficult it is to do work, take care of things at home, or get along with other people for the subject, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9QuestionnaireMode | PHQ-9 assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
This reflects the mode in which the assessment PHQ-9 Depression was performed; this could be "personal interview", "postal questionnaire", "telephone interview" or web-based. |
| Outcomes.PHQ9SleepProbScre | 3) Over the last 2 weeks, how often have you been bothered by falling or staying asleep, or sleeping too much? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been bothered with troubling falling/staying asleep or sleeping too much in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9SpdMovmntSpchScre | 8) Over the last 2 weeks, how often have you been bothered by moving or speaking so slowly that other people could have noticed, or the opposite - being so fidgety or restless that you have been moving around a lot more than usual? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been suffering with moving or speaking too slowly in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9TirdLckEnrgyScre | 4) Over the last 2 weeks, how often have you been bothered by feeling tired or having little energy? | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been feeling tired in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9TotlScre | PHQ-9 total score | Not scored by investigator, calculated score. Total score of the questionnaire, as the part of Patient Health Questionnaire Depression (PHQ-9). | |
| Outcomes.QoLIBRIAdlScore | QoLIBRI Total Score (Activities of daily living) | QoLIBRI Daily Life Autonomy Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRICogScore | QoLIBRI Total Score (Thinking/cognition) | QoLIBRI Cognition Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRIDate | Date of QoLIBRI assessment | Date of QoLIBRI outcome test. | |
| Outcomes.QoLIBRIEmoScore | QoLIBRI Total Score (Emotions) | QoLIBRI Emotional Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRIEmotAchievmnts | B5) How satisfied are you with what you have achieved since your brain injury? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with what they have achieved since the brain injury as part of the QoLIBRI test. |
| Outcomes.QoLIBRIEmotAppearnce | B4) How satisfied are you with the way you look? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with they way they look since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIEmotEnergy | B1) How satisfied are you with your level of energy? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with their level of energy, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIEmotFuture | B7) How satisfied are you with the way you see your future? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with the way he/she sees his/her future since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIEmotMotivtn | B2) How satisfied are you with your level of motivation to do things? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his level of motivation to do things since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIEmotSelfEstm | B3) How satisfied are you with your self-esteem, how valuable you feel? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his self-esteem, how valuable he/she feels since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIEmotSelfPerceptn | B6) How satisfied are you with the way you perceive yourself? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with the way he/she perceives himself/herself since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIFeelAngry | E5) How bothered are you by feeling angry or aggressive? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by feeling angry or aggressive, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIFeelAnxious | E3) How bothered are you by feeling anxious? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by feeling anxious, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIFeelBored | E2) How bothered are you by feeling bored? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by feeling bored, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIFeelLonely | E1) How bothered are you by feeling lonely, even when you are with other people? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by feeling lonely, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIFeelSad | E4) How bothered are you by feeling sad or depressed? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by feeling sad or depressed, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIIndpDomesticAct | C3) How satisfied are you with your ability to carry out domestic activities, for example cooking or repairing things? | This variable describes how satisfied the subject is with his ability to carry out domestic activities, for example cooking or repairing things, since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRIIndpExtent | C1) How satisfied are you with the extent of your independence from others? | This variable describes how satisfied the subject is with the extent of his independence from others, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRIIndpOutAbout | C2) How satisfied are you with your ability to get out and about? | This variable describes how satisfied the subject is with his ability to get out and about since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRIIndpOwnLife | C7) How satisfied are you with the extent to which you are in charge of your own life? | This variable describes how satisfied the subject is with the extent to which he/she is in charge of his/her own life, since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRIIndpPersonalFin | C4) How satisfied are you with your ability to run your personal finances? | This variable describes how satisfied the subject is with his ability to run his personal finances, since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRIIndpSocAct | C6) How satisfied are you with your participation in social and leisure activities, for example sports, hobbies, parties? | This variable describes how satisfied the subject is with his participation in social and leisure activities, for example sports, hobbies, parties, since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRIIndpWrkEd | C5) How satisfied are you with your participation in work or education? | This variable describes how satisfied the subject is with his participation in work or education since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRIOSBrainWorking | 2) Overall, how satisfied are you with how your brain is working, in terms of your concentration, memory, thinking? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied the subject is with how his brain is working, in terms of concentration, memory, thinking, since the brain injury, as part of the QoLIBRI-OS test. |
| Outcomes.QoLIBRIOSCompleteBy | QoLIBRI-OS (Part A) assessment completed by | 1 == Patient alone 2 == Relative or friend or carer alone 3 == Patient and relative, friend or carer together |
This variables describes who has filled out the QoLIBRI-OS form. |
| Outcomes.QoLIBRIOSCurrSituationFutureProspects | 6) Overall, how satisfied are you with your current situation and future prospects? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied the subject is with his current situation and future prospects, since the brain injury, as part of the QoLIBRI-OS test. |
| Outcomes.QoLIBRIOSDate | Date of QoLIBRI-OS (Part A) assessment | This variables reflects the date of QoLIBRI-OS test. | |
| Outcomes.QoLIBRIOSDayToDay | 4) Overall, how satisfied are you with your ability to carry out day to day activities? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied the subject is with his ability to carry out day to day activities, since the brain injury, as part of the QoLIBRI-OS test. |
| Outcomes.QoLIBRIOSFeelingsEmotions | 3) Overall, how satisfied are you with your feelings and emotions? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied the subject is with his feelings and emotions since the brain injury, as part of the QoLIBRI-OS test. |
| Outcomes.QoLIBRIOSPerformed | QoLIBRI-OS (Part A) assessment performed | 1 == Performed/Completed 0 == Not performed |
This variable describes if the QoLIBRI-OS questionnaire assessment is performed. |
| Outcomes.QoLIBRIOSPersonalSocialLife | 5) Overall, how satisfied are you with your personal and social life? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable described how satisfied a subject is with their personal and social life, as part of the QoLIBRI-OS test. |
| Outcomes.QoLIBRIOSPhysCondition | 1) Overall, how satisfied are you with your physical condition? | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied the subject is with your physical condition, as part of the QoLIBRI-OS test. |
| Outcomes.QoLIBRIOSQuestionnaireMode | QoLIBRI-OS (Part A) assessment mode | 4 == Personal interview 3 == Web-based completion 1 == Telephone interview 2 == Postal questionnaire |
This variable informs how the QoLIBRI-OS assessment was performed. Could be "Personal interview", "Postal questionnaire", "Telephone interview" or "Web-based completion". |
| Outcomes.QoLIBRIOStartTime | QoLIBRI-OS assessment start time | This variable reflects the QoLIBRI-OS assessment start time. | |
| Outcomes.QoLIBRIOStopTime | QoLIBRI-OS assessment stop time | This variable reflects the QoLIBRI-OS assessment stop time. | |
| Outcomes.QoLIBRIOSTotalScore | QoLIBRI-OS (Part A) total score | Total score for Qolibri-OS | |
| Outcomes.QoLIBRIOTimeSpent | Time spent for QoLIBRI-OS assessment | This variable reflects the time spent for the QoLIBRI-OS assessment. | |
| Outcomes.QoLIBRIPerformed | Is QoLIBRI assessment performed? | 1 == Performed/Completed 0 == Not performed |
This variable informs if the QoLIBRI assessment was performed or not |
| Outcomes.QoLIBRIPhysProbBrainInj | F5) Overall, how bothered are you by the effects of your brain injury? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by the effects of his brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIPhysProbInjs | F2) How bothered are you by effects of any other injuries you sustained at the same time as your brain injury? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by effects of any other injuries sustained at the same time as his brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIPhysProbPain | F3) How bothered are you by pain, including headaches? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by pain, including headaches, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIPhysProbSeeHear | F4) How bothered are you by problems with seeing or hearing? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by problems with seeing or hearing, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIPhysProbSlow | F1) How bothered are you by slowness and/or clumsiness of movement? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how bothered the subject is by slowness and/or clumsiness of movement, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIPhysScore | QoLIBRI Total Score (Physical problems) | QoLIBRI Physical Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRIQuestionnaireMode | QoLIBRI assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
The mode in which the QoLIBRI assessment was performed |
| Outcomes.QoLIBRISelfScore | QoLIBRI Total Score (Feelings) | QoLIBRI Self Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRISocRelAffectn | D1) How satisfied are you with your ability to feel affection towards others, for example your partner, family, friends? | This variable describes how satisfied the subject is with his ability to feel affection towards others, for example his partner, family, friends, since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRISocRelAttitudes | D6) How satisfied are you with the attitudes of other people towards you? | This variable describes how satisfied the subject is with the attitudes of other people towards him/her, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRISocRelFamily | D2) How satisfied are you with your relationships with members of your family? | This variable describes how satisfied the subject is with his/her relationships with members of his/her family since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRISocRelFriends | D3) How satisfied are you with your relationships with your friends? | This variable describes how satisfied the subject is with his relationships with his friends since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRISocRelPartner | D4) How satisfied are you with your relationship with a partner or with not having a partner? | This variable describes how satisfied the subject is with his/her relationship with a partner or with not having a partner, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRISocRelSexLife | D5) How satisfied are you with your sex life? | This variable describes how satisfied the subject is with his/her sex life since the brain injury, as part of the QoLIBRI test. | |
| Outcomes.QoLIBRISocScore | QoLIBRI Total Score (Social) | QoLIBRI Social Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRIThnkConcentrate | A1) How satisfied are you with your ability to concentrate, for example when reading or keeping track of a conversation? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his/her ability to concentrate, for example when reading or keeping track of a conversation, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIThnkDecisions | A5) How satisfied are you with your ability to make decisions? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his/her ability to make decisions since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIThnkExpress | A2) How satisfied are you with your ability to express yourself and understand others in a conversation? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his/her ability to express himself/herself and understand others in a conversation, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIThnkMemory | A3) How satisfied are you with your ability to remember everyday things, for example where you have put things? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his/her ability to remember everyday things, for example where you have put things, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIThnkNavigate | A6) How satisfied are you with your ability to find your way around? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his/her ability to find his/her way around, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIThnkSolns | A4) How satisfied are you with your ability to plan and work out solutions to everyday practical problems, for example what to do when you lose your keys? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his/her ability to plan and work out solutions to everyday practical problems, for example what to do when losing his/her keys, as part of the QoLIBRI test. |
| Outcomes.QoLIBRIThnkSpeed | A7) How satisfied are you with your speed of thinking? | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with his/her speed of thinking, since the brain injury, as part of the QoLIBRI test. |
| Outcomes.QoLIBRITotalScore | QoLIBRI Total Score | QoLIBRI Total Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.RAVLT20MinDelayPrincipalList7 | 20 min delay (No) of correct responses - Principal list recall trial 7) | This variable reflects the 20 minute delay for the principal list recall Trial 7 for the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTCompletionCode | RAVLT completed or not and the reason if not | Reflects if the RAVLT (The Rey Auditory Verbal Learning Test) was completed or not, and if not, why not. | |
| Outcomes.RAVLTDate | Date of RAVLT assessment | Reflects the date of the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTInterferenceList1 | No) of correct responses - Interference list recall trial 1 | This variable reflects the interference for the list recall Trial 1 for the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTNeuroPsychCompCode | RAVLT assessment completion code | 3.0 == 3.0 Test completed 2.0 == 2.0 Test attempted but not completed 1.0 == 1.0 Test not done |
Reflects the completion of the RAVLT (The Rey Auditory Verbal Learning Test). |
| Outcomes.RAVLTPrincipalList1 | No) of correct responses - Principal list recall trial 1 | This variable reflects the # of Correct Responses for the principal list recall Trial 1 for the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTPrincipalList2 | No) of correct responses - Principal list recall trial 2 | This variable reflects the # of Correct Responses for the principal list recall Trial 2 for the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTPrincipalList3 | No) of correct responses - Principal list recall trial 3 | This variable reflects the # of Correct Responses for the principal list recall Trial 3 for the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTPrincipalList4 | No) of correct responses - Principal list recall trial 4 | This variable reflects the # of Correct Responses for the principal list recall Trial 4 for the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTPrincipalList5 | No) of correct responses - Principal list recall trial 5 | This variable reflects the # of Correct Responses for the principal list recall Trial 5 for the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTPrincipalListRecall6 | No) of correct responses - Principal list recall trial 6 | This variable reflects the # of Correct Responses for the principal list recall Trial 6 for the RAVLT (The Rey Auditory Verbal Learning Test). | |
| Outcomes.RAVLTTestAttemptdNotCompOptions | Reason for attempting but not completing RAVLT assessment | 2.6 == Not completed - Logistical reasons, other reasons 2.5 == Not completed - Illness/fatigue 2.4 == Not completed - Language 2.3 == Not completed - Lack of effort/uncooperative 2.2 == Not completed - Non-neurological/physical reason 2.1 == Not completed - Cognitive/neurological deficits 2.7 == Not completed - Examiner error |
If the RAVLT test was attempted but not completed, this variable specifies the reason. |
| Outcomes.RAVLTTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing RAVLT assessment | If the reason why the RAVLT test was attempted but not completed, was another reason than pre-defined, the other reason must be specified here. | |
| Outcomes.RAVLTTestCompletedOptions | RAVLT assessment completion type | 3.2 == Non-standard administration - Other 3.1 == Test completed - Non-standard, results valid 3.0 == Test completed in full - results valid |
If the RAVLT Test was completed, this variable was to specify how it was completed. |
| Outcomes.RAVLTTestComplNonStandAdminOTHER | Other non-standard administration reason for RAVLT assessment (please specify) | ||
