| Variable | Lookup values | Description |
|---|---|---|
| AIS.InjAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
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 | 1 == Externa 2 == Head and Neck-Other 3 == Brain Injury 4 == Cervical Spine 5 == Face 6 == Thorax/Chest 7 == Thoracic Spine 8 == Abdomen/Pelvic Contents 9 == Lumbar Spine 10 == Upper Extremities 11 == Lower Extremities 12 == Pelvic Girdle |
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 | 1 == Brain Injury: Concussion 2 == Brain Injury: Contusions 3 == Brain Injury: EDH 4 == Brain Injury: Diffuse Injury 5 == Brain Injury: ASDH 6 == Brain Injury: Other 7 == Head and Neck-Other: Specify in comments box 8 == Cervical Spine: Fracture 9 == Cervical Spine: Dislocation 10 == Cervical Spine: Other 11 == Face: Maxillo-facial fracture le Fort I 12 == Face: Maxillo-facial fracture le Fort II 13 == Face: Maxillo-facial fracture le Fort III 14 == Face: Orbital fracture 15 == Face: Zygomatic arch fracture 16 == Face: Other 17 == Thorax/Chest: Rib fracture 18 == Thorax/Chest: Lung contusion 19 == Thorax/Chest: Cardiac contusion 20 == Thorax/Chest: Aorta dissection 21 == Thorax/Chest: Pneumo-thorax 22 == Thorax/Chest: Hemato-thorax 23 == Thorax/Chest: Other 24 == Thoracic Spine: Fracture 25 == Thoracic Spine: Dislocation 26 == Abdomen/Pelvic Contents: Spleen rupture 27 == Abdomen/Pelvic Contents: Liver rupture 28 == Abdomen/Pelvic Contents: Perforating abdominal injury 29 == Abdomen/Pelvic Contents: Kidney contusion 30 == Abdomen/Pelvic Contents: Retroperitoneal hematoma 31 == Abdomen/Pelvic Contents: Other 32 == Lumbar Spine: Fracture 33 == Lumbar Spine: Dislocation 34 == Lumbar Spine: Sacral fracture 35 == Lumbar Spine: Other 36 == Upper Extremities: Humerus fracture 37 == Upper Extremities: Radial and/or ulnar fracture 38 == Upper Extremities: Dislocation 39 == Upper Extremities: Hand 40 == Upper Extremities: Finger 41 == Lower Extremities: Femoral fracture 42 == Lower Extremities: Tibia plateau fracture 43 == Lower Extremities: Tibia fracture 44 == Lower Extremities: Ankle fracture 45 == Lower Extremities: Calcaneus fracture 46 == Lower Extremities: Metatarsal/tarsal fracture (toe fracture) 47 == Lower Extremities: Fibula fracture 48 == Pelvic Girdle: Pelvic fracture 49 == Pelvic Girdle: Hip fracture 50 == Pelvic Girdle: Hip dislocation 51 == Externa: Other 52 == Thoracic Spine: Other 53 == Upper Extremities: Other 54 == Lower Extremities: Other 55 == Pelvic Girdle: Other |
List of body regions with 55 subcategories describing the injury. |
| AIS.InjDesOther | Free text specifying the injury when AIS.InjDescription is "other" | |
| Brainmonitoring.DataAvailable | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.DataCollectionSoftware | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.DataEndTime | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.DataProcessingSoftware | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.DataStartTime | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.DateTimeFormat | ||
| Brainmonitoring.Duration | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.FormatVersion | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| Brainmonitoring.HDF5URL | URL to download high resolution ICU file | |
| Brainmonitoring.InvalidValue | Meta data from the High Resolution ICU data collected in a subcategory of patients in specific HR-ICU sites. | |
| CTMRI.CTAcuteSubdurHema | 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 | 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 | 0 == No 1 == Yes |
Assessment by clinician/investigator whether or not in his/her interpretation the basal cisterns are compressed. |
| CTMRI.CTContusion | 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 | 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 | 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 | 1 == GCS <= 14 2 == GCS = 15 + risk factors 3 == Head wound 4 == Exclusion of abnormalities prior to discharge 5 == Suspicion of maxillofacial injury 88 == Unknown 99 == Other |
WHY question: reason for performing CT; only applicable to initial scan (presentation). |
| CTMRI.CTERReasonOther | Specification, only applicable if "CTMRI.CTERReason" was "other" | |
| CTMRI.CTExtraduralHema | 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 | 0 == No 1 == Yes 88 == Unknown |
Assessment by clinician/investigator whether or not in his/her interpretation diffuse axonal injury is present. |
| CTMRI.CTIschemia | 0 == No 1 == Single arterial territory 2 == Multiple territories 3 == Hemisphere |
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 | TOSH == Toshiba SIEM == Siemens PHIL == Philips KONI == Konica Minolta AGFA == Agfa CARE == Carestream GE == GE HITA == Hitachi 99 == Other |
This variable describes the CT scans manufacturer. |
| CTMRI.CTMidlineShift | 0 == No 1 == Yes |
Assessment by Investigator |
| CTMRI.CTMidlineShiftMeasure | Assessment by Investigator | |
| CTMRI.CTMRICompleteStatus | INCNOSHOW == Incompletable - No Show INCPT == Incompletable - Pt Factors NOT == Queries Outstanding COM == Complete PRO == In Process NOSTART == Not Started |
This variable is populated when the CRF status is "complete". |
| CTMRI.CTMRIDate | Date of Imaging captured in CRF | |
| CTMRI.CTMRITime | Time of imaging captured in CRF | |
| CTMRI.CTNoOpMotiv | 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 88 == Unknown 99 == Lesion present, but Other |
WHY question: documents reason for not having an indication for (intra)cranial surgery. |
| CTMRI.CTNoOpMotivOther | Specification, only applicable if "CTMRI.CTNoOpMotiv" was "other" | |
| CTMRI.CTPatientLocation | ICU == ICU ADMIS == Ward/Admission ED == ER |
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 | ICUADM88 == Unknown ICUADM99 == Other LOP == Lack of improvement IICP == (Suspicion of) Increasing ICP CD == Clinical deterioration POC == Post-operative control SFU == Standard follow-up |
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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 16 == 16-slice 32 == 32-slice 64 == 64-slice 99 == Other 128 == 128-slice 256 == 256-slice 320 == 320-slice |
This variable specifies the type of CT-scanner by the number of slices. |
| CTMRI.CTSchedForOp | 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 | 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 | PCT == Perfusion CT CTA == CT Angiography CCT == Contrast CT NCCT == Non-contrast 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 | 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 | ||
| CTMRI.IcometrixImageId | Identifier generated for an imaging experiment when images are uploaded from site It's recommended to use: Imaging.CRFIcometrixImageId | |
| CTMRI.IcometrixPassedQA | 0 == No 1 == Yes |
Status of QA dome on images |
| CTMRI.IcometrixQADateTime | Date and time when central QA was done | |
| CTMRI.IcometrixUploadDateTime | Date and time when the images were uploaded from site | |
| CTMRI.InitialDataIcometrix | ||
| CTMRI.MRIDone | 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 | ER1 == ER only: Discrepancy between clinical symptomatology and (lack of) CT abnormalities ER3 == ER only: Instead of CT (limiting radiation exposure) ER2 == ER only: Suspicion non-metal foreign object ER4 == ER only: Suspicion spinal cord lesion 88 == Unknown 99 == Other |
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 nonĀmetal 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 | 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 | SIEM == Siemens PHIL == Philips GE == GE TOSH == Toshiba 99 == Other |
This variable describes the MRI-scan manufacturer. |
| CTMRI.MRIPatientLocation | ADMIS == Ward/Admission ED == ER ICU == ICU |
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 | ICUADM3 == Detection of brainstem lesions ICUADM2 == Standard Care ICUADM1 == Discrepancy between CT and clinical condition STUDYPROT == Study protocol 88 == Unknown 99 == Other |
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 |
| CTMRI.MRIReasonOther | 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 | |
| CTMRI.MRIResultPreExistAbnorm | 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. |
| CTMRI.MRIResultTraumaticAbnorm | 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. |
| CTMRI.MRIScannerStrength | This variable describes the MRI scanner strength. This is a text field. | |
| CTMRI.MRISequences | PWI == PWI MRSI == MRSI DTI == DTI SWI == SWI GRE == GRE DWI == DWI FLAIR == FLAIR T2 == T2 T1 == T1 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. |
| CTMRI.MRITraumAbnormASDH | 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. |
| CTMRI.MRITraumAbnormContusion | 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. |
| CTMRI.MRITraumAbnormDAI | 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. |
| CTMRI.MRITraumAbnormDAILesionLocBrainstem | 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. |
| CTMRI.MRITraumAbnormDAILesionLocCorpusCallosum | 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. |
| CTMRI.MRITraumAbnormDAILesionLocDiffuseWhiteMatter | 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. |
| CTMRI.MRITraumAbnormDAINumLesions | 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. |
| CTMRI.MRITraumAbnormEDH | 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. |
| CTMRI.MRIType | MRI == MRI MRA == MRA |
This variable describes the type of MRI scan that has been made. Options are: MRI, MRA |
| CTMRI.Timepoint | CT Followup == CT Followup CT Early == CT Early CT Post-Op == CT Post-Op MR Early == MR Early |
This variable describes the timepoint of imaging. Options are: CT Early, CT Followup, CT PostĀOp, 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 | This variable is populated when an X-ray angiography has been done. | |
| DailyTIL.TILCCSFDrainageVolume | Specification of volume drained, only applicable if "DailyTIL.TILCSFDrainage" was "yes" | |
| DailyTIL.TILCSFDrainage | 0 == No 1 == Yes |
|
| DailyTIL.TILDailyPhysConcSatisfNotDone | Daily physician concerns are documented for 9 aspects rated on a scale of 1 (not concerned) to 10 (very concerned) | |
| DailyTIL.TILDate | 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 | Calculated over a 24-hour period | |
| DailyTIL.TILDopamineDose | Calculated over a 24-hour period | |
| DailyTIL.TILFactorsCaloricIntakeEnteralKcal | ||
| DailyTIL.TILFactorsCaloricIntakeParenKcal | ||
| DailyTIL.TILFactorsCaloricIntakeRouteEnteral | Enteral route | |
| DailyTIL.TILFactorsCaloricIntakeRouteParen | Parenteral | 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 | ||
| DailyTIL.TILFactorsCoagHemoglobAfterOtherUnitSpecify | 1 == mmol/L 99 == Other |
|
| DailyTIL.TILFactorsCoagHemoglobBeforeOtherUnitAmt | ||
| DailyTIL.TILFactorsCoagHemoglobBeforeOtherUnitSpecify | 1 == mmol/L 99 == Other |
|
| DailyTIL.TILFactorsCoagulation | 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 | ||
| DailyTIL.TILFactorsCoagulationHemoglobinAfterNotDone | 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 | ||
| DailyTIL.TILFactorsCoagulationHemoglobinBeforeNotDone | 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 == 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 |
|
| DailyTIL.TILFactorsCoagulationType2 | 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 |
|
| DailyTIL.TILFactorsCoagulationType3 | 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 |
|
| DailyTIL.TILFactorsCoagulationType4 | 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 |
|
| DailyTIL.TILFactorsCoagulationVolume1 | ||
| DailyTIL.TILFactorsCoagulationVolume2 | ||
| DailyTIL.TILFactorsCoagulationVolume3 | ||
| DailyTIL.TILFactorsCoagulationVolume4 | ||
| DailyTIL.TILFactorsGenSuppCareDone | 0 == No 1 == Yes |
|
| DailyTIL.TILFactorsGlucoseManagement | 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]) |
|
| DailyTIL.TILFever | 0 == No 1 == Yes |
|
| DailyTIL.TILFeverHypothermia | 0 == No 1 == Yes |
|
| DailyTIL.TILFeverMildHypothermia | 0 == No 1 == Yes |
|
| DailyTIL.TILFluidBalanceNotDone | ||
| DailyTIL.TILFluidCalcStartDate | ||
| DailyTIL.TILFluidCalcStartTime | ||
| DailyTIL.TILFluidCalcStopDate | ||
| DailyTIL.TILFluidCalcStopTime | ||
| DailyTIL.TILFluidColloids | 0 == No 1 == Yes 88 == Unknown |
|
| DailyTIL.TILFluidColloidsTotalVolume | ||
| DailyTIL.TILFluidColloidsType | 1 == Albumin 5% 2 == Albumin 20% 3 == Dextran 4 == Gelatin (e.g. gelofusion) 5 == HES (hydroxyethyl starches) 6 == Tetrastarches (e.g. HES 130/04) |
|
| DailyTIL.TILFluidIn | Recorded preferably over 24-hour period, exact details to be derived from start and stop date/time for calculation | |
| DailyTIL.TILFluidLoading | 0 == No 1 == Yes |
|
| DailyTIL.TILFluidLoadingVasopressor | 0 == No 1 == Yes |
|
| DailyTIL.TILFluidOutCSFDrain | ||
| DailyTIL.TILFluidOutGastric | ||
| DailyTIL.TILFluidOutOther | ||
| DailyTIL.TILFluidOutUrine | ||
| DailyTIL.TILFluidsRenalReplacement | 0 == No 1 == Yes |
|
| DailyTIL.TILHyperosmolarThearpy | 0 == No 1 == Yes |
|
| DailyTIL.TILHyperosomolarTherapyHigher | 0 == No 1 == Yes |
|
| DailyTIL.TILHyperosomolarTherapyHypertonicLow | 0 == No 1 == Yes |
|
| DailyTIL.TILHyperosomolarTherapyMannitolGreater2g | 0 == No 1 == Yes |
|
| DailyTIL.TILHypertonicSalineDose | Calculated over a 24-hour period | |
| DailyTIL.TILHyperventilation | 0 == No 1 == Yes |
|
| DailyTIL.TILHyperventilationIntensive | 0 == No 1 == Yes |
|
| DailyTIL.TILHyperventilationModerate | 0 == No 1 == Yes |
|
| DailyTIL.TILICPSurgery | 0 == No 1 == Yes |
|
| DailyTIL.TILICPSurgeryDecomCranectomy | 0 == No 1 == Yes |
|
| DailyTIL.TILMannitolDose | Calculated over a 24-hour period | |
| DailyTIL.TILNoradrenalineDose | Calculated over a 24-hour period | |
| DailyTIL.TILOtherDose | ||
| DailyTIL.TILOtherTxt | ||
| DailyTIL.TILOtherVaso | 0 == No 1 == Yes |
|
| DailyTIL.TILPhenylephrineDose | Calculated over a 24-hour period | |
| DailyTIL.TILPhysicianConcernsContusionpregression | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianConcernsCPP | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianConcernsEpilepsy | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianConcernsFocalSwelling | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianConcernsHematomaProgression | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianConcernsHypoperfusion | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianConcernsICP | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianConcernsIntracranialInfection | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianConcernsVasospasm | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| DailyTIL.TILPhysicianOverallSatisfaction | 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 | 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 | 1 == Not at all 2 == Slightly 3 == Moderate 4 == Quite 5 == Very 77 == N/A (no ICP monitoring) |
Documents physician satisfaction with ICP control |
| DailyTIL.TILPosition | 0 == No 1 == Yes |
|
| DailyTIL.TILPositionNursedFlat | 0 == No 1 == Yes |
|
| DailyTIL.TILReasonForChange | 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) |
|
| DailyTIL.TILSedation | 0 == No 1 == Yes |
|
| DailyTIL.TILSedationHigher | 0 == No 1 == Yes |
|
| DailyTIL.TILSedationMetabolic | 0 == No 1 == Yes |
|
| DailyTIL.TILSedationNeuromuscular | 0 == No 1 == Yes |
|
| DailyTIL.TILSedationScaleUsed | 0 == No 1 == Yes 77 == N/A |
|
| DailyTIL.TILSedativesInterrupted | 0 == No 1 == Yes 77 == N/A |
|
| DailyTIL.TILTherapyIntensityNotDone | ||
| DailyTIL.TILTime | ||
| DailyTIL.TotalTIL | 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 | 1 == No angulation (volume scan) 2 == Orbital-meatal line 99 == Other |
|
| FollowUp.CTAtrophy | 0 == No D == Diffuse F == Focal 88 == Unknown |
Scored by investigator |
| FollowUp.CTHydrocephalus | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator |
| FollowUp.CTManuf | AGFA == Agfa CARE == Carestream GE == GE HITA == Hitachi KONI == Konica Minolta PHIL == Philips SIEM == Siemens TOSH == Toshiba 99 == Other |
Manufacturer of the CT scanner used |
| FollowUp.CTMidlineShift | 0 == No 1 == Yes |
Scored by investigator |
| FollowUp.CTMidlineShiftMeasure | Scored by investigator | |
| FollowUp.CTMRIDate | Imaging date captured in the CRF for followup images | |
| FollowUp.CTMRITime | Imaging time captured in CRF for followup images | |
| FollowUp.CTReason | RFU == Routine follow-up LOP == Absence of or slow improvement CD == Clinical deterioration |
Reason for follow up CT could be: Clinical deterioration, Absence of or slow improvement, Routine followĀup |
| FollowUp.CTScannerType | 16 == 16-slice 32 == 32-slice 64 == 64-slice 99 == Other 128 == 128-slice 256 == 256-slice 320 == 320-slice |
Type of scanner used for follow up CT |
| FollowUp.CTSubduralHaematomaHygroma | 0 == No R == Right L == Left B == Bilateral 88 == Unknown |
Scored by investigator |
| FollowUp.CTType | NCCT == Non-contrast CT CCT == Contrast CT CTA == CT Angiography PCT == Perfusion CT |
Type of CT scan for followup imaging |
| FollowUp.FUAttendance | 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 | 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 | 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 | 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 | 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 | 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 | 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 | CT == CT MRI == MRI XRay == X-Ray Angiography |
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 | 0 == No 1 == Yes 88 == Unknown |
|
| FollowUp.FUIntracranialSurgDate | ||
| FollowUp.FUIntracranialSurgOther | ||
| FollowUp.FUIntracranialSurgSpecifyType | 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 | ||
| FollowUp.FUMartlPartnerStatus | 1 == Never been married 2 == Married 3 == Living together/common law 4 == Divorced 5 == Separated 6 == Widowed 88 == Unknown 99 == Other |
Only recorded if change in SES; This variable needs to be related to the pre-injury situation: Subject.MartlPartnerStatus |
| FollowUp.FUMedAmantidine | ||
| FollowUp.FUMedAmantidineReason | 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 |
|
| FollowUp.FUMedAntibiotics | ||
| FollowUp.FUMedAntibioticsReason | 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 |
|
| FollowUp.FUMedAntiConv | ||
| FollowUp.FUMedAntiConvReason | 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 |
|
| FollowUp.FUMedAntidep | ||
| FollowUp.FUMedAntidepReason | 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 |
|
| FollowUp.FUMedAntipsycho | ||
| FollowUp.FUMedAntipsychoReason | 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 |
|
| FollowUp.FUMedAnxiolytics | ||
| FollowUp.FUMedAnxiolyticsReason | 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 |
|
| FollowUp.FUMedCholinergic | ||
| FollowUp.FUMedCholinergicReason | 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 |
|
| FollowUp.FUMedClonidine | ||
| FollowUp.FUMedClonidineReason | 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 |
|
| FollowUp.FUMedComplAutonomicInstability | 0 == No 1 == Yes 88 == Unknown |
|
| FollowUp.FUMedComplAutonomicInstabilityTreatment | BPUMP == Baclofen pump DRUGS == Drugs |
|
| FollowUp.FUMedComplDVT | 0 == No 1 == Yes 88 == Unknown |
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 alsewhere: Hospital.HospComplDVT |
| FollowUp.FUMedComplHeteroOss | 0 == No 1 == Yes 88 == Unknown |
|
| FollowUp.FUMedComplHeteroOssTreatment | PLAN == Planned PERF == Performed |
|
| FollowUp.FUMedComplPressureSores | 0 == No 1 == Yes 88 == Unknown |
|
| FollowUp.FUMedComplPulmonaryEmbolus | 0 == No 1 == Yes 88 == Unknown |
Intent is to record here only Pulmonary embolism (PE) occurring post-discharge. PE that occurred before/at presentation or during hospital stay is recorded alsewhere: Hospital.HospComplPumlEmb |
| FollowUp.FUMedComplSeizurePostDischarge | 0 == No 1 == Yes 88 == Unknown |
Intent is to record here only seizures occurring post-discharge.seizures that occurred before/at presentation or during hospital stay are recorded alsewhere: InjuryHx.EDComplEventSeizures; Vitals.HosComplEventSeizures; Hospital.HospComplSeizures; Vitals.HosComplEventSeizures; Hospital.ICUDisComplSeizure; Outcomes.GOSEEpilepsyFits; Subjective reporting also in: Outcomes.PartQuestACurHltSeiz |
| FollowUp.FUMedComplSpasticity | 0 == No 1 == Yes 88 == Unknown |
|
| FollowUp.FUMedComplSpasticityTreatment | PHYS == Physiotherapy IBAC == Intrathecal baclofen pump OBAC == Oral baclofen BENZ == Benzodiazepines |
|
| FollowUp.FUMedication | 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 | ||
| FollowUp.FUMedNarcReason | 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 |
|
| FollowUp.FUMedOther | ||
| FollowUp.FUMedOtherPain | ||
| FollowUp.FUMedOtherPainReason | 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 |
|
| FollowUp.FUMedOtherReason | 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 |
|
| FollowUp.FUMedOtherText | ||
| FollowUp.FUMedPsycho | ||
| FollowUp.FUMedPsychoReason | 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 |
|
| FollowUp.FUMedSteroids | ||
| FollowUp.FUMedSteroidsReason | 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 |
|
| FollowUp.FUPrincipalDeathCause | 1 == Head injury/initial injury 2 == Head injury/secondary intracranial damage 3 == Systemic trauma 4 == Medical complications 88 == Unknown 99 == Other |
|
| FollowUp.FUPrincipalDeathCauseOther | ||
| FollowUp.FUPtStillInICU | This variable reflects if the patient was still in ICU at the time of a scheduled follow up visit. | |
| FollowUp.FUReasonNoAttendance | 1 == Not contactable 2 == Forgotten 3 == Refused 99 == Other |
Documents reason if subject did not undergo assessment |
| FollowUp.FURehabGenLongTermAcuteCUInPat | ||
| FollowUp.FURehabGenRehabUnitInPat | ||
| FollowUp.FURehabGeriatricRehabUnitInPat | ||
| FollowUp.FURehabInPat | Documents that patient received in-patient rehab care at the time of this assessment. | |
| FollowUp.FURehabInPatAdmisDate | ||
| FollowUp.FURehabInPatDischDate | ||
| FollowUp.FURehabInPatOngoingRehab | 0 == No 1 == Yes |
|
| FollowUp.FURehabInPatShortTermInterrup1EndDate | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup1StartDate | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup2EndDate | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup2StartDate | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup3EndDate | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabInPatShortTermInterrup3StartDate | Only applicable in case the inpatient rehab was interrupted for specific reasons | |
| FollowUp.FURehabNo | Documents that patient received no rehab at the time of this assessment. | |
| FollowUp.FURehabOutPat | Documents that patient received out-patient rehab care at the time of this assessment. | |
| FollowUp.FURehabOutPatAdmisDate | ||
| FollowUp.FURehabOutPatTherpyCog | ||
| FollowUp.FURehabOutPatTherpyCogFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyCompDayTreatmnt | ||
| FollowUp.FURehabOutPatTherpyCompDayTreatmntFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyHomeHealth | ||
| FollowUp.FURehabOutPatTherpyHomeHealthFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyIndLivngTrainng | ||
| FollowUp.FURehabOutPatTherpyIndLivngTrainngFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyNursServ | ||
| FollowUp.FURehabOutPatTherpyNursServFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyOcc | ||
| FollowUp.FURehabOutPatTherpyOccFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyOther | ||
| FollowUp.FURehabOutPatTherpyOtherFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyOtherText | ||
| FollowUp.FURehabOutPatTherpyPeerMentor | ||
| FollowUp.FURehabOutPatTherpyPeerMentorFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyPhysicianInvolved | 0 == No 1 == Yes 88 == Unknown |
|
| FollowUp.FURehabOutPatTherpyPsychSer | ||
| FollowUp.FURehabOutPatTherpyPsychSerFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyPT | ||
| FollowUp.FURehabOutPatTherpyPTFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyRec | ||
| FollowUp.FURehabOutPatTherpyRecFreq | 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 |
|
| FollowUp.FURehabOutPatTherpySocWrkCaseMgmt | ||
| FollowUp.FURehabOutPatTherpySocWrkCaseMgmtFreq | 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 |
|
| FollowUp.FURehabOutPatTherpySpeech | ||
| FollowUp.FURehabOutPatTherpySpeechFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyStructure | 1 == Mono-disciplinary (little/nocollaboration between care providers 2 == Multi-disciplinary |
|
| FollowUp.FURehabOutPatTherpyUnknown | ||
| FollowUp.FURehabOutPatTherpyUnknownFreq | 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 |
|
| FollowUp.FURehabOutPatTherpyVocServ | ||
| FollowUp.FURehabOutPatTherpyVocServFreq | 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 |
|
| FollowUp.FURehabTBIRehabUnitInPat | ||
| FollowUp.FURehabTherpyEndDate | ||
| FollowUp.FURehabTherpyOngoingInd | 0 == No 1 == Yes |
|
| FollowUp.FURehabUnknown | ||
