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 | Data URL | URL to download high resolution ICU file | |
| 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 URL | This variable is an URL towards the generated Bval file. | |
| Imaging.BvecURL | Bvec URL | This variable is an URL towards the generated Bvec file. | |
| 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 | NIfTI URL | 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 is a URL towards the header file. | |
| 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 generated nifti file. R: Open source tool to convert dicom to nifti https://github.com/icometrix/dicom2nifti | |
| Imaging.QCResultsURL | QC results URL | S: A json file containing MR quality measures. B: All different quality measures that have been applied are being collected in one json file. The comprises at least a protocol check, snr, cnr, head coverage, GM/WM, FA/MD, tensor residuals, ... A: Url to the .json file | |
| 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 on the data, a snapshot of the mid-slice in 3 planes is provided. A: Url to .png screenshot of generated nifti images. R: Screenshot 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 URL | S: Screenshot are automatically generated. B: Thumbnails are reduced-size versions of pictures. A: Url to .png screenshot of generated nifti images. R: You can find higher resolution image at the URL provided by Imaging.SnaphshotURL. Screenshot 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? |