| Outcomes.RAVLTTestNotDoneOptions | Reason for not attempting RAVLT assessment | 1.6 == Not attempted - Logistical reasons, other reasons 1.5 == Not attempted - Illness/fatigue 1.4 == Not attempted - Language 1.3 == Not attempted - Lack of effort/uncooperative 1.2 == Not attempted - Non-neurological/physical reasons 1.1 == Not attempted - Cognitive/neurological deficits 1.7 == Not attempted - Examiner error 1.8 == Not attempted - Patient not available |
This variable described why the RAVLT test is not done. |
| Outcomes.RAVLTTestNotDoneOptionsOTHER | Other reason for not attempting RAVLT assessment | This variable described the "other" reason why the RAVLT test is not done. | |
| Outcomes.RAVLTTotalScorePrincipal | Total of all words recalled from all principal lists trials | Rey Auditory Verbal Learning Test Total Score. Calculated centrally. | |
| Outcomes.RAVLTWordListNum | RAVLT Word List Form Number | 1 == 1 2 == 2 3 == 3 |
Indicates which RAVLT Word List Form was used for the asessment |
| Outcomes.RPQ13Score | RPQ-13 score | Score for the Rivermead Assessment RPQ-13. Score for the Not scored by investigator, calculated score. Baseline RPQ documents complaints and symptoms commonly reported after TBI. Baseline RPQ can only be assessed in conscious subjects who are out of PTA. Provides further details on AOC. | |
| Outcomes.RPQ3Score | RPQ-3 score | Score for the Rivermead Assessment RPQ-3. Not scored by investigator, calculated score. Baseline RPQ documents complaints and symptoms commonly reported after TBI. Baseline RPQ can only be assessed in conscious subjects who are out of PTA. Provides further details on AOC. | |
| Outcomes.RPQBlurredVision | Blurred vision | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from blurred vision, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQDate | Date of RPQ assessment | Date of the Rivermead RPQ assessment. Baseline RPQ documents complaints and symptoms commonly reported after TBI. Baseline RPQ can only be assessed in conscious subjects who are out of PTA. Provides further details on AOC. | |
| Outcomes.RPQDepressed | Feeling depressed or tearful | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from feeling depressed or tearful, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQDizziness | Feelings of dizziness | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from feelings of dizziness, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQDoubleVision | Double vision | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from double vision, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQFatigue | Fatigue, tiring more easily | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Fatigue, tiring more easily, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQForgetful | Forgetfulness, poor memory | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Forgetfulness, poor memory, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQFrustrated | Feeling frustrated or impatient | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Feeling frustrated or impatient, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQHeadaches | Headaches | 0 == 0-Not experienced at all 1 == 1- No more of a problem 2 == 2- A mild problem 3 == 3- A moderate problem 4 == 4- A severe problem |
This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Headaches, as part of the Rivermead RPQ assessment. |
| Outcomes.RPQIrritable | Being irritable, easily angered | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Being irritable, easily angered, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQLightSensitivity | Light sensitivity (easily upset by bright light) | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Light sensitivity (easily upset by bright light), as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQLongerToThink | Taking longer to think | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Taking longer to think, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQNausea | Nausea and/or vomiting | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Nausea and/or vomiting, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQNoiseSensitivity | Noise sensitivity (easily upset by loud noise) | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Noise sensitivity (easily upset by loud noise), as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQOther1 | (1) Any other difficulty being experienced (please rate) | 0 == 0-Not experienced at all 1 == 1-No more of a problem 2 == 2-A mild problem 3 == 3-A moderate problem 4 == 4-A severe problem |
This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Other difficulties than the pre-defined list, as part of the Rivermead RPQ assessment. |
| Outcomes.RPQOther1Text | (1) Any other difficulty being experienced (please specify) | This variable reflects which other difficulties, if the subject, compared with before the accident, now (over the last 24 hours) suffers from Other difficulties than the pre-defined list, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQOther2 | (2) Any other difficulty being experienced (please rate) | 0 == 0-Not experienced at all 1 == 1-No more of a problem 2 == 2-A mild problem 3 == 3-A moderate problem 4 == 4-A severe problem |
This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Other difficulties than the pre-defined list, as part of the Rivermead RPQ assessment. |
| Outcomes.RPQOther2Text | (2) Any other difficulty being experienced (please specify) | This variable reflects which other difficulties, if the subject, compared with before the accident, now (over the last 24 hours) suffers from Other difficulties than the pre-defined list, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQPerformed | Is RPQ assessment performed? | 1 == Performed/Completed 0 == Not performed |
Reflects if the Rivermead RPQ assessment was performed or not |
| Outcomes.RPQPoorConcentration | Poor concentration | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Poor concentration, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQQuestionnaireMode | RPQ assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
The mode in which the Rivermead RPQ assessment was performed; could be "Personal interview", "Postal questionnaire", "Telephone interview", "Web-based completion" |
| Outcomes.RPQRestless | Restlessness | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Restlessness, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQSleepDisturbance | Sleep disturbance | This variable reflects if the subject, compared with before the accident, now (over the last 24 hours) suffers from Sleep disturbance, as part of the Rivermead RPQ assessment. | |
| Outcomes.RPQTime | Time of the Rivermead RPQ assessment | Reflects the time of the Rivermead RPQ assessment. | |
| Outcomes.RPQTotalScore | RPQ Total Score | RPQ (Rivermead post-concussion symptoms questionnaire) Total Score. Calculated centrally. | |
| Outcomes.SF12Date | Date of SF-12 assessment | SF-12 v2 Date of assessment. | |
| Outcomes.SF12EmotProbLessAccomp | 4a) During the past 4 weeks, have you accomplished less than you would like as a result of emotional problems? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-12 v2 question relating to the past 4 weeks: how much time have you had any of the following problems with your work or daily activities AS A RESULT OF ANY EMOTIONAL PROBLEMS (such as feeling depressed or anxious)? --> ACCOMPLISHED LESS than you would like |
| Outcomes.SF12EmotProbWkLessCare | 4b) During the past 4 weeks, have you not done work or other activities less carefully than usual as a result of emotional problems? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-12 v2 question relating to the past 4 weeks: how much time have you had any of the following problems with your work or daily activities AS A RESULT OF ANY EMOTIONAL PROBLEMS (such as feeling depressed or anxious)? --> Didn't do work or other activities LESS CAREFULLY than usual |
| Outcomes.SF12GenHlth | 1) In general, would you say your health is: | 1 == 1 - Excellent 2 == 2 - Very Good 3 == 3 - Good 4 == 4 - Fair 5 == 5 - Poor |
SF-12 v2 question relating to the subjects' view of his/her health: In general, would you say your health is... |
| Outcomes.SF12HlthLmtClmbSvrlFlStair | 2b) Does your health limit you in climbing several flights of stairs? | 1 == 1 - Yes, Limited A Lot 2 == 2 - Yes, Limited A Little 3 == 3 - No, Not Limited At All |
SF-12 v2 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Climbing SEVERAL flights of stairs |
| Outcomes.SF12HlthLmtModAct | 2a) Does your health limit you in moderate activities, such as moving a table, pushing a vacuum cleaner, bowling, or playing golf? | 1 == 1 - Yes, Limited A Lot 2 == 2 - Yes, Limited A Little 3 == 3 - No, Not Limited At All |
SF-12 v2 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> MODERATE ACTIVITIES, such as moving a table, pushing a vacuum cleaner, bowling, or playing golf |
| Outcomes.SF12PainInterfWrk | 5) During the past 4 weeks, how much did pain interfere with your normal work (including both work outside the home and housework)? | 1 == 1 - Not At All 2 == 2 - A Little Bit 3 == 3 - Moderately 4 == 4 - Quite A Bit 5 == 5 - Extremely |
SF-12 v2 question relating to the past 4 weeks: how much did PAIN interfere with your normal work (including both work outside the home and housework)? |
| Outcomes.SF12Performed | Is SF-12 assessment performed? | 1 == Performed/Completed 0 == Not performed |
Reflects if SF12 v2 assessment was performed or not. |
| Outcomes.SF12PhyEmotInterfSoc | 7) During the past 4 weeks, how much of the time has your physical health or emotional problems interfered with your social activities (like visiting with friends, relatives, etc.)? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-12 v2 question relating to the past 4 weeks: how much of the time has your PHYSICAL HEALTH OR EMOTIONAL PROBLEMS interfered with your social activities (like visiting with friends, relatives, etc.)? |
| Outcomes.SF12PhyHlthLessAccomp | 3a) During the past 4 weeks, have you accomplished less than you would like as a result of your physical health? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-12 v2 question relating to the past 4 weeks: how much of the time have you had any of the following problems with your work or other regular activities AS A RESULT OF YOUR PHYSICAL HEALTH? --> ACCOMPLISHED LESS than you would like |
| Outcomes.SF12PhyHlthLmtWrkAct | 3b) During the past 4 weeks, were you limited in the kind of work or other activities as a result of your physical health? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-12 v2 question relating to the past 4 weeks: how much of the time have you had any of the following problems with your work or other regular activities AS A RESULT OF YOUR PHYSICAL HEALTH? --> Were limited in the KIND of work or other activities |
| Outcomes.SF12QuestionnaireMode | SF-12 assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
This variable reflects the mode of the SF-12 v2 assessment: it could be "Personal interview", "Postal questionnaire", "Telephone interview" or "Web-based completion" |
| Outcomes.SF12ScoreBP | Bodily Pain (BP) score | SF-12v2. Bodily Pain - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreBPNBS | Bodily Pain (BP) norm-based score | SF-12v2. Bodily Pain Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreGH | General Health (GH) score | SF-12v2. General Health (GH) - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreGHNBS | General Health (GH) norm-based score | SF-12v2. General Health (GH) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreHMNBS | Mental Health (MH) norm-based score | SF-12v2. Mental Health (MH) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreMCS | Mental Component Summary | SF-12v2. Mental Component Summary - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreMH | Mental Health (MH) score | SF-12v2. Mental Health (MH) - Scored on a 0-100 scale | |
| Outcomes.SF12ScorePCS | Physical Component Summary | SF-12v2. Physical Component Summary - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScorePF | Physical Functioning (PF) score | SF-12v2. Physical Functioning - Scored on a 0-100 scale | |
| Outcomes.SF12ScorePFNBS | Physical Functioning (PF) norm-based score | SF-12v2. Physical Functioning Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreRE | Role Emotional (RE) score | SF-12v2. Role-Emotional (RE) - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreRENBS | Role Emotional (RE) norm-based score | SF-12v2. Role-Emotional (RE) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreRP | Role Physical (RP) score | SF-12v2. Role-Physical (RP) - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreRPNBS | Role Physical (RP) norm-based score | SF-12v2. Role-Physical (RP) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreSF | Social Functioning (SF) score | SF-12v2. Social Functioning - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreSFNBS | Social Functioning (SF) norm-based score | SF-12v2. Social Functioning Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreVT | Vitality (V) score | SF-12v2. Vitality - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreVTNBS | Vitality (V) norm-based score | SF-12v2. Vitality Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12TimesFeelCalmPcful | 6a) During the past 4 weeks, how much of the time have you felt calm and peaceful ? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-12 v2 question relating to the past 4 weeks: How much of the time during the PAST 4 WEEKS --> Have you felt calm and peaceful? |
| Outcomes.SF12TimesFeelDown | 6c) During the past 4 weeks, how much of the time have you felt downhearted and low? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-12 v2 question relating to the past 4 weeks: Have you felt downhearted and low? |
| Outcomes.SF12TimesFeelEnergetic | 6b) During the past 4 weeks, how much of the time have did you have a lot of energy? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-12 v2 question relating to the past 4 weeks: Did you have a lot of energy? |
| Outcomes.SF36AsHlthy | 11b) I am as healthy as anybody I know | 1 == 1 - Definitely true 2 == 2 - Mostly true 3 == 3 - Don't know 4 == 4 - Mostly false 5 == 5 - Definitely false |
Reflects as part of the SF-36 assessment how true or false a statement is for the subject: I am as healthy as anybody I know |
| Outcomes.SF36Date | Date of SF-36 assessment | Date of the SF-36 assessment. | |
| Outcomes.SF36EmotProbLessAccomp | 5b) During the past 4 weeks, have you accomplished less than you would like as a result of your emotional problems (such as feeling depressed or anxious) ? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: how much time have you had any of the following problems with your work or daily activities AS A RESULT OF ANY EMOTIONAL PROBLEMS (such as feeling depressed or anxious)? --> Accomplished less than you would like |
| Outcomes.SF36EmtProbCutTimeWrk | 5a) During the past 4 weeks, have you cut down on the amount of time you spent on work or other activities as a result of your emotional problems (such as feeling depressed or anxious) ? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: how much time have you had any of the following problems with your work or daily activities AS A RESULT OF ANY EMOTIONAL PROBLEMS (such as feeling depressed or anxious)? --> Cut down on the amount of time you spent on work or other activities |
| Outcomes.SF36EmtProbLessCare | 5c) During the past 4 weeks, did you work or did other activities less carefully than usual as a result of your emotional problems (such as feeling depressed or anxious) ? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: how much time have you had any of the following problems with your work or daily activities AS A RESULT OF ANY EMOTIONAL PROBLEMS (such as feeling depressed or anxious)? --> Did work or other activities less carefully than usual |
| Outcomes.SF36ExpctWrseHlth | 11c) I expect my health to get worse | 1 == 1 - Definitely true 2 == 2 - Mostly true 3 == 3 - Don't know 4 == 4 - Mostly false 5 == 5 - Definitely false |
Reflects as part of the SF-36 assessment how true or false a statement is for the subject: I expect my health to get worse |
| Outcomes.SF36GenHlth | 1) In general, would you say your health is: | 1 == 1 - Excellent 2 == 2 - Very good 3 == 3 - Good 4 == 4 - Fair 5 == 5 - Poor |
SF-36 question relating to the subjects' view of his/her health: In general, would you say your health is... |
| Outcomes.SF36HlthExcllnt | 11d) My health is excellent | 1 == 1 - Definitely true 2 == 2 - Mostly true 3 == 3 - Don't know 4 == 4 - Mostly false 5 == 5 - Definitely false |
Reflects as part of the SF-36 assessment how true or false a statement is for the subject: My health is excellent |
| Outcomes.SF36HlthLmtBathDress | 3j) How much does your health limit you in bathing or dressing yourself? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Bathing or dressing yourself |
| Outcomes.SF36HlthLmtBendKneel | 3f) How much does your health limit you in bending, kneeling or stooping? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Bending, kneeling or stooping |
| Outcomes.SF36HlthLmtClmbOneFlStair | 3e) How much does your health limit you in climbing one flight of stairs? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Climbing ONE flight of stairs |
| Outcomes.SF36HlthLmtClmbSvrlFlStair | 3d) How much does your health limit you in climbing several flights of stairs? | 3 == 3 - No, not limited at all. 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Climbing SEVERAL flights of stairs |
| Outcomes.SF36HlthLmtLiftCarry | 3c) How much does your health limit you in lifting or carrying groceries? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Lifting or carrying groceries |
| Outcomes.SF36HlthLmtModAct | 3b) How much does your health limit you in moderate activities, such as moving a table, pushing a vacuum cleaner, bowling or playing golf? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> MODERATE ACTIVITIES, such as moving a table, pushing a vacuum cleaner, bowling or playing golf |
| Outcomes.SF36HlthLmtVigAct | 3a) How much does your health limit you in vigorous activities, such as running lifting heavy objects, participating in strenuous sports? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> VIGOROUS ACTIVITIES, such as running lifting heavy objects, participating in strenuous sports |
| Outcomes.SF36HlthLmtWalkHndrdYards | 3i) How much does your health limit you in walking one hundred yards? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Walking ONE HUNDRED yards |
| Outcomes.SF36HlthLmtWalkMile | 3g) How much does your health limit you in walking more than a mile? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Walking MORE THAN a mile |
| Outcomes.SF36HlthLmtWalkSvrlHndrdYards | 3h) How much does your health limit you in walking several hundred yards? | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
SF-36 question relating to activities the subject might do during a typical day: Does YOUR HEALTH NOW LIMIT YOU in these activities? If so, how much? --> Walking SEVERAL HUNDRED yards |