| FollowUp.FUResdncType | 1 == Living at home independently 2 == Living at home supported by family/carers 6 == Living in a long-stay patient ward(hospital) 7 == Rehabilitation centre 10 == Living in nursing home 11 == Living in shelteed + housing/community care 99 == Other |
Only recorded if change in SES |
| FollowUp.FUResdncTypeOther | Only recorded if change in SES | |
| FollowUp.FURtrnToOtherAct | 0 == No 1 == Full return to previous level 2 == Reduced level 88 == Unknown |
|
| FollowUp.FURtrnWrkSchlStatus | NA == N/A 1 == Returned to previous job / school at same level and hours 2 == Unable to work / go to school 5 == Looking for work / go to school 7 == Retired 8 == Returned to previous job / school at increased levels or hours from pre-injury 9 == Returned to previous job / school at reduced level or hours 10 == Change of job / different work or school 11 == Special employment / sheltered employment 88 == Unknown |
|
| FollowUp.FUSESChange | 0 == No 1 == Yes 88 == Unknown |
This variable aims to document any change in socio-economic status following the TBI |
| FollowUp.FUSESPeopleLivingWith | Only recorded if change in SES | |
| FollowUp.FUSESPrimAdultAlone | Only recorded if change in SES; These variables need to be related to the pre-injury situation. | |
| FollowUp.FUSESPrimAdultCarerUnrelated | Only recorded if change in SES | |
| FollowUp.FUSESPrimAdultChildren | Only recorded if change in SES | |
| FollowUp.FUSESPrimAdultOther | Only recorded if change in SES | |
| FollowUp.FUSESPrimAdultParents | Only recorded if change in SES | |
| FollowUp.FUSESPrimAdultSiblings | Only recorded if change in SES | |
| FollowUp.FUSESPrimAdultSignOther | Only recorded if change in SES | |
| FollowUp.FUSESPrimAdultSpousePartner | Only recorded if change in SES | |
| FollowUp.FUSESPrimAdultUnknown | Only recorded if change in SES | |
| FollowUp.FUSurgCranioplastyPerformed | 0 == No 1 == Yes 2 == No, but scheduled |
Only applicable in case a decompressive craniectomy was performed during the in-hospital period |
| FollowUp.FUSurgExtracranialSurg | 0 == No 1 == Yes 88 == Unknown |
|
| FollowUp.FUSurgExtracranialSurgDate | ||
| FollowUp.FUSurgExtracranialSurgSpecify | ||
| FollowUp.FUSurgExtracranialSurgTime | ||
| FollowUp.FUVisitDate | ||
| FollowUp.FUVisitTime | ||
| FollowUp.FUVisitType | SCHED == Scheduled study follow-up UNSCHED == Unscheduled 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 | 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 | Identifier generated for an imaging experiment when images are uploaded from site It's recommended to use: Imaging.CRFIcometrixImageId | |
| FollowUp.IcometrixPassedQA | 0 == No 1 == Yes |
|
| FollowUp.IcometrixQADateTime | Date and time when central QA was done for followup images | |
| FollowUp.IcometrixUploadDateTime | ||
| FollowUp.InitialDataIcometrix | ||
| FollowUp.MRIManuf | SIEM == Siemens PHIL == Philips GE == GE TOSH == Toshiba 99 == Other |
This variable reflects the manufacturer of the MRI scanner used. |
| FollowUp.MRIReason | CR == Clinical routine ISC == Ischemia SBL == Suspicious brainstem lesions LOP == Lack of improvement CD == Clinical deterioration SP == Study protocol 88 == Unknown 99 == Other |
|
| FollowUp.MRIReasonOther | ||
| FollowUp.MRIResultPreExistAbnorm | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator |
| FollowUp.MRIResultTraumaticAbnorm | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator |
| FollowUp.MRIScannerStrength | ||
| FollowUp.MRISequences | T1 == T1 T2 == T2 DWI == DWI FLAIR == FLAIR GRE == GRE DTI == DTI SWI == SWI MRSI == MRSI PWI == PWI 99 == Other |
|
| FollowUp.MRITraumAbnormASDH | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator |
| FollowUp.MRITraumAbnormContusion | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator |
| FollowUp.MRITraumAbnormDAI | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator |
| FollowUp.MRITraumAbnormDAILesionLocBrainstem | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator; only applicable if DAI scored "yes" |
| FollowUp.MRITraumAbnormDAILesionLocCorpusCallosum | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator; only applicable if DAI scored "yes" |
| FollowUp.MRITraumAbnormDAILesionLocDiffuseWhiteMatter | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator; only applicable if DAI scored "yes" |
| FollowUp.MRITraumAbnormDAINumLesions | 1 == 1 2 == 2 3 == 3 4 == 4 5 == >= 5 |
Scored by investigator; only applicable if DAI scored "yes" |
| FollowUp.MRITraumAbnormEDH | 0 == No 1 == Yes 88 == Unknown |
Scored by investigator |
| FollowUp.MRIType | MRI == MRI MRA == MRA |
Type of MRI for followup imaging |
| FollowUp.TimePoint | 2wk == 2 weeks 3mo == 3 months 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. |
| Hospital.AdditionalStudiesCoag | 0 == No 1 == Yes |
Intended to provide a definitive documentation if the patient was enrolled in the MR substudy or not. Would need to verify if MR data are indeed available for this patients. |
| Hospital.AdditionalStudiesECoG | 0 == No 1 == Yes |
|
| Hospital.AdditionalStudiesEEG | 0 == No 1 == Yes |
|
| Hospital.AdditionalStudiesTEGRotem | 0 == No 1 == Yes |
Intended to provide a definitive documentation if the patient was enrolled in the MR substudy or not. Would need to verify if MR data are indeed available for this patients. |
| Hospital.BrainDeathDate | ||
| Hospital.BrainDeathTime | ||
| Hospital.ComplCRBSIDateDiagnosis | ||
| Hospital.DeadAge | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.DeadCoMorbidities | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.DeadDeterminationOfBrainDeath | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.DeadOrganDonation | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.DeadPatWill | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.DeadRequestRelatives | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.DeadSeverityofTBI | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.DeathAutopsy | 0 == No 1 == Yes, forensic 2 == Yes, clinical 88 == Unknown |
|
| Hospital.DeathCause | 1 == Head injury/initial injury 2 == Head injury/secondary intracranial damage 3 == Systemic trauma 4 == Medical complications 99 == Other |
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.DeathCauseOther | ||
| Hospital.DischargeStatus | 0 == Dead 1 == Alive 88 == Unknown |
Assessment by investigator |
| Hospital.DispHosp | 1 == Other hospital 2 == Rehab unit 3 == Nursing home 5 == Home 88 == Unknown 99 == Other |
Documents destination upon hospital discharge |
| Hospital.DispHospOther | ||
| Hospital.GCSHospDischargeEyes | UN == Unknown S == Untestable (swollen) O == Untestable (other) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously |
|
| Hospital.GCSHospDischargeMotor | UN == Unknown O == Untestable (Other) P == Untestable (Deep sedation/paralyzed) 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 |
|
| Hospital.GCSHospDischargeScore | ||
| Hospital.GCSHospDischargeVerbal | UN == Unknown T == Untestable (tracheotomy/endotracheal tube) O == Untestable (Other) 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
|
| Hospital.HospComplCardio | 0 == No 1 == Yes |
|
| Hospital.HospComplCRBSI | 0 == No 1 == Yes |
CRBSI: catheter related blood stream infection |
| Hospital.HospComplDelayedHaema | 0 == No 1 == Yes |
|
| Hospital.HospComplDVT | 0 == No 1 == Yes |
DVT: deep venous thrombosis |
| Hospital.HospComplIntraCranOther | 0 == No 1 == Yes |
|
| Hospital.HospComplIntraCranOtherTxt | ||
| Hospital.HospComplMeningitis | 0 == No 1 == Yes |
|
| Hospital.HospComplMetabolic | 0 == No 1 == Yes |
|
| Hospital.HospComplPressureSore | 0 == No 1 == Yes |
|
| Hospital.HospComplPumlEmb | 0 == No 1 == Yes |
|
| Hospital.HospComplRasiedICP | 0 == No 1 == Yes |
|
| Hospital.HospComplResp | 0 == No 1 == Yes |
|
| Hospital.HospComplSeizures | 0 == No 1 == Yes |
|
| Hospital.HospComplSystemOther | 0 == No 1 == Yes |
|
| Hospital.HospComplSystemOtherTxt | ||
| Hospital.HospComplUTI | 0 == No 1 == Yes |
|
| Hospital.HospDischargeBodyWeightkg | ||
| Hospital.HospDischargeBodyWeightlbs | ||
| Hospital.HospDischargeBodyWeightMeasure | 1 == Estimated 2 == Measured |
|
| Hospital.HospDischargeBodyWeightUnit | 1 == kgs 2 == lbs |
|
| Hospital.HospDischargeCTProgression | 0 == No 1 == Yes |
|
| Hospital.HospDischargeCTProgressionYes | 1 == Increase in initial lesion 2 == Development of new lesion |
|
| Hospital.HospDischargeNumberCT | 0 == No 1 == Yes |
|
| Hospital.HospDischargeReason | 0 == No institutional care necessary 1 == No institutional care in trauma center necessary 2 == Clinical rehab required but not approved 3 == Waiting list for rehab 4 == Clinical rehab required and approved 5 == No benefit of clinical rehab anticipated 99 == Other |
WHY question: documents reason for choice of discharge destination;WHY question: documents reason for choice of hospital discharge destination. |
| Hospital.HospDischargeReasonOther | ||
| Hospital.HospDischargeTimeToObeyCommands | ||
| Hospital.HospDischargeTimeToObeyCommandsNotApplic | 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 | 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 | 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 | 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 | Intended to designate patients who are still in PTA at the moment of discharge of hospital | |
| Hospital.HospDischTime | 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 | 0 == No 1 == Yes |
|
| Hospital.ICDCode1 | 16 fields available to enter diagnosis as recorded by hospital administration according to ICD codes; applicable to patients admitted/discharged from hospital. | |
| Hospital.ICDCode10 | ||
| Hospital.ICDCode11 | ||
| Hospital.ICDCode12 | ||
| Hospital.ICDCode13 | ||
| Hospital.ICDCode14 | ||
| Hospital.ICDCode15 | ||
| Hospital.ICDCode16 | ||
| Hospital.ICDCode2 | For patients discharged directly from the ER, ICD codes are documented in: InjuryHx.ERDestICDCodes1 | |
| Hospital.ICDCode3 | ||
| Hospital.ICDCode4 | ||
| Hospital.ICDCode5 | ||
| Hospital.ICDCode6 | ||
| Hospital.ICDCode7 | ||
| Hospital.ICDCode8 | ||
| Hospital.ICDCode9 | ||
| Hospital.ICDCodeVersion | 9 == ICD-9 10 == ICD-10 |
|
| Hospital.ICPDevice | 1 == Ventricular 2 == Ventricular +inbuilt sensor 3 == Parenchymal 99 == Other |
Type of ICP monitoring device used. |
| Hospital.ICPDeviceOther | 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 | ||
| Hospital.ICPInsTime | ||
| Hospital.ICPMonitorNo | Indicates if a patient does not have intracranial pressure (ICP) monitoring. If Hospital.ICPMonitorNo=1, see Hospital.ICUReasonNoICP. | |
| Hospital.ICPMonitorStop | 0 == No 1 == Yes |
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.ICPMonitorStopReason. |
| Hospital.ICPMonitorStopReasonOther | ||
| Hospital.ICPMonitorYes | 0 == No 1 == Yes |
Indicates if a patient has intracranial pressure (ICP) monitoring. If yes, see Hospital.ICUReasonICP and Hospital.ICPDevice. |
| Hospital.ICPMontDuration | The duration of ICP monitoring. Calculated variable: Hospital.ICPRemDateTime-Hospital.ICPInsDateTime. | |
| Hospital.ICPRemDate | Date for stopping ICP monitoring. | |
| Hospital.ICPRemTime | Time of stopping ICP monitoring. | |
| Hospital.ICPStopReason | 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 | 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 | 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 | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.ICUAdmisStatusIntubated | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.ICUAdmisStatusMechVent | 0 == No 1 == Yes 88 == Unknown |
|
| Hospital.ICUAdmReason | 1 == Mechanical ventilation 2 == Frequent neurological observations 3 == Haemodynamic invasive monitoring 4 == Extracranial injuries 5 == Neurological operation 6 == Clinical deterioration 99 == Other |
|
| Hospital.ICUAdmReasonOther | ||
| Hospital.ICUAdmTime | ||
| Hospital.ICUCardiacOutput | 0 == No 1 == Yes |
|
| Hospital.ICUCatheterICP | 0 == No 1 == Yes |
|
| Hospital.ICUCatheterICPDate | ||
| Hospital.ICUCatheterICPTime | ||
| Hospital.ICUCentralVenousPress | 0 == No 1 == Yes |
|
| Hospital.ICUComplUTI | 0 == No 1 == Yes |
|
| Hospital.ICUDisAdditionalStudiesCoag | 0 == No 1 == Yes |
|
| Hospital.ICUDisAdditionalStudiesTEGRotem | 0 == No 1 == Yes |
|
| Hospital.ICUDischargeICDCode1 | 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 fuurther captured at ER discharge and at hospital discharge. | |
| Hospital.ICUDischargeICDCode10 | ||
| Hospital.ICUDischargeICDCode11 | ||
| Hospital.ICUDischargeICDCode12 | ||
| Hospital.ICUDischargeICDCode13 | ||
| Hospital.ICUDischargeICDCode14 | ||
| Hospital.ICUDischargeICDCode15 | ||
| Hospital.ICUDischargeICDCode16 | ||
| Hospital.ICUDischargeICDCode2 | ||
| Hospital.ICUDischargeICDCode3 | ||
| Hospital.ICUDischargeICDCode4 | ||
| Hospital.ICUDischargeICDCode5 | ||
| Hospital.ICUDischargeICDCode6 | ||
| Hospital.ICUDischargeICDCode7 | ||
| Hospital.ICUDischargeICDCode8 | ||
| Hospital.ICUDischargeICDCode9 | ||
| Hospital.ICUDischargeICDCodeVersion | 9 == 9 10 == 10 |
|
| Hospital.ICUDischargeStatus | 1 == Alive 2 == Dead 88 == Unknown |
Documents data on discharge from ICU |
| Hospital.ICUDischargeTo | 1 == General ward 2 == Other ICU 3 == Other hospital 4 == Rehab unit 5 == Home 6 == Nursing home 7 == Step down/high care unit 88 == Unknown 99 == Other |
Documents data on discharge from ICU |
| Hospital.ICUDischargeToOther | ||
| Hospital.ICUDischDate | ||
| Hospital.ICUDischPTADays | ||
| Hospital.ICUDischPTADaysNA | ||
| Hospital.ICUDischPTAOngoing | ||
| Hospital.ICUDischTime | ||
| Hospital.ICUDisComplCardiacArrest | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplCRBSI | 0 == No 1 == Yes |
CRBSI: catheter-related bloodstream infection |
| Hospital.ICUDisComplDVT | 0 == No 1 == Yes |
DVT: Deep venous thrombosis |
| Hospital.ICUDisComplIntraCranOther | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplIntraCranOtherTxt | ||
| Hospital.ICUDisComplMeningitis | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplMetabolic | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplPE | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplPressureSores | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplRaisedICP | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplRespiratoryFailure | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplSeizure | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplSeromaHematoma | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplSystemOther | 0 == No 1 == Yes |
|
| Hospital.ICUDisComplSystemOtherTxt | ||
| Hospital.ICUDisComplVAP | 0 == No 1 == Yes |
VAP: Ventilator associated pneumonia |
| Hospital.ICUDisCTProg | 0 == No 1 == Yes |
|
| Hospital.ICUDisCTProgYes | 1 == Increase in initial lesion 2 == Development of new lesion |
|
| Hospital.ICUDishDurVent | ||
| Hospital.ICUDishDurVentNA | ||
| Hospital.ICUDisNeuroworseEpisode | 0 == No 1 == Yes |
|
| Hospital.ICUDisNososcomialPneumNum | ||
| Hospital.ICUDisNumCT | ||
| Hospital.ICUDisPatDeadAtICU | 0 == No 1 == Yes |
Intended as an introductory question for the following details on withdrawal of treatment, brain death and organ donation |
| Hospital.ICUDisPneumAntibiotic1StartDate | ||
| Hospital.ICUDisPneumAntibiotic2StartDate | ||
| Hospital.ICUDisPneumAntibiotic3StartDate | ||
| Hospital.ICUDisPneumAntibiotic4StartDate | ||
| Hospital.ICUDisPneumAntibioticTreat | 0 == No 1 == Yes |
|
| Hospital.ICUDisPneumBacteriaSmpl | 1 == BAL 2 == Tracheal suction 3 == PDP 4 == Brush |
|
| Hospital.ICUDisPneumBloodFiO2pc | ||
| Hospital.ICUDisPneumBloodPaCO2mmHg | ||
| Hospital.ICUDisPneumBloodPaO2mmHg | ||
| Hospital.ICUDisPneumBloodPEPcmH2O | ||
| Hospital.ICUDisPneumBloodPF | ||
| Hospital.ICUDisPneumChestX | 1 == New pneumonia 2 == Modification of an old one 3 == No infiltrate 4 == Diffuse (or patchy) infiltrate 5 == Localized infiltrate |
|
| Hospital.ICUDisPneumClinical | 1 == Fever >=38degC or hypothermia <=36degC 2 == Purulent trachea aspirations 3 == Leukocytes >=12000/ml or <=4000/ml |
|
| Hospital.ICUDisPneumDate | The variables on ventilator associated pneumonia concern a substudy initiated by Luciana Mascia for the PROLABI study | |
| Hospital.ICUDisPneumPathogen1 | ||
| Hospital.ICUDisPneumPathogen1QuantUCFml | ||
| Hospital.ICUDisPneumPathogen2 | ||
| Hospital.ICUDisPneumPathogen2QuantUCFml | ||
| Hospital.ICUDisPneumPathogen3 | ||
| Hospital.ICUDisPneumPathogen3QuantUCFml | ||
| Hospital.ICUDisPneumPathogen4 | ||
| Hospital.ICUDisPneumPathogen4QuantUCFml | ||
| Hospital.ICUDisPneumSepsis | 0 == No 1 == Yes |
|
| Hospital.ICUDisSixMonthOutcomeDate | ||
| Hospital.ICUDisSixMonthOutcomeGOS | GR == Good Recovery MD == Moderate Disability SD == Severe Disability V == Vegetative state D == Death |
This variable aims to collect information of the anticipated outcome of this patient as determined on discharge from the ICU by the treating physician. Documents the level of experience of physician who provided prognostic estimate on discharge from ICU. |
| Hospital.ICUDisSixMonthOutcomeQualification | 1 == Resident 2 == Junior staff (< 5 years) 3 == Senior staff ( >5 years) 4 == Head of department |
Documents the level of experience of physician who provided prognostic estimate on discharge from ICU |
| Hospital.ICUDisSixMonthOutcomeType | 1 == ER physician 2 == Intensive care physician 3 == Neurology 4 == Neurosurgery 5 == Traumatology 88 == Unknown 99 == Other |
Documents the specialty of physician who provided prognostic estimate on discharge from ICU |
| Hospital.ICUDisSixMonthOutcomeUnfavourable | ||
| Hospital.ICUDisSupportWithdrawnDate | This variable documents date and time at which life prolonging therapy was withdrawn | |
| Hospital.ICUDisSupportWithdrawnTime | ||
| Hospital.ICUDisTimeToObeyCommands | ||
| Hospital.ICUDisTimeToObeyCommandsNA | ||
| Hospital.ICUDisWithdrawalTreatmentDecisionDate | Investigators were requested to record the date and time of "a do not resuscitate (DNR)" policy | |
| Hospital.ICUDisWithdrawalTreatmentDecisionTime | ||
| Hospital.ICUDisWithdrawlTreatmentDecision | 1 == Multi disciplinary 2 == By a single physician 3 == With relatives |
|
| Hospital.ICUEndTidalCO2 | 0 == No 1 == Yes |
|
| Hospital.ICUGCSDischargeEyes | O == Untestable (other) S == Untestable (swollen) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously 88 == Unknown |
|
| Hospital.ICUGCSDischargeMotor | UN == Unknown P == Untestable (Deep sedation/paralyzed) O == Untestable (Other) 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 |
|
| Hospital.ICUGCSDischargeScore | ||
| Hospital.ICUGCSDischargeVerbal | UN == Unknown O == Untestable (Other) P == Untestable (tracheotomy/endotracheal tube) T == Untestable (tracheotomy/endotracheal tube) 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
|
| Hospital.ICUInvasiveBP | 0 == No 1 == Yes |
|
| Hospital.ICUProblemsICP | 0 == No 1 == Yes |
|
| Hospital.ICUProblemsICPYes | 1 == Accidental catheter removal 2 == Catheter obstruction/failure 3 == Suspicion of inaccurate measurement |
|
| Hospital.ICUPulseOximetry | 0 == No 1 == Yes |
|
| Hospital.ICURaisedICP | 0 == No 1 == Yes, controlled 2 == Yes, refractory |
|
| Hospital.ICUReasonForTypeICPMont | 1 == Routine in our department 2 == Not routine, but enlarged ventricles 3 == No parenchymal device available 99 == Other |
WHY Question: reason for choosing ventricular monitor |
| Hospital.ICUReasonForTypeICPMontPare | 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 |
WHY Question: reason for choosing parenchymal monitor |
| Hospital.ICUReasonForTypeICUMontOther | ||
| Hospital.ICUReasonForTypeICUMontParOther | ||
| Hospital.ICUReasonICP | 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 |
WHY Question: documents reason for monitoring ICP in patient admitted to ICU |
| Hospital.ICUReasonICPOther | 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 | 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 |
WHY Question: documents reason for not monitoring ICP in patient admitted to ICU |
| Hospital.ICUReasonNoICPOther | 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 | 0 == No 1 == Yes |
|
| Hospital.MonContEGGDuration | ||
| Hospital.MonECoG | 0 == No 1 == Yes |
|
| Hospital.MonECoGDuration | ||
| Hospital.MonJugularDesatEpisodes | 0 == No 1 == Yes 77 == N/A |
|
| Hospital.MonJugularSatDuration | ||
| Hospital.MonJugularSatStopReason | 1 == Monitor/catheter failure 2 == Patient considered unsalvageable 3 == Patient died 4 == Clinically no longer required |
|
| Hospital.MonJugularSatUsed | 0 == No 1 == Yes |
|
| Hospital.MonLicoxDuration | ||
| Hospital.MonLicoxPO2 | 0 == No 1 == Yes 77 == N/A |
|
| Hospital.MonLicoxStopReason | 1 == Monitor/catheter failure 2 == Patient considered unsalvageable 3 == Patient died 4 == Clinically no longer required |
|
| Hospital.MonLicoxUsed | 0 == No 1 == Yes |
|
| Hospital.MonMicrodialysisDuration | ||
| Hospital.MonMicrodialysisStopReason | 1 == Monitor/catheter failure 2 == Patient considered unsalvageable 3 == Patient died 4 == Clinically no longer required |
|
| Hospital.MonMicrodialysisUsed | 0 == No 1 == Yes |
|
| Hospital.MonTranscranDoppler | 0 == No 1 == Yes |
|
| Hospital.OrganDonationDate | ||
| Hospital.OrganDonationTime | ||
| Hospital.SixMonthOutcomeDate | ||
| Hospital.SixMonthOutcomeGOS | GR == Good Recovery MD == Moderate Disability SD == Severe Disability V == Vegetative state D == Death |
Documents the level of experience of physician who provided prognostic estimate on discharge from hospital |
| Hospital.SixMonthOutcomeQualification | 1 == Resident 2 == Junior staff (< 5 years) 3 == Senior staff ( >5 years) 4 == Head of department |
Documents the level of experience of physician who provided prognostic estimate on discharge from hospital |
| Hospital.SixMonthOutcomeType | 1 == ER physician 2 == Intensive care physician 3 == Neurology 4 == Neurosurgery 5 == Traumatology 88 == Unknown 99 == Other |
Documents the specialty of physician who provided prognostic estimate on discharge from hospital |
| Hospital.SixMonthOutcomeUnfavourable | ||
| Hospital.SupportWithdrawnDate | ||
| Hospital.SupportWithdrawnTime | ||
| Hospital.TimeSinceICUAdmisDeath | ||
| Hospital.WardAdmDate | 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 | 4 == Extracranial injuries 7 == CT abnormalities 8 == Clinical observation for TBI 9 == No ICU bed available 10 == Could be discharged home, but no adequate supervision 99 == Other |
WHY question: documents main reason for admission to ward (and not to ICU or discharge home) |
| Hospital.WardAdmReasonOther | 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 the ward | |
| Hospital.WithdrawalTreatmentDecision | 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 | ||
| Hospital.WithdrawalTreatmentDecisionTime | ||
| HourlyMeasurements.DaySinceInjury | Calculated from HourlyValues.HVDate and Subject.DateInj | |
| HourlyMeasurements.HVCPP | Normalized data for HVCPP2, HVCPP 4 etc. Calculated from MAP-ICP (HVSBP+2*HVDBP)/3-HVICP. | |
| HourlyMeasurements.HVDateTime | 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 into one variable, measured twice hourly. To get intended measurement time, see HourlyMeasurements.HVMeasurementDateTime. | |
| HourlyMeasurements.HVICP | All intracranial pressures combined into one variable, measured twice hourly. To get intended measurement time, see HourlyMeasurements.HVMeasurementDateTime. | |
| HourlyMeasurements.HVMeasurementDateTime | 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 into one variable, measured twice hourly. To get intended measurement time, see HourlyMeasurements.HVMeasurementDateTime. | |
| HourlyMeasurements.HVTIL | 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 | 0 == No 1 == Yes 2 == Doubtful |
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 | 0 == No 1 == Yes |
Answer to the question: "Was active ICP treatment discontinued (due to poor prognosis)?" |
| HourlyValues.HourlyValueLevelABP | 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 | A free text description of the level of ABP transducer if HourlyValues.HourlyValueLevelABP is "other". | |
| HourlyValues.HourlyValueLevelICP | 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 | Explanation in free text of the variable HourlyValues.HourlyValueAccurate. Associated with the date in HourlyValues.HVDate. | |
| HourlyValues.HVCPP10 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | The date the hourly values are measured. | |
| HourlyValues.HVDBP10 | The diastolic blood pressure associated with HourlyValues.HVDateTime10. | |
| HourlyValues.HVDBP12 | The diastolic blood pressure associated with HourlyValues.HVDateTime12. | |
| HourlyValues.HVDBP14 | The diastolic blood pressure associated with HourlyValues.HVDateTime14. | |
| HourlyValues.HVDBP16 | The diastolic blood pressure associated with HourlyValues.HVDateTime16. | |
| HourlyValues.HVDBP18 | The diastolic blood pressure associated with HourlyValues.HVDateTime18. | |
| HourlyValues.HVDBP2 | The diastolic blood pressure associated with HourlyValues.HVDateTime2. | |
| HourlyValues.HVDBP20 | The diastolic blood pressure associated with HourlyValues.HVDateTime20. | |
| HourlyValues.HVDBP22 | The diastolic blood pressure associated with HourlyValues.HVDateTime22. | |
| HourlyValues.HVDBP24 | The diastolic blood pressure associated with HourlyValues.HVDateTime24. | |
| HourlyValues.HVDBP4 | The diastolic blood pressure associated with HourlyValues.HVDateTime4. | |
| HourlyValues.HVDBP6 | The diastolic blood pressure associated with HourlyValues.HVDateTime6. | |
| HourlyValues.HVDBP8 | The diastolic blood pressure associated with HourlyValues.HVDateTime8. | |
| HourlyValues.HVICP10 | The intracranial pressure associated with HourlyValues.HVDateTime10. | |
| HourlyValues.HVICP12 | The intracranial pressure associated with HourlyValues.HVDateTime12. | |
| HourlyValues.HVICP14 | The intracranial pressure associated with HourlyValues.HVDateTime14. | |
| HourlyValues.HVICP16 | The intracranial pressure associated with HourlyValues.HVDateTime16. | |
| HourlyValues.HVICP18 | The intracranial pressure associated with HourlyValues.HVDateTime18. | |
| HourlyValues.HVICP2 | The intracranial pressure associated with HourlyValues.HVDateTime2. | |
| HourlyValues.HVICP20 | The intracranial pressure associated with HourlyValues.HVDateTime20. | |
| HourlyValues.HVICP22 | The intracranial pressure associated with HourlyValues.HVDateTime22. | |
| HourlyValues.HVICP24 | The intracranial pressure associated with HourlyValues.HVDateTime24. | |
| HourlyValues.HVICP4 | The intracranial pressure associated with HourlyValues.HVDateTime4. | |
| HourlyValues.HVICP6 | The intracranial pressure associated with HourlyValues.HVDateTime6. | |
| HourlyValues.HVICP8 | The intracranial pressure associated with HourlyValues.HVDateTime8. | |
| HourlyValues.HVSBP10 | The systolic blood pressure associated with HourlyValues.HVDateTime10. | |
| HourlyValues.HVSBP12 | The systolic blood pressure associated with HourlyValues.HVDateTime12. | |
| HourlyValues.HVSBP14 | The systolic blood pressure associated with HourlyValues.HVDateTime14. | |
| HourlyValues.HVSBP16 | The systolic blood pressure associated with HourlyValues.HVDateTime16. | |
| HourlyValues.HVSBP18 | The systolic blood pressure associated with HourlyValues.HVDateTime18. | |
| HourlyValues.HVSBP2 | The systolic blood pressure associated with HourlyValues.HVDateTime2. | |
| HourlyValues.HVSBP20 | The systolic blood pressure associated with HourlyValues.HVDateTime20. | |
| HourlyValues.HVSBP22 | The systolic blood pressure associated with HourlyValues.HVDateTime22. | |
| HourlyValues.HVSBP24 | The systolic blood pressure associated with HourlyValues.HVDateTime24. | |
| HourlyValues.HVSBP4 | The systolic blood pressure associated with HourlyValues.HVDateTime4. | |
| HourlyValues.HVSBP6 | The systolic blood pressure associated with HourlyValues.HVDateTime6. | |
| HourlyValues.HVSBP8 | The systolic blood pressure associated with HourlyValues.HVDateTime8. | |
| HourlyValues.HVTIL12 | 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 | 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 | 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 | 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 | 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 | 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 | 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) |
|
| HourlyValues.HVTILChangeReason16 | 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) |
|
| HourlyValues.HVTILChangeReason20 | 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) |
|
| HourlyValues.HVTILChangeReason24 | 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) |
|
| HourlyValues.HVTILChangeReason4 | 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 | 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) |
|
| HourlyValues.HVTime10 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | ||
| Imaging.AcquisitionTime | ||
| Imaging.AnyIntracranTraumaticAbnormality | 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 | ||
| Imaging.BvecURL | ||
| Imaging.CisternalCompression | 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 | 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 | ||
| Imaging.CRFCTManuf | ||
| Imaging.CRFCTMidlineShift | ||
| Imaging.CRFCTMidlineShiftMeasure | ||
| Imaging.CRFCTMRIDate | ||
| Imaging.CRFCTMRITime | ||
| Imaging.CRFCTReason | ||
| Imaging.CRFCTScannerType | ||
| Imaging.CRFCTType | ||
| Imaging.CRFForm | ||
| Imaging.CRFIcometrixImageId | This variable combines data from CTMRI.IcometrixImageId and FollowUp.IcometrixImageId. Identifier generated for an imaging experiment when images are uploaded from site. | |
| Imaging.CRFIcometrixPassedQA | ||
| Imaging.CRFIcometrixQADateTime | ||
| Imaging.CRFIcometrixUploadDateTime | ||
| Imaging.CRFInitialDataIcometrix | ||
| Imaging.CRFMRIManuf | ||
| Imaging.CRFMRIReason | ||
| Imaging.CRFMRIReasonOther | ||
| Imaging.CRFMRIResultPreExistAbnorm | ||
| Imaging.CRFMRIResultTraumaticAbnorm | ||
| Imaging.CRFMRIScannerStrength | ||
| Imaging.CRFMRISequences | ||
| Imaging.CRFMRITraumAbnormASDH | ||
| Imaging.CRFMRITraumAbnormContusion | ||
| Imaging.CRFMRITraumAbnormDAI | ||
| Imaging.CRFMRITraumAbnormDAILesionLocBrainstem | ||
| Imaging.CRFMRITraumAbnormDAILesionLocCorpusCallosum | ||
| Imaging.CRFMRITraumAbnormDAILesionLocDiffuseWhiteMatter | ||
| Imaging.CRFMRITraumAbnormDAINumLesions | ||
| Imaging.CRFMRITraumAbnormEDH | ||
| Imaging.CRFMRIType | ||
| Imaging.CRFTimePoint | Imaging.CRFTimepoint = CTMRI.Timepoint + FollowUp.Timepoint Imaging related data from CTMRI table and Followup is combined under Imaging table so that all data is available in a single place. We only combine the ones with a valid IcometrixImageId | |
| Imaging.DicomHeaderURL | DICOM header 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 | 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 | ||
| Imaging.ExperimentDateTime | S: Date and time at which one images are acquired. B: An experiment is an entire session of images acquisition with multiple scans. Source of the date is the dicom tag '(0008,0020) Study Date'. Source of the time is the dicom tag '(0008,0030), Study Time' A: Date and time of the experiment in iso-8601 format. (YYYY-MM-DD hh:mm:ss) R: If Study Time tag was empty, we used '(0008,0031), Series Time'. If Study and Series Time was empty, we used '(0008,0032), Acquisition Time'. If time not available at all, time is replaced with 00:00:00. If date is anterior to 01-01-1970, the date has not been provided by the center. (not available in Study Date dicom header tag) | |
| Imaging.ExperimentId | 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 | 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 | ||
| Imaging.ExtraaxialHematoma | 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 | 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 | B: Scan are acquired in dicom format. A: Number of dicom files that compose the scan. | |
| Imaging.GreenCTGrade | 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 | 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 | 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 | 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, uinterpretable, not interpreted). | |
| Imaging.Manufacturer | S: Imaging scanner manufacturer. R: Tag (0008,0070) from dicom header available in Imaging.DicomHeaderURL | |
| Imaging.MarshallCTClassification | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 scanner This information is available from the Imaging.DicomHeaderURL | |
| Imaging.ScanNotes | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | S: Subject stratum B: Possible options are: ER, ADMISSION, ICU | |
| Imaging.TAI | 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 | 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 | 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 | 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.UploadDateTime | S: Date and time of upload of the scans to the imaging repository R: UploadDateTime can only be after ExperimentDateTime. | |
| Imaging.WindowDetectionComment | 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 | 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 | 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 | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.AbdomenPelvicContentsDesc | 1 == Spleen rupture 2 == Liver rupture 3 == Perforating abdominal injury 4 == Kidney contusion 5 == Retroperitoneal hematoma 99 == Other |
|
| InjuryHx.AbdomenPelvicContentsISS | ||
| InjuryHx.ACEFocalNeuroDeficit | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.ACEFocalNeuroDeficitDysphasia | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.ACEFocalNeuroDeficitOther | ||
| InjuryHx.ACEFocalNeuroDeficitOtherTxt | ||
| InjuryHx.ACEFocalNeuroDeficitParesis | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.ACEOverallRating | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.ACEOverallRatingUnknown | ||
| InjuryHx.ACERatedBy | 1 == Proxy 2 == Subject 3 == Both proxy and subject 4 == Not done |
|
| InjuryHx.AlcPriorUseInd | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.AlcUseDur | Only applicable if use marked "yes" | |
| InjuryHx.AlcUseLstMoDaysDrankNum | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.AUDITCAlcDrnkTypclDayNumScore | 1 == 1-2 2 == 3-4 3 == 5-6 4 == 7-9 5 == 10 or more 88 == Unknown |
|
| InjuryHx.AUDITCDrnkContainAlcFreqScore | 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.) |
| InjuryHx.AUDITCMoreThan6AlcDrnkFreqScore | 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) 5 == Less than monthly 6 == Monthly 7 == Weekly 8 == Daily or almost daily 88 == Unknown |
|
| InjuryHx.BaselineGCSMostReliableAssessmentCondition | 0 == No sedation/paralysis 1 == Under sedation 3 == After stopping sedation 4 == After pharmacological reversal |
|
| InjuryHx.BaselineGCSMostReliableAssessmentTime | 1 == Admission 2 == Post-stabilization 3 == First hospital 4 == Scene of accident 5 == Other |
|
| InjuryHx.BaselineGCSMostReliableMotorScore | Most reliable baseline Motor score of the GCS as given by sites for use in prognostic models. | |
| InjuryHx.BaselineGOS6MoDateOfPrognosticEstimate | ||
| InjuryHx.BaselineGOS6MoExpectedDeathRisk | ||
| InjuryHx.BaselineGOS6MoExpectedOutcome | GR == GR - Good Recovery MD == MD - Moderate Disability SD == SD - Severe Disability V == V - Vegetative State D == D - Death |
Documents expected outcome at time of discharge from ER (home or to ward/ICU) |
| InjuryHx.BaselineGOS6MoUnfavourableOutcomeRisk | ||
| InjuryHx.BaselinePhysEstOf6MoOutcomePhysicianQual | 1 == Resident 2 == Junior staff (< 5 years) 3 == Senior staff (>= 5 years) 4 == Head of department |
|
| InjuryHx.BaselinePhysEstOf6MoOutcomePhysicianType | 1 == ER Physician 2 == Intensive Care 3 == Neurology 4 == Neurosurgery 5 == Traumatology 88 == Unknown |
|
| InjuryHx.BestOfAbdomenPelvicLumbarISS | AbdomenPelvicLumbar region (Highest AIS of the region)^2 compare AbdomenPelvicContentsAIS, LumbarSpineAIS. This score is taken forward for ISS calculation | |
| InjuryHx.BestOfChestSpineISS | (highest AIS of the region)^2 Compare ThoraxChestAIS, ThoracicSpineAIS and select the highest for ISS calculation | |
| InjuryHx.BestOfExternaISS | External region (ExternaAIS)^2 select the highest external AIS severity code for ISS calculation. | |
| InjuryHx.BestOfExtremitiesISS | Extremities region (Highest AIS of the region)^2 compare UpperExtremitiesAIS, LowerExtremitiesAIS, PelvicGirdleAIS select the highest for ISS calculation | |
| InjuryHx.BestOfFaceISS | Face region (FaceAIS)^2 select the highest facial injury for ISS calculation | |
| InjuryHx.BestOfHeadBrainCervicalISS | 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 | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.BrainInjuryDesc | 1 == Concussion 2 == Contusions 3 == EDH 4 == Diffuse Injury 5 == ASDH 99 == Other |
Injury description is coded by drop-down menus for each body region |
| InjuryHx.CannabisCurrentUse | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.CannabisPriorUse | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.CannabisPriorUseDuration | Only applicable if use marked "yes" | |
| InjuryHx.CervicalSpineAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.CervicalSpineDesc | 1 == Fracture 2 == Dislocation 99 == Other |
|
| InjuryHx.DispER | 1 == Discharge home 2 == Discharge other facility 3 == Hospital admission--Ward 4 == Hospital admission--Intermediate/high care unit 5 == Hospital admission--ICU 6 == Hospital admission--OR for immediate surgical procedure 7 == Death 8 == Hospital admission--Other (e.g. observation unit) 88 == Unknown |
|
| InjuryHx.DrgSubIllctCurntUseInd | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.DrgSubIllctUseCatOther | ||
| InjuryHx.DrgSubIllctUseDur | Only applicable if use marked "yes" | |
| InjuryHx.DrgSubPriorIllctUseInd | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.DrugIllicitCurrentUseOther | ||
| InjuryHx.EDAirway | 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 Tx performed in the ER/on admission. Pre-hospital inteventions are documented at:InjuryHx.PresEmergencyCare |
| InjuryHx.EDArrDBP | ||
| InjuryHx.EDArrHR | ||
| InjuryHx.EDArrivalAirway | 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 | ||
| InjuryHx.EDArrivalArtpCO2mmhg | ||
| InjuryHx.EDArrivalArtpCO2unit | 1 == kPa 2 == mmHg |
|
| InjuryHx.EDArrivalArtpCO2Unknown | ||
| InjuryHx.EDArrivalArtpO2kPa | ||
| InjuryHx.EDArrivalArtpO2mmhg | ||
| InjuryHx.EDArrivalArtpO2unit | 1 == kPa 2 == mmHg |
|
| InjuryHx.EDArrivalArtpO2Unknown | ||
| InjuryHx.EDArrivalBaseExcess | ||
| InjuryHx.EDArrivalBaseExcessUnit | 1 == mEq/l 99 == Other |
|
| InjuryHx.EDArrivalBaseExcessUnitSpecify | ||
| InjuryHx.EDArrivalBaseExcessUnknown | ||
| InjuryHx.EDArrivalBloodGasDone | 0 == No 1 == Yes |
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 | 88 == Unknown | |
| InjuryHx.EDArrivalBMI | BMI using height in inches (EDArrivalHeightInches) and weight in pounds (EDArrivalBodyWeightLbs) BMI=((weight/(height*height)) * 704.5469 | |
| InjuryHx.EDArrivalBMIKgCm | BMI using height in cm (EDArrivalHeightCm) and weight (EDArrivalBodyWeightKg) BMI= (Weight/(Height*Height))) * 10000 | |
| InjuryHx.EDArrivalBodyWeightKg | ||
| InjuryHx.EDArrivalBodyWeightLbs | ||
| InjuryHx.EDArrivalBodyWeightMeasured | 1 == Estimated 2 == Self reported 3 == Measured 4 == Proxy reported 88 == Unknown |
Provides an indication of accuracy of reported weight |
| InjuryHx.EDArrivalBodyWeightUnit | 1 == kg 2 == lbs |
|
| InjuryHx.EDArrivalBreathing | 1 == Spontaneous, adequate 2 == Spontaneous, insufficient 3 == Manual support with bag, valve, mask 4 == Mechanical ventilation 88 == Unknown |
|
| InjuryHx.EDArrivalCirculation | 0 == No specific therapy 1 == IV Fluids 2 == Vasopressors 3 == CPR 88 == Unknown |
|
| InjuryHx.EDArrivalFiO2 | 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 | ||
| InjuryHx.EDArrivalHeartRateUnknown | ||
| InjuryHx.EDArrivalHeightCm | ||
| InjuryHx.EDArrivalHeightInches | ||
| InjuryHx.EDArrivalHeightMeasured | 1 == Estimated 2 == Self reported 3 == Measured 4 == Proxy reported 88 == Unknown |
Provides an indication of accuracy of reported height |
| InjuryHx.EDArrivalHeightUnit | 1 == cm 2 == inch |
|
| InjuryHx.EDArrivalLactate | ||
| InjuryHx.EDArrivalLactateUnit | 1 == mEq/l 99 == Other |
|
| InjuryHx.EDArrivalLactateUnitSpecify | ||
| InjuryHx.EDArrivalLactateUnknown | ||
| InjuryHx.EDArrivalOxygenSatUnknown | ||
| InjuryHx.EDArrivalpH | ||
| InjuryHx.EDArrivalpHUnknown | ||
| InjuryHx.EDArrivalRespRateUnknown | 1 == Spontaneous 2 == Ventilated 88 == Unknown |
|
| InjuryHx.EDArrivalSpinalImmob | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.EDArrivalSupplementalOxygen | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.EDArrivalTemperatureUnknown | ||
| InjuryHx.EDArrPupilLftEyeMeasr | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| InjuryHx.EDArrPupilLftEyeMeasrUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.EDArrPupilReactivityLghtLftEyeReslt | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
|
| InjuryHx.EDArrPupilReactivityLghtRtEyeReslt | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
|
| InjuryHx.EDArrPupilRtEyeMeasr | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| InjuryHx.EDArrPupilRtEyeMeasrUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.EDArrPupilSymmetry | 1 == Equal 2 == Unequal R>L 3 == Unequal L>R 66 == Untestable 88 == Unknown |
|
| InjuryHx.EDArrRespRate | ||
| InjuryHx.EDArrSBP | The vital signs reported here are intended to document the first values obtained on presentation to study hospital | |
| InjuryHx.EDArrSpO2 | ||
| InjuryHx.EDArrTempCelsius | ||
| InjuryHx.EDArrTempFahrenheit | ||
| InjuryHx.EDArrTempUnit | 1 == C 2 == F |
|
| InjuryHx.EDBloodGasConditions | 1 == Pre-intubation, room air 2 == Pre-intubation, +O2 3 == Post-intubation, not ventilated 4 == Post-intubation, ventilated |
|
| InjuryHx.EDBloodGasDate | ||
| InjuryHx.EDBloodGasTime | ||
| InjuryHx.EDBloodTrans | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.EDCircCPR | ||
| InjuryHx.EDCircIV | ||
| InjuryHx.EDCircNone | Records Tx performed in the ER/on admission. Pre-hospital inteventions are documented at: InjuryHx.PresCirculationTreatmentNone | |
| InjuryHx.EDCircUnknown | ||
| InjuryHx.EDCircVaso | ||
| InjuryHx.EDCoagulopathyType1 | 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 15 == Vitamin K (Konakion) |
|
| InjuryHx.EDCoagulopathyType2 | 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 15 == Vitamin K (Konakion) |
|
| InjuryHx.EDCoagulopathyType3 | 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 15 == Vitamin K (Konakion) |
|
| InjuryHx.EDCoagulopathyType4 | 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 15 == Vitamin K (Konakion) |
|
| InjuryHx.EDCoagulopathyVolume1 | ||
| InjuryHx.EDCoagulopathyVolume2 | ||
| InjuryHx.EDCoagulopathyVolume3 | ||
| InjuryHx.EDCoagulopathyVolume4 | ||
| InjuryHx.EDCompEventHypothermia | 0 == No 1 == Definite 2 == Suspect 88 == Unknown |
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 | 0 == No 1 == Yes |
|
| InjuryHx.EDComplEventHypotension | 0 == No 1 == Definite 2 == Suspect 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 | 0 == No 1 == Definite 2 == Suspect 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 | 0 == No 1 == Partial/Focal 2 == Generalized 3 == Status epilepticus 88 == Unknown |
|
| InjuryHx.EDCorrCoagulopathy | 0 == No 1 == Yes 88 == Unknown |
Documents blood transfusions and treatment of coagulopathy in the acute phase at presentation. |
| InjuryHx.EDDischDate | ||
| InjuryHx.EDDischPupilLftEyeMeasr | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| InjuryHx.EDDischPupilLftEyeMeasrUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.EDDischPupilReactivityLghtLftEyeReslt | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
|
| InjuryHx.EDDischPupilReactivityLghtRtEyeReslt | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
|
| InjuryHx.EDDischPupilRtEyeMeasr | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| InjuryHx.EDDischPupilRtEyeMeasrUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.EDDischPupilSymmetry | 1 == Equal 2 == Unequal R>L 3 == Unequal L>R 66 == Untestable 88 == Unknown |
|
| InjuryHx.EDDischTime | ||
| InjuryHx.EDICPMonitoring | 0 == No 1 == Yes 88 == Unknown |
Scheduled for ICP monitoring; e.g. may not accurately reflect if ICP monitoring was indeed performed |
| InjuryHx.EDIVAlbumin | ||
| InjuryHx.EDIVBlood | ||
| InjuryHx.EDIVColloids | ||
| InjuryHx.EDIVCrystalloids | ||
| InjuryHx.EDIVMannitol | ||
| InjuryHx.EDIVSaline | ||
| InjuryHx.EDSecondInsultsNeuroWorse | 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 | 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 | 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 | 0 == No 1 == Yes 88 == Unknown |
Records Tx performed in the ER/on admission |
| InjuryHx.EmergSurgInterventionsExtraCran | 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 | 1 == Damage control thoracotomy 2 == Damage control laparotomy 3 == Extraperitoneal pelvic packing 4 == External fixation limb 5 == Cranio-maxillo-facial reconstruction 99 == Other |
|
| InjuryHx.EmergSurgInterventionsExtraCranYesOther | ||
| InjuryHx.EmergSurgInterventionsIntraCran | 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 | 1 == Craniotomy for haematoma/contusion 2 == Decompressive Craniectomy 3 == Depressed skull fracture 99 == Other intracranial procedure |
|
| InjuryHx.EmerSurgIntraCranSurviveNoSurg | 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. | |
| 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. | |
| InjuryHx.ERDestICDCodes1 | ||
| InjuryHx.ERDestICDCodes10 | ||
| InjuryHx.ERDestICDCodes11 | ||
| InjuryHx.ERDestICDCodes12 | ||
| InjuryHx.ERDestICDCodes13 | ||
| InjuryHx.ERDestICDCodes14 | ||
| InjuryHx.ERDestICDCodes15 | ||
| InjuryHx.ERDestICDCodes16 | ||
| InjuryHx.ERDestICDCodes2 | ||
| InjuryHx.ERDestICDCodes3 | ||
| InjuryHx.ERDestICDCodes4 | ||
| InjuryHx.ERDestICDCodes5 | ||
| InjuryHx.ERDestICDCodes6 | ||
| InjuryHx.ERDestICDCodes7 | ||
| InjuryHx.ERDestICDCodes8 | ||
| InjuryHx.ERDestICDCodes9 | ||
| InjuryHx.ERDestICDCodesVersion | 9 == ICD-9 10 == ICD-10 |
Intent is to document ICD codes as reported by hospital administration. Up to 16 diagnoses can be entered; only applicable to subjects discharged from ER |
| InjuryHx.ERDischHomeSchedApptOutpatient | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.ERDischHomeSchedApptOutpatientDate | ||
| InjuryHx.ERDischHomeSchedApptReferToGP | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.ERDischHomeSchedApptStudyProtoFU | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.ERDischHomeTypeOfCarePlanned | 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 |
|
| InjuryHx.ERDischMotivForDestChoice | 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. |
| InjuryHx.ERDischMotivForDestChoiceOther | ||
| InjuryHx.ExternaAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.ExternaDesc | 1 == No values yet | |
| InjuryHx.FaceAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.FaceDesc | 1 == Maxillo-facial fracture le Fort I 2 == Maxillo-facial fracture le Fort II 3 == Maxillo-facial fracture le Fort III 4 == Orbital fracture 5 == Zygomatic arch fracture 99 == Other |
|
| InjuryHx.FirstHospAssmtCondition | 0 == No sedation or paralysis 1 == Sedated 2 == Paralyzed 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
Describes the condition under which the GCS was assessed. |
| InjuryHx.GcsEDArrAssmtCond | 0 == No sedation or paralysis 1 == Sedated 2 == Paralyzed 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
Describes the condition under which the GCS was assessed. |
| InjuryHx.GCSEDArrEyes | O == Untestable (other) UN == Unknown S == Untestable (swollen) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously |
GCSĀ EyeĀ opening at arrival to ER of study hospital |
| InjuryHx.GCSEDArrMotor | UN == Unknown O == Untestable (Other) P == Untestable (Deep sedation/paralyzed) 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 |
GCS Motor at arrival to ER of study hospital |
| InjuryHx.GcsEDArrNotDone | 77 == Not done / Results not available | Indication that GCS at arrival to Study hospital was not done. |
| InjuryHx.GCSEDArrScore | Calculated score: GCSEDArrEyes + GCSEDArrMotor + GCSEDArrVerbal. If one or more of these is Untestable or unknown then = "No Sum" | |
| InjuryHx.GcsEDArrScoreDate | ||
| InjuryHx.GcsEDArrScoreTime | ||
| InjuryHx.GCSEDArrVerbal | UN == Unknown O == Untestable (Other) T == Untestable (Tracheotomy/endotracheal tube) 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
GCS ED Verbal at arrival to ER of study hospital |
| InjuryHx.GcsEDDischAssmtCond | 0 == No Sedation or Paralysis 1 == Sedated 2 == Paralyzed 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
Describes the condition under which the GCS was assessed. |
| InjuryHx.GCSEDDischEyes | S == Untestable (swollen) UN == Unknown O == Untestable (other) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously |
|
| InjuryHx.GCSEDDischMotor | O == Untestable (Other) UN == Unknown P == Untestable (Deep sedation/paralyzed) 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 |
|
| InjuryHx.GcsEDDischNotDone | 77 == Not done / Results not available | Indication that GCS at post-stabilization was not done. |
| InjuryHx.GCSEDDischScore | Calculated score: GCSEDDischEyes + GCSEDDischMotor + GCSEDDischVerbal. If one or more of these is Untestable or unknown then = "No Sum" | |
| InjuryHx.GcsEDDischScoreDate | ||
| InjuryHx.GcsEDDischScoreTime | ||
| InjuryHx.GCSEDDischVerbal | UN == Unknown O == Untestable (Other) T == Untestable (Tracheotomy/endotracheal tube) 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
|
| InjuryHx.GCSFirstHospEyes | UN == Unknown O == Untestable (other) S == Untestable (swollen) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously |
|
| InjuryHx.GCSFirstHospMotor | UN == Unknown P == Untestable (Deep sedation/paralyzed) O == Untestable (Other) 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 |
|
| InjuryHx.GCSFirstHospNotDone | 77 == Not done / Results not available | Indication that GCS at First hospital was not done. |