| Outcomes.SF36HlthOneYrAgo | 2) Compared to one year ago, how would you rate your health in general now? | 1 == 1 - Much better now than a year ago 2 == 2 - Somewhat better now than a year ago 3 == 3 - About the same as one year ago 4 == 4 - Somewhat worse now than one year ago 5 == 5 - Much worse now than one year ago |
SF-36 question relating to COMPARED TO ONE YEAR AGO: how would you rate your health in general NOW? |
| Outcomes.SF36IllMoreEasily | 11a) I seem to get ill more easily than other people | 1 == 1 - Definitely true 2 == 2 - Mostly true 3 == 3 - Don't know 4 == 4 - Mostly false 5 == 5 - Definitely false |
Reflects as part of the SF-36 assessment how true or false a statement is for the subject: I seem to get ill more easily than other people |
| Outcomes.SF36LvlBodPain | 7) How much bodily pain have you had during the past 4 weeks? | 1 == 1 - None 2 == 2 - Very mild 3 == 3 - Mild 4 == 4 - Moderate 5 == 5 - Severe 6 == 6 - Very severe |
SF-36 question relating to the past 4 weeks: How much BODILY pain have you had during the PAST 4 WEEKS? |
| Outcomes.SF36PainInterfWrk | 8) During the past 4 weeks, how much did pain interfere with your normal work (including both work outside the home and housework) ? | 1 == 1 - Not at all 2 == 2 - A little bit 3 == 3 - Moderately 4 == 4 - Quite a bit 5 == 5 - Extremely |
SF-36 question relating to the past 4 weeks: how much did PAIN interfere with your normal work (including both work outside the home and housework)? |
| Outcomes.SF36Performed | Is SF-36 assessment performed? | 1 == Performed/Completed 0 == Not performed |
Indicates if the SF-36 assessment was performed or not |
| Outcomes.SF36PhysEmotInterfNormSoc | 6) During the past 4 weeks, to what extent has your physical health or emotional problems interfered with your normal social activities with family, friends neighbours or groups? | 1 == 1 - Not at all 2 == 2 - Slightly 3 == 3 - Moderately 4 == 4 - Quite a bit 5 == 5 - Extremely |
SF-36 question relating to the past 4 weeks: to what extent has your PHYSICAL HEALTH OR EMOTIONAL PROBLEMS interfered with your normal social activities with family, friends neighbors or groups? |
| Outcomes.SF36PhysEmotInterfSoc | 10) During the past 4 weeks, how much of the time has your physical health or emotional problems interfered with your social activities (like visiting with friends, relatives, etc) ? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: how much of the time has your PHYSICAL HEALTH OR EMOTIONAL PROBLEMS interfered with your social activities (like visiting with friends, relatives, etc.)? |
| Outcomes.SF36PhysHlthCutTimeWrk | 4a) During the past 4 weeks, have you cut down on the amount of time you spent on work/other activities as a result of your physical health? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: how much of the time have you had any of the following problems with your work or other regular activities AS A RESULT OF YOUR PHYSICAL HEALTH? --> Cut down on the amount of time you spent on work/other activities |
| Outcomes.SF36PhysHlthDiffWrkAct | 4d) During the past 4 weeks, have you had difficulty performing work or other activities (example, it took extra effort) as a result of your physical health? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: how much of the time have you had any of the following problems with your work or other regular activities AS A RESULT OF YOUR PHYSICAL HEALTH? --> Had difficulty performing work or other activities (for example, it took extra effort) |
| Outcomes.SF36PhysHlthLessAccomp | 4b) During the past 4 weeks, have you accomplished less than you would like as a result of your physical health? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: how much of the time have you had any of the following problems with your work or other regular activities AS A RESULT OF YOUR PHYSICAL HEALTH? --> Accomplished less than you would like |
| Outcomes.SF36PhysHlthLmtWrkAct | 4c) During the past 4 weeks, were you limited in the kind of work or other activities as a result of your physical health? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: how much of the time have you had any of the following problems with your work or other regular activities AS A RESULT OF YOUR PHYSICAL HEALTH? --> Were limited in the kind of work or other activities |
| Outcomes.SF36QuestionnaireMode | SF-36 assessment mode | 4 == Personal interview 3 == Web-based completion 2 == Postal questionnaire 1 == Telephone interview |
The mode of SF-36 questionnaire assessment ; this could be "Personal interview", "Postal questionnaire", "Telephone interview" or "Web-based completion" |
| Outcomes.SF36ScoreBP | Bodily Pain (BP) score | SF-36v2. Bodily Pain - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreBPNBS | Bodily Pain (BP) norm-based score | SF-36v2. Bodily Pain Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreGH | General Health (GH) score | SF-36v2. General Health (GH) - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreGHNBS | General Health (GH) norm-based score | SF-36v2. General Health (GH) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreHMNBS | Mental Health (MH) norm-based score | SF-36v2. Mental Health (MH) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreMCS | Mental Component Summary | SF-36v2. Mental Component Summary - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreMH | Mental Health (MH) score | SF-36v2. Mental Health (MH) - Scored on a 0-100 scale | |
| Outcomes.SF36ScorePCS | Physical Component Summary | SF-36v2. Physical Component Summary - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScorePF | Physical Functioning (PF) score | SF-36v2. Physical Functioning - Scored on a 0-100 scale | |
| Outcomes.SF36ScorePFNBS | Physical Functioning (PF) norm-based score | SF-36v2. Physical Functioning Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreRE | Role Emotional (RE) score | SF-36v2. Role-Emotional (RE) - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreRENBS | Role Emotional (RE) norm-based score | SF-36v2. Role-Emotional (RE) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreRP | Role Physical (RP) score | SF-36v2. Role-Physical (RP) - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreRPNBS | Role Physical (RP) norm-based score | SF-36v2. Role-Physical (RP) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreSF | Social Functioning (SF) score | SF-36v2. Social Functioning - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreSFNBS | Social Functioning (SF) norm-based score | SF-36v2. Social Functioning Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreVT | Vitality (V) score | SF-36v2. Vitality - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreVTNBS | Vitality (V) norm-based score | SF-36v2. Vitality Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36TimesFeelCalmPcful | 9d) During the past 4 weeks, how much of the time have you felt calm and peaceful? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: Have you felt calm and peaceful? |
| Outcomes.SF36TimesFeelDown | 9f) During the past 4 weeks, how much of the time have you felt downhearted and low? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: Have you felt downhearted and low? |
| Outcomes.SF36TimesFeelDumps | 9c) During the past 4 weeks, how much of the time have you felt so down in the dumps that nothing could cheer you up? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: Have you felt so down in the dumps that nothing could cheer you up? |
| Outcomes.SF36TimesFeelEnergetic | 9e) During the past 4 weeks, how much of the time did you have a lot of energy? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: Did you have a lot of energy? |
| Outcomes.SF36TimesFeelFullLife | 9a) During the past 4 weeks, how much of the time did you feel full of life? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 5 == 5 - None of the time 4 == 4 - A little of the time |
SF-36 question relating to the past 4 weeks: how you feel and how things have been DURING THE PAST 4 WEEKS. For each question, please give the one answer that comes closest to the way you have been feeling. How much of the time during the PAST 4 WEEKS – --> Did you feel full of life? |
| Outcomes.SF36TimesFeelHappy | 9h) During the past 4 weeks, how much of the time have you been happy? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: Have you been happy? |
| Outcomes.SF36TimesFeelNerv | 9b) During the past 4 weeks, how much of the time have you been very nervous? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: Have you been very nervous? |
| Outcomes.SF36TimesFeelTired | 9i) During the past 4 weeks, how much of the time did you feel tired? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: Did you feel tired? |
| Outcomes.SF36TimesFeelWornOut | 9g) During the past 4 weeks, how much of the time did you feel worn out? | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
SF-36 question relating to the past 4 weeks: Did you feel worn out? |
| Outcomes.Timepoint | Outcome assessment timepoint | 2wk == 2 weeks 3mo == 3 months 6mo == 6 months 12mo == 12 months 24mo == 24 months Base == Baseline |
Outcome timepoints are 2-3 weeks, 3 months, 6 months, 12 months and 24 months. Depending on the stratum and sub-studies of a patient, follow up was performed at some of these time points or at all timepoints. For an overview, please check the SOP Manual. |
| Outcomes.TMTCompletionCode | TMT completed or not and the reason if not | Reflects the completion of the TMT (trail making test) testing, and if not completed, reason why not. | |
| Outcomes.TMTDate | Date of Trail Making Test (TMT) assessment | Reflects the Date of the TMT (trail making test) testing. | |
| Outcomes.TMTHandedness | Hand used | 1 == Dominant 2 == Non-Dominant |
This variable reflects for the TMT (Trail Making Test) if the patient used his dominant or non-dominant hand to perform the test. |
| Outcomes.TMTNeuroPsychCompCode | TMT assessment completion code | 3.0 == 3.0 Test completed 2.0 == 2.0 Test attempted but not completed 1.0 == 1.0 Test not done |
Completion code for the TMT (Trail Making Test). |
| Outcomes.TMTPartATime | Trail Making Part A | Time (in sec) for the TMT Trail Making Test Part A. | |
| Outcomes.TMTPartBTime | Trail Making Part B | Time (in sec) for the TMT Trail Making Test Part B. | |
| Outcomes.TMTTestAttemptdNotCompOptions | Reason for attempting but not completing TMT assessment | 2.6 == Not completed - Logistical reasons, other reasons 2.5 == Not completed - Illness/fatigue 2.4 == Not completed - Language 2.3 == Not completed - Lack of effort/uncooperative 2.2 == Not completed - Non-neurological/physical reason 2.1 == Not completed - Cognitive/neurological deficits 2.7 == Not completed - Examiner error |
Reason why TMT test was not completed. |
| Outcomes.TMTTestAttemptdNotCompOptionsOTHER | Other reason for attempting but not completing TMT assessment | "Other" reason why TMT test was not completed. | |
| Outcomes.TMTTestCompletedOptions | TMT assessment completion type | 3.2 == Non-standard administration - Other 3.1 == Test completed - Non-standard, results valid 3.0 == Test completed in full - results valid |
Reflects if TMT test was completed. |
| Outcomes.TMTTestComplNonStandAdminOTHER | Other non-standard administration reason for TMT assessment (please specify) | ||
| Outcomes.TMTTestNotDoneOptions | Reason for not attempting TMT assessment | 1.6 == Not attempted - Logistical reasons, other reasons 1.5 == Not attempted - Illness/fatigue 1.4 == Not attempted - Language 1.3 == Not attempted - Lack of effort/uncooperative 1.2 == Not attempted - Non-neurological/physical reasons 1.1 == Not attempted - Cognitive/neurological deficits 1.7 == Not attempted - Examiner error 1.8 == Not attempted - Patient not available |
Reason why TMT test was not attempted. |
| Outcomes.TMTTestNotDoneOptionsOTHER | Other reason for not attempting TMT assessment | "Other" reason why TMT test was not attempted. | |
| Outcomes.TUGDate | Date of TUG assessment | Date of the TUG (Timed Up and Go) test. | |
| Outcomes.TUGTimedResult | Timed result (< 10 seconds = normal, < 20 seconds = good mobility; can go out alone, mobile without a gait aid, < 30 seconds = problems, cannot go outside alone, requires a gait aid) | Times results of the TUG (Timed Up and Go) test. Interpretation: < 10 sec = normal; < 20 sec: good mobility, can go out alone, mobile without gait aid; < 30 sec: problems, cannot go outside alone, requires a gait aid | |
| PriorMeds.PmMedicalCode | Medical History Code | Medical History of patients has been recorded under MedHx.MedHx* A number of predefined medical conditions were coded in the e-CRF. If the patient was taking medication for this predefined medical condition, the same code needed to be entered here. An option other was also available for conditions not listed. Please check MedHx.MedHx* for the information on the medical condition(s) corresponding to this variable. | |
| PriorMeds.PmMedicationName | Medication Name | These fields capture information on medication taken pre-injury. For each medication taken, the corresponding Medical History code is listed to document the reason for which this med was taken. If the medication taken was not linked to one of the recorded medication history codes, Investigators were asked to enter "777" as related history code. | |
| Registry.AbdomenPelvicContentsAIS | Abdomen/pelvic contents AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Abdomen/Pelvic Contents In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.AbdomenPelvicContentsISS | Abdomen Pelvic Content AIS | ISS score for the Abdomen/Pelvic Contents | |
| Registry.AbdomenPelvicLumbarRegionAIS | Abdomen Pelvic Lumbar Region AIS | AIS score for the Pelvic Lumbar Region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| Registry.Age | Age | Age, recorded in years. | |
| Registry.Anticoagulants | Anticoagulants | 0 == No 1 == Yes 88 == Unknown |
Reflects use of anticoagulants. |
| Registry.BrainInjuryAIS | Brain injury AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Brain Injury In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.BrainInjuryISS | Brain Injury ISS | ISS score for the Brain Injury | |
| Registry.CervicalSpineAIS | Cervical spine AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Cervical Spine region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.CervicalSpineISS | Cervical Spince ISS | ISS score for the Cervical Spine region | |
| Registry.ChestSpineRegionAIS | Chest Spine Region AIS | AIS score for the Chest Thoracic Spine region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| Registry.CraniotomyForHaematoma | Craniotomy for haematoma | Reflects if a Craniotomy for haematoma was performed as Key emergency interventions. | |
| Registry.CraniotomyForHaematomaDate | Date of craniotomy for haematoma | Reflects the Date if a Craniotomy for haematoma was performed as Key emergency interventions. | |
| Registry.CraniotomyForHaematomaDateTime | Date and time of Craniectomy for haematoma | Calculated from Registry.CraniotomyForHaematomaDate and Registry.CraniotomyForHaematomaTime | |
| Registry.CraniotomyForHaematomaTime | Time of craniotomy for haematoma | Reflects the time if a Craniotomy for haematoma was performed as Key emergency interventions. | |
| Registry.CT1Date | Date of first CT Brain | Date of the first Brain CT | |
| Registry.CT1DateTime | CT1 date and time | Calculated value from Registry.CT1Date and Registry.CT1Time | |
| Registry.CT1Time | Time of first CT Brain | Time of the first Brain CT | |
| Registry.CT1TimeSinceInj | Time between injury and CT1 | Calculated value from Registry.CT1Date, Registry.CT1Time and Registry.DateInj, Registry.TimeInj | |
| Registry.CTAbnormalBasalCisterns | Basal cisterns | 1 == Open 2 == Compressed/obliterated 88 == Unknown |
These details record the investigators score of the first CT brain concerning Basal cisterns. |
| Registry.CTIntracranialLesions | Intracranial lesions | 0 == No 1 == Yes 88 == Unknown |
These details record the investigators score of the first or subsequent CT brain scans as to whether or not TBI or intracranial bleeding is visible. |
| Registry.CTIntracranialLesionsPresentASDH | Intracranial lesions: ASDH | 0 == No 1 == Small 2 == Large (mass) 88 == Unknown |
These details record the investigators score of the first or subsequent CT brain scans related to presence or absence of an ASDH. |
| Registry.CTIntracranialLesionsPresentContusions | Intracranial lesions: Contusions | 0 == No 1 == Small 2 == Large (mass) 88 == Unknown |
These details record the investigators score of the first or subsequent CT brain scans related to presence or absence of a Contusion. |
| Registry.CTIntracranialLesionsPresentEDH | Intracranial lesions: EDH | 0 == No 1 == Small 2 == Large (mass) 88 == Unknown |
These details record the investigators score of the first or subsequent CT brain scans related to presence or absence of an EDH. |
| Registry.CTResult | CT result | 0 == Normal 1 == Abnormal |
These details record the investigators score of the first CT brain concerning normal or abnormal results. |
| Registry.CTShift | Shift | 0 == No 1 == 0-4 mm 2 == >=5 mm 88 == Unknown |
These details record the investigators score of the first CT brain concerning Shift. |
| Registry.CTtSAH | tSAH | 0 == No 1 == Yes 88 == Unknown |
These details record the investigators score of the first CT brain concerning TSAH. |
| Registry.DamageControlLaparotomy | Damage control laparotomy | Reflects if a Damage control laparotomy was performed as Key emergency intervention. | |
| Registry.DamageControlLaparotomyDate | Date of damage control laparotomy | Reflects the Date if a Damage control laparotomy was performed as Key emergency intervention. | |
| Registry.DamageControlLaparotomyDateTime | Date and time of Damage Control Laparotomy | Calculated from Registry.DamageControlLaparotomyDate and Registry.DamageControlLaparotomyTime | |
| Registry.DamageControlLaparotomyTime | Time of damage control laparotomy | Reflects the Time if a Damage control laparotomy was performed as Key emergency intervention. | |
| Registry.DamageControlThoracotomy | Damage control thoracotomy | Reflects if a Damage control thoracotomy was performed as Key emergency intervention. | |
| Registry.DamageControlThoracotomyDate | Date of damage control thoracotomy | Reflects the Date if a Damage control thoracotomy was performed as Key emergency intervention. | |
| Registry.DamageControlThoracotomyDateTime | Date and time of Damage Control Thoracotomy | Calculated from Registry.DamageControlThoracotomyDate and Registry.DamageControlThoracotomyTime | |
| Registry.DamageControlThoracotomyTime | Time of damage control thoracotomy | Reflects the Time if a Damage control thoracotomy was performed as Key emergency intervention. | |
| Registry.DateInj | Date of injury | Date of Injury. Anonymised and saved as 1970-01-01 for all patients. All other dates are converted relative to date of Injury. | |
| Registry.DateTimeInj | Date and time of injury | Derived from Registry.DateInj and Registry.TimeInj | |
| Registry.DateTimeInjReliable | Reliability of time of injury | 1 == Verified 2 == Estimate |