| InjuryHx.GCSFirstHospPupilLftEyeMeasure | ||
| InjuryHx.GCSFirstHospPupilLftEyeMeasureUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.GCSFirstHospPupilReactivityLightLftEyeReslt | 1 == + (Sluggish) 2 == + (Brisk) 3 == - (Negative) |
|
| InjuryHx.GCSFirstHospPupilReactivityLightRghtEyeReslt | 1 == + (Sluggish) 2 == + (Brisk) 3 == - (Negative) |
|
| InjuryHx.GCSFirstHospPupilRightEyeMeasure | ||
| InjuryHx.GCSFirstHospPupilRightEyeMeasureUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.GCSFirstHospPupilSymmetry | 1 == Equal 2 == Unequal R>L 3 == Unequal L>R 66 == Untestable 88 == Unknown |
|
| InjuryHx.GCSFirstHospReportedTotalScore | 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 |
Score by investigators in case component scores not available, but GCS sum score available |
| InjuryHx.GCSFirstHospScore | Calculated Score: 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 | ||
| InjuryHx.GCSFirstHospScoreTime | ||
| InjuryHx.GCSFirstHospVerbal | UN == Unknown O == Untestable (Other) T == Untestable (tracheotomy/endotracheal tube) 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
|
| InjuryHx.GCSMotorBaselineDerived | 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 | 0 == No Sedation or Paralysis 1 == Sedated 2 == Paralyzed 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
Describes the condition under which the GCS was assessed. |
| InjuryHx.GCSOtherDate | ||
| InjuryHx.GCSOtherEyes | S == Untestable (swollen) UN == Unknown O == Untestable (other) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously |
|
| InjuryHx.GCSOtherMotor | UN == Unknown O == Untestable (Other) P == Untestable (Deep sedation/paralyzed) 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 |
|
| InjuryHx.GCSOtherNotDone | 77 == Not done / Results not available | Indication that GCS otherl was not done. |
| InjuryHx.GCSOtherPupilLftEyeMeasure | ||
| InjuryHx.GCSOtherPupilLftEyeMeasureUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.GCSOtherPupilReactivityLightLftEyeReslt | 1 == + (Sluggish) 2 == + (Brisk) 3 == - (Negative) |
|
| InjuryHx.GCSOtherPupilRightEyeMeasure | ||
| InjuryHx.GCSOtherPupilSymmetry | 1 == Equal 2 == Unequal R>L 3 == Unequal L>R 66 == Untestable 88 == Unknown |
|
| InjuryHx.GCSOtherReactivityLightRghtEyeReslt | 1 == + (Sluggish) 2 == + (Brisk) 3 == - (Negative) |
|
| InjuryHx.GCSOtherRightEyeMeasureUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.GCSOtherScore | Calculated Score: 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 | ||
| InjuryHx.GCSOtherVerbal | UN == Unknown O == Untestable (Other) T == Untestable (tracheotomy/endotracheal tube) 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
|
| InjuryHx.GcsPreHospBestDate | ||
| InjuryHx.GCSPreHospBestEyes | UN == Unknown O == Untestable (Other) S == Untestable (swollen) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously |
|
| InjuryHx.GCSPreHospBestMotor | UN == Unknown O == Untestable (Other) P == Untestable (Deep sedation/paralyzed) 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 |
|
| InjuryHx.GCSPreHospBestReportedTotalScore | 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 |
Score by investigators in case the component scores are not available, but GCS sum score available |
| InjuryHx.GCSPreHospBestScore | Calculated Score: 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 | ||
| InjuryHx.GCSPreHospBestVerbal | O == Untestable (Other) UN == Unknown T == Untestable (Tracheotomy/endotracheal tube) 1 == 1-None 2 == 2-Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
|
| InjuryHx.GcsPreHospLftEyeMeasr | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 |
|
| InjuryHx.GcsPreHospNotDone | 77 == Not Done / Results not available | The initial GCS and pupillary reactivity can be scored at 4 pre-defined moments in the pre-hospital/presentation phase: 1.: scene of accident; 2: first hospital (in case of secondary referral; 3.: arrival to Er of study hospital; 4.: post-stabilization; In addition, assessment at a different time point is possible (designated as other). A derived variable captures the highest available GCS score across these time periods. Indication that GCS at Scene of accident was not done. |
| InjuryHx.GCSPreHospPupilLftEyeMeasureUnkUnt | 66 == Untestable 88 == Unknown |
Only applicable to size of pupils |
| InjuryHx.GCSPreHospPupilReactivityLghtLftEyeResult | 1 == + (Sluggish) 2 == + (Brisk) 3 == - (Negative) |
|
| InjuryHx.GCSPreHospPupilReactivityLghtRghtEyeResult | 1 == + (Sluggish) 2 == + (Brisk) 3 == - (Negative) |
|
| InjuryHx.GCSPreHospPupilRightEyeMeasureUnkUnt | 66 == Untestable 88 == Unknown |
|
| InjuryHx.GCSPreHospPupilSymmetry | 1 == Equal 2 == Unequal R>L 3 == Unequal L>R 66 == Untestable 88 == Unknown |
|
| InjuryHx.GcsPreHospRghtEyeMeasr | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 |
|
| InjuryHx.GCSScoreBaselineDerived | 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 | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.HeadNeckDesc | ||
| InjuryHx.HighestGCSMotorDerived | This is a derived variable calculated centrally. It represents the GCS motor score for baseline risk adjustment with missing values imputed using āhighestā 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 | This is a derived variable calculated centrally. Total GCS (single timepoint) for baseline risk adjustment with missing values imputed using āhighestā 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 | This is a derived variable calculated centrally. Number of reactive pupils for baseline risk adjustment with missing values imputed using āhighestā 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 | 1 == Urban (city) 2 == Rural 88 == Unknown |
|
| InjuryHx.InjCause | 1 == Road traffic incident 2 == Incidental fall 3 == Other non-intentional injury 4 == Violence/assault 5 == Act of mass violence 6 == Suicide attempt 88 == Unknown 99 == Other |
|
| InjuryHx.InjCauseOther | ||
| InjuryHx.InjIndContactSportType | 1 == Boxing 2 == Martial Arts 99 == Other |
Only applicable for sports/recreational injuries |
| InjuryHx.InjIndSportTypeOther | Only applicable for sports/recreational injuries | |
| InjuryHx.InjIntention | 1 == Intentional 2 == Unintentional 3 == Undetermined |
|
| InjuryHx.InjMech | 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 |
Applicable for closed TBI |
| InjuryHx.InjMechOther | ||
| InjuryHx.InjOtherPartyInvolved | 77 == N/A | If no other party: N/A |
| InjuryHx.InjOtherPartySleepingPills | 0 == No 1 == Suspect 2 == Definite 88 == Unknown |
|
| InjuryHx.InjPenetratingType | 1 == Gunshot wound 2 == Fragment (incl. shell/shrapnel) 99 == Other penetrating brain injury |
Only applicable if penetrating brain injury |
| InjuryHx.InjPenetratingTypeOther | ||
| InjuryHx.InjPlace | 1 == Street/highway 2 == Home/domestic 3 == Work/school 4 == Sport/Recreational 5 == Military deployment 6 == Public location (eg. bar, station, nightclub) 88 == Unknown 99 == Other |
|
| InjuryHx.InjPlaceOther | ||
| InjuryHx.InjRecSportType | 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 88 == Unknown 99 == Other |
Only applicable for sports/recreational injuries |
| InjuryHx.InjRecSportTypeOther | Only applicable for sports/recreational injuries | |
| InjuryHx.InjRoadAccEjectedFromVehicle | 0 == No 1 == Yes 88 == Unknown |
Only applicable if subject was motor vehicle occupant |
| InjuryHx.InjRoadAccOtherParty | 1 == Motor vehicle 2 == Pedestrian 3 == Cyclist 4 == Moped/Scooter 5 == Tram/Bus 6 == Train/Metro 7 == Obstacle 10 == Motor Bike 11 == Lorry (camion) 88 == Unknown 99 == Other |
|
| InjuryHx.InjRoadAccOtherPartyInvolved | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.InjRoadAccOtherPartyOther | ||
| InjuryHx.InjRoadAccVictim | 1 == Motor vehicle occupant 2 == Pedestrian 3 == Cyclist 4 == Moped/Scooter 5 == Motor Bike 99 == Other |
Only if traffic accident |
| InjuryHx.InjRoadAccVictimOther | ||
| InjuryHx.InjRoadAccVictimVehiclePlace | 1 == Driver 2 == Front seat passenger 3 == Back seat passenger |
|
| InjuryHx.InjSafetyAirbag | 0 == No 1 == Yes 77 == Not Applicable 88 == Unknown |
Only applicable if subject was motor vehicle occupant |
| InjuryHx.InjSafetyHelmet | 0 == No 1 == Yes 77 == Not Applicable 88 == Unknown |
Only applicable in case of cyclist, scooter, motorbike incident. However, may also have been scored for various sports injuries |
| InjuryHx.InjSafetySeatbelt | 0 == No 1 == Yes 77 == Not Applicable 88 == Unknown |
Only applicable if subject was motor vehicle occupant |
| InjuryHx.InjTeamSportType | 1 == Football (soccer) 2 == Rugby 3 == Field Hockey 4 == Ice Hockey 5 == Lacrosse 99 == Other |
Only applicable for sports/recreational injuries |
| InjuryHx.InjTeamSportTypeOther | Only applicable for sports/recreational injuries | |
| InjuryHx.InjType | 1 == Closed 2 == Blast 3 == Crush 5 == Penetrating 6 == Penetrating-perforating 7 == Penetrating-tangential 8 == Closed with open depressed skull fracture 88 == Unknown |
Details of Injury are captured in 4 different variables: Type of Injury, Place of Injury, Cause of Injury and Mechanism of injury. |
| InjuryHx.InjVictimAlcoholTestType | Breath == Breath Test Blood == Blood Test |
|
| InjuryHx.InjVictimBloodAlcoholmgdL | ||
| InjuryHx.InjVictimBloodAlcoholpermil | ||
| InjuryHx.InjVictimBloodAlcoholUnit | 1 == mg/dL 2 == per mil (0/00) |
|
| InjuryHx.InjVictimDrugsTypeOther | ||
| InjuryHx.InjVictimSleepingPills | 0 == No 1 == Suspect 2 == Definite 88 == Unknown |
|
| InjuryHx.InjVictimTypeDrugs | 1 == Cannabis 2 == Cocaine 3 == Methamphetamine's 4 == Opioids 5 == XTC 88 == Unknown 99 == Other |
|
| InjuryHx.InjViolence | 1 == Robbery 2 == Interpersonal violence (fight) 3 == Domestic assault 4 == Child abuse 5 == Gang violence 6 == Military deployment 88 == Unknown 99 == Other |
Only applicable if violence cause of injury |
| InjuryHx.InjViolenceOther | ||
| InjuryHx.InjViolenceOtherPartyAlcohol | 0 == No 1 == Definite 2 == Suspect 88 == Unknown |
|
| InjuryHx.InjViolenceOtherPartyDrugs | 0 == No 1 == Definite 2 == Suspect 88 == Unknown |
|
| InjuryHx.InjViolenceVictimAlcohol | 0 == No 1 == Definite 2 == Suspect 88 == Unknown |
Information drug and alcohol abuse of possible influence on the incident is different for victim versus "other party" (if involved) |
| InjuryHx.InjViolenceVictimDrugs | 0 == No 1 == Definite 2 == Suspect 88 == Unknown |
|
| InjuryHx.InterventRadiology | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.LOCAOC | 0 == No 1 == Yes, immediate 2 == Not tested due to LOC 3 == Suspected 4 == Yes, delayed onset 88 == 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. Details of symptoms are captured in the Rivermead Questionnaire. |
| InjuryHx.LOCAOCDelayedHrs | Only in case of delayed onset | |
| InjuryHx.LOCAOCDelayedHrsUnk | ||
| InjuryHx.LOCAOCDuration | 0 == None 2 == <1 minute 3 == 1-29 minutes 4 == 30-59 minutes 5 == 1-24 hours 6 == 1-7 days 7 == >7 days 88 == Unknown |
|
| InjuryHx.LOCAOCReportedBy | 1 == Patient 2 == Witness 3 == Clinical interview 4 == Medical chart 5 == Not available |
|
| InjuryHx.LOCDuration | 0 == No return of consciousness 2 == <1 minute 3 == 1-29 minutes 4 == 30-59 minutes 5 == 1-24 hours 6 == 1-7 days 7 == >7 days 88 == Unknown |
Note: for patients admitted to hospital, the time to obeying commands is documented on hospital discharge: Hospital.HospDischargeTimeToObeyCommands |
| InjuryHx.LOCGCSSumDet | 0 == None 1 == 1 point 2 == 2 or more points 88 == Unknown |
|
| InjuryHx.LOCLossOfConsciousness | 0 == No 1 == Yes 3 == Suspected 88 == Unknown |
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 | 0 == No 1 == Yes 88 == Unknown |
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 | ||
| InjuryHx.LOCLucidIntervalHrsUnk | ||
| InjuryHx.LOCPTA | 0 == No 1 == Yes, ongoing 2 == Yes, resolved 3 == Suspected 88 == Unknown |
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 | 0 == None 2 == <1 hour 5 == 1-24 hours 6 == 1-7 days 7 == 7-28 days 8 == 1-2 hours 9 == 2-4 hours 10 == 4-24 hours 11 == >1 day 28 == >28 77 == N/A (e.g. death) 88 == Unknown |
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 | 1 == Patient 2 == Witness 3 == Retrospective assessment/ clinical interview 4 == Medical chart 5 == Not available 6 == Prospective assessment with PTA scale |
|
| InjuryHx.LOCPTAScale | 1 == GOAT 2 == Westmead 3 == O-Log 4 == Nijmegen PTA scale 99 == Other |
In some centres, prospective assessment of amnesia after TBI is performed using a dedicated scale. This variable documents the scale used. |
| InjuryHx.LOCReportedBy | 1 == Self report 2 == Witness 3 == Clinical interview 4 == Medical chart 5 == Not available |
Documentation of LOC can be subjective. We therefore asked for "source of verification" |
| InjuryHx.LOCRGA | 0 == No 1 == Yes 88 == Unknown |
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 | 0 == None 1 == <30 2 == >= 30 minutes 88 == Unknown |
|
| InjuryHx.LOCRGAReportBy | 1 == Self report 2 == Witness 3 == Clinical interview 4 == Medical chart 5 == Not available |
|
| InjuryHx.LowerExtremitiesAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
Lower extremities as subdomain of Extremities and pelvic girdle |
| InjuryHx.LowerExtremitiesDesc | 1 == Femoral fracture 2 == Tibia plateau fracture 3 == Tibia fracture 4 == Ankle fracture 5 == Calcaneus fracture 6 == Metatarsal/tarsal fracture (toe fracture) 7 == Fibula fracture |
|
| InjuryHx.LumbarSpineAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
Lumbar spine as subdomain of Abdomen/Pelvic contents |
| InjuryHx.LumbarSpineDesc | 1 == Fracture 2 == Dislocation 3 == Sacral fracture 99 == Other |
|
| InjuryHx.NeuroAssmtsAVPU | U == The patient is completely unresponsive A == Patient is awake V == Patient responds to verbal stimulation P == The patient responds to painful stimulation 88 == Unknown |
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 | ||
| InjuryHx.PainScaleUnk | 77 == Untestable 88 == Unknown |
|
| InjuryHx.PelvicGirdleAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
Pelvic Girdle as subdomain of Extremities and pelvic girdle |
| InjuryHx.PelvicGirdleDesc | 1 == Pelvic fracture 2 == Hip fracture 3 == Hip dislocation |
|
| InjuryHx.PreHospAssmtConditions | 0 == No sedation or paralysis 1 == Sedated 2 == Paralyzed 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
Describes the condition under which the GCS was assessed. |
| InjuryHx.PresArrivalMethod | 1 == Ambulance 2 == Helicopter 3 == Medical mobile team 4 == Walk in or drop off 99 == Other |
|
| InjuryHx.PresCirculationTreatmentCPR | CPR = Cardio-pulmonary resuscitation | |
| InjuryHx.PresCirculationTreatmentIVFluids | ||
| InjuryHx.PresCirculationTreatmentNone | ||
| InjuryHx.PresCirculationTreatmentUnknown | ||
| InjuryHx.PresCTBrain | 0 == No 1 == Yes 88 == Unknown |
Procedure performed at first hospital (not study hospital). |
| InjuryHx.PresEmergencyCare | 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 |
|
| InjuryHx.PresEmergencyCareIntubation | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.PresEmergencyCareSuppOxygen | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.PresEmergencyCareVentilation | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.PresEmergencyServiceAmbuBasic | ||
| InjuryHx.PresEmergencyServiceAmbuSpec | ||
| InjuryHx.PresEmergencyServiceFirefighter | ||
| InjuryHx.PresEmergencyServiceHelicopter | ||
| InjuryHx.PresEmergencyServiceNone | ||
| InjuryHx.PresEmergencyServicePolice | ||
| InjuryHx.PresERExtracranialSurg | 0 == No 1 == Yes 88 == Unknown |
Procedure performed at first hospital (not study hospital). |
| InjuryHx.PresERIntracranialSurg | 0 == No 1 == Yes 88 == Unknown |
Procedure performed at first hospital before arrival to the study hospital. Surgical procedures decided on to perform directly on arrival to the study hospital are recorded within InjuryHx.EmergSurgInterventionsIntraCran. |
| InjuryHx.PresFHospDate | First hospital is defined as the initial hospital to which the patient was brought before being transferred to Study hospital. Consequently, only applicable in case of secondary transferral. However, in some sites data for first hospital may have been entered also when the patient was brought directly to the study hospital.. | |
| InjuryHx.PresFHospTime | ||
| InjuryHx.PresFirstOnSceneDate | ||
| InjuryHx.PresFirstOnSceneDepartUnknownTime | 77 == N/A if emergency service=none 88 == Unknown |
|
| InjuryHx.PresFirstOnSceneDepartureDate | ||
| InjuryHx.PresFirstOnSceneDepartureTime | ||
| InjuryHx.PresFirstOnSceneTime | ||
| InjuryHx.PresFirstOnSceneUnknownTime | 77 == N/A if emergency service=none 88 == Unknown |
Time of arrival of EMS to incident scene unknown or N/A (f.e. if no EMS involved) |
| InjuryHx.PresIntubation | 0 == No 1 == Yes 88 == Unknown |
Procedure performed at first hospital (not study hospital). |
| InjuryHx.PresSTHospDate | ||
| InjuryHx.PresSTHospTime | ||
| InjuryHx.PresTBIRef | 1 == Primary 2 == Secondary |
|
| InjuryHx.PupilsBaselineDerived | 0 - Both reacting 1 - One reacting (other pupil is either unreactive, missing or untestable) 2 - Both unreacting |
This is a derived variable calculated centrally. Number of reactive 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 | Pupil symmetry derived variable calculated from (GCSFirstHospPupilSymmetry,EDArrPupilSymmetry,GCSPreHospPupilSymmetry,EDDischPupilSymmetry,PupilsNonSymmetric) | |
| InjuryHx.SedativeCurrentUse | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.SedativePriorUse | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.SedativePriorUseDuration | Only applicable if use marked "yes" | |
| InjuryHx.SympSkullFract | 0 == No 1 == Yes 88 == Unknown |
|
| InjuryHx.SympVomiting | 0 == No 1 == Once 2 == More than once 88 == Unknown |
|
| InjuryHx.ThoracicSpineAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.ThoracicSpineDesc | 1 == Fracture 2 == Dislocation |
Thoracic spine as subdomain of Thorax/Chest |
| InjuryHx.ThoraxChestAIS | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
|
| InjuryHx.ThoraxChestDesc | 1 == Rib fracture 2 == Lung contusion 3 == Cardiac contusion 4 == Aorta dissection 5 == Pneumo-thorax 6 == Hemato-thorax 99 == Other |
|
| InjuryHx.TobcoCurntUseInd | 0 == No 1 == Yes 88 == Unknown |
Use in the past 3 months |
| InjuryHx.TobcoPriorUseInd | 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 | ||
| InjuryHx.TotalISS | 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 | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 |
Upper extremities as subdomain of Extremities and pelvic girdle |
| InjuryHx.UpperExtremitiesDesc | 1 == Humerus fracture 2 == Radial and/or ulnar fracture 3 == Dislocation 4 == Hand 5 == Finger |
|
| Labs.DLA10Extem | Only applicable to sites doing ROTEM studies | |
| Labs.DLA10Fibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLA10NotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLA5Extem | Only applicable to sites doing ROTEM studies | |
| Labs.DLA5Fibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLA5NotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLaAngleExtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLaAngleFibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLaAngleNotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLACT | Only applicable to sites doing ROTEM/TEG studies | |
| Labs.DLACTNotDone | Only applicable to sites doing ROTEM/TEG studies | |
| Labs.DLADPAggreg | Only applicable to sites doing multiplate studies | |
| Labs.DLADPAUC | Only applicable to sites doing multiplate studies | |
| Labs.DLADPAUCU | Only applicable to sites doing multiplate studies | |
| Labs.DLADPVelocity | Only applicable to sites doing multiplate studies | |
| Labs.DLAlatSgptNotDone | ||
| Labs.DLAlatSgptOther | Preferred unit for ALAT/SGPT was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAlatSgptOtherUnit | Preferred unit for ALAT/SGPT was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAlatSgptUL | Recorded in "preferred" units | |
| Labs.DLAlbumingL | Recorded in "preferred" units | |
| Labs.DLAlbuminNotDone | ||
| Labs.DLAlbuminOther | Preferred unit for Albumin was g/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAlbuminOtherUnit | Preferred unit for Albumin was g/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAlkalinePhosphataseNotDone | ||
| Labs.DLAlkalinePhosphataseOther | Preferred unit for Alkaline Phosphatase was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAlkalinePhosphataseOtherUnit | Preferred unit for Alkaline Phosphatase was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAlkalinePhosphataseUL | Recorded in "preferred" units | |
| Labs.DLAmylaseNotDone | ||
| Labs.DLAmylaseOther | Preferred unit for Amylase was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAmylaseOtherUnit | Preferred unit for Amylase was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAmylaseUL | Recorded in "preferred" units | |
| Labs.DLaPttNotDone | ||
| Labs.DLaPttOther | Preferred unit for aPTT was sec. When sites used another unit, the value was recorded here. | |
| Labs.DLaPttOtherUnit | Preferred unit for aPTT was sec. When sites used another unit, the other unit was recorded here. | |
| Labs.DLaPttsec | Recorded in "preferred" units | |
| Labs.DLAsatSgotNotDone | ||
| Labs.DLAsatSgotOther | Preferred unit for ASAT/SGOT was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLAsatSgotOtherUnit | Preferred unit for ASAT/SGOT was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLAsatSgotUL | Recorded in "preferred" units | |
| Labs.DLASPIAggreg | Only applicable to sites doing multiplate studies | |
| Labs.DLASPIAUC | Only applicable to sites doing multiplate studies | |
| Labs.DLASPIAUCU | Only applicable to sites doing multiplate studies | |
| Labs.DLASPIVelocity | Only applicable to sites doing multiplate studies | |
| Labs.DLBloodChemDone | ||
| Labs.DLCalciummmolL | Recorded in "preferred" units | |
| Labs.DLCalciumNotDone | ||
| Labs.DLCalciumOther | Preferred unit for Calcium was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLCalciumOtherUnit | Preferred unit for Calcium was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLCFTExtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLCFTFibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLCFTNotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLCL30 | ||
| Labs.DLCL30NotDone | ||
| Labs.DLCL60 | ||
| Labs.DLCL60NotDone | ||
| Labs.DLCLTExtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLCLTFibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLCLTNotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLCOLAggreg | Only applicable to sites doing multiplate studies | |
| Labs.DLCOLAUC | Only applicable to sites doing multiplate studies | |
| Labs.DLCOLAUCU | Only applicable to sites doing multiplate studies | |
| Labs.DLCOLVelocity | Only applicable to sites doing multiplate studies | |
| Labs.DLCreatinineNotDone | ||
| Labs.DLCreatinineOther | Preferred unit for Creatinine was Āµmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLCreatinineOtherUnit | Preferred unit for Creatinine was Āµmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLCreatinineumolL | Recorded in "preferred" units | |
| Labs.DLCRPmgL | Recorded in "preferred" units | |
| Labs.DLCRPNotDone | ||
| Labs.DLCRPOther | Preferred unit for CRP was mg/L. When sites used another unit, the value was recorded here. | |
| Labs.DLCRPOtherUnit | Preferred unit for CRP was mg/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLCTExtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLCTFibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLCTNotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLDate | ||
| Labs.DLDdimersNotDone | ||
| Labs.DLDdimersOther | Preferred unit for D-dimers was Āµg/L. When sites used another unit, the value was recorded here. | |
| Labs.DLDdimersOtherUnit | Preferred unit for D-dimers was Āµg/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLDdimersugL | Recorded in "preferred" units | |
| Labs.DLEosinophilsNotDone | ||
| Labs.DLEosinophilsOther | Preferred unit for Eosinophils was %. When sites used another unit, the value was recorded here. | |
| Labs.DLEosinophilsOtherUnit | Preferred unit for Eosinophils was %. When sites used another unit, the other unit was recorded here. | |
| Labs.DLEosinophilspct | Recorded in "preferred" units | |
| Labs.DLEPL | ||
| Labs.DLEPLNotDone | ||
| Labs.DLFibrinogenmgdL | Recorded in "preferred" units | |
| Labs.DLFibrinogenNotDone | ||
| Labs.DLFibrinogenOther | Preferred unit for Fibrinogen was mg/dL. When sites used another unit, the value was recorded here. | |
| Labs.DLFibrinogenOtherUnit | Preferred unit for Fibrinogen was mg/dL. When sites used another unit, the other unit was recorded here. | |
| Labs.DLGlucosemmolL | Recorded in "preferred" units | |
| Labs.DLGlucoseNotDone | ||
| Labs.DLGlucoseOther | Preferred unit for Glucose was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLGlucoseOtherUnit | Preferred unit for Glucose was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLHaematologyDone | ||
| Labs.DLHematocritNotDone | ||