This variable documents if the time of injury is accurate, or is based on "best possible estimate", in case exact time of injury not known. |
| Registry.DayInjury | Day of injury | Day of injury. (Sunday - Saturday) | |
| Registry.DeathCause | Principle cause of death | 1 == Head injury/initial injury 2 == Head injury/secondary intracranial damage 3 == Systemic trauma 4 == Medical complications 99 == Other 88 == Unknown |
Principle cause of death |
| Registry.DeathDate | Date of death | Death date. | |
| Registry.DeathDateTime | Death date and time | Calculated from Registry.DeathDate and Registry.DeathTime | |
| Registry.DeathTime | Time of death | Time of death | |
| Registry.DeathTimeSinceInj | Time between injury and death | Calculated death time since injury. | |
| Registry.DecompressionCraniectomy | Decompression craniectomy | Reflects if a Decompression craniectomy was performed as Key emergency interventions. | |
| Registry.DecompressionCraniectomyDate | Date of decompression craniectomy | Reflects the Date if a Decompression craniectomy was performed as Key emergency interventions. | |
| Registry.DecompressionCraniectomyDateTime | Date and time of Decompression Craniectomy | Calculated from Registry.DecompressionCraniectomyDate and Registry.DecompressionCraniectomyTime | |
| Registry.DecompressionCraniectomyTime | Time of decompression craniectomy | Reflects the Time if a Decompression craniectomy was performed as Key emergency interventions. | |
| Registry.DischargeDate | Date of discharge | Discharge Date. | |
| Registry.DischargeDateTime | Discharge date and time | Calculated from Registry.DischargeDate and Registry.DischargeTime | |
| Registry.DischargeDestination | Discharge destination | 8 == Discharged to home and self-care with some reservations 1 == Discharged to other hospital 3 == Discharged to nursing home 2 == Discharged to rehabilitation 5 == Discharged to home with carer 6 == Discharged to home and self-care but judged unfit for work 7 == Discharged to home and self-care without reservations 88 == Unknown |
Documents destination upon hospital discharge |
| Registry.DischargeTime | Time of discharge | Time of discharge. | |
| Registry.EDArrDBP | Diastolic | Reflects Clinical Exam (on arrival at Study Center) --> BP (mmHg) --> Diastolic | |
| Registry.EDArrivalBloodPressureUnknown | BP (unknown) | 88 == Unknown | Reflects Clinical Exam (on arrival at Study Center) --> BP (mmHg) --> Unknown |
| Registry.EDArrivalOxygenSatUnknown | Oxygen saturation (unknown) | 88 == Unknown | Reflects Clinical Exam (on arrival at Study Center) --> Oxygen saturation --> Unknown |
| Registry.EDArrivedIntubated | Arrived intubated | Reflects procedures in study center (< 24 hours) --> Intubation N/A (arrived intubated) | |
| Registry.EDArrPupilLftEyeMeasr | Left eye | Reflects Clinical Exam (on arrival at Study Center) --> Left eye Size | |
| Registry.EDArrPupilLftEyeMeasrUnkUnt | Left eye (unknown) | 66 == Untestable 88 == Unknown |
Reflects Clinical Exam (on arrival at Study Center) --> Left eye untestable or measurement unknown |
| Registry.EDArrPupilRtEyeMeasr | Right eye | Reflects Clinical Exam (on arrival at Study Center) --> Right eye size | |
| Registry.EDArrPupilRtEyeMeasrUnkUnt | Right eye (unknown) | 66 == Untestable 88 == Unknown |
Reflects Clinical Exam (on arrival at Study Center) --> Right eye untestable of measurement unknown |
| Registry.EDArrSBP | Systolic | Reflects Clinical Exam (on arrival at Study Center) --> BP (mmHg) --> Systolic | |
| Registry.EDArrSpO2 | Oxygen saturation | Reflects Clinical Exam (on arrival at Study Center) --> Oxygen saturation (in %) | |
| Registry.EDCTBrain | CT Brain | 0 == No 1 == Yes 88 == Unknown |
Reflects if a CT brain was performed. |
| Registry.EDIntubation | Intubation | 0 == No 1 == Yes 88 == Unknown |
Reflects Procedures in study center (< 24 hours) --> Intubation performed or not |
| Registry.EnrollDate | Date of Enrolment | Records the date of enrollment to the Registry Data Collection. | |
| Registry.ExternaAIS | External (skin) AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the External skin In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.ExternaISS | Externa ISS | ISS score for the External skin | |
| Registry.ExternalFixationLimb | External fixation limb | Reflects if an External fixation of the limb was performed as Key emergency interventions. | |
| Registry.ExternalFixationLimbDate | Date of external fixation limb | Reflects the Date if an External fixation of the limb was performed as Key emergency interventions. | |
| Registry.ExternalFixationLimbDateTime | Date and time of External Limb Fixation | Calculated from Registry.ExternalFixationLimbDate and Registry.ExternalFixationLimbTime | |
| Registry.ExternalFixationLimbTime | Time of external fixation limb | Reflects the Time if an External fixation of the limb was performed as Key emergency interventions. | |
| Registry.ExternalVentricularCSFDrainage | External ventricular CSF drainage | Reflects if External ventricular CSF drainage was performed as Key emergency interventions. | |
| Registry.ExternalVentricularCSFDrainageDate | Date of external ventricular CSF drainage | Reflects the Date if External ventricular CSF drainage was performed as Key emergency interventions. | |
| Registry.ExternalVentricularCSFDrainageDateTime | Date and time of External Ventricular CSF Drainage | Calculated from Registry.ExternalVentricularCSFDrainageDate and Registry.ExternalVentricularCSFDrainageTime | |
| Registry.ExternalVentricularCSFDrainageTime | Time of external ventricular CSF drainage | Reflects the Time if External ventricular CSF drainage was performed as Key emergency interventions. | |
| Registry.ExternaRegionAIS | Externa Region AIS | AIS score for the External (skin) region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| Registry.ExtraperitonealPelvicPacking | Extraperitoneal pelvic packing | Reflects if a Extraperitoneal pelvic packing was performed as Key emergency intervention. | |
| Registry.ExtraperitonealPelvicPackingDate | Date of extraperitoneal pelvic packing | Reflects the Date if Extraperitoneal pelvic packing was performed as Key emergency intervention. | |
| Registry.ExtraperitonealPelvicPackingDateTime | Date and time of Extraperitoneal Pelvic Packing | Calculated from Registry.ExtraperitonealPelvicPackingDate and Registry.ExtraperitonealPelvicPackingTime | |
| Registry.ExtraperitonealPelvicPackingTime | Time of extraperitoneal pelvic packing | Reflects the Time if Extraperitoneal pelvic packing was performed as Key emergency intervention. | |
| Registry.ExtremitiesRegionAIS | Extremities Region AIS | AIS score for Extremities Region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| Registry.FaceAIS | Face (incl.maxillofacial) AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for Face (incl.maxillofacial) In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.FaceISS | Face ISS | ISS score for Face (incl.maxillofacial) | |
| Registry.FaceRegionAIS | Face Region AIS | AIS score for Face (incl.maxillofacial) region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| Registry.GcsEDArrEyes | Eye opening score | 4 == 4 - Spontaneously 3 == 3 - To speech 2 == 2 - To pain 1 == 1 - None S == Untestable (swollen) O == Untestable (Other) UN == Unknown |
Reflects Clinical Exam (on arrival at Study Center) --> Eye opening |
| Registry.GcsEDArrMotor | Motor score | 1 == 1- None 2 == 2 - Abnormal extension 3 == 3 - Abnormal flexion 4 == 4 - Normal flexion/withdrawal 5 == 5 - Localizes to pain 6 == 6 - Obeys command P == Untestable (Deep sedation/paralyzed) UN == Unknown O == Untestable (Other) |
Reflects Clinical Exam (on arrival at Study Center) --> Glasgow Coma Scale (GCS) --> Motor score |
| Registry.GcsEDArrPupils | Pupils | 1 == One reacting 2 == Both reacting 0 == None reacting |
Reflects Clinical Exam (on arrival at Study Center) --> Pupils reactivity |
| Registry.GcsEDArrScore | GCS score | Reflects Clinical Exam (on arrival at Study Center) --> Glasgow Coma Scale (GCS) --> Total Score. Scored by investigators in case component scores not available, but GCS sum score available | |
| Registry.GcsEDArrVerbal | Verbal score | 1 == 1- None 2 == 2 - Incomprehensible sound 3 == 3 - Inappropriate words 4 == 4 - Confused 5 == 5 - Oriented T == Untestable (Tracheotomy/endotracheal tube) O == Untestable (Other) UN == Unknown |
Reflects Clinical Exam (on arrival at Study Center) --> Glasgow Coma Scale (GCS) --> Verbal score |
| Registry.HeadBrainCervicalRegionAIS | Head Brain Cervical Region AIS | AIS score for the Head and Neck (Brain injury and Cervical Spine) region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. | |
| Registry.HeadNeckAIS | Head and Neck AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Head Neck region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.HeadNeckISS | Head Neck ISS | ISS score for the Head Neck region. | |
| Registry.HospitalAdm | Admission to Hospital | 0 == No 1 == Yes 88 == Unknown |
Reflects if subject was admitted to hospital or not. |
| Registry.ICPDeviceInsertion | Intracranial pressure (ICP) device insertion | Reflects if a Intracranial pressure (ICP) device was inserted as Key emergency interventions. | |
| Registry.ICPDeviceInsertionDate | Date of Intracranial pressure (ICP) device insertion | Reflects the Date if a Intracranial pressure (ICP) device was inserted as Key emergency interventions. | |
| Registry.ICPDeviceInsertionDateTime | Date and time of ICP device insertion | Calculated from Registry.ICPDeviceInsertionDate and Registry.ICPDeviceInsertionTime | |
| Registry.ICPDeviceInsertionTime | Time of Intracranial pressure (ICP) device insertion | Reflects the Time if a Intracranial pressure (ICP) device was inserted as Key emergency interventions. | |
| Registry.ICUAdm | Admission to ICU | 0 == No 1 == Yes 88 == Unknown |
Reflects if the subject was admitted to the ICU. |
| Registry.ICUAdmDate | Date of admission to ICU | Reflects the Date if the subject was admitted to the ICU. | |
| Registry.ICUAdmDateTime | Date and time of admission to the ICU | Calculated from Registry.ICUAdmDate and Registry.ICUAdmTime | |
| Registry.ICUAdmTime | Time of admission to ICU | Reflects the Time if the subject was admitted to the ICU. | |
| Registry.ICUAdmTimeSinceInj | Time between injury and admission to the ICU | Reflects the Time Since injury if the subject was admitted to the ICU. | |
| Registry.ICUDischDate | Date of discharge from ICU | Reflects ICU discharge date (if the subject had been admitted to ICU) | |
| Registry.ICUDischDateTime | Date and time of dischagre from the ICU | Calculated from Registry.ICUDischDate and Registry.ICUDischTime | |
| Registry.ICUDischTime | Time of discharge from ICU | Reflects ICU discharge time (if the subject had been admitted to ICU) | |
| Registry.ICUDishcTimeSinceInj | Time between injury and discharge from the ICU | Reflects Time since injury for discharge from ICU (if the subject had been admitted to ICU) | |
| Registry.InjMech | Mechanism of injury | 1 == RTA Pedestrian 2 == RTA Cyclist 3 == RTA Motorcyclist 4 == RTA Driver 5 == RTA Other vehicle occupant 6 == Fall standing height 7 == Fall from height 8 == Assault fists 9 == Assault blunt instrument 10 == Assault knife 11 == Assault firearm 12 == Self Harm 99 == Other violence 13 == Sport/recreational activity 88 == Unknown 14 == Other, please specify |
Reflects the mechanism of injury |
| Registry.InjPlace | Location of incident | 1 == Street/traffic 2 == Home 6 == Public place 3 == Work 4 == Sports field/hall 99 == Other 88 == Unknown |
Reflects the place where the TBI injury occurred. |
| Registry.InjType | Type of injury | 1 == Blunt/closed 4 == Penetrating 2 == Blast 3 == Crush 88 == Unknown |
Details of Injury are captured in 3 different variables: Type of Injury, Place of Injury and Mechanism of injury. This reflects the type of injury. |
| Registry.InterventionalRadiology | Interventional radiology | Reflects if Interventional radiology was performed as Key emergency interventions. | |
| Registry.InterventionalRadiologyDate | Date of interventional radiology | Reflects the Date if Interventional radiology was performed as Key emergency interventions. | |
| Registry.InterventionalRadiologyDateTime | Date and time of Interventional Radiology | Calculated from Registry.InterventionalRadiologyDate and Registry.InterventionalRadiologyTime | |
| Registry.InterventionalRadiologyTime | Time of interventional radiology | Reflects the Time if Interventional radiology was performed as Key emergency interventions. | |
| Registry.InterventionsOther | Other intervention | Reflects if another Intervention than the predefined list was performed as Key emergency interventions. | |
| Registry.InterventionsOtherDate | Date of other intervention | Reflects the Date if another Intervention than the predefined list was performed as Key emergency interventions. | |
| Registry.InterventionsOtherDateTime | Date and time of Other interventions | Calculated from Registry.InterventionsOtherDate and Registry.InterventionsOtherTime | |
| Registry.InterventionsOtherTime | Time of other intervention | Reflects the Time if another Intervention than the predefined list was performed as Key emergency interventions. | |
| Registry.KeyEmergencyInterventions | Key emergency interventions | 0 == No 1 == Yes 88 == Unknown |
Reflects if any Key emergency intervention was performed. |
| Registry.LowerExtremitiesAIS | Lower extremities AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Lower extremities. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.LowerExtremitiesISS | Lower Extremities ISS | ISS score for the Lower extremities. | |
| Registry.LumbarSpineAIS | Lumbar spine AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Lumbar Spine region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.LumbarSpineISS | Lumbar Spine ISS | ISS score for the Lumbar Spine region. | |
| Registry.MonthInjury | Month of injury | Month of Injury (January - December) | |
| Registry.PatientType | Stratum | Stratum coded from ICUAdm, ERAdm, HospitalAdm | |
| Registry.PelvicGirdleAIS | Pelvic girdle AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Pelvic Girdle region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.PelvicGirdleISS | Pelvic Girdle ISS | ISS score for the Pelvic Girdle region. | |
| Registry.PlateletAggregInhibitors | Platelet aggregation inhibitors | 0 == No 1 == Yes 88 == Unknown |
Reflects if the subject is taking Platelet aggregation inhibitors |
| Registry.PreInjuryASAPSClassification | Pre-injury ASA-PS Classification system | 1 == A normal healthy patient 2 == A patient with mild systemic disease 3 == A patient with severe systemic disease 4 == A patient with severe systemic disease that is a constant threat to life 88 == Unknown |
Reflects the Pre-injury ASA-PS Classification system. This is a common classification system used in anesthesia; denotes overall health. |
| Registry.PresCTBrain | Procedures: CT Brain | 0 == No 1 == Yes 88 == Unknown |
Only applicable in case of secondary referral. Reflects CT brain procedure performed at first hospital (not study hospital). |
| Registry.PresEmergencyCare | Emergency care: Intubation | 0 == No professional care 1 == Ambulance service (no physician) 2 == Helicopter service 3 == Medical mobile team 98 == N/A (for example injury in hospital) |
Reflects if and by whom emergency medical care was given at the scene of accident (highest level of assistance) |
| Registry.PresEmergencyCareIntubation | Emergency care: Mechanical ventilation | 0 == No 1 == Yes 88 == Unknown |
Reflects if intubation was performed on scene. |
| Registry.PresEmergencyCareVentilation | Emergency care: Referral | 0 == No 1 == Yes 88 == Unknown |
Reflects if Mechanical Ventilation was done on scene. |
| Registry.PresERExtracranialSurg | Procedures: Emergency extracranial surgery | 0 == No 1 == Yes 88 == Unknown |
Only applicable in case of secondary referral. Reflects Emergency Extracranial surgery procedure performed at first hospital (not study hospital). |
| Registry.PresERIntracranialSurg | Procedures: Emergency intracranial surgery | 0 == No 1 == Yes 88 == Unknown |
Only applicable in case of secondary referral. Reflects the Emergency intracranial surgery Procedure performed at first hospital (not study hospital). |
| Registry.PresFHospDate | Date of arrival to first hospital | Date of arrival first hospital. First hospital is defined as the initial hospital to which the patient was brought before being transferred to Study hospital. Consequently, only applicable in case of secondary transferal. However, in some sites data for first hospital may have been entered also when the patient was brought directly to the study hospital. | |
| Registry.PresFHospDateTime | Date and time of arrival at first hospital | Calculated from Registry.PresFHospDate and Registry.PresFHospTime | |
| Registry.PresFHospTime | Time of arrival to first hospital | Time of arrival first hospital. First hospital is defined as the initial hospital to which the patient was brought before being transferred to Study hospital. Consequently, only applicable in case of secondary transferal. However, in some sites data for first hospital may have been entered also when the patient was brought directly to the study hospital. | |
| Registry.PresFHospTimeSinceInj | Time between injury and presentation at first hospital | Time since injury till arrival at first hospital. First hospital is defined as the initial hospital to which the patient was brought before being transferred to Study hospital. Consequently, only applicable in case of secondary transferal. However, in some sites data for first hospital may have been entered also when the patient was brought directly to the study hospital. | |
| Registry.PresIntubation | Procedures: Intubation | 0 == No 1 == Yes 88 == Unknown |
Only applicable in case of secondary referral. Reflects procedure of intubation performed at first hospital (not study hospital). |
| Registry.PresSTHospDate | Date of arrival to study center | Date of arrival at study center. | |
| Registry.PresSTHospDateTime | Date and time of arrival at study hospital | Calculated from Registry.PresSTHospDate and Registry.PresSTHospTime | |
| Registry.PresSTHospTime | Time of arrival to study center | Time of arrival at study center. | |
| Registry.PresSTHospTimeSinceInj | Time between injury and presentation at study hospital | Time since injury till arrival at study center. | |
| Registry.PresTBIRef | Referral | 1 == Primary referral 2 == Secondary referral from other hospital |
Reflects if the subject was transported from the scene of accident immediately to the study hospital (primary referral) or if secondary referral occurred from a first hospital to the Study hospital. |
| Registry.RegistryCompleteStatus | Registry form completion status | NOSTART == Not Started PRO == In Process COM == Complete NOT == Not Complete INCPT == Incompletable |
Completion Status of the Registry data. |
| Registry.Sex | Sex | M == Male F == Female |
The difference between male and female, based upon the interactions between genes and between the genotype and the environment. Gender of Subject. |
| Registry.SiteCode | Site | Anonymized site code. | |
| Registry.StatusOnDischarge | Status on discharge | 0 == Dead 1 == Alive |
Status on discharge - assessed by the investigator. |
| Registry.ThoracicSpineAIS | Thoracic spine AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Thoracic spine Region In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.ThoracicSpineISS | Thoracic Spine ISS | ISS score for the Thoracic spine Region | |
| Registry.ThoraxChestAIS | Thorax/chest AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Thorax Chest region. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.ThoraxChestISS | Thorax Chest ISS | ISS score for the Thorax Chest region. | |
| Registry.TimeInj | Time of injury | Time of injury. | |
| Registry.TotalISS | Total ISS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
Represents the quadratic sum of the three AIS regions with the highest score. |
| Registry.UpperExtremitiesAIS | Upper extremities AIS | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 0 == 0 |
AIS score for the Upper extremities. In the original AIS classification of injury severity, the grading is from 1 (minor) to 6 (unsurvivable). We added a score of 0 to designate absence of injuries. |
| Registry.UpperExtremitiesISS | Upper Extremities ISS | ISS score for the Upper extremities. | |
| Registry.WardAdm | Admission to Ward | 0 == No 1 == Yes 88 == Unknown |
The intent here was to record direct admission to the ward versus direct admission to the ICU (Registry.ICUAdm). However, the possibility that this variable was also checked for patients discharged from the ICU to the Ward cannot be excluded. |
| Registry.WardAdmDate | Date of admission to ward | Ward admission date (if subject had been admitted to ward) | |
| Registry.WardAdmDateTime | Date and time of admission to the Ward | Calculated from Registry.WardAdmDate and Registry.WardAdmTime | |
| Registry.WardAdmTime | Time of admission to ward | Ward admission time (if subject had been admitted to ward) | |
| Registry.WardAdmTimeSinceInj | Time between injury and admission to the Ward | Time since injury till Ward admission (if subject had been admitted to ward) | |
| Subject.Age | Age | Age in years | |
| Subject.AnytimeGOSECompleteStatus | Anytime GOSE completion status | INCPT == Not performed INCNOSHOW == Incompletable - No Show COM == Complete NOT == Queries Outstanding PRO == In Process NOSTART == Not Started |
Reflects the completion status for the "Anytime GOSE". For patients with missing GOSE (no GOSE obtained at all), we developed an “anytime GOSE”. This is intended to be completed if no other GOSE has been obtained at any of the predefined timepoint and should reflect a general GOSE Score obtained through discussion with family and clinicians caring for the patient or personal knowledge of the study nurse/investigator. |
| Subject.AnytimeGOSEDate | Anytime GOSE date | Reflects the Date for the "Anytime GOSE". For patients with missing GOSE (no GOSE obtained at all), we developed an “anytime GOSE”. This is intended to be completed if no other GOSE has been obtained at any of the predefined timepoint and should reflect a general GOSE Score obtained through discussion with family and clinicians caring for the patient or personal knowledge of the study nurse/investigator. | |
| Subject.AnytimeGOSEMethod | Anytime GOSE method | 3 == Patient Chart 2 == Structured 1 == Postal 99 == Other 4 == Personal knowledge |
Reflects the method for obtaining the "Anytime GOSE". For patients with missing GOSE (no GOSE obtained at all), we developed an “anytime GOSE”. This is intended to be completed if no other GOSE has been obtained at any of the predefined timepoint and should reflect a general GOSE Score obtained through discussion with family and clinicians caring for the patient or personal knowledge of the study nurse/investigator. |
| Subject.AnytimeGOSEPtAlive | Anytime GOSE patient status | 88 == Unknown 0 == No 1 == Yes |
Reflects the patient status for the "Anytime GOSE". For patients with missing GOSE (no GOSE obtained at all), we developed an “anytime GOSE”. This is intended to be completed if no other GOSE has been obtained at any of the predefined timepoint and should reflect a general GOSE Score obtained through discussion with family and clinicians caring for the patient or personal knowledge of the study nurse/investigator. |
| Subject.AnytimeGOSEReasonMissing | Anytime GOSE reason for missing | Reflects reason for missing the "Anytime GOSE". For patients with missing GOSE (no GOSE obtained at all), we developed an “anytime GOSE”. This is intended to be completed if no other GOSE has been obtained at any of the predefined timepoint and should reflect a general GOSE Score obtained through discussion with family and clinicians caring for the patient or personal knowledge of the study nurse/investigator. | |
| Subject.AnytimeGOSEScore | Anytime GOSE score | 8 == 8-Upper Good Recovery (Upper GR) 7 == 7-Lower Good Recovery (Lower GR) 6 == 6-Upper Moderate Disability (Upper MD) 5 == 5-Lower Moderate Disability (Lower MD) 4 == 4-Upper Severe Disability (Upper SD) 1 == 1-Dead 2 == 2-Vegetative State (VS) 3 == 3-Lower Severe Disability (Lower SD) |
Reflects the score for the "Anytime GOSE". For patients with missing GOSE (no GOSE obtained at all), we developed an “anytime GOSE”. This is intended to be completed if no other GOSE has been obtained at any of the predefined timepoint and should reflect a general GOSE Score obtained through discussion with family and clinicians caring for the patient or personal knowledge of the study nurse/investigator. |
| Subject.ApptPtShowOutcomes12Mo | 12 month outcomes – Did the patient show up? | Reflects of the patient show up for the 12 months Follow up appointment. | |
| Subject.ApptPtShowOutcomes24mo | 24 month outcomes – Did the patient show up? | 1 == Yes 0 == No |
Reflects of the patient show up for the 24 months Follow up appointment. |
| Subject.ApptPtShowOutcomes2Wk | 2 weeks outcomes – Did the patient show up? | 1 == Yes 0 == No 77 == N/A |
Reflects of the patient show up for the 2 weeks Follow up appointment. |
| Subject.ApptPtShowOutcomes3Mo | 3 month outcomes – Did the patient show up? | Reflects of the patient show up for the 3 months Follow up appointment. | |
| Subject.ApptPtShowOutcomes6Mo | 6 month outcomes – Did the patient show up? | Reflects of the patient show up for the 6 months Follow up appointment. | |
| Subject.ApptQuestComplOutcomes12Mo | Outcome questionnaires completed for the 12 months FU or not | 1 == Yes 0 == No 77 == N/A |
Reflects if the outcome questionnaires were completed for the 12 months Follow up appointment. |
| Subject.ApptQuestComplOutcomes24Mo | Outcome questionnaires completed for the 24 months FU or not | 1 == Yes 0 == No 77 == N/A |
Reflects if the outcome questionnaires were completed for the 24 months Follow up appointment. |
| Subject.ApptQuestComplOutcomes2Wk | Outcome questionnaires completed for the 2 wk FU or not | 1 == Yes 0 == No 77 == N/A |
Reflects if the outcome questionnaires were completed for the 2 week Follow up appointment. |
| Subject.ApptQuestComplOutcomes3Mo | Outcome questionnaires completed for the 3 months FU or not | 1 == Yes 0 == No 77 == N/A |
Reflects if the outcome questionnaires were completed for the 3 months Follow up appointment. |
| Subject.ApptQuestComplOutcomes6Mo | Outcome questionnaires completed for the 6 months FU or not | 1 == Yes 0 == No 77 == N/A |
Reflects if the outcome questionnaires were completed for the 6 months Follow up appointment. |
| Subject.ApptQuestLangUsed12Mo | Language used for the 12 months FU (if not local language) | ENG == English GER == German FRE == French DUT == Dutch DAN == Danish FIN == Finnish HUN == Hungarian ITA == Italian LIT == Lithuanian NOR == Norwegian ROM == Romanian SER == Serbian SLO == Slovakian SPA == Spanish RUS == Russian HEB == Hebrew ARA == Arabic SWE == Swedish |
Reflects the language used for the 12 months Follow up appointment (only applicable if the questionnaires were administered in another language than the local language). |
| Subject.ApptQuestLangUsed24Mo | Language used for the 24 months FU (if not local language) | ENG == English GER == German FRE == French DUT == Dutch DAN == Danish FIN == Finnish HUN == Hungarian ITA == Italian LIT == Lithuanian NOR == Norwegian ROM == Romanian SER == Serbian SLO == Slovakian SPA == Spanish RUS == Russian HEB == Hebrew ARA == Arabic SWE == Swedish |
Reflects the language used for the 24 months Follow up appointment (only applicable if the questionnaires were administered in another language than the local language). |
| Subject.ApptQuestLangUsed2Wk | Language used for the 2 wk FU (if not local language) | ENG == English DUT == Dutch FRE == French DAN == Danish FIN == Finnish GER == German HUN == Hungarian ITA == Italian LIT == Lithuanian NOR == Norwegian ROM == Romanian SER == Serbian SLO == Slovakian SPA == Spanish RUS == Russian HEB == Hebrew ARA == Arabic SWE == Swedish |
Reflects the language used for the 2 weeks Follow up appointment (only applicable if the questionnaires were administered in another language than the local language). |
| Subject.ApptQuestLangUsed3Mo | Language used for the 3 months FU (if not local language) | ENG == English GER == German FRE == French DUT == Dutch DAN == Danish FIN == Finnish HUN == Hungarian ITA == Italian LIT == Lithuanian NOR == Norwegian ROM == Romanian SER == Serbian SLO == Slovakian SPA == Spanish RUS == Russian HEB == Hebrew ARA == Arabic SWE == Swedish |
Reflects the language used for the 3 months Follow up appointment (only applicable if the questionnaires were administered in another language than the local language). |
| Subject.ApptQuestLangUsed6Mo | Language used for the 6 months FU (if not local language) | ENG == English GER == German FRE == French DUT == Dutch DAN == Danish FIN == Finnish HUN == Hungarian ITA == Italian LIT == Lithuanian NOR == Norwegian ROM == Romanian SER == Serbian SLO == Slovakian SPA == Spanish RUS == Russian HEB == Hebrew ARA == Arabic SWE == Swedish |
Reflects the language used for the 6 months Follow up appointment (only applicable if the questionnaires were administered in another language than the local language). |
| Subject.ApptQuestLocLang12Mo | Local language used for the 12 months FU or not | 1 == Yes 0 == No 99 == Unknown |
Reflects if the local language was used for the 12 months Follow up appointment. |
| Subject.ApptQuestLocLang24Mo | Local language used for the 24 months FU or not | 1 == Yes 0 == No 99 == Unknown |
Reflects if the local language was used for the 24 months Follow up appointment. |
| Subject.ApptQuestLocLang2Wk | Local language used for the 2 wk FU or not | 1 == Yes 0 == No 99 == Unknown |
Reflects if the local language was used for the 2 weeks Follow up appointment. |
| Subject.ApptQuestLocLang3Mo | Local language used for the 3 months FU or not | 1 == Yes 0 == No 99 == Unknown |
Reflects if the local language was used for the 3 months Follow up appointment. |
| Subject.ApptQuestLocLang6Mo | Local language used for the 6 months FU or not | 1 == Yes 0 == No 99 == Unknown |
Reflects if the local language was used for the 6 months Follow up appointment. |
| Subject.ApptScheduledDateOutcomes12mo | 12 month outcomes – Scheduled date | Milestone Window: 12month outcomes must be completed 10 - 14 months from DOI. | |
| Subject.ApptScheduledDateOutcomes24mo | 24 month outcomes – Scheduled date | Milestone Window: 24month outcomes must be completed 22 - 28 months from DOI | |
| Subject.ApptScheduledDateOutcomes2wk | 2 weeks outcomes – Scheduled date | Milestone window: 2week outcomes must be completed 10 - 27 days from DOI (Date Of Injury) | |
| Subject.ApptScheduledDateOutcomes3mo | 3 month outcomes – Scheduled date | Milestone Window: 3month outcomes must be completed 11 - 18 weeks from DOI (Date of Injury). | |
| Subject.ApptScheduledDateOutcomes6mo | 6 month outcomes – Scheduled date | Milestone Window: 6month outcomes must be completed 5 - 8 months from DOI (Date of Injury). | |
| Subject.ApptScheduledTimeOutcomes12mo | 12 month outcomes – Scheduled time | Scheduled time for the 12 months outcome. | |
| Subject.ApptScheduledTimeOutcomes24mo | 24 month outcomes – Scheduled time | Scheduled time for the 24 months outcome. | |
| Subject.ApptScheduledTimeOutcomes2wk | 2 weeks outcomes – Scheduled time | Scheduled time for the 2 weeks outcome. | |
| Subject.ApptScheduledTimeOutcomes3mo | 3 month outcomes – Scheduled time | Scheduled time for the 3 months outcome. | |
| Subject.ApptScheduledTimeOutcomes6mo | 6 month outcomes – Scheduled time | Scheduled time for the 6 months outcome. | |
| Subject.ApptTargetDateOutcomes12Mo | 12 month outcomes – Best appointment date | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.ApptTargetDateOutcomes24mo | 24 month outcomes – Best appointment date | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.ApptTargetDateOutcomes2Wk | 2 weeks outcomes – Best appointment date | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.ApptTargetDateOutcomes3Mo | 3 month outcomes – Best appointment date | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.ApptTargetDateOutcomes6Mo | 6 month outcomes – Best appointment date | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.AssociatedStudy | Associated study | 1 == RESCUE-ASDH 2 == TAHITI-B 3 == PROLABI |
Documents if a subject was enrolled in an associated CENTER-TBI study: RESCUE ASDH/Tahiti/Prolabi |
| Subject.Comments | Any comments about the patients (No PHI) | Free text box allowing to enter any comments about the patient. | |
| Subject.ConsentWithdrawn | Is consent withdrawn? | Reflects if Informed Consent was withdrawn | |
| Subject.ConsentWithdrawnDate | Date consent withdrawn | Reflects the date of withdrawal if Informed Consent was withdrawn | |
| Subject.ConsentWithdrawnReason | Reason for withdrawing consent | WHY Question: documents the reason for withdrawing subject | |
| Subject.ConsentWithdrawnTime | Time consent withdrawn | Reflects the time of withdrawal if Informed Consent was withdrawn | |
| Subject.ConsentWithdrawnTimeSinceInj | Time since injury until withdrawal of consent | Reflects time since injury till withdrawal of consent (if applicable). | |
| Subject.DateInj | Date of Injury | Date of Injury. Anonymised and saved as 1970-01-01 for all patients. All other dates are converted relative to date of Injury. | |
| Subject.DateOfAdmission | Date of admission (ICU or Ward) | This variable denotes date of admission to hospital; Therefore not applicable to subjects in ER stratum. In principle the date of injury; date of enrollment and Date of Admission to ICU or Ward will match, but in some cases there can be a difference of 1 or 2 days. For example when a patient was injured late at night, it is possible that the consent was only obtained in the morning, hence the date of Study Enrollment will be 1 day later than the date of injury. Or in some hospitals a patient is kept for 24 hours in observation at the ER in a specific unit before being transferred to ICU or Ward. Hence the Date of Admission to ICU or Ward can be 1 or 2 days later. Or if there is no bed available on ICU or Ward for a patient being injured late at night, there can be a delay in admitting the patient. Also, in some countries, Enrollment Date > 24h was accepted according to local regulations and IRB. | |
| Subject.DateTimeInjReliable | Reliability of time of injury | 1 == Verified 2 == Estimated |
This variable documents if the time of injury is accurate, or is based on "best possible estimate", in case exact time of injury not known. |
| Subject.DayInjury | Day of injury (1-7) | Day of injury. (Sunday - Saturday) | |
| Subject.DeathCause | Principal cause of death | 1 == Head injury/initial injury 2 == Head injury/secondary intracranial damage 3 == Systemic trauma 4 == Medical complications 88 == Unknown 99 == Other |
Cause of death in or outside the hospital |
| Subject.DeathCauseOther | Other cause of death (please specify) | "Other" cause of death in or outside the hospital (than predefined list). | |
| Subject.DeathDate | Date of death | Date of death also recorded on hospital discharge and at followup: FollowUp.FUPrincipalDeathCause;Death may also have been recorded in the ER forms: Subject.DeathDate | |
| Subject.DeathERDeclaredBrainDeadFollowingNationalCriteria | Declared brain dead following national criteria | 0 == No 1 == Yes 88 == Unknown |
Reflects if patient was declared brain dead following national criteria. Only applicable if patient declared "dead" on the ER |
| Subject.DeathERDOA | Was the patient dead on arrival (DOA) at ER? | 0 == No 1 == Yes 88 == Unknown |
Reflects if patient is declared dead on the ER --> Dead on arrival (DOA). Only applicable if patient declared "dead" on the ER. |
| Subject.DeathERUnsuccResusForExtraCranInj | Unsuccessful resuscitation for extra cranial injuries | 0 == No 1 == Yes 88 == Unknown |
Reflects unsuccessful resuscitation for extra cranial injuries if patient is declared dead on the ER. Only applicable if patient declared "dead" on the ER |
| Subject.DeathERWithdrawalLifeSuppForSeverityOfTBI | Withdrawal of life-sustaining measures for severity of TBI | 0 == No 1 == Yes 88 == Unknown |
Reflects Withdrawal of lifesustaining measures for severity of TBI if patient is declared dead on the ER. Only applicable if patient declared "dead" on the ER |
| Subject.DeathTime | Time of death | Time of death | |
| Subject.DerivedImputed180DaysGOSE | Derived imputed 6 month GOSE | This variable contains a GOSE that has been imputed at exactly 180 days after injury. Imputation is based on the composite GOSE recorded at different timepoints 2 weeks to one year. The imputation of the GOSE uses a multi-state model. The model does not include any baseline covariates. Since the imputation uses GOSE information across time points, the imputed 6 month GOSE does not necessarily correspond to outcomes that are observed at 6 months. Apart from deaths, imputed values of the GOSE are subject to uncertainty, and this is reflected in the companion variables that give the probabilities that a given outcome is in each of the GOSE categories 1 to 8. (Subject.DerivedImputed180DaysGOSE_1_probability, Subject.DerivedImputed180DaysGOSE_2_3_probability, Subject.DerivedImputed180DaysGOSE_4_probability, Subject.DerivedImputed180DaysGOSE_5_probability, Subject.DerivedImputed180DaysGOSE_6_probability, Subject.DerivedImputed180DaysGOSE_7_probability, Subject.DerivedImputed180DaysGOSE_8_probability). The category with the highest probability is taken as the final imputed value. Deaths have been added to this variable where a date of death is recorded on or before 180 days. The GOSE is a character/ string variable (not numeric) with the following categories: “1”= Dead, “2_or_3”= VS / Lower Severe Disability, “4”= Upper Severe Disability, “5” = Lower Moderate Disability, “6” = Upper Moderate Disability, “7” = Lower Good Recovery, “8” =Upper Good Recovery. This variable should NOT be combined with outcomes.timepoint! | |