| Labs.DLHematocritOther | Preferred unit for Hematocrit was %. When sites used another unit, the value was recorded here. | |
| Labs.DLHematocritOtherUnit | Preferred unit for Hematocrit was %. When sites used another unit, the other unit was recorded here. | |
| Labs.DLHematocritpct | Recorded in "preferred" units | |
| Labs.DLHemoglobingdL | Recorded in "preferred" units | |
| Labs.DLHemoglobinNotDone | ||
| Labs.DLHemoglobinOther | Preferred unit for Hemoglobin was g/dL. When sites used another unit, the value was recorded here. | |
| Labs.DLHemoglobinOtherUnit | Preferred unit for Hemoglobin was g/dL. When sites used another unit, the other unit was recorded here. | |
| Labs.DLInr | ||
| Labs.DLInrNotDone | Recorded in "preferred" units | |
| Labs.DLInrOther | ||
| Labs.DLInrOtherUnit | ||
| Labs.DLK | ||
| Labs.DLKNotDone | ||
| Labs.DLLabsNotDone | Only hospital labs | |
| Labs.DLLabsNotDoneOther | ||
| Labs.DLLdhNotDone | ||
| Labs.DLLdhOther | Preferred unit for LDH was U/L. When sites used another unit, the value was recorded here. | |
| Labs.DLLdhOtherUnit | Preferred unit for LDH was U/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLLdhUL | Recorded in "preferred" units | |
| Labs.DLLY30Extem | Only applicable to sites doing ROTEM studies | |
| Labs.DLLY30Fibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLLY30NotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLLY60Extem | Only applicable to sites doing ROTEM studies | |
| Labs.DLLY60Fibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLLY60NotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLLymphocytesNotDone | ||
| Labs.DLLymphocytesOther | Preferred unit for Lymphocytes was %. When sites used another unit, the value was recorded here. | |
| Labs.DLLymphocytesOtherUnit | Preferred unit for Lymphocytes was %. When sites used another unit, the other unit was recorded here. | |
| Labs.DLLymphocytespct | Recorded in "preferred" units | |
| Labs.DLMA | ||
| Labs.DLMagnesiummmolL | Recorded in "preferred" units | |
| Labs.DLMagnesiumNotDone | ||
| Labs.DLMagnesiumOther | Preferred unit for Magnesium was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLMagnesiumOtherUnit | Preferred unit for Magnesium was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLMANotDone | ||
| Labs.DLMCFExtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLMCFFibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLMCFNotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLMCFtExtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLMCFtFibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLMCFtNotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLMLExtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLMLFibtem | Only applicable to sites doing ROTEM studies | |
| Labs.DLMLNotDone | Only applicable to sites doing ROTEM studies | |
| Labs.DLMultiplateDone | Only in selected sites | |
| Labs.DLNeutrophilsNotDone | ||
| Labs.DLNeutrophilsOther | Preferred unit for Neutrophils was %. When sites used another unit, the value was recorded here. | |
| Labs.DLNeutrophilsOtherUnit | Preferred unit for Neutrophils was %. When sites used another unit, the other unit was recorded here. | |
| Labs.DLNeutrophilspct | Recorded in "preferred" units | |
| Labs.DLPlatelet10_5L | Recorded in "preferred" units | |
| Labs.DLPlateletNotDone | ||
| Labs.DLPlateletOther | Preferred unit for Platelet was X109/L or X103/Ī¼L. When sites used another unit, the value was recorded here. | |
| Labs.DLPlateletOtherUnit | Preferred unit for Platelet was X109/L or X103/Ī¼. When sites used another unit, the other unit was recorded here. | |
| Labs.DLPotassiummmolL | Recorded in "preferred" units | |
| Labs.DLPotassiumNotDone | ||
| Labs.DLPotassiumOther | Preferred unit for Potassium was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLPotassiumOtherUnit | Preferred unit for Potassium was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLProthrombineTimeNotDone | ||
| Labs.DLProthrombineTimeOther | Preferred unit for Prothrombine Time was sec. When sites used another unit, the value was recorded here. | |
| Labs.DLProthrombineTimeOtherUnit | Preferred unit for Prothrombine Time was sec. When sites used another unit, the other unit was recorded here. | |
| Labs.DLProthrombineTimeSec | Recorded in "preferred" units | |
| Labs.DLR | ||
| Labs.DLRISTOAggreg | Only applicable to sites doing multiplate studies | |
| Labs.DLRISTOAUC | Only applicable to sites doing multiplate studies | |
| Labs.DLRISTOAUCU | Only applicable to sites doing multiplate studies | |
| Labs.DLRISTOVelocity | Only applicable to sites doing multiplate studies | |
| Labs.DLRNotDone | Only applicable to sites doing TEG studies | |
| Labs.DLROTEMDone | Only applicable to sites doing ROTEM tests | |
| Labs.DLS100BNotDone | ||
| Labs.DLS100BOther | Preferred unit for S100B was Āµg/L. When sites used another unit, the value was recorded here. | |
| Labs.DLS100BOtherUnit | Preferred unit for S100B was Āµg/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLS100BugL | Recorded in "preferred" units | |
| Labs.DLSodiummmolL | Recorded in "preferred" units | |
| Labs.DLSodiumNotDone | ||
| Labs.DLSodiumOther | Preferred unit for Sodium mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLSodiumOtherUnit | Preferred unit for Sodium mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLTEGA10 | ||
| Labs.DLTEGA10NotDone | ||
| Labs.DLTEGA5 | ||
| Labs.DLTEGA5NotDone | ||
| Labs.DLTEGaAngle | ||
| Labs.DLTEGaAngleNotDone | ||
| Labs.DLTEGDone | Only applicable for sites doing TEG | |
| Labs.DLTEGType | ||
| Labs.DLTime | ||
| Labs.DLTMA | ||
| Labs.DLTMANotDone | ||
| Labs.DLTotalBilirubinNotDone | ||
| Labs.DLTotalBilirubinOther | Preferred unit for Total Bilirubin was Āµmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLTotalBilirubinOtherUnit | Preferred unit for Total Bilirubin was Āµmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLTotalBilirubinumolL | Recorded in "preferred" units | |
| Labs.DLToxScreen | Only if performed as part of clinical routine | |
| Labs.DLToxScreenDone | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosAmphet | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosBarb | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosBenzo | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosCannabis | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosCocaine | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosMeth | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosMethaqual | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosOpiate | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosOther | Only if performed as part of clinical routine | |
| Labs.DLToxScreenPosOtherTxt | ||
| Labs.DLToxScreenPosPhency | Only if performed as part of clinical routine | |
| Labs.DLToxScreenType | Only if performed as part of clinical routine | |
| Labs.DLTRAPAggreg | Only applicable to sites doing multiplate studies | |
| Labs.DLTRAPAUC | Only applicable to sites doing multiplate studies | |
| Labs.DLTRAPAUCU | Only applicable to sites doing multiplate studies | |
| Labs.DLTRAPVelocity | Only applicable to sites doing multiplate studies | |
| Labs.DLTTL | ||
| Labs.DLTTLNotDone | ||
| Labs.DLUreammolL | Recorded in "preferred" units | |
| Labs.DLUreaNotDone | ||
| Labs.DLUreaOther | Preferred unit for Urea was mmol/L. When sites used another unit, the value was recorded here. | |
| Labs.DLUreaOtherUnit | Preferred unit for Urea was mmol/L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLWhiteBloodCellNotDone | ||
| Labs.DLWhiteBloodCellOther | Preferred unit for White Blood Cell was X109/L or X103/Ī¼L. When sites used another unit, the value was recorded here. | |
| Labs.DLWhiteBloodCellOtherUnit | Preferred unit for White Blood Cell was X109/L or X103/Ī¼L. When sites used another unit, the other unit was recorded here. | |
| Labs.DLWhiteBloodCellpct | Recorded in "preferred" units | |
| LabSampling.LSBiomarkersCollctnDate | Protein biomarker sampling is planned in all 5400 subjects. 1 x 9ml blood sample was collected in a serum separator tube. After 45 minutes (Ā±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 that blood sampling required specific informed consent. This was not provided by all subjects, and in others was not possible for logistic reasons. | |
| LabSampling.LSBiomarkersCollctnTime | ||
| LabSampling.LSBiomarkersFreezerCollctnDate | ||
| LabSampling.LSBiomarkersFreezerCollctnTime | ||
| LabSampling.LSBiomarkersNotCollReason | 1 == No informed consent 2 == Blood draw not successful 3 == Logistic reasons |
|
| LabSampling.LSBloodTransBfSampl | 0 == No 1 == Yes 99 == Unknown |
|
| LabSampling.LSCoagulationCollctnDate | Central haemostasis investigations are complementary to routine tests performed by local laboratories at participating sites and were performed in selected centres. This involves 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 enrolment time points for 600 subjects from the admission stratum and 600 subjects from the ICU stratum. Post-op samples (300 cases) and Day 2 samples will also be obtained in the same two sodium citrate tubes from 600 ICU subjects (at this sampling point no potassium EDTA tubes/samples are requested). | |
| LabSampling.LSCoagulationCollctnTime | ||
| LabSampling.LSCoagulationFreezerDate | ||
| LabSampling.LSCoagulationFreezerTime | ||
| LabSampling.LSGeneticCollctnDate | Two genetic samples should be obtained in all CENTER-TBI participants. It is recognised by the CENTER-TBI coordinators that obtaining genetic samples post transfusion could result in āchimerismā 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 participantās transfusion status is essential for future analysis. In some cases blood sampling for genetic analysis were obtained later. | |
| LabSampling.LSGeneticCollctnTime | ||
| LabSampling.LSGeneticFreezerDate | ||
| LabSampling.LSGeneticFreezerTime | ||
| LabSampling.LSGeneticNotCollReason | 1 == No informed consent 2 == Blood draw not successful 3 == Logistic reasons |
|
| LabSampling.LSHospitalCollctnDate | 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 | ||
| LabSampling.LSPointOfCareCollctnDate | ||
| LabSampling.LSPointOfCareCollctnTime | ||
| LabSampling.LSTissueCollctnDate | ||
| LabSampling.LSTissueCollctnTime | ||
| MedHx.AnticoagAntiThrombinProtein | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of antithrombin protein therapeutics (Atryn). | |
| MedHx.AnticoagCoumarin | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of Coumarin derivative (Coumadin, Warfarin). | |
| MedHx.AnticoagDirectThrombinInhib | 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 | 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 | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of heparin. | |
| MedHx.AnticoagLowMolHeparin | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of low molecular weight heparin | |
| MedHx.AnticoagulantOther | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of Xarelto | |
| MedHx.BetaBlocker | 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 | 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 | 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 | 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 | 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 | 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 | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, specifically Carteolol. | |
| MedHx.BetaBlockerNonSelectNadolol | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, specifically Nadolol | |
| MedHx.BetaBlockerNonSelectOther | 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 | 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 | Medical history. Use of anticoagulant or platelet aggregation inhibitor by the patient. This variable describes the use of beta blockers, specifically Penbutolo. | |
| MedHx.BetaBlockerNonSelectPindolol | 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 | Medical history. This variable describes the use of beta blockers, specifically Propranolol | |
| MedHx.BetaBlockerNonSelectSotalol | Medical history. This variable describes the use of beta blockers, specifically Sotalol (Sotacor) | |
| MedHx.BetaBlockerSelectAcebutolol | Medical history. This variable describes the use of beta blockers, specifically Acebutolol (Sectral) | |
| MedHx.BetaBlockerSelectAtenolol | Medical history. This variable describes the use of beta blockers, specifically Atenolol (Tenormin) | |
| MedHx.BetaBlockerSelectBetaxolol | Medical history. This variable describes the use of beta blockers, specifically Betaxolol (Kerlon) | |
| MedHx.BetaBlockerSelectBisoprolol | Medical history. This variable describes the use of beta blockers, specifically Bisoprolol (Emcor) | |
| MedHx.BetaBlockerSelectCeliprolol | Medical history. This variable describes the use of beta blockers, specifically Celiprolol (Dilanorm) | |
| MedHx.BetaBlockerSelectEsmolol | Medical history. This variable describes the use of beta blockers, specifically Esmolol (Brevibloc) | |
| MedHx.BetaBlockerSelectMetoprolol | Medical history. This variable describes the use of beta blockers, specifically Metoprolol (Selokeen). | |
| MedHx.BetaBlockerSelectNebivolol | Medical history. This variable describes the use of beta blockers, specifically Nebivolol (Nebilet) | |
| MedHx.BetaBlockerSelectOther | Medical history. This variable describes the use of beta blockers, specifically selective beta1blockers not specified elsewhere. | |
| MedHx.BetaBlockerSelectOtherTxt | Medical history. This variable describes the use of beta blockers, specifically selective beta1blockers not specified elsewhere (text field). | |
| MedHx.MedHxAnticoagulantsOrPlatelet | 0 == No 1 == Yes anticoagulants 2 == Yes platelet aggregation inhibitors 3 == Yes, both 88 == Unknown |
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 | 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 | 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 | 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 | 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 | ||
| MedHx.MedHxCardioNYHA | IV == IV III == III II == II I == I |
A classification system for severity of cardiac disease - generally used for ischaemia, but used here in broader sense. |
| MedHx.MedHxCardioOther | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 1 == Well controlled 2 == Difficult controlled 88 == Unknown |
|
| MedHx.MedHxEndocrineNIDDM | NIDDM: Non-insulin dependent diabetes mellitus | |
| MedHx.MedHxEndocrineNIDDMControl | 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 endocrine diseases, specifically how well IDDM (Insulin dependent diabetes mellitus) is controlled. |
| MedHx.MedHxEndocrineOther | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | ||
| MedHx.MedHxNeuroMigraineFamHist | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 oncologic, specifically prostate cancer. |
| MedHx.MedHxOtherTxt | 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 | 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 88 == Unknown |
Preinjury ASAPS classification. Common classification system used in anaesthesia; denotes overall health |
| MedHx.MedHxPreTBIConcussions | 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 | 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 | 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 | 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 total number of hospital admissions for previous TBI/ concussions |
| MedHx.MedHxPsychiatricAnx | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of ADP receptor inhibitors. | |
| MedHx.PltAggregADPReceptInhibEffient | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of Parasugrel (Effient) | |
| MedHx.PltAggregADPReceptInhibOther | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of ADP receptor inhibitors, not specified elsewhere. | |
| MedHx.PltAggregADPReceptInhibOtherTxt | 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 | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of Clopidogrel (Plavix). | |
| MedHx.PltAggregADPReceptInhibTiclid | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of Ticlopidine (Ticlid). | |
| MedHx.PltAggregAspirin | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of Aspirin | |
| MedHx.PltAggregGlycoproteinInhib | Medical history. Use of platelet aggregation inhibitor by the patient. This variable describes the use of glycoprotein IIB/IIIA inhibitors (eg. Aggrastat). | |
| Medication.Agent | 1 == Analgesic: paracetamol 2 == Analgesic: NSAIDs 3 == Analgesic: tramadol 4 == Analgesic: opioids (morphine, ect) 5 == Sedatives/treatment of agitation: barbiturates (penthothal, ect) 6 == Sedatives/treatment of agitation: clondine 7 == Sedatives/treatment of agitation: dexmedetomidine 8 == Sedatives/treatment of agitation: diazepam 9 == Sedatives/treatment of agitation: fentanyl 10 == Sedatives/treatment of agitation: haloperidol (haldol) 11 == Sedatives/treatment of agitation: lorazepam (tenesta, ect) 12 == Sedatives/treatment of agitation: midazolam 13 == Sedatives/treatment of agitation: morphine 14 == Sedatives/treatment of agitation: propofol 15 == Sedatives/treatment of agitation: other 16 == Neuromuscular blockade: pancuronium (pavulon) 17 == Neuromuscular blockade: atracurium (tracium) 18 == Neuromuscular blockade: cisatracurium (nimbex) 19 == Neuromuscular blockad: gallamine (flaxedil) 20 == Neuromuscular blockade: rocuronium (zemuron) 21 == Neuromuscular blockade: vecuronium (norcuron) 22 == Neuromuscular blockade: other 23 == Anti- epileptic: carbamazepine (tegretol) 24 == Anti- epileptic: lamotrigine (lamectal) 25 == Anti- epileptic: levetirazetam (keppra) 26 == Anti- epileptic: phenytoine (diphantoine) 27 == Anti- epileptic: valproate (depakine) 28 == Anti- epileptic: other 29 == Antibiotics: aminoglycoside (amikacine, gentamicine etc) 30 == Antibiotics: carbapemens (meronem etc) 31 == Antibiotics: cephalosporin 1st gen (cefalexin etc) 32 == Antibiotics: cephalosporin 2nd gen (cefuroxim etc) 33 == Antibiotics: cephalosporin 3rd gen (cefotaxine etc) 34 == Antibiotics: cephalosporin 4th gen (cefepime, maxipime etc) 35 == Antibiotics: cephalosporin 5th gen (ceftasoline etc) 36 == Antibiotics: glycopeptides (vancomycine) 37 == Antibiotics: lincosamides (clindamycine etc) 38 == Antibiotics: macrolidis (erythromycine etc) 39 == Antibiotics: nitrofurones (furoxone, furadantine etc) 40 == Antibiotics: penicillines (ampicilline, cloxacilline) 41 == Antibiotics: amoxycilline/clavulanic acid (augmentin, tyclav etc) 42 == Antibiotics: quinolones (ciprofloxacine etc) 43 == Antibiotics: sulfonamides (co-trimoxazole, doxycycline) 44 == Antibiotics: other 45 == Anti- hypertensive: ACE blockers (captopril, perindopril etc) 46 == Anti- hypertensive: angiotensininhibitors (cardesartan etc) 47 == Anti- hypertensive: bĆĀØtablockers (propanolol) 48 == Anti- hypertensive: clonidine 49 == Anti- hypertensive: diuretics 50 == Calcium channel blockers: nimodipine 51 == Calcium channel blockers: nicardipine 52 == Calcium channel blockers: verapamil 53 == Steroids: methylprednisolone 54 == Steroids: bĆĀ©tametasone 55 == Steroids: dexametasone 56 == Steroids: hydrocortisone/cortisone 57 == Antacids: Aluminium hydroxide 58 == Antacids: other 59 == H2 receptor antagonist: Cimetidine 60 == H2 receptor antagonist: Ranitidine (Zantac) 61 == Proton pump inhibitors: Omeprazol (Losec) 62 == Proton pump inhibitors: Esomeprazol (Nexium) 63 == Proton pump inhibitors: Pantoprazole (Pantozol) 64 == Prokinetics: Domperidon (Motilium) 65 == Prokinetics: Erythromycin 66 == Prokinetics: Metoclopramide (Primperan) 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 99 == Other, specify in Agent Other: Other |
|
| Medication.AgentOther | ||
| Medication.Class | 1 == Analgesic 2 == Sedatives/treatment of agitation 3 == Neuromuscular blockade 4 == Anti- epileptic 5 == Antibiotics 6 == Anti- hypertensive 7 == Calcium channel blockers 8 == Steroids 9 == Antacids 10 == H2 receptor antagonist 11 == Proton pump inhibitors 12 == Prokinetics 99 == Other, specify in Agent Other |
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 | These details should be entered for each agent | |
| Medication.Ongoing | These details should be entered for each agent; records if medication was still ongoing on discharge | |
| Medication.Reason | 1 == Sedatives/treatment of agitation: mechanical ventilation 2 == Sedatives/treatment of agitation: metabolic suppression 3 == Anti- epileptic: prophylaxis 4 == Anti- epileptic: treatment of overt seizure 6 == Anti- epileptic: treatment of (silent) seizure activity 7 == Antibiotics: fever, no clear focus 8 == Antibiotics: pneumonia 9 == Antibiotics: urinary tract infection 10 == Antibiotics: catheter related bloodstream infection 11 == Antibiotics: intracranial abces/empyeme 12 == Antibiotics: periprocedural prophylaxis 13 == Antibiotics: meningitis 14 == Anti- hypertensive: to lower blood pressure 15 == Anti- hypertensive: treatment agitation 16 == Calcium channel blockers: prevention of vasospasm 17 == Calcium channel blockers: treatment of vasospasm 18 == Calcium channel blockers: anti- hypertensive 19 == Calcium channel blockers: cardiac indication 20 == Steroids: traumatic brain injury 21 == Steroids: ARDS 22 == Steroids: hypopituitarism 23 == Steroids: sepsis 24 == Antacids: gastric protection 25 == Antacids: reflux 26 == H2 receptor antagonist: gastric protection 27 == H2 receptor antagonist: treatment of ulcer 28 == Proton pump inhibitors: gastric protection 29 == Proton pump inhibitors: treatment of ulcer 30 == Prokinetics: gastric retention 31 == Prokinetics: vomiting 32 == Prokinetics: constipation 33 == Prokinetics: routine care 35 == Analgesic: other 36 == Neuromuscular blockade: other 37 == Sedatives/treatment of agitation: Other 38 == Anti- epileptic: Other 39 == Antibiotics: Other 40 == Anti- hypertensive: Other 41 == Calcium channel blockers: Other 42 == Steroids: Other 43 == Antacids: Other 44 == H2 receptor antagonist: Other 45 == Proton pump inhibitors: Other 46 == Prokinetics: Other 99 == Other, specify in Agent Other: Other |
These details should be entered for each agent |
| Medication.ReasonOther | These details should be entered for each agent | |
| Medication.Route | ED == Epidural IvCont == Continuous IV IvInt == Intermittent IV Ih == Inhaled Re == Rectal Im == Intramuscular PO == Oral Pv == Vaginal To == Topical Sc == Subcutaneous |
These details should be entered for each agent |
| Medication.StartDate | These details should be entered for each agent | |
| Medication.StopDate | These details should be entered for each agent | |
| Meds.DVTMechOngoing | ||
| Meds.DVTPharmOngoing | ||
| Meds.DVTPharmType | 1 == Heparin 2 == Low molecular weight Heparin 3 == Dalteparin (Fragmin) 4 == Enoxaparin 5 == Nadroparin (Fraxiparine, Fraxodil) 6 == Parnaparin 7 == Reviparin 8 == Tinzaparin |
|
| Meds.DVTProphylaxisMech | 0 == No 1 == Yes |
|
| Meds.DVTProphylaxisMechStartDate | ||
| Meds.DVTProphylaxisMechStopDate | ||
| Meds.DVTProphylaxisMechType | ||
| Meds.DVTProphylaxisPharm | 0 == No 1 == Yes |
These variables aim to document specific information on the use of DVT prophylaxis. Little evidence exists on the use and timing of DVT prophylaxis after TBI, and considerable practice variation exists. |
| Meds.DVTProphylaxisStartDate | ||
| Meds.DVTProphylaxisStopDate | ||
| Meds.EnteralNutrition | 0 == No 1 == Yes |
|
| Meds.EnteralNutritionRoute | 1 == Nasogastric tube 2 == Transpyloric tube 3 == Gastrostomy |
|
| Meds.EnteralNutritionStartDate | ||
| Meds.EnteralNutritionStopDate | ||
| Meds.Intubation | 0 == No 1 == Yes |
|
| Meds.IntubationStartDate | ||
| Meds.IntubationStartTime | ||
| Meds.IntubationStop | 0 == No 1 == Yes |
|
| Meds.IntubationStopDate | ||
| Meds.IntubationStopReason | 1 == Respiratory stable 2 == Accidental 3 == Withdrawal of care |
|
| Meds.IntubationStopTime | ||
| Meds.MechVentilation | 0 == No 1 == Yes |
|
| Meds.MechVentilationStartDate | ||
| Meds.MechVentilationStartTime | ||
| Meds.MechVentilationStopDate | ||
| Meds.MechVentilationStopTime | ||
| Meds.Nasogastric | 0 == No 1 == Yes |
|
| Meds.NasogastricOngoing | ||
| Meds.NasogastricStartDate | ||
| Meds.NasogastricStopDate | ||
| Meds.OxygenAdm | 0 == No 1 == Yes 88 == Unknown |
|
| Meds.OxygenAdmOngoing | ||
| Meds.OxygenAdmStartDate | ||
| Meds.OxygenAdmStopDate | ||
| Meds.ParenteralNutrition | 0 == No 1 == Yes |
|
| Meds.ParenteralNutritionStartDate | These variables aim to document specific information on nutritional support, provided by parenteral and/or enteral routes. | |
| Meds.ParenteralNutritionStopDate | ||
| Meds.PEGTube | 0 == No 1 == Yes |
|
| Meds.PEGTubeOngoing | ||
| Meds.PEGTubeStartDate | ||
| Meds.PEGTubeStopDate | ||
| Meds.ReIntubation | 0 == No 1 == Yes |
|
| Meds.ReIntubationStartDate | ||
| Meds.ReIntubationStartTime | ||
| Meds.ReMechVentilation | 0 == No 1 == Yes |
|
| Meds.ReMechVentilationReason | 1 == Respiratory failure 2 == Neurologic deterioration 3 == Spontaneous hyperventilation 4 == Sepsis 99 == Other |
|