| Subject.DerivedImputed180DaysGOSE_1_probability | Derived imputed 6 month GOSE probablity - 1 | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_2_or_3_probability | Derived imputed 6 month GOSE probablity - 2 or 3 | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_4_probability | Derived imputed 6 month GOSE probablity - 4 | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_5_probability | Derived imputed 6 month GOSE probablity - 5 | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_6_probability | Derived imputed 6 month GOSE probablity - 6 | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_7_probability | Derived imputed 6 month GOSE probablity - 7 | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_8_probability | Derived imputed 6 month GOSE probablity - 8 | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed360DaysGOSE | Derived imputed 12 month GOSE | This variable contains a GOSE that has been imputed at exactly 360 days after injury. Imputation is based on the composite GOSE recorded at different timepoints 2 weeks to one year. The imputation of the GOSE uses a multi-state model. The model does not include any baseline covariates. Since the imputation uses GOSE information across time points, the imputed 12 month GOSE does not necessarily correspond to outcomes that are observed at 12 months. Apart from deaths, imputed values of the GOSE are subject to uncertainty, and this is reflected in the companion variables that give the probabilities that a given outcome is in each of the GOSE categories 1 to 8. (Subject.DerivedImputed360DaysGOSE_1_probability, Subject.DerivedImputed360DaysGOSE_2_3_probability, Subject.DerivedImputed360DaysGOSE_4_probability, Subject.DerivedImputed360DaysGOSE_5_probability, Subject.DerivedImputed360DaysGOSE_6_probability, Subject.DerivedImputed360DaysGOSE_7_probability, Subject.DerivedImputed360DaysGOSE_8_probability). The category with the highest probability is taken as the final imputed value. Deaths have been added to this variable where a date of death is recorded on or before 360 days. The GOSE is a character/ string variable (not numeric) with the following categories: “1”= Dead, “2_or_3”= VS / Lower Severe Disability, “4”= Upper Severe Disability, “5” = Lower Moderate Disability, “6” = Upper Moderate Disability, “7” = Lower Good Recovery, “8” =Upper Good Recovery. REMARK for OzENTER: this variable does not include imputed values in the OzENTER dataset This variable should NOT be combined with outcomes.timepoint! | |
| Subject.DerivedImputed360DaysGOSE_1_probability | Derived imputed 12 month GOSE probablity - 1 | See "Subject.DerivedImputed360DaysGOSE" | |
| Subject.DerivedImputed360DaysGOSE_2_or_3_probability | Derived imputed 12 month GOSE probablity - 2 or 3 | See "Subject.DerivedImputed360DaysGOSE" | |
| Subject.DerivedImputed360DaysGOSE_4_probability | Derived imputed 12 month GOSE probablity - 4 | See "Subject.DerivedImputed360DaysGOSE" | |
| Subject.DerivedImputed360DaysGOSE_5_probability | Derived imputed 12 month GOSE probablity - 5 | See "Subject.DerivedImputed360DaysGOSE" | |
| Subject.DerivedImputed360DaysGOSE_6_probability | Derived imputed 12 month GOSE probablity - 6 | See "Subject.DerivedImputed360DaysGOSE" | |
| Subject.DerivedImputed360DaysGOSE_7_probability | Derived imputed 12 month GOSE probablity - 7 | See "Subject.DerivedImputed360DaysGOSE" | |
| Subject.DerivedImputed360DaysGOSE_8_probability | Derived imputed 12 month GOSE probablity - 8 | See "Subject.DerivedImputed360DaysGOSE" | |
| Subject.DerivedImputed90DaysGOSE | Derived imputed 3 month GOSE | This variable contains a GOSE that has been imputed at exactly 90 days after injury. Imputation is based on the composite GOSE recorded at different timepoints 2 weeks to one year. The imputation of the GOSE uses a multi-state model. The model does not include any baseline covariates. Since the imputation uses GOSE information across time points, the imputed 3 month GOSE does not necessarily correspond to outcomes that are observed at 3 months. Apart from deaths, imputed values of the GOSE are subject to uncertainty, and this is reflected in the companion variables that give the probabilities that a given outcome is in each of the GOSE categories 1 to 8. (Subject.DerivedImputed90DaysGOSE_1_probability, Subject.DerivedImputed90DaysGOSE_2_3_probability, Subject.DerivedImputed90DaysGOSE_4_probability, Subject.DerivedImputed90DaysGOSE_5_probability, Subject.DerivedImputed90DaysGOSE_6_probability, Subject.DerivedImputed90DaysGOSE_7_probability, Subject.DerivedImputed90DaysGOSE_8_probability). The category with the highest probability is taken as the final imputed value. Deaths have been added to this variable where a date of death is recorded on or before 90 days. The GOSE is a character/ string variable (not numeric) with the following categories: “1”= Dead, “2_or_3”= VS / Lower Severe Disability, “4”= Upper Severe Disability, “5” = Lower Moderate Disability, “6” = Upper Moderate Disability, “7” = Lower Good Recovery, “8” =Upper Good Recovery. This variable should NOT be combined with outcomes.timepoint! | |
| Subject.DerivedImputed90DaysGOSE_1_probability | Derived imputed 3 month GOSE probablity - 1 | See "Subject.DerivedImputed90DaysGOSE" | |
| Subject.DerivedImputed90DaysGOSE_2_or_3_probability | Derived imputed 3 month GOSE probablity - 2 or 3 | See "Subject.DerivedImputed90DaysGOSE" | |
| Subject.DerivedImputed90DaysGOSE_4_probability | Derived imputed 3 month GOSE probablity - 4 | See "Subject.DerivedImputed90DaysGOSE" | |
| Subject.DerivedImputed90DaysGOSE_5_probability | Derived imputed 3 month GOSE probablity - 5 | See "Subject.DerivedImputed90DaysGOSE" | |
| Subject.DerivedImputed90DaysGOSE_6_probability | Derived imputed 3 month GOSE probablity - 6 | See "Subject.DerivedImputed90DaysGOSE" | |
| Subject.DerivedImputed90DaysGOSE_7_probability | Derived imputed 3 month GOSE probablity - 7 | See "Subject.DerivedImputed90DaysGOSE" | |
| Subject.DerivedImputed90DaysGOSE_8_probability | Derived imputed 3 month GOSE probablity - 8 | See "Subject.DerivedImputed90DaysGOSE" | |
| Subject.DNRDateTime | Date and time of DNR (Do Not Resucitate) | Reflects date and time of DNR (do not resuscitate) if DNR is the reason for end of study participation. | |
| Subject.EduLvlEUROFather | Highest level of education completed by father | 0 == None, not currently in school 1 == Currently in diploma or degree-oriented program 2 == Primary school 3 == Secondary school / High school 4 == Post-high school training (e.g. trade/technical certificate) 5 == College / University (diploma or degree) 88 == Unknown |
Father Highest level of education completed. Only if patient age <18 |
| Subject.EduLvlEUROMother | Highest level of education completed by mother | Mother Highest level of education completed. Only if patient age <18 | |
| Subject.EduLvlUSATyp | Highest level of education completed | 88 == Unknown 5 == College / University (diploma or degree) 4 == Post-high school training (e.g. trade/technical certificate) 3 == Secondary school / High school 2 == Primary school 1 == Currently in diploma or degree-oriented program 0 == None, not currently in school |
Highest level of education of patient. |
| Subject.EduYrCt | Number of years completed in education | Number of years of education completed. | |
| Subject.EmplmtStatus | Employment status before injury | 2 == Working (20-34 hours per week) 10 == Homemaker, keeping house 8 == Retired 9 == Student / schoolgoing 1 == Working (35 hours or more per week) 3 == Working (less than 20 hours per week) 4 == In working force, but currently on sick leave 5 == Special employment / sheltered employment 6 == Looking for work, unemployed 7 == Unable to work 88 == Unknown |
Employment status before injury. |
| Subject.EnrollDate | Date of enrollment | Date of Study Enrollment. In principle the date of injury and date of enrollment will match, but in some cases there can be a difference of 1 or 2 days. For example when a patient was injured late at night, it is possible that the consent was only obtained in the morning, hence the date of Study Enrollment will be 1 day later than the date of injury. | |
| Subject.EnrolledInOtherStudy | Is patient enrolled in other study? | 1 == Yes 0 == No 99 == Unknown |
Denotes if a subject was also enrolled in a concomitant study |
| Subject.EOSDate | Date of the end of study participation | Date for end of study participation | |
| Subject.EOSFormCompletion | Have all forms pertaining to the study been completed? | 0 == No 1 == Yes |
Reflects if all forms pertaining to the study have been completed |
| Subject.EOSFormNotCompleteOtherReasonTxt | Other reason why the study forms have not been completed (please specify) | Specifies the "other" reason for not completing all study forms. | |
| Subject.EOSFormNotCompletePrimReason | Primary reason why the study forms have not been completed | 1 == Consent withdrawn 2 == Violation study conduct 99 == Other |
Specifies the primary reason for not completing all study forms. |
| Subject.EOSFormNotCompleteViolateStudyConductTxt | Any violation because of which the study forms have not been completed (please specify) | Specifies the violation for not completing all study forms. | |
| Subject.EOSReason | Reason for the end of study participation | 1 == Completion of study 2 == Inability to obtain follow-up 3 == Withdrawal from study (by patient or representative) 4 == Adverse event(s) 5 == Decision for DNR*: 6 == Withdrawal of support 7 == Death 99 == Other |
Reason for end of study participation |
| Subject.EOSReasonOtherTxt | Other reason for the end of study participation (please specify) | "Other" reason for end of study participation than the predefined list. | |
| Subject.FUConsentForContStudyPart | Does patient consent to continue their participation in the study? | This variable documents written consent obtained from the patient for continued study participation | |
| Subject.FUConsentForContStudyPartDate | Date of written informed consent by patient | This variable documents the date of written consent obtained from the patient for continued study participation | |
| Subject.GOSE12monthEndpointDerived | GOSE 12 month endpoint (derived) | A twelve month GOSE endpoint that uses both observed ratings and imputed values. The variable is constructed as follows: (1) “Dead” is recorded for those with a date of death on or before 360 days post injury. (2) If there is an observed GOSE in the range 300 to 420 days (i.e. in the per protocol time window for twelve month assessment) then this rating is used. (3) If there is no per-protocol rating, then then an imputed 360 day GOSE is used where available. For a description of the imputation method see the variable ‘Subject.DerivedImputed360DaysGOSE’. The GOSE is a character/ string variable (not numeric) with the following categories: “1”= Dead, “3" = 2_or_3= VS / Lower Severe Disability, “4”= Upper Severe Disability, “5” = Lower Moderate Disability, “6” = Upper Moderate Disability, “7” = Lower Good Recovery, “8” =Upper Good Recovery. REMARK for OzENTER: this variable does not include imputed values in the OzENTER dataset. This variable should NOT be combined with outcomes.timepoint! | |
| Subject.GOSE3monthEndpointDerived | GOSE 3 month endpoint (derived) | A three month GOSE endpoint that uses both observed ratings and imputed values. The variable is constructed as follows: (1) “Dead” is recorded for those with a date of death on or before 90 days post injury. (2) If there is an observed GOSE in the range 76 to 125 days (i.e. in the per protocol time window for three month assessment) then this rating is used. (3) If there is no per-protocol rating, then then an imputed 90 day GOSE is used where available. For a description of the imputation method see the variable ‘Subject.DerivedImputed90NDaysGOSE’. The GOSE is a character/ string variable (not numeric) with the following categories: “1”= Dead, “3" = 2_or_3= VS / Lower Severe Disability, “4”= Upper Severe Disability, “5” = Lower Moderate Disability, “6” = Upper Moderate Disability, “7” = Lower Good Recovery, “8” =Upper Good Recovery. REMARK for OzENTER: this variable does not include imputed values in the OzENTER dataset. This variable should NOT be combined with outcomes.timepoint! | |
| Subject.GOSE6monthEndpointDerived | GOSE 6 month endpoint (derived) | A six month GOSE endpoint that uses both observed ratings and imputed values. The variable is constructed as follows: (1) “Dead” is recorded for those with a date of death on or before 180 days post injury. (2) If there is an observed GOSE in the range 150 to 240 days (i.e. in the per protocol time window for six month assessment) then this rating is used. (3) If there is no per-protocol rating, then then an imputed 180 day GOSE is used where available. For a description of the imputation method see the variable ‘Subject.DerivedImputed180DaysGOSE’. The GOSE is a character/ string variable (not numeric) with the following categories: “1”= Dead, “3" = 2_or_3= VS / Lower Severe Disability, “4”= Upper Severe Disability, “5” = Lower Moderate Disability, “6” = Upper Moderate Disability, “7” = Lower Good Recovery, “8” =Upper Good Recovery. REMARK for OzENTER: this variable does not include imputed values in the OzENTER dataset. REMARK for CINTER (India): As questionnaires were only interview based, no composite or derived variable is available for the Indian dataset, the variable “Outcomes.GOSEScore” should be used. REMARK: This variable should NOT be combined with outcomes.timepoint! | |
| Subject.GUPI | Global Unique Patient Identifier (GUPI) | The Global Unique Patient Identifier (GUPI) is a unique identifier that meets protection requirements in the EU and in Member States. This process takes patient specific characteristics (such as the first name, middle name, last name, place of birth, country of birth, date of birth, and gender) to generate a unique GUPI for each patient using an irreversible process, referred to as a “one way hash”. This process replicates an approach taken by the Federal Inter-agency Traumatic Brain Injury Research initiative (FITBIR; https://fitbir.nih.gov/) in the USA to create a similar construct, which they term a Global Unique Identifier (GUID; see https://fitbir.nih.gov/jsp/contribute/guid-overview.jsp). This process is one of the options considered by rulings on EU Data Protection requirements at the start of the study (see http://ec.europa.eu/justice/data-protection/article-29/documentation/opinion-recommendation/files/2014/wp216_en.pdf). | |
| Subject.InfConsBy | Consent obtained by | 99 == Other 4 == Research assistant 2 == Nurse 1 == Doctor (MD) |
Type of health care professional who requested and obtained consent |
| Subject.InfConsDate | Date of written consent | Confirmation of consent date; denotes written confirmation | |
| Subject.InfConsentBlood | Has consented for Blood? | This variable documents if informed consent was obtained specifically for Blood sampling. | |
| Subject.InfConsentData | Has consented for Data? | Explicit consent was requested for broad use and possible transfer of clinical data, blood samples, genetics, MRI and outcome. | |
| Subject.InfConsentDNA | Has consented for DNA? | This variable documents if informed consent was obtained specifically for DNA sampling. | |
| Subject.InfConsentMRI | Has consented for MRI? | This variable documents if informed consent was obtained specifically for MRI. | |
| Subject.InfConsentOutcomeAssmts | Has consented for Outcome assessments? | This variable documents if continued informed consent was obtained for the outcome assessments. | |
| Subject.InfConsInitialDate | Date of initial consent | Date of initial informed consent. | |
| Subject.InfConsInitialTime | Time of initial consent | Time of initial informed consent. | |
| Subject.InfConsTime | Time of written consent | Confirmation of consent time; denotes written confirmation | |
| Subject.InfConsTyp | Type of initial consent | 1 == Informed consent (by subject) oral 2 == Informed consent (by subject) written 3 == Proxy consent verbal 4 == Proxy consent written 5 == Deferred consent 6 == Waiver of consent |
Designates the initial form of consent used |
| Subject.InfConsWhen | Confirmation of consent | 2 == Written proxy consent AFTER enrolment 1 == Written proxy consent BEFORE enrolment 3 == Written informed consent by patient |
Reflects when informed consent was obtained. |
| Subject.JobclassCat | Job category | 5 == Manual worker 3 == Clerk / Sales 0 == None 4 == Skilled manual worker 2 == Technician / Supervisor / Associate Professional 1 == Manager / Professional 99 == Other |
Reflects job category. Only displayed if employment status (Subject.EmplmtStatus) is 1-4 |
| Subject.JobclassCatOther | Other job category (please specify) | Specifies the "other" job category than predefined list. Only displayed if employment status (Subject.EmplmtStatus) is 1-4 | |
| Subject.LengthOfStay | Patient's length of stay at the study hospital | This variable reflects the length of stay of the patient at the study hospital. It has been derived using the information of the date and time of arrival at the study hospital and date and time of (study) hospital discharge. | |
| Subject.MartlPartnerStatus | Marital status | 5 == Separated 4 == Divorced 3 == Living together/common law 2 == Married 1 == Never been married 88 == Unknown 99 == Other 6 == Widowed |
Marital status. |
| Subject.MonthInjury | Month of injury (1-12) | Month of Injury (January - December) | |
| Subject.ObservStudyOtherObservStudy | Other observational study patient is enrolled in (please specify) | Specifies in which other observational study patient is enrolled (if enrolled in another study). | |
| Subject.ObservStudyOtherRegistry | Other registry patient is enrolled in (please specify) | Specifies in which other registry study patient is enrolled (if enrolled in another study). | |
| Subject.ObservStudyRegistry | Observational Study/Registry patient is enrolled in | 1 == CREACTIVE 2 == TARN or EuroTARN registry 3 == German Trauma registry 99 == Other Observational Study 98 == Other Registry 4 == Net-QuRe |
Specifies if subject is also enrolled in another observational study/registry |
| Subject.PatientType | Stratum | 1 == ER 2 == Admission 3 == ICU |
Subjects enrolled in the Core data collection of CENTER are differentiated by stratum (3 strata): ER: discharged directly from ER (dead or alive); Adm: admitted to hospital ward from the ER (may be transferred later to ICU); ICU: directly admitted from ER (or other hospital) to ICU. Patients remain in the stratum allocated, even though they may be internally transferred after admission. This means that the stratum is allocated at presentation based on planned care paths. But possibility exists that a patient allocated to for example the ER stratum, was still admitted to WARD or ICU in a later stage of his care path due to worsening. General enrollment criteria for Core study: Patients with a clinical diagnosis of TBI and clinical indication for CT scan. |
| Subject.Race | Race | Race of Subject | |
| Subject.RandomizedControlTrial | RCT (Randomized Controlled Trial) patient is enrolled in | 2 == EPO-TBI 4 == POLAR (Oxy-TC) 1 == CRASH-3 3 == Eurotherm 99 == Other Randomized Clinical Trial 5 == NOSTRA |
This variables is to ask if the patient is enrolled in another randomized controlled trial |
| Subject.RandomizedControlTrialOther | Other RCT (Randomized Controlled Trials) patient is enrolled in (please specify) | Specifies which RCT if the patient is enrolled in another randomized controlled trial | |
| Subject.SesEduNoFather | Number of years completed in education by father | Father's number of years education completed. Only if patient age <18 | |
| Subject.SesEduNoMother | Number of years completed in education by mother | Mother's number of years of education completed. Only if patient age <18 | |
| Subject.SesNumberPeopleLivingWith | No. of living people living with | Living together and number of people living with provides an indication of "social support" - important to recovery and social re-integration. | |
| Subject.SESPrimAdultAlone | Persons living with: Alone | Reflects living situation prior to the injury: --> Alone | |
| Subject.SESPrimAdultChildren | Persons living with: Child/children | Reflects living situation prior to the injury: --> with Child/children | |
| Subject.SESPrimAdultParents | Persons living with: Parents | Reflects living situation prior to the injury: --> with parents | |
| Subject.SESPrimAdultSiblings | Persons living with: Siblings | Reflects living situation prior to the injury: --> with siblings | |
| Subject.SESPrimAdultSignOther | Persons living with: Significant other partner | Reflects living situation prior to the injury: --> with a significant other partner | |
| Subject.SESPrimAdultSpousePartner | Persons living with: Spouse | Reflects living situation prior to the injury: --> with spouse | |
| Subject.SESPrimAdultUnknown | living situation prior to the injury "other" than the predefined list | Reflects living situation prior to the injury: --> "other" than the predefined list | |
| Subject.Sex | Sex | F == Female M == Male |
The difference between male and female, based upon the interactions between genes and between the genotype and the environment. Gender of Subject. |
| Subject.SiteCode | Site | Anonymized site code. | |
| Subject.StudentStatus | School status (if student) | 88 == Unknown 0 == None 3 == Other school 2 == Part time, diploma / degree oriented 1 == Full time, diploma / degree oriented |
Only displayed if employment status is student/school going |
| Subject.SurgeriesNotes | Notes or additional information about surgeries | Notes or additional information about surgeries if Decompressive Craniectomy wad Performed | |
| Subject.TimeInj | Time of Injury | If exact time of injury is unknown, Investigators were asked to approximate the closest time and code "estimation" in the following variable: Subject.DateTimeInjReliable | |
| Subject.TransOfCareCompleteStatusNotes | Any notes for Transitions of care | Notes on the transition of care. | |
| Subject.ValidGUPI | Validates the GUPI of the patient | Validates the GUPI of the patient. This field got set automatically. | |
| Subject.WithdrawalOption | Withdrawal option | 2 == No further study related activities, but consent to access of clinical notes and use of existing data 1 == Complete Withdrawal (no further contact, destruction of all data and samples collected up to that point) |
In case of complete withdrawal, all data have been deleted from the database |
| Subject.WithdrawSuppDateTime | Date and time of withdrawal of support | Withdrawal of Support Date & Time if Withdrawal of life-sustaining support was the reason for end of study participation. | |
| Surgeries.CranialSurgDone | Cranial surgical procedures done during the hospital stay | 0 == No 1 == Yes 88 == Unknown |
These variables document cranial surgical procedures performed during the hospital stay. Up to 5 different surgical sessions can be recorded; Start date/time, stop date/time, reason for surgery and any delays in starting surgery are recorded. Life-saving emergency procedures performed immediately after presentation are recorded in the ER section: InjuryHx.EmergSurgInterventionsIntraCran. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERIntracranialSurg. |
| Surgeries.DecompressiveCran | Is Decompressive craniectomy performed? | 0 == No 1 == Yes |
These variables specifically focus on decompressive craniectomy (DC). Considerable uncertainty exists on which patients may benefit from DC, as well as on the timing. Previous studies have shown that in approximately one third of cases the DC was too small in size. |
| Surgeries.DecompressiveCranLocation | Location of Decompressive craniectomy | 1 == Bifrontal 2 == Hemicraniectomy- left side 3 == Hemicraniectomy- right side 4 == Posterior fossa |
Documents type of decompressive craniectomy. |
| Surgeries.DecompressiveCranReason | Reason for Decompressive craniectomy | 1 == Pre-emptive approach to treatment of (suspected) raised ICP (not last resort) 2 == Raised ICP, refractory to medical management (last resort) 3 == ICP not monitored, but CT evidence of raised ICP 4 == Not directly planned, but decided on because of intra-operative brain swelling 5 == Routinely performed with every ASDH or Contusion evacuation 6 == Development of cerebral infarction |
WHY question: documents main reason for performing DC |
| Surgeries.DecompressiveCranType | Type of Decompressive craniectomy | 1 == Isolated procedure 2 == In association with ASDH removal 3 == In association with contusion/ICH removal 4 == In association with ASDH and contusion/ICH removal |
The indications for the decompressive craniectomy can be documented here. |
| Surgeries.DecompressiveSize | Size of Decompressive craniectomy | In some sites, the size of DC was recorded by Investigators. No generable way of calculating was proposed. | |
| Surgeries.ExtraCranialSurgDone | Extracranial surgical procedures done during the hospital stay | 0 == No 1 == Yes 88 == Unknown |
These variables document extracranial surgical procedures performed during the hospital stay. Up to 5 different surgical sessions can be recorded; Start date/time, stop date/time, reason for surgery and any delays in starting surgery are recorded. Life-saving emergency procedures performed immediately after presentation are recorded in the ER section: InjuryHx.EmergSurgInterventionsExtraCran. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERExtracranialSurg. |
| Surgeries.SurgIntervenAppro | How strongly do you feel that this surgical intervention is appropriate in terms of the expected benefit to final clinical outcome? | 10 == 10 9 == 9 8 == 8 7 == 7 6 == 6 5 == 5 4 == 4 3 == 3 2 == 2 1 == 1 0 == 0 |
WHY question: How strongly does the surgeon feels that this surgical intervention is appropriate in terms of the expected benefit to final clinical outcome? |
| SurgeriesCranial.ShortTermSurvivalNoSurg | The short term survival chances of the patient if I do not operate (1-100) | Aims to capture information on the surgeon's expectations, eg if the surgeon considers a realistic expectation of benefit, or performs the surgery as a "last resort" in a likely hopeless case --> The short term survival chances of the patient if I DO NOT operate (1-100) | |
| SurgeriesCranial.ShortTermSurvivalYesSurg | The short term survival chances of the patient if I do operate (1-100) | Aims to capture information on the surgeon's expectations, eg if the surgeon considers a realistic expectation of benefit, or performs the surgery as a "last resort" in a likely hopeless case --> The short term survival chances of the patient if I DO operate (1-100) | |
| SurgeriesCranial.SurgeryCranialDelay | Reason for delay in performing cranial surgery | 99 == Other 5 == No delay 1 == Transferral from other hospital 2 == Haemodynamic instability 3 == No OR available 4 == Surgeon delayed |
Reflects reason for delay of cranial surgery (if any). |
| SurgeriesCranial.SurgeryCranialReason | Reason for performing cranial surgery | 1 == Emergency/Life saving 2 == Clinical deterioration 3 == Mass effect on CT 4 == Radiological progression 5 == suspicion of) raised ICP 6 == Guideline adherence 7 == To prevent deterioration |
WHY Question: aims to document the reason for intracranial surgery |
| SurgeriesCranial.SurgeryDescCranial | Cranial surgery code | 01 == Aneurysm (non trauma) 02 == Acute subdural hematoma 03 == Contusion 04 == Craniofacial surgery 05 == CSF shunt 06 == Chronic subdural hematoma 07 == Decompressive craniectomy-hemicraniectomy 08 == Depressed skull fracture 09 == Epidural hematoma 10 == Intracerebral hematoma 11 == Infection 12 == Optic nerve decompression 13 == Posterior fossa surgery 14 == Skull base fracture 15 == Ventriculostomy for CSF drainage 16 == Debridement &ndash minimal for penetrating injuries 17 == Debridement &ndash extensive for penetrating injuries 18 == Foreign body removal 19 == Bone flap replacement 20 == Cranioplasty 21 == Other 071 == Decompressive craniectomy - bifrontal 072 == Decompressive craniectomy - removal previous bone flap |
The cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Cranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate For the “code” there was a choice of 23 values in a drop-down box. For each row you entered in the table, you could select only 1 code in the drop-down. But, if a patient had several surgical options that were applicable, you could enter several rows with each the same start and end date, but marking the different applicable surgical codes in each row separately. |
| SurgeriesCranial.SurgeryEndDate | Date cranial surgery ended | The cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Cranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate | |
| SurgeriesCranial.SurgeryEndTime | Time cranial surgery ended | The cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Cranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate | |
| SurgeriesCranial.SurgeryStartDate | Date cranial surgery started | The cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Cranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate | |
| SurgeriesCranial.SurgeryStartTime | Time cranial surgery started | The cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Cranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate | |
| SurgeriesExtraCranial.SurgeryDescExtraCranial | Extracranial surgery code | 22 == Maxillofacial 23 == Extremity fracture lower limb (internal fixation) 24 == Extremity fracture lower limb (external fixation) 25 == Extremity fracture upper limb (internal fixation) 26 == Extremity fracture upper limb (external fixation) 27 == Fasciotomy 28 == Laparotomy (abdomen) 29 == Pelvic fracture (internal fixation) 30 == Pelvic fracture (external fixation) 31 == Spinal stabilisation/cervical 32 == Spinal stabilisation/thoracic 33 == Spinal stabilisation/lumbar 34 == Thoracotomy 35 == Tracheostomy 36 == Vascular (operative) 37 == Vascular (endovascular treatment) 38 == Wound closure/graft 39 == Other |
The extra-cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Extracranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate For the “code” there was a choice of 18 values in a drop-down box. For each row you entered in the table, you could select only 1 code in the drop-down. But, if a patient had several surgical options that were applicable, you could enter several rows with each the same start and end date, but marking the different applicable surgical codes in each row separately. |
| SurgeriesExtraCranial.SurgeryEndDate | Date extracranial surgery ended | The extra-cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Extracranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate | |
| SurgeriesExtraCranial.SurgeryEndTime | Time extracranial surgery ended | The extra-cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Extracranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate | |
| SurgeriesExtraCranial.SurgeryExtraCranialDelay | Reason for delay in performing extracranial surgery | 1 == Transferral from other hospital 2 == Haemodynamic instability 3 == No OR available 4 == Surgeon delayed 99 == Other 5 == No Delay |
The extra-cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Extracranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate |
| SurgeriesExtraCranial.SurgeryExtraCranialReason | Reason for performing extracranial surgery | 1 == Emergency/Lifesaving 2 == Elective 3 == Treatment of complication 4 == Airway management 99 == Other |
The extra-cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Extracranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate |
| SurgeriesExtraCranial.SurgeryStartDate | Date extracranial surgery started | The extra-cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Extracranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate | |
| SurgeriesExtraCranial.SurgeryStartTime | Time extracranial surgery started | The extra-cranial surgeries information was to be entered in the e-CRF in tables for which you could add as many rows as you wish. The tables consisted of - Surgery start date - Surgery start time - Surgery end date - Surgery end time - Extracranial surgery code - Reason - Delay - Short time survival if you do not operate - Short time survival if you do operate | |
| TransitionsOfCare.CauseOfDelay | Cause of delay in transfer | 1 == Unavailability of beds in the receiving unit 2 == Unavailability of transport 3 == Wish of patient/proxies 4 == Need for isolation due to multi resistant bacteria 5 == Funding issues 6 == Bureaucratic causes 99 == Other |
WHY question: documents reason for delayed transition of care |
| TransitionsOfCare.CauseOfDelayOther | Other cause of delay in transfer (please specify) | WHY question: documents "other" reason for delayed transition of care than predefined list | |
| TransitionsOfCare.DateClinReadyForTransfer | Date clinically ready for transfer | This variable documents the date at which the patient is considered ready for transfer; the date of "effective" transfer documents the date to which this transfer actually occured. In case of a substantial difference, the cause of delay should be recorded | |
| TransitionsOfCare.DateEffectiveTransfer | Date of effective transfer | This variable documents the date of "effective" transfer (versus the date at which the patient was considered ready for transfer). In case of a substantial difference, the cause of delay should be recorded. | |
| TransitionsOfCare.Location | Location | PostDisch == Post Discharge InHosp == In Hospital |
Reflects if transition of care occurred in hospital or post-discharge |
| TransitionsOfCare.TransFrom | Transfer from | RU == Rehab Unit HCU == High Care Unit WNS == Ward - Neurosurgery WN == Ward - Neurology WS == Ward - Surgery WO == Ward - Other ICU == ICU OR == OR CT == CT MRI == MRI IHR == In-hospital Rehab 99 == Other 98 == Other Hospital HOME == Home SRU == Rehab Unit, specialized in Brain Injury NSRU == Non-specialized rehab unit NH == Nursing Home ER == ER PSY == Psychiatric Unit SMCH == Substance misuse Care Unit RSH == Readmission Study Hospital RSHICU == Readmission Study Hosp - ICU |
This informs on the care pathway of the patient. It is important to also check the ER, ADM and/or ICU admission and discharge forms for information on the care pathway. |
| TransitionsOfCare.TransReason | Reason for transfer | 25 == Neurological complication 10 == Could be discharged home, but no adequate supervision 8 == Clinical observation for TBI 6 == Clinical deterioration 99 == Other 9 == No ICU bed available 7 == CT abnormalities 5 == Neurological operation 11 == Improvement 12 == Neurological deterioration 13 == Systemic compilation 14 == CT progression 4 == Extracranial injuries 21 == Lack of improvement 15 == Planned surgery 16 == Condition stable 17 == (acute) Treatment goals accomplished 18 == Need to free a bed 19 == Further improvement 20 == Clinical rehab completed 3 == Haemodynamic invasive monitoring 1 == Mechanical ventilation 2 == Frequent neurological observations 22 == Late neurological deterioration 23 == Problems unrelated to trauma 24 == Post operative care |
WHY question: documents reason for transition of care |
| TransitionsOfCare.TransTiming | Time of transfer | DEL == Delayed APP == Appropriate PRE == Premature |
Transitions of care may be premature or delayed because of logistic problems. This variable aims to capture such information. |
| TransitionsOfCare.TransTo | Transfer to | HCU == High Care Unit WNS == Ward - Neurosurgery WN == Ward - Neurology WS == Ward - Surgery WO == Ward - Other ICU == ICU OR == OR CT == CT MRI == MRI IHR == In-hospital Rehab 99 == Other HOME == Home RU == Rehab Unit NH == Nursing Home 98 == Other Hospital PSY == Psychiatric Unit SMCH == Substance misuse Care Unit RSH == Readmission Study Hospital RSHICU == Readmission Study Hosp - ICU ER == ER SRU == Rehab Unit, specialized in Brain Injury NSRU == Non-specialized rehab unit |
Reflects to which location transition of care occurred. |
| Vitals.DailyGCSTime | Time of worst GCS | For each Day of assessment, a Best and Worst score of GCS and pupillary reactivity is requested. If both scores are the same, only the Worst is reported. | |
| Vitals.DVAssmtConditions | Best GCS: Assessment conditions | 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other 1 == Sedated 3 == Temporary stop of sedation/paralysis 0 == No sedation or paralysis 4 == Reversal of sedation/paralysis 2 == Paralyzed |
Reflects the assessment condition for the best GCS assessments as part of the daily vitals. Only applicable to ICU stratum. |
| Vitals.DVAssmtConditionsWorst | Worst GCS: Assessment conditions | 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 2 == Paralyzed 1 == Sedated 0 == No sedation or paralysis |
Reflects the assessment condition for the worst GCS assessments as part of the daily vitals. Only applicable to ICU stratum. |
| Vitals.DVBestPupilSymmetry | Best pupils: Pupil symmetry | 3 == Unequal L>R 1 == Equal 2 == Unequal R>L |
Reflects if the pupil are of equal size (symmetry) during the day as part of the Daily vitals. |
| Vitals.DVBloodGasNotDone | Daily Vitals: Blood gas analysis Not done | Reflects if Blood Gas Analysis was Not done as part of the Daily Vitals. | |
| Vitals.DVBloodOxySatHigh | Lowest Oxygen saturation | Reflects Highest oxygen saturation (in %) as determined from Arterial Blood Gas | |
| Vitals.DVBloodOxySatHighNotDone | Daily Vitals: Highest oxygen saturation Not done | Reflects if Highest oxygen saturation was Not done. | |
| Vitals.DVBloodOxySatLow | Highest Oxygen saturation | Reflects Lowest oxygen saturation (in %) as determined from Arterial Blood Gas | |
| Vitals.DVBloodOxySatLowNotDone | Daily Vitals: Lowest oxygen saturation Not done | Reflects if Lowest oxygen saturation was Not done | |
| Vitals.DVBrainTempCLow | Brain temperature at the time of lowest body temperature | Brain temperature at the timepoint of the lowest body temperature of the day, degrees Celsius. | |