| Meds.ReMechVentilationReasonOther | ||
| Meds.ReMechVentilationStartDate | ||
| Meds.ReMechVentilationStartTime | ||
| Meds.TakenMeds | 0 == No 1 == Yes |
Documentation of concomitant medication largely follows a pre-defined structure: A total of 12 classes of drugs are pre-defined, each with a drop-down menu of 1-15 most commonly used agents. The reason for prescribing, the highest daily dose&units as well as route of administration is documented. For agents not listed in the drop-down menu's, the option "other" permits free text entries. |
| Meds.Tracheostomy | 0 == No 1 == Yes |
|
| Meds.TracheostomyOngoing | ||
| Meds.TracheostomyStartDate | ||
| Meds.TracheostomyStopDate | ||
| Meds.UrineCath | 0 == No 1 == Yes |
|
| Meds.UrineCathOngoing | ||
| Meds.UrineCathStartDate | ||
| Meds.UrineCathStopDate | ||
| Meds.VentilationMgmtNA | ||
| Outcomes.10mWALKBestTestTime | ||
| Outcomes.10mWALKCompletionCode | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
|
| Outcomes.10mWALKDate | ||
| Outcomes.10mWALKTest1 | ||
| Outcomes.10mWALKTest2 | ||
| Outcomes.10mWALKTest3 | ||
| Outcomes.10mWALKTestAttemptdNotCompOptions | 2.1 == Not completed - Cognitive/neurological deficits 2.2 == Not completed - Non-neurological/physical reason 2.3 == Not completed - Lack of effort/uncooperative 2.4 == Not completed - Language 2.5 == Not completed - Illness/fatigue 2.6 == Not completed - Logistical reasons, other reasons 2.7 == Not completed - Examiner error |
This variable describes why the test is attempted, but not completed. |
| Outcomes.10mWALKTestAttemptdNotCompOptionsOTHER | This variable describes why the test is attempted, but not completed. | |
| Outcomes.10mWALKTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
|
| Outcomes.10mWALKTestComplNonStandAdminOTHER | ||
| Outcomes.10mWALKTestNotDoneOptions | 1.1 == Not attempted - Cognitive/neurological deficits 1.2 == Not attempted - Non-neurological/physical reasons 1.3 == Not attempted - Lack of effort/uncooperative 1.4 == Not attempted - Language 1.5 == Not attempted - Illness/fatigue 1.6 == Not attempted - Logistical reasons, other reasons 1.7 == Not attempted - Examiner error 1.8 == Not attempted - Patient not available |
This variable describes the reason why the test is not done. |
| Outcomes.10mWALKTestNotDoneOptionsOTHER | This variable describes why the test is not done. | |
| Outcomes.10mWALKTUGNeuroPsychCompCode | 1.0 == 1.0 Test not done 2.0 == 2.0 Test attempted but not completed 3.0 == 3.0 Test completed |
This variable describes the completion status of the assessment. |
| Outcomes.CANTABAST | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABASTCompCode | 1.0 == Test not done 2.0 == Test attempted, but not completed 3.0 == Test completed |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABASTCongruencyCostMeanBlock3Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Mean for correct trials in Block 3. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMeanBlock5Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Mean for correct trials in Block 5. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMeanBlock7Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Mean for correct trials in Block 7. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMeanCorrect | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Mean for all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMedianBlock3Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Median for correct trials in Block 3. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMedianBlock5Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Median for correct trials in Block 5. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMedianBlock7Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Median for correct trials in Block 7. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostMedianCorrect | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Median for all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostSDBlock3Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Standard deviation for correct trials in Block 3. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostSDBlock5Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Standard deviation for correct trials in Block 5. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostSDBlock7Correct | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Standard deviation for correct trials in Block 7. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTCongruencyCostSDCorrect | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) on the trials that were congruent versus the trials that were incongruent. Standard deviation for all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatency | Attention Switching Task (AST): Mean response latency on all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencyCongruent | Attention Switching Task (AST): Mean response latency on correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencyDirection | Attention Switching Task (AST): Mean response latency on correct direction task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencyIncongruent | Attention Switching Task (AST): Mean response latency on correct incongruent task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencyNonSwitched | Attention Switching Task (AST): Mean response latency on correct task non-switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencySide | Attention Switching Task (AST): Mean response latency on correct side task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMeanCorrectLatencySwitched | Attention Switching Task (AST): Mean response latency on correct task switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatency | Attention Switching Task (AST): Median response latency on all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencyCongruent | Attention Switching Task (AST): Median response latency on correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencyDirection | Attention Switching Task (AST): Median response latency on correct direction task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencyIncongruent | Attention Switching Task (AST): Median response latency on correct incongruent task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencyNonSwitched | Attention Switching Task (AST): Median response latency on correct task non-switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencySide | Attention Switching Task (AST): Median response latency on correct side task trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTMedianCorrectLatencySwitched | Attention Switching Task (AST): Median response latency on correct task switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSDCorrectLatency | Attention Switching Task (AST): Standard deviation of response latency on all correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSDCorrectLatencyCongruent | Attention Switching Task (AST): Standard deviation of response latency on correct congruent trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencyDirection | Attention Switching Task (AST): Standard deviation of response latency on correct direction task trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencyIncongruent | Attention Switching Task (AST): Standard deviation of response latency on correct incongruent task trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencyNonSwitched | Attention Switching Task (AST): Standard deviation of response latency on correct task non-switched trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencySide | Attention Switching Task (AST): Standard deviation of response latency on correct side task trials. Time in msec. | |
| Outcomes.CANTABASTSDCorrectLatencySwitched | Attention Switching Task (AST): Standard deviation of response latency on correct task switched trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMeanCorrect | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMeanCorrectCongruent | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Mean for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMeanCorrectIncongruent | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Mean for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMedianCorrect | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Median for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMedianCorrectCongruent | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Median for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostMedianCorrectIncongruent | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Median for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostSDCorrect | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Standard deviation for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostSDCorrectCongruent | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Standard deviation for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTSwitchingCostSDCorrectIncongruent | Attention Switching Task (AST): The difference between the median latency of response (from stimulus appearance to button press) during assessed blocks in which the rule is switching versus assessed blocks in which the rule remains constant. Standard deviation for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestAttemptdNotCompOptions | 2.7 == NotĀ completedĀ Ā- Examinor Error 2.1 == NotĀ completedĀ Ā- Cognitive/neurologicalĀ deficits 2.2 == NotĀ completedĀ -Ā NonĀneurological/physicalĀ reason 2.3 == NotĀ completed -Ā LackĀ ofĀ effort/uncooperative 2.4 == NotĀ completedĀ -ĀĀ Language 2.5 == NotĀ completed -ĀĀ Illness/fatigue 2.6 == NotĀ completedĀ ĀĀ LogisticalĀ reasons,Ā otherĀ reasons |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABASTTestAttemptdNotCompOptionsOTHER | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestCompletedOptions | 1.0 == Test not done 2.3 == Test attempted, but not completed 3.0 == Test completed |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABASTTestComplNonStandAdminOTHER | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTestNotDoneOptions | 1.8 == NotĀ attemptedĀ -ĀĀ PatientĀ not available 1.1 == NotĀ attemptedĀ -ĀĀ Cognitive/neurologicalĀ deficits 1.2 == NotĀ attemptedĀ -ĀĀ NonĀneurological/physicalĀ reasons 1.3 == NotĀ attemptedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 1.4 == NotĀ attemptedĀ -ĀĀ Language 1.5 == NotĀ attemptedĀ -ĀĀ Illness/fatigue 1.6 == NotĀ attemptedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons 1.7 == NotĀ attempted - ReturnĀ toĀ allĀ normalĀ activities |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABASTTestNotDoneOptionsOTHER | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCommissionErrors | Attention Switching Task (AST): This is the total number of trials for which the trial outcome was a commission error āwhere the subject responded too soon; either prior to the end of the pre-empt window or prior to the appearance of the stimulus. Total errors in all blocks. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCommissionErrorsBlock3 | Attention Switching Task (AST): This is the total number of trials for which the trial outcome was a commission error āwhere the subject responded too soon; either prior to the end of the pre-empt window or prior to the appearance of the stimulus. Total errors in block 3. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCommissionErrorsBlock5 | Attention Switching Task (AST): This is the total number of trials for which the trial outcome was a commission error āwhere the subject responded too soon; either prior to the end of the pre-empt window or prior to the appearance of the stimulus. Total errors in block 5. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCommissionErrorsBlock7 | Attention Switching Task (AST): This is the total number of trials for which the trial outcome was a commission error āwhere the subject responded too soon; either prior to the end of the pre-empt window or prior to the appearance of the stimulus. Total errors in block 7. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct all trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsBlock3 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct Block 3. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsBlock5 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct Block 5. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsBlock7 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct Block 7. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsCongruent | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct congruent trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsDirection | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsIncongruent | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct incongruent trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsLeftDirection | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct left direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsLeftSide | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct left side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsNonSwitched | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct non-switched trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsRightDirection | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct right direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsRightSide | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct right side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsSide | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalCorrectTrialsSwitched | Attention Switching Task (AST): This is the total number of trials which the trial outcome was a correct response. Total correct switched trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrials | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect all trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsBlock3 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect Block 3. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsBlock5 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect Block 5. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsBlock7 | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect Block 7. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsCongruent | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect congruent trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsDirection | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsIncongruent | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect incongruent trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsLeftDirection | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect left direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsLeftSide | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect left side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsNonSwitched | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect non-switched trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsRightDirection | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect right direction trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsRightSide | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect right side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsSide | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect side trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalIncorrectTrialsSwitched | Attention Switching Task (AST): This is the total number of trials which the trial outcome was an incorrect response. Total incorrect switched trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalOmissionErrors | Attention Switching Task (AST): This is the total number of This is the total number of trials, for which the trial outcome was an omission error which the trial outcome was an omission error ā where the subject responded too late, after end where the subject responded too late, after end of the response window. Total errors all trials. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalOmissionErrorsBlock3 | Attention Switching Task (AST): This is the total number of This is the total number of trials, for which the trial outcome was an omission error which the trial outcome was an omission error ā where the subject responded too late, after end where the subject responded too late, after end of the response window. Total errors Block 3. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalOmissionErrorsBlock5 | Attention Switching Task (AST): This is the total number of This is the total number of trials, for which the trial outcome was an omission error which the trial outcome was an omission error ā where the subject responded too late, after end where the subject responded too late, after end of the response window. Total errors Block 5 For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABASTTotalOmissionErrorsBlock7 | Attention Switching Task (AST): This is the total number of This is the total number of trials, for which the trial outcome was an omission error which the trial outcome was an omission error ā where the subject responded too late, after end where the subject responded too late, after end of the response window. Total errors Block 7 For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABBattery | Test battery used. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABDaysPost | Test session days post-injury For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPAL | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABPALCompCode | 1.0 == 1.0 Test not done 2.0 == 2.0 Test attempted but not completed 3.0 == 3.0 Test completed |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABPALFirstTrialMemoryScore | Paired Associate Learning (PAL): The number of correct box choices that were made on the first attempt during assessment problems For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALMeanErrorsToSuccess | Paired Associate Learning (PAL): This measure summarises, for all stages, the mean number of errors made before the stage was successfully completed. It is calculated by summing the total errors for all attempted stages and dividing the result by the number of successfully completed stages. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALMeanTrialsToSuccess | Paired Associate Learning (PAL): This is calculated by calculating the total number of trials required (maximum score=10 trials per stage) to locate all the patterns correctly in all stages attempted, and dividing the result by the number of successfully completed stages. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALNumberOfPatternsReached | Paired Associate Learning (PAL): This is calculated by calculating the total number of trials required (maximum score=10 trials per stage) to locate all the patterns correctly in all stages attempted, and dividing the result by the number of successfully completed stages. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALStagesCompleted | Paired Associate Learning (PAL): This is a key indicator of the subjectās overall success, recording how many stages were successfully completed. When analysing other outcome measures from PAL it is crucial that analyses are conducted with reference to the number of stages completed. Clearly a subject that fails prior to the successful completion of the 8-pattern stage will have had less opportunity to make errors than a subject who completes the test. Higher is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALStagesCompletedOnFirstTrial | Paired Associate Learning (PAL): This is the number of stages passed on the first trial (out of a maximum of 8 stages in the clinical mode). This relates to the PAL first trial memory score. Higher is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestAttemptdNotCompOptions | 2.7 == NotĀ completedĀ Ā- Examinor Error 2.1 == NotĀ completedĀ Ā- Cognitive/neurologicalĀ deficits 2.2 == NotĀ completedĀ -Ā NonĀneurological/physicalĀ reason 2.3 == NotĀ completed -Ā LackĀ ofĀ effort/uncooperative 2.4 == NotĀ completedĀ -ĀĀ Language 2.5 == NotĀ completed -ĀĀ Illness/fatigue 2.6 == NotĀ completedĀ ĀĀ LogisticalĀ reasons,Ā otherĀ reasons |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABPALTestAttemptdNotCompOptionsOTHER | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABPALTestComplNonStandAdminOTHER | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTestNotDoneOptions | 1.8 == NotĀ attemptedĀ -ĀĀ PatientĀ not available 1.1 == NotĀ attemptedĀ -ĀĀ Cognitive/neurologicalĀ deficits 1.2 == NotĀ attemptedĀ -ĀĀ NonĀneurological/physicalĀ reasons 1.3 == NotĀ attemptedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 1.4 == NotĀ attemptedĀ -ĀĀ Language 1.5 == NotĀ attemptedĀ -ĀĀ Illness/fatigue 1.6 == NotĀ attemptedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons 1.7 == Not attempted - ReturnĀ toĀ allĀ normalĀ activities |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABPALTestNotDoneOptionsOTHER | Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors | Paired Associate Learning (PAL): This measure reports the total number of errors across all assessed problems and all stages. Note that subjects failing at any stage of the test have had less opportunity to make errors than subjects who complete the test. The PAL Total errors (adjusted) measure attempts to compensate for this. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors2Shapes | Paired Associate Learning (PAL): Total errors on 2-pattern trials For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors2ShapesAdjusted | Paired Associate Learning (PAL): This measure reports the total number of errors made at the two 2-pattern stages (when there is a stimulus in two of the 6 boxes), with an adjustment for those who have not reached these stages. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors3Shapes | Paired Associate Learning (PAL): Total errors on 3-pattern trials For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors3ShapesAdjusted | Paired Associate Learning (PAL): This measure reports the total number of errors made at the two 3-pattern stages (when there is a stimulus in three of the 6 boxes), with an adjustment for those who have not reached these stages. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors6Shapes | Paired Associate Learning (PAL): Total errors on 6-pattern trials For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors6ShapesAdjusted | Paired Associate Learning (PAL): This measure reports the total number of errors made at the 6 -pattern stage (when there is a stimulus in each the 6 boxes), with an adjustment for those who have not reached these stage. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors8Shapes | Paired Associate Learning (PAL): Total errors on 8-pattern trials For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABPALTotalErrors8ShapesAdjusted | Paired Associate Learning (PAL): This measure reports the total number of errors made at the 8-pattern stage (when there is a stimulus in each the 8 boxes), with an adjustment for those who have not reached these stage. | |
| Outcomes.CANTABPALTotalErrorsAdjusted | Paired Associate Learning (PAL): This measure reports the total number of errors across all assessed problems and all stages, with an adjustment for each stage not attempted due to previous failure. | |
| Outcomes.CANTABPALTotalTrials | Paired Associate Learning (PAL): This measure represents the total number of trials required. | |
| Outcomes.CANTABPALTotalTrials2Shapes | Paired Associate Learning (PAL): This measure represents the number of trials required at the 2-pattern stage. | |
| Outcomes.CANTABPALTotalTrials3Shapes | Paired Associate Learning (PAL): This measure represents the number of trials required at the 3-pattern stage. | |
| Outcomes.CANTABPALTotalTrials6Shapes | Paired Associate Learning (PAL): This measure represents the number of trials required at the 6-pattern stage. | |
| Outcomes.CANTABPALTotalTrials8Shapes | Paired Associate Learning (PAL): This measure represents the number of trials required at the 8-pattern stage. | |