| Vitals.DVBrainTempLowNotDone | Daily Vitals:Brain temperature at the time of lowest body temp Not done | Reflects if recording of Brain temperature at the time of lowest body temp was Not done | |
| Vitals.DVBrainTempUnit | Daily Vitals: Unit used (C or F) for Brain temperature at the time of lowest body temp | F == F C == C |
Reflects the unit used (C or F) for measuring Brain temperature at the time of lowest body temp as part of the Daily Vitals. |
| Vitals.DVChangeCauseWorst | Worst GCS: Cause of change | 3 == Both to an equal extent 2 == Mainly extracranial 1 == Mainly intracranial 88 == Unknown |
Reflects the cause of change for the worst GCS as part of the Daily Vitals. |
| Vitals.DVChangeInOneDay | Best GCS: Change over past 24 hours | 0 == No change 1 == Improving 2 == Episode of deterioration 4 == Fluctuating 3 == Sustained deterioration |
Reflects presence or absence of change over past 24 hours for the Best GCS as part of the Daily Vitals. |
| Vitals.DVChangeInOneDayWorst | Worst GCS: Change over past 24 hours | 3 == Sustained deterioration 4 == Fluctuating 0 == No change 1 == Improving 2 == Episode of deterioration |
Reflects presence or absence of change over past 24 hours for the Worst GCS as part of the Daily Vitals. |
| Vitals.DVDate | Date of Vitals assessment | Daily Vitals Date. Daily vitals are documented in both the Adm and ICU strata on Day 1-7, Day 10, Day 14, Day 21 and Day 28. Note: FOUR score only applicable to patients in the ICU. | |
| Vitals.DVDBP | Highest Diastolic | The diastolic blood pressure at the timepoint of the highest systolic blood pressure. | |
| Vitals.DVDBPLow | Lowest Diastolic | The diastolic blood pressure at the timepoint of the lowest systolic blood pressure. | |
| Vitals.DVFiO2AtHighPaO2 | FiO2 at highest PaO2 | FiO2 at time of sampling - Highest PaO2/FiO3 (in %) | |
| Vitals.DVFiO2AtHighPaO2NotDone | Daily Vitals: Highest PaO2/FiO2 Not done | Recording of Highest PaO2/FiO2 Not done | |
| Vitals.DVFiO2AtLowPaO2 | FiO2 at lowest PaO2 | FiO2 at time of sampling - Lowest PaO2/FiO3 (in %) | |
| Vitals.DVFiO2AtLowPaO2NotDone | Daily Vitals: Lowest PaO2/FiO2 Not done | Recording of Lowest PaO2/FiO2 Not done | |
| Vitals.DVFourScoreBraintstem | Four score: Brainstem reflexes | 3 == One pupil wide and fixed 4 == Pupil and corneal reflexes present 88 == Unknown 1 == Pupil and corneal reflexes absent 2 == Pupil or corneal reflexes absent 0 == Absent pupil, corneal, and cough reflex |
Four Score for the Brainstem reflexes |
| Vitals.DVFourScoreEye | Four Score: Eye response | 0 == Eyelids remain closed with pain 1 == Eyelids closed but opens to pain 2 == Eyelids closed but opens to loud voice 3 == Eyelids open but not tracking 4 == Eyelids open or opened tracking or blinking to command 88 == Unknown |
Four Score for the Eye response |
| Vitals.DVFourScoreMotor | Four score: Motor response | 0 == No response to pain or generalized myoclonus status epilepticus 1 == Extensor posturing 3 == Localizing to pain 2 == Flexion response to pain 88 == Unknown 4 == Thumbs up, fist, or peace sign to command |
Four Score for the Motor response |
| Vitals.DVFourScoreNotDone | Daily Vitals: Four Score Not done | Four Score Not Done | |
| Vitals.DVFourScoreRespiration | Four score: Respiration | 0 == Breathes at ventilator rate or apnea 88 == Unknown 1 == Breathes above ventilator rate 2 == Not intubated, irregular breathing pattern 3 == Not intubated, Cheyne- Stokes breathing pattern 4 == Not intubated, regular breathing pattern |
Four Score for the Respiration |
| Vitals.DVFourScoreTotal | Four score | DVFourScoreEye + DVFourScoreMotor + DVFourScoreBraintstem + DVFourScoreRespiration. No score if any of the components =88 (unknown) or NULL | |
| Vitals.DVGCSBest | Is the worst GCS same as best GCS? | 1 == Yes 0 == No |
Reflects if the Worst GCS is the same as the best GCS as part of the Daily Vitals. |
| Vitals.DVGCSBestChangeCause | Best GCS: Cause of change | 1 == Mainly intracranial 2 == Mainly extracranial 3 == Both to an equal extent 88 == Unknown |
Cause of change for the Best GCS as part of the Daily Vitals. |
| Vitals.DVGCSBestTime | Time of best GCS | Time of Best GCS score, as part of the Daily Vitals. | |
| Vitals.DVGCSEyes | Best GCS: Eye opening (E) response | 2 == 2-To pain O == Untestable (Other) UN == Unknown 1 == 1-None S == Untestable (swollen) 4 == 4-Spontaneously 3 == 3-To speech |
Best GCS eye opening as part of the Daily Vitals. |
| Vitals.DVGCSMotor | Best GCS: Motor (M) response | 4 == 4-Normal flexion/withdrawal 5 == 5-Localizes to pain 6 == 6-Obeys command 3 == 3-Abnormal flexion P == Untestable (Deep sedation/paralyzed) UN == Unknown O == Untestable (Other) 1 == 1-None 2 == 2-Abnormal extension |
Best GCS motor score as part of the Daily Vitals. |
| Vitals.DVGCSPupilsNotDone | Daily Vitals: GCS and Pupils recording Not done | Reflects if GCS and pupil recording was not done as part of the daily vitals. | |
| Vitals.DVGCSScore | Best GCS: Score | Best GCS Score: DVGCSEyes + DVGCSMotor + DVGCSVerbal. If one or more of these is Untestable or unknown then = "No Sum" | |
| Vitals.DVGCSVerbal | Best GCS: Verbal (V) response | 4 == 4-Confused 5 == 5-Oriented 3 == 3-Inappropriate words 2 == 2- Incomprehensible sound 1 == 1-None UN == Unknown O == Untestable (Other) T == Untestable (Tracheotomy/endotracheal tube) |
Best GCS verbal score as part of the daily vitals. |
| Vitals.DVGCSWorstEyes | Worst GCS: Eye opening (E) response | 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously S == Untestable (swollen) O == Untestable (Other) UNK == Unknown 1 == 1-None |
Worst GCS eye opening as part of the daily vitals. |
| Vitals.DVGCSWorstMotor | Worst GCS: Motor (M) response | 1 == 1-None 2 == 2-Abnormal extension 3 == 3-Abnormal flexion 4 == 4-Normal flexion/withdrawal 5 == 5-Localizes to pain 6 == 6-Obeys command P == Untestable (Deep sedation/paralyzed) O == Untestable (Other) UN == Unknown |
Worst GCS motor score as part of the daily vitals. |
| Vitals.DVGCSWorstScore | Worst GCS: Score | Worst GCS: DVGCSWorstEyes + DVGCSWorstMotor + DVGCSWorstVerbal. If one or more of these is Untestable or unknown then = "No Sum" | |
| Vitals.DVGCSWorstVerbal | Worst GCS: Verbal (V) response | UN == Unknown 2 == 2- Incomprehensible sound T == Untestable (Tracheotomy/endotracheal tube) 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented 1 == 1-None O == Untestable (Other) |
Worst GCS Verbal score as part of the daily vitals |
| Vitals.DVHighestPaCO2 | Highest PaCO2 | Highest PaCO2 on a day, in mmHg. | |
| Vitals.DVHighestPaCO2kPa | Daily Vitals: highest value of PaCO2 measured on each day, in kPa | The highest value of PaCO2 measured on each day, in kPa. | |
| Vitals.DVHighestPaCO2NotDone | Daily Vitals: highest value of PaCO2 measurement Not done | Highest PaCO2 measurement was Not done | |
| Vitals.DVHighestPaCO2Unit | Daily Vitals: Unit used for highest value of PaCO2 measurement | kPa == kPa mmHg == mmHg |
The unit in which the highest PaCO2 on a day is measured. |
| Vitals.DVHighestPaO2 | Highest PaO2 | Highest PaO2 on a day, in mmHg | |
| Vitals.DVHighestPaO2kPa | Daily Vitals: highest value of PaO2 measured on each day, in kPa | Highest PaO2 in a day, in Kpa | |
| Vitals.DVHighestPaO2NotDone | Daily Vitals: highest value of PaO2 measurement Not done | Highest PaO2 measurement Not done | |
| Vitals.DVHighestPaO2OverHighestFiO2 | Highest PaO2/FiO2 | FiO2 at time of sampling - Highest PaO2/FiO4 | |
| Vitals.DVHighestPaO2Unit | Daily Vitals: Unit used for highest value of PaO2 measurement | kPa == kPa mmHg == mmHg |
Unit used for Highest PaO2 measurement (mmHg or kPa) |
| Vitals.DVHighestpH | Highest pH | Highest pH as part of the Daily vitals Blood Gas Analysis | |
| Vitals.DVHighestpHNotDone | Daily Vitals: Highest pH measurement Not done | Highest pH measurement Not Done | |
| Vitals.DVHR | Highest Heart Rate | The highest heart rate during the day. | |
| Vitals.DVHRHighTime | Time of highest Heart Rate | The timepoint for the highest heart rate of a day. | |
| Vitals.DVHRLow | Lowest Heart Rate | The lowest heart rate of a day. | |
| Vitals.DVHRLowTime | Time of lowest Heart Rate | The time of the lowest heart rate of a day | |
| Vitals.DVIntracranialSecondInsultsNotDone | Daily Vitals: Intracranial Second Insults recording Not done | Intracranial Second Insults recording Not done | |
| Vitals.DVLowestPaCO2 | Lowest PaCO2 | The lowest value of PaCO2 measured on each day, in mmHg. | |
| Vitals.DVLowestPaCO2kPa | Daily Vitals: lowest value of PaCO2 measured on each day, in kPa | The lowest value of PaCO2 measured on each day, in kPa. | |
| Vitals.DVLowestPaCO2NotDone | Daily Vitals: lowest value of PaCO2 measurement Not done | Lowest PaCO2 measurement Not done | |
| Vitals.DVLowestPaCO2Unit | Daily Vitals: Unit used for lowest value of PaCO2 measurement | kPa == kPa mmHg == mmHg |
The unit in which PaCO2 is measured. |
| Vitals.DVLowestPaO2 | Lowest PaO2 | Lowest PaO2 in mmHg as part of the Daily Vitals Blood Gas Analysis | |
| Vitals.DVLowestPaO2kPa | Daily Vitals: lowest value of PaO2 measured on each day, in kPa | Lowest PaO2 in kPa as part of the Daily Vitals Blood Gas Analysis | |
| Vitals.DVLowestPaO2NotDone | Daily Vitals: lowest value of PaO2 measurement Not done | Lowest PaO2 measurement Not Done. | |
| Vitals.DVLowestPaO2OverLowestFiO2 | Lowest PaO2/FiO2 | FiO2 at time of sampling - Lowest PaO2/FiO4 as part of the Daily Vitals | |
| Vitals.DVLowestPaO2Unit | Daily Vitals: Unit used for lowest value of PaO2 measurement | kPa == kPa mmHg == mmHg |
Unit used (mmHg or kPa) for the measurement of Lowest PaO2 as part of the Daily Vitals Blood Gas Analysis |
| Vitals.DVLowestpH | Lowest pH | Lowest pH as part of the Daily Vitals Blood Gas Analysis | |
| Vitals.DVLowestpHNotDone | Daily Vitals: Lowest pH measurement Not done | Lowest pH measurement Not Done | |
| Vitals.DVPupilLftEyeMeasr | Best pupils: Left eye pupil size | 2 == 2 5 == 5 3 == 3 1 == 1 4 == 4 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
Best Pupil Left eye size |
| Vitals.DVPupilLftEyeMeasrUnkUnt | Daily Vitals: best pupil left eye size untestable/unknown | 66 == Untestable 88 == Unknown |
Best pupil left eye size is untestable or unknown. |
| Vitals.DVPupilReactivityLghtLftEyeReslt | Best pupils: Left eye pupil reactivity | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
The best pupillary reactivity of the left eye during the day |
| Vitals.DVPupilReactivityLghtRtEyeReslt | Best pupils: Right eye pupil reactivity | 3 == - (Negative) 1 == + (Brisk) 2 == + (Sluggish) |
Best pupillary reactivity of the right eye during the day |
| Vitals.DVPupilRtEyeMeasr | Best pupils: Right eye pupil size | 8 == 8 9 == 9 7 == 7 5 == 5 6 == 6 1 == 1 3 == 3 2 == 2 10 == 10 4 == 4 |
Best Pupil Right eye Size |
| Vitals.DVPupilRtEyeMeasrUnkUnt | Daily Vitals: best pupil right eye size untestable/unknown | 88 == Unknown 66 == Untestable |
Best Pupil Right eye Size is untestable or unknown |
| Vitals.DVSBP | Highest Systolic | The highest systolic blood pressure for each day where vitals are recorded. | |
| Vitals.DVSBPHighTime | Time of highest Blood Pressure | Time of the the highest systolic blood pressure, for each day where vitals are recorded. | |
| Vitals.DVSBPLow | Lowest Systolic | The lowest systolic blood pressure for each day. | |
| Vitals.DVSBPLowTime | Time of lowest Blood Pressure | The time at which the lowest systolic blood pressure and its associated diastolic blood pressure is recorded. | |
| Vitals.DVSpO2 | Highest Oxygen saturation (Pulse oximetry) | Highest Oxygen saturation (pulse oximetry) in % for each day where vitals are recorded. | |
| Vitals.DVSpO2HighTime | Time of highest Oxygen saturation (Pulse oximetry) | Time of the Highest Oxygen saturation (pulse oximetry) for each day where vitals are recorded. | |
| Vitals.DVSpO2Low | Lowest Oxygen saturation (Pulse oximetry) | Lowest Oxygen saturation (pulse oximetry) in % for each day where vitals are recorded. | |
| Vitals.DVSpO2LowTime | Time of lowest Oxygen saturation (Pulse oximetry) | Time for the lowest Oxygen saturation (pulse oximetry) for each day where vitals are recorded. | |
| Vitals.DVTempBrainC | Brain temperature at the time of highest body temperature | Brain temperature at the timepoint of the highest body temperature of the day, degrees Celsius. | |
| Vitals.DVTempBrainNotDone | Daily Vitals: brain temperature measurement not done | Brain temperate measurement not done. | |
| Vitals.DVTempBrainUnit | Daily Vitals: unit used for brain temperature at timepoint of highest body temperature of the day | C == C F == F |
Unit used (C or F) for Brain temperature at the timepoint of the highest body temperature of the day. |
| Vitals.DVTempHighC | Highest body temperature | The highest body temperature of the day in degrees Celsius. For the associated time point, see Vitals.DVTempHighDateTime. For location of where the temperature was measured, see Vitals.DVTempLocation. | |
| Vitals.DVTempHighTime | Time of highest temperature | Time when the highest temp of the day was recorded. | |
| Vitals.DVTempLocation | Where was temperature measured? | 5 == Core- oesophageal 6 == Core- tympanic 7 == Core- nasopharynx 3 == Core- rectal 4 == Core-bladder 1 == External-axillary 2 == External-skin |
Location of thermometer probe for temperature measurement. |
| Vitals.DVTempLowC | Lowest body temperature | The lowest temperature of a day in degrees Celsius. For the timepoint, see Vitals.DVTempLowDateTime. For location of where the temperature was measured, see Vitals.DVTempLocation. | |
| Vitals.DVTempLowTime | Time of lowest temperature | Time when the lowest temp of the day was recorded. | |
| Vitals.DVTempNotDone | Daily Vitals: temperature measurement not done | Temperature measurement Not done | |
| Vitals.DVTempUnitHigh | Daily Vitals: Unit used for highest temperature measurement | F == F C == C |
The unit in which the highest temperature is measured |
| Vitals.DVTempUnitLow | Daily Vitals: Unit used for lowest temperature measurement | F == F C == C |
The unit in which the lowest body temperature of the day is measured. |
| Vitals.DVTimepoint | Day of recording of vital signs (Day 1 is the day of admission to ICU/Ward) | 28 == Day 28 21 == Day 21 14 == Day 14 10 == Day 10 6 == Day 6 7 == Day 7 4 == Day 4 5 == Day 5 2 == Day 2 3 == Day 3 1 == Day 1 |
Intended day after injury when the vitals are recorded |
| Vitals.DVVitalsNotDone | Daily Vitals measurement Not done | Reflects if daily vitals measurement was Not Done. | |
| Vitals.DVWorstPupilLftEyeMeasr | Worst pupils: Left eye pupil size | Worst Pupils Left eye Size | |
| Vitals.DVWorstPupilLftEyeMeasrUnkUnt | Daily Vitals: worst pupil left eye size untestable/unknown | 88 == Unknown 66 == Untestable |
Worst Pupils Left eye Size is untestable or unknown |
| Vitals.DVWorstPupilReactivityLghtLftEyeResult | Worst pupils: Left eye pupil reactivity | 3 == - (Negative) 1 == + (Brisk) 2 == + (Sluggish) |
Worst Pupils Left eye Reactivity |
| Vitals.DVWorstPupilReactivityLghtRghtEyeResult | Worst pupils: Right eye pupil reactivity | 2 == + (Sluggish) 1 == + (Brisk) 3 == - (Negative) |
Worst Pupils Right eye Reactivity |
| Vitals.DVWorstPupilRghtEyeMeasr | Worst pupils: Right eye pupil size | Worst Pupils Right eye Size | |
| Vitals.DVWorstPupilRghtEyeMeasrUnkUnt | Daily Vitals: worst pupil right eye size untestable/unknown | 88 == Unknown 66 == Untestable |
Worst Pupils Right eye Size is untestable or unknown |
| Vitals.DVWorstPupilSymmetry | Worst pupils: Pupil symmetry | 3 == Unequal L>R 2 == Unequal R>L 1 == Equal |
Worst Pupil symmetry |
| Vitals.HosComplEventHypocapnia | Systemic Second Insults: Inadvertent hypocapnia | 0 == No 1 == Single episode, short duration 2 == Multiple episodes or prolonged duration 88 == Unknown |
Reflects Inadvertent hypocapnia. Second Insults reported in Vitals relate to the the hospital phase (both ward and ICU). Inadvertent hypocapnia is defined as a PaCO2 <=3.3 kPa (25 mmHg) |
| Vitals.HosComplEventHypotension | Systemic Second Insults: Hypotension | 0 == No 1 == Single episode, short duration 88 == Unknown 2 == Multiple episodes or prolonged duration |
Reflects Hypotensive Episodes. Second Insults reported in Vitals relate to the the hospital phase (both ward and ICU). Pre-hospital hypoxia is documented at: InjuryHx.EDComplEventHypotension. Definite hypotension is defined as a documented systolic BP < 90 mm Hg (adults) |
| Vitals.HosComplEventHypoxia | Systemic Second Insults: Hypoxic Episode | 88 == Unknown 2 == Multiple episodes or prolonged duration 1 == Single episode, short duration 0 == No |
Reflects Hypoxic Episodes. Second Insults reported in Vitals relate to the hospital phase (both ward and ICU). Pre-hospital hypoxia is documented at: InjuryHx.EDComplEventHypoxia. Definite hypoxia is defined as a documented PaO2 <8 kPa (60 mm Hg) and/or SaO2<90% |
| Vitals.HosComplEventSeizures | Intracranial Second Insults: Seizures | 5 == Silent seizure activity (only electrical, no clinical manifestation) 4 == Status epilepticus 88 == Unknown 0 == No 1 == Single episode, short duration 2 == Partial/Focal 3 == Generalized |
Reflects absence or presence of seizures as Intracranial Second Insult. Second Insults reported in Vitals relate to the the hospital phase (both ward and ICU). |
| Vitals.HospSecondInsultsNeuroWorse | Neuroworsening | 0 == No 1 == Yes 88 == Unknown |
The importance of Neuroworsening was first described by Morris and Marshall. The occurrence of neuroworsening is related to poorer outcome in subjects with moderate to severe TBI. Neuroworsening is defined as 1) a decrease in GCS motor score of 2 or more points; 2) a new loss of pupillary reactivity or development of pupillary assymmetry >= 2mm; 3) deterioration in neurological or CT status sufficient to warrant immediate medical or surgical intervention |
| Vitals.HospSecondInsultsNeuroWorseAction | Action taken towards Neuroworsening | 3 == Change in medical therapy 4 == Surgical intervention 1 == None 2 == Unscheduled CT scan |
Action taken in case of Neuroworsening. The importance of Neuroworsening was first described by Morris and Marshall. The occurrence of neuroworsening is related to poorer outcome in subjects with moderate to severe TBI. Neuroworsening is defined as 1) a decrease in GCS motor score of 2 or more points; 2) a new loss of pupillary reactivity or development of pupillary assymmetry >= 2mm; 3) deterioration in neurological or CT status sufficient to warrant immediate medical or surgical intervention |
| Vitals.HospSecondInsultsNeuroWorseYes | Neuroworsening (please describe) | 1 == Decrease in motor score >= 2 points 2 == Development of pupillary abnormalities 3 == Other neurological and/or CT deterioration |
This variable provides a specification of the type of neuroworsening if it occurs. |
| Vitals.PatientLocation | Location of patient at the time of daily vitals assessment | ICU == ICU Ward == Ward |
Location of the patient (Ward or ICU) at time of Daily Vitals measurement. |
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