| Outcomes.CANTABPALTotalTrialsAdjusted | Paired Associate Learning (PAL): This measure represents the total number of presentations required to locate all the patterns correctly in all stages. When using this measure it is important to analyse the data with reference to the PAL Stages completed score. This is because subjects who fail to complete the test will have had fewer PAL Total trials simply because they had less opportunity to make errors than subjects who completed the test. One possible way of dealing with this is to add the maximum score of 10 trials (or 6, depending on the mode) for each stage not attempted due to an earlier failure and this is what this measure shows. Please note that if this adjustment is made to a dataset in which large numbers of subjects have failed, this will have the effect of markedly reducing variance in later stages. Note that for aborted runs, the adjustment is made based on the subject failing the stage on which the test was aborted, so each of the 10 trials(or 6, depending on the mode) from that stage will count as part of the adjusted score. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTI | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRTICompCode | 1.0Ā == TestĀ notĀ done 2.0Ā == TestĀ attemptedĀ butĀ notĀ completed 3.0Ā == TestĀ completed |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRTIFiveChoiceErrorScoreAll | Reaction time (RTI): This is the total number of trials where the response status is recorded as an error, for assessment trials where the stimuli appear in one of five locations. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScoreInaccurate | Reaction time (RTI): This is the total number of trials where the response status is recorded as the specified error type, for assessment trials where the stimuli appear in one of five locations. Error types: inaccurate, incorrect location, premature, or no response settings. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScoreIncorrectLocation | Reaction time (RTI): This is the total number of trials where the response status is recorded as the specified error type, for assessment trials where the stimuli appear in one of five locations. Error types: inaccurate, incorrect location, premature, or no response settings. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScoreNoResponse | Reaction time (RTI): This is the total number of trials where the response status is recorded as the specified error type, for assessment trials where the stimuli appear in one of five locations. Error types: inaccurate, incorrect location, premature, or no response settings. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIFiveChoiceErrorScorePremature | Reaction time (RTI): This is the total number of trials where the response status is recorded as the specified error type, for assessment trials where the stimuli appear in one of five locations. Error types: inaccurate, incorrect location, premature, or no response settings. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMeanFiveChoiceMovementTime | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one of five possible locations. Lower is better. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMeanFiveChoiceReactionTime | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in any one of five locations. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMeanSimpleMovementTime | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one location. Lower is better. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMeanSimpleReactionTime | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in one location. Mean for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMedianFiveChoiceMovementTime | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one of five possible locations. Lower is better. Median for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMedianFiveChoiceReactionTime | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in any one of five locations. Median for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMedianSimpleMovementTime | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one location. Lower is better. Median for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTIMedianSimpleReactionTime | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in one location. Median for correct incongruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTISDFiveChoiceMovementTime | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one of five possible locations. Lower is better. Standard deviation for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTISDFiveChoiceReactionTime | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in any one of five locations. Standard deviation for correct congruent trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTISDSimpleMovementTime | Reaction time (RTI): This is the time taken to touch the stimulus after the press pad button has been released in trials where the stimulus has been presented in one location. Lower is better. Standard deviation for correct trials. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTISDSimpleReactionTime | Reaction time (RTI): This is the speed with which the subject releases the press pad button in response to a stimulus in one location. Standard deviation for correct congruent trials. Time in msec. | |
| Outcomes.CANTABRTISimpleAccuracyScore | Reaction time (RTI): This is the total number of trials where the response is recorded as correct, for assessment trials where the stimuli appear in one location only. Higher is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestAttemptdNotCompOptions | 2.7 == NotĀ completedĀ Ā- Examinor Error 2.1 == NotĀ completedĀ Ā- Cognitive/neurologicalĀ deficits 2.2 == NotĀ completedĀ -Ā NonĀneurological/physicalĀ reason 2.3 == NotĀ completed -Ā LackĀ ofĀ effort/uncooperative 2.4 == NotĀ completedĀ -ĀĀ Language 2.5 == NotĀ completed -ĀĀ Illness/fatigue 2.6 == NotĀ completedĀ ĀĀ LogisticalĀ reasons,Ā otherĀ reasons |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRTITestAttemptdNotCompOptionsOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRTITestComplNonStandAdminOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRTITestNotDoneOptions | 1.8 == NotĀ attemptedĀ -ĀĀ PatientĀ not available 1.1 == NotĀ attemptedĀ -ĀĀ Cognitive/neurologicalĀ deficits 1.2 == NotĀ attemptedĀ -ĀĀ NonĀneurological/physicalĀ reasons 1.3 == NotĀ attemptedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 1.4 == NotĀ attemptedĀ -ĀĀ Language 1.5 == NotĀ attemptedĀ -ĀĀ Illness/fatigue 1.6 == NotĀ attemptedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons 1.7 == NotĀ attempted - ReturnĀ toĀ allĀ normalĀ activities |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRTITestNotDoneOptionsOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVP | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRVPA | Rapid Visual Information Processing (RVP): Aā² (A prime) is the signal detection measure of sensitivity to the target, regardless of response tendency (range 0.00 to 1.00; bad to good). In essence, this measure is a measure of how good the subject is at detectingtarget sequences using p(hit) and p(fa). For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPB | Rapid Visual Information Processing (RVP): Bā³ (B double prime) is the signal detection measure of the strength of trace required to elicit a response (range ā1.00 to +1.00). Thus, it is the tendency to respond regardless of whether the target sequence is present, and uses the p(hit) and p(fa) results. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPCompCode | 1.0Ā == TestĀ notĀ done 2.0Ā == TestĀ attemptedĀ butĀ notĀ completed 3.0Ā == TestĀ completed |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRVPMeanLatency | Rapid Visual Information Processing (RVP): This measure details the mean time taken to respond and is reported in milliseconds. It only includes correct responses made within the response window of 1800 milliseconds. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPMedianLatency | Rapid Visual Information Processing (RVP): This measure details the median time taken to respond and is reported in milliseconds. It only includes correct responses made within the response window of 1800 milliseconds. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPProbabilityOfFalseAlarm | Rapid Visual Information Processing (RVP): The probability of a false alarm or p(fa) (the subject responding inappropriately), is equal to total false alarms/(total false alarms + total correct rejections). For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPProbabilityOfHit | Rapid Visual Information Processing (RVP): The probability of a āhitā or p(hit), (the subject responding correctly), is calculated from hits/(hits+misses). For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPSDLatency | Rapid Visual Information Processing (RVP): This measure details the standard deviation of the time taken to respond and is reported in milliseconds. It only includes correct responses made within the response window of 1800 milliseconds. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestAttemptdNotCompOptions | 2.7 == NotĀ completedĀ Ā- ExaminerĀ error 2.1 == NotĀ completedĀ -ĀĀ Cognitive/neurologicalĀ deficits 2.2 == NotĀ completedĀ -ĀĀ NonĀneurological/physicalĀ reason 2.3 == NotĀ completedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 2.4 == NotĀ completedĀ -ĀĀ Language 2.5 == NotĀ completedĀ -ĀĀ Illness/fatigue 2.6 == NotĀ completedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRVPTestAttemptdNotCompOptionsOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRVPTestComplNonStandAdminOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTestNotDoneOptions | 1.8 == NotĀ attemptedĀ -ĀĀ PatientĀ not available 1.1 == NotĀ attemptedĀ -ĀĀ Cognitive/neurologicalĀ deficits 1.2 == NotĀ attemptedĀ -ĀĀ NonĀneurological/physicalĀ reasons 1.3 == NotĀ attemptedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 1.4 == NotĀ attemptedĀ -ĀĀ Language 1.5 == NotĀ attemptedĀ -ĀĀ Illness/fatigue 1.6 == NotĀ attemptedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons 1.7 == NotĀ attempted - ReturnĀ toĀ allĀ normalĀ activities |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABRVPTestNotDoneOptionsOTHER | ||
| Outcomes.CANTABRVPTotalCorrectRejections | Rapid Visual Information Processing (RVP): This is the number of stimuli that were correctly rejected, i.e., the number of stimuli that were not part of a target sequence and were not responded to. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTotalFalseAlarms | Rapid Visual Information Processing (RVP): This records the number of times the subject responds outside the response window of a target sequence. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTotalHits | Rapid Visual Information Processing (RVP): This score represents the number of occasions upon which the target sequence is correctly responded to. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABRVPTotalMisses | Rapid Visual Information Processing (RVP): This score reports the number of occasions the subject fails to respond to a target sequence within the response window For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSessionStartDate | Session test date For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCCompCode | 1.0Ā == TestĀ notĀ done 2.0Ā == TestĀ attemptedĀ butĀ notĀ completed 3.0Ā == TestĀ completed |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSOCMeanInitialThinkingTime2Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanInitialThinkingTime3Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanInitialThinkingTime4Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanInitialThinkingTime5Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanMoves2Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanMoves3Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanMoves4Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanMoves5Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanSubsequentThinkingTime2Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanSubsequentThinkingTime3Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanSubsequentThinkingTime4Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCMeanSubsequentThinkingTime5Moves | Stockings of Cambridge (SOC): Outcome only available when tested in clinical mode. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves | Stockings of Cambridge (SOC): This is a fundamental measure, recording the number of occasions upon which the subject has successfully completed a test problem in the minimum possible number of moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves2Moves | Stockings of Cambridge (SOC): Describes the mean number of moves required by the subject to solve problems where the solution can be reached in a minimum of 2 moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves3Moves | Stockings of Cambridge (SOC): Describes the mean number of moves required by the subject to solve problems where the solution can be reached in a minimum of 3 moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves4Moves | Stockings of Cambridge (SOC): Describes the mean number of moves required by the subject to solve problems where the solution can be reached in a minimum of 4 moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCProblemsSolvedInMinimumMoves5Moves | Stockings of Cambridge (SOC): Describes the mean number of moves required by the subject to solve problems where the solution can be reached in a minimum of 5 moves. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestAttemptdNotCompOptions | 2.7 == NotĀ completedĀ Ā- ExaminerĀ error 2.1 == NotĀ completedĀ -ĀĀ Cognitive/neurologicalĀ deficits 2.2 == NotĀ completedĀ -ĀĀ NonĀneurological/physicalĀ reason 2.3 == NotĀ completedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 2.4 == NotĀ completedĀ -ĀĀ Language 2.5 == NotĀ completedĀ -ĀĀ Illness/fatigue 2.6 == NotĀ completedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSOCTestAttemptdNotCompOptionsOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSOCTestComplNonStandAdminOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSOCTestNotDoneOptions | 1.8 == NotĀ attemptedĀ -ĀĀ PatientĀ not available 1.1 == NotĀ attemptedĀ -ĀĀ Cognitive/neurologicalĀ deficits 1.2 == NotĀ attemptedĀ -ĀĀ NonĀneurological/physicalĀ reasons 1.3 == NotĀ attemptedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 1.4 == NotĀ attemptedĀ -ĀĀ Language 1.5 == NotĀ attemptedĀ -ĀĀ Illness/fatigue 1.6 == NotĀ attemptedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons 1.7 == NotĀ attempted - ReturnĀ toĀ allĀ normalĀ activities |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSOCTestNotDoneOptionsOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABStockingsOfCambridge | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSWM | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSWMBetweenErrors | Spatial Working Memory (SWM): Between errors are defined as times the subject revisits a box in which a token has previously been found. This is calculated for all trials of four or more tokens only. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMBetweenErrors4Boxes | Spatial Working Memory (SWM): Between errors are defined as times the subject revisits a box in which a token has previously been found. This is calculated for trials of four tokens only. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMBetweenErrors6Boxes | Spatial Working Memory (SWM): Between errors are defined as times the subject revisits a box in which a token has previously been found. This is calculated for trials of six tokens only. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMBetweenErrors8Boxes | Spatial Working Memory (SWM): Between errors are defined as times the subject revisits a box in which a token has previously been found. This is calculated for trials of eight tokens only. Lower is better. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMCompCode | 1.0Ā == TestĀ not done 2.0Ā == TestĀ attemptedĀ butĀ notĀ completed 3.0Ā == TestĀ completed |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSWMMeanTimeToFirstResponse | Spatial Working Memory (SWM): This is the mean time between the problem being presented to the subject and the subject first touching the screen to open a box. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToFirstResponse4Boxes | Spatial Working Memory (SWM): This is the mean time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 4 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToFirstResponse6Boxes | Spatial Working Memory (SWM): This is the mean time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 6 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToFirstResponse8Boxes | Spatial Working Memory (SWM): This is the mean time between the problem being presented to the subject and the subject first touching the screen to open a box, for problems with 8 boxes. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToLastResponse | Spatial Working Memory (SWM): This is the mean time for the subjectās last response for a problem. Time in msec. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToLastResponse4Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToLastResponse6Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTimeToLastResponse8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTokenSearchPreparationTime | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTokenSearchPreparationTime4Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTokenSearchPreparationTime6Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMeanTokenSearchPreparationTime8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToFirstResponse | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToFirstResponse4Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToFirstResponse6Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToFirstResponse8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToLastResponse | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToLastResponse4Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToLastResponse6Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTimeToLastResponse8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTokenSearchPreparationTime | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTokenSearchPreparationTime4Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTokenSearchPreparationTime6Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMMedianTokenSearchPreparationTime8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMProblemReached | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToFirstResponse | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToFirstResponse4Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToFirstResponse6Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToFirstResponse8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToLastResponse | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToLastResponse4Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToLastResponse6Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTimeToLastResponse8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTokenSearchPreparationTime | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTokenSearchPreparationTime4Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTokenSearchPreparationTime6Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMSDTokenSearchPreparationTime8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMStrategy | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMStrategy6To8Boxes | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestAttemptdNotCompOptions | 2.7 == NotĀ completedĀ Ā- ExaminerĀ error 2.1 == NotĀ completedĀ -ĀĀ Cognitive/neurologicalĀ deficits 2.2 == NotĀ completedĀ -ĀĀ NonĀneurological/physicalĀ reason 2.3 == NotĀ completedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 2.4 == NotĀ completedĀ -ĀĀ Language 2.5 == NotĀ completedĀ -ĀĀ Illness/fatigue 2.6 == NotĀ completedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSWMTestAttemptdNotCompOptionsOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
Completion codes of CANTAB testings are not automatically filled in in the outcome assessment form. For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSWMTestComplNonStandAdminOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABSWMTestNotDoneOptions | 1.8 == NotĀ attemptedĀ -ĀĀ PatientĀ not available 1.1 == NotĀ attemptedĀ -ĀĀ Cognitive/neurologicalĀ deficits 1.2 == NotĀ attemptedĀ -ĀĀ NonĀneurological/physicalĀ reasons 1.3 == NotĀ attemptedĀ -ĀĀ LackĀ ofĀ effort/uncooperative 1.4 == NotĀ attemptedĀ -ĀĀ Language 1.5 == NotĀ attemptedĀ -ĀĀ Illness/fatigue 1.6 == NotĀ attemptedĀ -ĀĀ LogisticalĀ reasons,Ā otherĀ reasons 1.7 == NotĀ attempted - ReturnĀ toĀ allĀ normalĀ activities |
For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! |
| Outcomes.CANTABSWMTestNotDoneOptionsOTHER | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.CANTABTestingLanguage | For more detailed information on CANTAB outcome measures, we strongly recommend to check the User Manual -Appendix 3! | |
| Outcomes.DerivedCompositeGOSE | 1 == 1-Dead 3 == 2 / 3- Vegetative State (VS) / Lower Severe Disability (Lower SD) 4 == 4-Upper Severe Disability (Upper SD) 5 == 5-Lower Moderate Disability (Lower MD) 6 == 6-Upper Moderate Disability (Upper MD) 7 == 7-Lower Good Recovery (Lower GR) 8 == 8-Upper Good Recovery (Upper GR) |
This GOSE rating is a derived composite score based on central review. The categories of Vegetative State and Lower Severe Disability are collapsed in the ratings assigned. Available information is used in the following order of precedence for the composite: (1) Central scoring of GOSE interview questionnaires completed by investigators (2) Central scoring based on GOSE postal questionnaires completed by patients and carers (3) Interviewer ratings for survivors, when neither of the GOSE questionnaires have been completed. (4) Deaths recorded in the eCRF where the date of death is on or before the end of the window for follow-up. |
| Outcomes.DerivedCompositeGOSEDaysPostInjury | Days post-injury for composite GOSE assessment calculated from the date recorded for the corresponding interview or self-report questionnaire. A date is only included for ratings in survivors (i.e Outcomes.DerivedCompositeGOSE >1). | |
| Outcomes.Derived_SF12ScoreBP | ||
| Outcomes.Derived_SF12ScoreBPNBS | ||
| Outcomes.Derived_SF12ScoreGH | ||
| Outcomes.Derived_SF12ScoreGHNBS | ||
| Outcomes.Derived_SF12ScoreHMNBS | ||
| Outcomes.Derived_SF12ScoreMCS | Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScoreMH | ||
| Outcomes.Derived_SF12ScorePCS | Derived variable (i.e. SF-12 scores derived from SF-36 questionnaires). | |
| Outcomes.Derived_SF12ScorePF | ||
| Outcomes.Derived_SF12ScorePFNBS | ||
| Outcomes.Derived_SF12ScoreRE | ||
| Outcomes.Derived_SF12ScoreRENBS | ||
| Outcomes.Derived_SF12ScoreRP | ||
| Outcomes.Derived_SF12ScoreRPNBS | ||
| Outcomes.Derived_SF12ScoreSF | ||
| Outcomes.Derived_SF12ScoreSFNBS | ||
| Outcomes.Derived_SF12ScoreVT | ||
| Outcomes.Derived_SF12ScoreVTNBS | ||
| Outcomes.GAD7Afraid | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
|
| Outcomes.GAD7Annoyed | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
|
| Outcomes.GAD7Date | ||
| Outcomes.GAD7Nervous | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
|
| Outcomes.GAD7NonStopWorry | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
|
| Outcomes.GAD7Performed | 0 == Not performed 1 == Performed/Completed |
Responses for the GAD-7 relate to how oftent the subject has been bothered in the last 2 weeks |
| Outcomes.GAD7QuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
|
| Outcomes.GAD7Restless | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
|
| Outcomes.GAD7TotalScore | Not scored by investigator, calculated score. | |
| Outcomes.GAD7TrblRelax | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
|
| Outcomes.GAD7WorryTooMuch | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
|
| Outcomes.GOATBrnDate | -4 == Error (-4) 0 == No Error |
|
| Outcomes.GOATBuldngLoc | -5 == Error (-5) 0 == No Error |
|
| Outcomes.GOATCityLoc | -5 == Error (-5) 0 == No Error |
|
| Outcomes.GOATCompletionCode | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
Neuropsych testing was scheduled for all scheduled follow-up visits according to study protocol. Subjects were only considered testable if the GOAT was >=65. Neuropsych testing included: GOAT, RAVLT, TMT, CANTAB subtests, 10 m walk, Timed up-and-go, as well as Participant Questionnaire B.. "Untestable" patients received the GOAT and JFK-Coma Recovery Scale-revised. |
| Outcomes.GOATCrntTm | -5 == Two and one-half hour + error (-5) -4 == Two hour error (-4) -3 == One and one-half hour error (-3) -2 == One hour error (-2) -1 == Half-hour error (-1) 0 == No Error |
|
| Outcomes.GOATDate | Assessment of the GOAT was requested on discharge from the ER for all subjects who had regained consciousness and were able to undergo the test. A main research interest was to explore if - and how many - patients were still in PTA on discharge home. Patients are considered out of PTA if they have a total score of 78 or more. | |
| Outcomes.GOATDayDate | -3 == Three day error (-3) -2 == Two day error (-2) -1 == One day error (-1) 0 == No Error |
|
| Outcomes.GOATDayMnthDate | -5 == Five day + error (-5) -4 == Four day error (-4) -3 == Three day error (-3) -2 == Two day error (-2) -1 == One day error (-1) 0 == No Error |
|
| Outcomes.GOATDtlRslt | -5 == Error (-5) 0 == No Error |
|
| Outcomes.GOATFirEvntRslt | -5 == Error (-5) 0 == No Error |
|
| Outcomes.GOATFirEvntRsltTxt | ||
| Outcomes.GOATHospAdmDate | -5 == Error (-5) 0 == No Error |
|
| Outcomes.GOATLiveLoc | -4 == Error (-4) 0 == No Error |
|
| Outcomes.GOATLstEvntDtlRslt | -5 == Error (-5) 0 == No Error |
|
| Outcomes.GOATLstEvntRslt | -5 == Error (-5) 0 == No Error |
|
| Outcomes.GOATLstEvntRsltTxt | ||
| Outcomes.GOATMnthDate | -15 == Three or more month error (-15) -10 == Two month error (-10) -5 == One month error (-5) 0 == No Error |
|
| Outcomes.GOATNeuroPsychCompCode | 1.0 == 1.0 Test not done 2.0 == 2.0 Test attempted but not completed 3.0 == 3.0 Test completed |
Neuropsych testing was conducted during scheduled follow-up visits to hospital according to study protocol. Cross-sectional assessments across all strata was performed at 6 mnths after injury. For patients included in the MR substudy full testing was conducted for ER patients at: 2-3 weeks, 3 mnths and 6 mnths; Adm and ICU strata: 6 mnths, 12 mnths and 24 mnths Subjects were only considered testable if the GOAT was >=65. Neuropsych testing included: GOAT, RAVLT, TMT, CANTAB subtests, 10 m walk, Timed up-and-go, as well as Participant Questionnaire B.. "Untestable" patients received the GOAT and JFK-Coma Recovery Scale-revised.. |
| Outcomes.GOATNm | -2 == Error (-2) 0 == No Error |
|
| Outcomes.GOATOutcome | The total GOAT score is calculated as 100 - Total error points; Interpretation: 76-100 = Normal / 66-75 = Borderline / <66 = Impaired | |
| Outcomes.GOATTestAttemptdNotCompOptions | 2.1 == Not completed - Cognitive/neurological deficits 2.2 == Not completed - Non-neurological/physical reason 2.3 == Not completed - Lack of effort/uncooperative 2.4 == Not completed - Language 2.5 == Not completed - Illness/fatigue 2.6 == Not completed - Logistical reasons, other reasons 2.7 == Not completed - Examiner error |
Documents reasons why GOAT was not completed when it was initially attempted (7 categories) |
| Outcomes.GOATTestAttemptdNotCompOptionsOTHER | ||
| Outcomes.GOATTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
Test completed in full results valid/Test completed Nonstandard, results valid/Nonstandard administration/Other |
| Outcomes.GOATTestComplNonStandAdminOTHER | ||
| Outcomes.GOATTestNotDoneOptions | 1.1 == Not attempted - Cognitive/neurological deficits 1.2 == Not attempted - Non-neurological/physical reasons 1.3 == Not attempted - Lack of effort/uncooperative 1.4 == Not attempted - Language 1.5 == Not attempted - Illness/fatigue 1.6 == Not attempted - Logistical reasons, other reasons 1.7 == Not attempted- Return to all normal activities 1.8 == Not attempted - Patient not available |
Documents reasons why GOAT was not attempted (8 categories) |
| Outcomes.GOATTestNotDoneOptionsOTHER | ||
| Outcomes.GOATTime | ||
| Outcomes.GOATTotError | The total error score is calculated automatically. | |
| Outcomes.GOATTotScr | The total GOAT score is calculated as 100 - Total error points; Interpretation: 76-100 = Normal / 66-75 = Borderline / <66 = Impaired | |
| Outcomes.GOATTranspTyp | -5 == Error (-5) 0 == No Error |
|
| Outcomes.GOATYrDate | -30 == Three or more year error (-30) -20 == Two year error (-20) -10 == One year error (-10) 0 == No Error |
|
| Outcomes.GOSEAssistanceNeeded | 0 == No 1 == Yes |
Indicator if the participant needs another person at home essentially every day for some activities of daily living as part of Glasgow Outcome Scale Extended (GOS-E). |
| Outcomes.GOSEDate | Date when Glasgow Outcome Scale Extended (GOS-E) (1-8) was administered. | |
| Outcomes.GOSEEpilepsyFits | 1 == No 2 == Yes |
These 2 questions on epilepsy do not form part of the GOSE rating, but are included in the questionnaire as very relevant variables. Subjective reporting also in: Outcomes.PartQuestACurHltSeiz. Seizures that occurred before/at presentation or during hospital stay are recorded alsewhere: InjuryHx.EDComplEventSeizures; Vitals.HosComplEventSeizures; Hospital.HospComplSeizures; Vitals.HosComplEventSeizures; Hospital.ICUDisComplSeizure; |
| Outcomes.GOSEEpilepsyRisk | 1 == No 2 == Yes |
These 2 questions on epilepsy do not form part of the GOSE rating, but are included in the questionnaire as very relevant variables |
| Outcomes.GOSEFamilyDisrupt | 0 == No 1 == Yes |
Indicator if the participant faces any rifts in family relationships or friendships caused by psychological problems. |
| Outcomes.GOSEFamilyDisruptChange | 0 == No 1 == Yes |
Indicator if the level of disruption or strain in family and friendships depicts a change in respect to pre-injury situation |
| Outcomes.GOSEFamilyDisruptExtent | 1 == Occasional - less than weekly (Lower GR) 2 == Frequent - once a week or more, but tolerable (Upper MD) 3 == Constant - daily and intolerable (Lower MD) |
Frequency of the extent of the rifts in relationships, including family and friendships, due to psychological problems. |
| Outcomes.GOSEIndependentBefore | 0 == No 1 == Yes |
Indicator if the assistance at home was essential for the patient before the injury, as part of Glasgow Outcome Scale Extended (GOS-E). |
| Outcomes.GOSENeedFreqHelp | 0 == No (upper SD) 1 == Yes (lower SD) |
Indicator if the participant is in need of frequent help of someone to be around at home as part of Glasgow Outcome Scale Extended (GOS-E). |
| Outcomes.GOSEOtherCurrentProb | 0 == No (upper GR) 1 == Yes (lower GR) |
Indicator if the participant faces any other current problems currently due to injury |
| Outcomes.GOSEOtherCurrentProbWorse | 0 == No 1 == Yes |
Indicator if the similar problems were present before injury and have these become markedly worse. |
| Outcomes.GOSEOutcomeFactor | 1 == Effects of head injury 2 == Effects of illness or injury to another part of the body 3 == A mixture of these |
Provides an indication how much disability is not due to TBI |
| Outcomes.GOSEPerformed | 0 == Not performed 1 == Performed/Completed |
|
| Outcomes.GOSEPostalPerformed | 0 == Not performed 1 == Performed |
|
| Outcomes.GOSEPOSTAssistanceNeededFreq | 1 == I do not need help or supervision in the home 2 == I need some help in the home, but not every day 3 == I need help in the home every day, but I could look after myself for at least 8 hours if necessary 4 == I could not look after myself for 8 hours during the day 5 == I need help in the home, but not because of the injury |
|
| Outcomes.GOSEPOSTComments | ||
| Outcomes.GOSEPOSTCompletionCode | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logistical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Not attempted - Other |
|
| Outcomes.GOSEPOSTDate | ||
| Outcomes.GOSEPOSTFamilyDisruptBefore | 1 == No 2 == Yes |
|
| Outcomes.GOSEPOSTFamilyDisruptChange | 1 == Things are still much the same 2 == There are occasional problems (less than once a week) 3 == There are frequent problems (once a week or more) 4 == There are constant problems (problems every day) 5 == There are problems for some other reason, not because of the injury |
|
| Outcomes.GOSEPOSTIndependentBefore | 1 == No 2 == Yes |
|
| Outcomes.GOSEPOSTOtherCurrentProbs | 1 == I have no current problems 2 == I have some problems, but these do not interfere with my daily life 3 == I have some problems, and these have affected my daily life 4 == I have some problems for other reasons, not because of the head injury |
|
| Outcomes.GOSEPOSTOtherCurrentProbsBefore | 1 == I had no problems before, I had minor problems 2 == I had similar problems before |
|
| Outcomes.GOSEPOSTPatientLocn | 1 == Out of hospital 2 == In hospital or residential care |
This variable describes the location of the subject (in or out hospital). |
| Outcomes.GOSEPOSTResponse | 1 == Patient alone 2 == Relative or friend or carer alone 3 == Patient and relative, friend or carer together |
This variable describes the respondent that completed the questionnaire. |
| Outcomes.GOSEPOSTShopAloneBefore | 1 == No 2 == Yes |
This variable describes if a subject is able to buy things at shops without help. |
| Outcomes.GOSEPOSTShopAssistance | 1 == I do not need help to shop 2 == I need some help, but I can go to local shops on my own 3 == I need help to shop even locally, or I cannot shop at all 4 == I need help to shop, but not because of the injury |
This variable describes if a subject needs help to buy things at shops as a result of the injury. |
| Outcomes.GOSEPOSTSocialActivityBefore | 1 == No 2 == Yes |
This variable describes if a subject did take part in regular social and leisure activities outside home (at least once a week) before the injury. |
| Outcomes.GOSEPOSTSocialActivityChange | 1 == I take part about as often as before (the activities may be different from before) 2 == I take part a bit less, but at least half as often 3 == I take part much less, less than half as often 4 == I do not take part at all 5 == My ability to take part has changed for some other reason, not because of the injury |
This variable describes if there has been a change in the subject's ability to take part in social and leisure activities outside home as a result of the injury. |
| Outcomes.GOSEPOSTTravelAloneBefore | 1 == No 2 == Yes |
This variable describes if a subject was able to travel without help before the injury. |
| Outcomes.GOSEPOSTTravelAssistance | 1 == I do not need help to travel 2 == I need some help, but can travel locally on my own (eg. by arranging a taxi) 3 == I need help to travel even locally, or I cannot travel at all 4 == I need help to travel but not because of the injury |
This variable describes if a subject needs help to travel as a result of the injury. |
| Outcomes.GOSEPOSTWorkBefore | 1 == Working 2 == Looking for work 3 == Looking after family 4 == Studying as a student 5 == Retired 6 == None of these (eg. unfit for work) |
This variable describes the employment before the injury. |
| Outcomes.GOSEPOSTWorkChange | 1 == I still do the same work 2 == I still do the same work, but have some problems (e.g. tiredness, lack of concentration). 3 == I still work, but at a reduced level (e.g. change from full-time to part-time, or change in level of responsibility) 4 == I am unable to work, or only able to work in sheltered workshop 5 == My ability to work has changed, but not because of the injury |
This variable describes the change in ability to work as a result of the injury. |
| Outcomes.GOSEQuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
This questionnaire describes the mode in which the questionnaire is completed. |
| Outcomes.GOSEResponse | 0 == Patient alone 1 == Relative/friend/caretaker alone 2 == Patient plus relative/friend/caretaker |
This variable describes who completed the questionnaire. |
| Outcomes.GOSEResumeSocialActivity | 0 == No 1 == Yes |
This variable describes if a subject is able to resume regular social and leisure activities outside home. |
| Outcomes.GOSEScore | 1 == 1-Dead 2 == 2-Vegetative State (VS) 3 == 3-Lower Severe Disability (Lower SD) 4 == 4-Upper Severe Disability (Upper SD) 5 == 5-Lower Moderate Disability (Lower MD) 6 == 6-Upper Moderate Disability (Upper MD) 7 == 7-Lower Good Recovery (Lower GR) 8 == 8-Upper Good Recovery (Upper GR) |
This GOSE rating is assigned by the rater. In addition, a central review score will be allocated. |
| Outcomes.GOSEShopAlone | 0 == No (upper SD) 1 == Yes |
This variable describes if a subject is able to shop without assistance. |
| Outcomes.GOSEShopAloneBefore | 0 == No 1 == Yes |
This variable describes if a subject was able to shop without assistance before the injury. |
| Outcomes.GOSESimpleCommands | 0 == No (VS) 1 == Yes |
This variable describes if the subject is able to obey simple commands or say any words. |
| Outcomes.GOSESocialActivityRestrict | 1 == Participate a bit less, at least half as often as before injury (Lower GR) 2 == Participate much less,less than half as often (Upper MD) 3 == Unable to participate,rarely, if ever, take part (Lower MD) |
This variable describes the extent of restriction on the social and leisure activities. |
| Outcomes.GOSESocialActivityRestrictChange | 0 == No 1 == Yes |
This variable describes the engagement in regular social and leisure activities outside home before the injury. |
| Outcomes.GOSETravelAlone | 0 == No (upper SD) 1 == Yes |
This variable describes if the subject is able to travel locally without assistance. |
| Outcomes.GOSETravelAloneBefore | 0 == No 1 == Yes |
This variable describes if a subject was able to travel locally without assistance before the injury. |
| Outcomes.GOSEWork | 0 == No 1 == Yes |
This variable describes if a subject is currently able to work to the previous capacity. |
| Outcomes.GOSEWorkRestrictChange | 0 == No 1 == Yes |
This variable describes whether the subject was either working or seeking employment before the injury or was doing neither. |
| Outcomes.GOSEWorkRestriction | 1 == Reduced work capacity (upper MD) 2 == Able to work only in a sheltered workshop or non-competitive job or currently unable to work (Lower MD) |
Work restriction type experienced by the participant as a result of injury |
| Outcomes.JFKCRSRAdtyFuncScaleScore | 0 == 0 - None 1 == 1 - Auditory Startle 2 == 2 - Localization to Sound 3 == 3 - Reproducible Movement to Command * 4 == 4 - Consistent Movement to Command * |
|
| Outcomes.JFKCRSRArousalScaleScore | 0 == 0 - Unarousable 1 == 1 - Eye Opening with Stimulation 2 == 2 - Eye Opening w/o Stimulation 3 == 3 - Attention |
|
| Outcomes.JFKCRSRBrainStemCornRflx | 1 == Absent 2 == Present Unilateral 3 == Present Bilateral |
|
| Outcomes.JFKCRSRBrainStemNotes | ||
| Outcomes.JFKCRSRBrainStemOculocRflx | 1 == None 2 == Abnormal 3 == Full 4 == Normal |
|
| Outcomes.JFKCRSRBrainStemPosturalResp | 1 == Abnormal Extension 2 == Abnormal Flexion |
|
| Outcomes.JFKCRSRBrainStemPosturalRespLimb | ||
| Outcomes.JFKCRSRBrainStemPupilLight | 1 == Reactive 2 == Equal 3 == Constricted 4 == Dilated 5 == Pinpoint 6 == Accommodation |
|
| Outcomes.JFKCRSRBrainStemSpontEyeMvmt | 1 == None 2 == Skew Deviation 3 == Conjugate Gaze Deviation 4 == Roving 5 == Dysconjugate |
|
| Outcomes.JFKCRSRCommScaleScore | 0 == 0 - None 1 == 1 - Non-Functional, Intentional * 2 == 2 - Functional, Accurate &dagger |
|
| Outcomes.JFKCRSRContngntBehvrElicitgStim | Supplementary item | |
| Outcomes.JFKCRSRContngntBehvrNumElicitdOccur | Supplementary item | |
| Outcomes.JFKCRSRContngntBehvrNumSpontOccur | Supplementary item | |
| Outcomes.JFKCRSRContngntBehvrTargtBehvr | Supplementary item | |
| Outcomes.JFKCRSRDate | ||
| Outcomes.JFKCRSRMotrFuncScaleScore | 0 == 0 - None/Flaccid 1 == 1 - Abnormal Posturing 2 == 2 - Flexion Withdrawal 3 == 3 - Localization to Noxious Stimulation * 4 == 4 - Object Manipulation * 5 == 5 - Automatic Motor Response * 6 == 6 - Functional Object Useā |
|
| Outcomes.JFKCRSRNeuroPsychCompCode | 1.0 == 1.0 Test not done 2.0 == 2.0 Test attempted but not completed 3.0 == 3.0 Test completed |
JFK Coma Recovery Scale: only applicable for patients in a minimally conscious/vegatative state |
| Outcomes.JFKCRSROrmtrVerbFuncScaleScore | 0 == 0 - None 1 == 1 - Oral Reflexive Movement 2 == 2 - Vocalization/Oral Movement 3 == 3 - Intelligible Verbalization * |
|
| Outcomes.JFKCRSRTestAttemptdNotCompOptions | 2.1 == Not completed - Cognitive/neurological deficits 2.2 == Not completed - Non-neurological/physical reason 2.3 == Not completed - Lack of effort/uncooperative 2.4 == Not completed - Language 2.5 == Not completed - Illness/fatigue 2.6 == Not completed - Logistical reasons, other reasons 2.7 == Not completed - Examiner error |
|
| Outcomes.JFKCRSRTestAttemptdNotCompOptionsOTHER | ||
| Outcomes.JFKCRSRTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
|
| Outcomes.JFKCRSRTestComplNonStandAdminOTHER | ||
| Outcomes.JFKCRSRTestNotDoneOptions | 1.1 == Not attempted - Cognitive/neurological deficits 1.2 == Not attempted - Non-neurological/physical reasons 1.3 == Not attempted - Lack of effort/uncooperative 1.4 == Not attempted - Language 1.5 == Not attempted - Illness/fatigue 1.6 == Not attempted - Logistical reasons, other reasons 1.7 == Not attempted - Examiner error 1.8 == Not attempted - Patient not available |
|
| Outcomes.JFKCRSRTestNotDoneOptionsOTHER | ||
| Outcomes.JFKCRSRTotalScore | ||
| Outcomes.JFKCRSRVislFuncScaleScore | 0 == 0 - None 1 == 1 - Visual Startle 2 == 2 - Fixation * 3 == 3 - Visual Pursuit * 4 == 4 - Object Localization, Reaching * 5 == 5 - Object Recognition * |
|
| Outcomes.OneHundred | 100 == 100 | |
| Outcomes.PartQuestACurHltBack | 0 == No 1 == Yes |
This variable describes if the subject currently has back pain. |
| Outcomes.PartQuestACurHltHead | 0 == No 1 == Yes |
This variable describes if the subject currently has headaches. |
| Outcomes.PartQuestACurHltHear | 0 == No 1 == Yes |
This variable describes if the subject currently has trouble hearing. |
| Outcomes.PartQuestACurHltMob | 0 == No 1 == Yes |
This variable describes if the subject has problems with mobility/ walking. |
| Outcomes.PartQuestACurHltMove | 0 == No 1 == Yes |
This variable describes if the subject has problems with movement of hands or arms. |
| Outcomes.PartQuestACurHltNeck | 0 == No 1 == Yes |
This variable describes if the subject has neck pain or restricted neck movement. |
| Outcomes.PartQuestACurHltOther | 0 == No 1 == Yes |
This variable describes if the subject currently has any other health problems. |
| Outcomes.PartQuestACurHltOthertxt | This variable describes any other health problems the subject currently has. | |
| Outcomes.PartQuestACurHltSeiz | 0 == No 1 == Yes |
This variable describes if the subject currently has seizures (epileptic fits). |
| Outcomes.PartQuestACurHltSmell | 0 == No 1 == Yes |
This variable describes if the subject has trouble smelling or tasting. |
| Outcomes.PartQuestACurHltSpeech | 0 == No 1 == Yes |
This variable describes if the subject currently has problems with speaking or understanding others. |
| Outcomes.PartQuestACurHltVis | 0 == No 1 == Yes |
This variable describes if the subject currently has trouble with eye sight/vision (even with glasses). |
| Outcomes.PartQuestACurrSitChange | 1 == Better 2 == About the same 3 == A little worse 4 == Worse 5 == Much worse |
This variable describes how the subject compares their current situation to that before injury. |
| Outcomes.PartQuestACurrSitChangeReason | 1 == Because of the head injury 2 == Because of other injuries received at the same time 3 == Because of illness related to the injury 4 == Some other reason, not the injury |
This variable describes the reason for change in situation to that before the injury. |
| Outcomes.PartQuestAEmplmtStatus | 1 == Return to previous job (increased level or hours from pre-injury) 2 == Return to previous job (reduced level or hours) 3 == Change of job, different work 4 == Special employment/ sheltered employment 5 == Looking for work, unemployed 6 == Unable to work 7 == Retired 8 == Student 9 == Homemaker, keeping house 88 == Unknown |
This variable describes the current employment of a subject in case there was a change because of the injury. |
| Outcomes.PartQuestAEmplmtStatusChange | 0 == No 1 == Yes |
This variable describes if the subject's employment status is the same as before the injury. |
| Outcomes.PartQuestAMaritalStat | 1 == Single (never married) 2 == Married 3 == Partnered (other than married) 4 == Separated/Divorced 5 == Widowed |
This variable describes the current marital status in case there was a change because of the injury. |
| Outcomes.PartQuestAMaritalStatChange | 0 == No 1 == Yes |
This variable describes if there is a change in marital status. |
| Outcomes.PartQuestASatHospInj | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied a subject is with the hospital care at the time of the injury. |
| Outcomes.PartQuestASatHospPostInj | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied a subject is with the health service care afterwards (including rehabilitation). |
| Outcomes.PartQuestASatSupport | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable describes how satisfied a subject is with the availability of support from people close to them. |
| Outcomes.PartQuestASesPrimAdultChange | 0 == No 1 == Yes |
This variable describes if the living arrangements of a subject are the same as before the injury. |
| Outcomes.PartQuestASesPrimAdultChangePlace | 1 == At home- Supported 2 == At home- Not-supported 3 == Rehabilitation centre 4 == Nursing Home 5 == Hospital 99 == Other |
This variable describes the current living arrangement of a subject, in case the living arrangements are not the same as before the injury. |
| Outcomes.PartQuestASupHelp | 1 == Information from the hospital concerning the effects of head injury 2 == Help for problems with speaking or making yourself understood (e.g. speech therapy) 3 == Help for problems with memory, attention etc (e.g. cognitive rehabilitation) 4 == Help for problems with movement (e.g. physiotherapy) 5 == Help for problems with looking after yourself in daily life (washing, cooking, toileting, mobility) (e.g. occupational therapy) 6 == Help for emotional difficulties, such as anxiety, depression, or stress 7 == Help for problems with behaviour, such as anger 8 == Help for problems with fatigue 9 == Help for managing money 10 == Help returning to work (e.g. vocational rehabilitation or employment services) |
This variable describes any professional help in specific areas being given because of the injury. |
| Outcomes.PartQuestASupPeopleQty | 0 == None 1 == 1 2 == 2-5 6 == 6-9 10 == 10 or more |
This variable describes how many people a subject has near them they can readily count on for real help in times of trouble or difficulty, such as watch over children or pets, give rides to hospital or store, or help if they are sick. |
| Outcomes.PartQuestASupRehab | 0 == No rehabilitation 1 == In-patient / residential rehabilitation 2 == Out-patient/ community rehabilitation |
This variable denotes the patient perspective. Objective documentation is recorded at variable: FollowUp.FURehabNo; FollowUp.FURehabInPat; FollowUp.FURehabOutPat |
| Outcomes.PartQuestASupRehabNow | 0 == No 1 == Yes |
This variable describes if received rehabilitation is still ongoing. |
| Outcomes.PartQuestASupRehabTime | 1 == Within 1 month of injury 2 == Between 1 and 3 months of injury 3 == Later than 3 months after injury |
This variable describes when rehabilition as a result of head injury began. |
| Outcomes.PartQuestASupServices | 1 == Hospital services 2 == Community health services 3 == Private practice 4 == Social services (e.g. social work, housing) 5 == Legal services 6 == Charity services (e.g. head injury support group) 99 == Other |
|
| Outcomes.PartQuestBAUDITCAlcDrnkTypclDayNumScore | 1 == 1-2 2 == 3-4 3 == 5-6 4 == 7-9 5 == 10 or more |
This variable describes the amount of drinks containing alcohol consumed on a typical day. |
| Outcomes.PartQuestBAUDITCDrnkContainAlcFreqScore | 0 == Never 1 == Monthly or less 2 == 2-4 times a month 3 == 2-3 times a week 4 == 4 or more times a week |
Detailed questions on the use of alcohol are derived from the first 3 questions of the "AUDIT" questionnaire,a screening tool developed by the World Health Organization (WHO) to assess alcohol consumption, drinking behaviors, and alcohol-related problems. The same questions are asked on in the forms on Behavioral history: InjuryHx.AUDITCDrnkContainAlcFreqScore. This aims to facilitate comparison between post- and pre-injury use. |
| Outcomes.PartQuestBAUDITCMoreThan6AlcDrnkFreqScore | 0 == Never 1 == Less than monthly 2 == Monthly 3 == Weekly 4 == Daily or almost daily |
This variable describes how often the subject has six or more drinks on one occasion. |
| Outcomes.PartQuestBBeforeInjAdmitHosPsy | 0 == No 1 == Yes |
This variable describes if the subject has been admitted to hospital for psychiatric reasons before the injury. |
| Outcomes.PartQuestBBeforeInjEmoDis | 0 == No 1 == Yes |
This variable describes if the subject ever sought treatment for emotional disorders (e.g. depression or anxiety) before the injury. |
| Outcomes.PartQuestBBeforeInjFamMigraine | 0 == No 1 == Yes |
This variable describes if the subject's parents and/or any brothers/sisters suffer from migraine. |
| Outcomes.PartQuestBBeforeInjLearnDis | 0 == No 1 == Yes |
This variable describes if the subject ever had any learning disabilities or attended special classes. |
| Outcomes.PartQuestBBeforeInjMentalHlt | 0 == No 1 == Yes |
This variable describes if the subject ever sought treatment for any other mental or health problem before the injury. |
| Outcomes.PartQuestBBeforeInjMob | 1 == Yes 2 == No |
This variable describes if the subject had mobility problems before the injury. |
| Outcomes.PartQuestBBeforeInjNeuro | 0 == No 1 == Yes |
This variable describes if the subject ever had a brain or neurological illness before the injury (e.g. epilepsy, tumour, stroke). |
| Outcomes.PartQuestBBeforeInjPhysLim | 0 == No 1 == Yes |
This variable describes if the subject had any other physical limitations before injury. |
| Outcomes.PartQuestBBeforeInjPrevConcus | 0 == No 1 == Yes |
This variable describes if the subject ever had a concussion or brain injury before the injury. |
| Outcomes.PartQuestBBeforeInjPrevConcusSport | 0 == No 1 == Yes |
This variable describes if the subject previously ever had a concussion or brain injury as a result of sports or recreational activities. |
| Outcomes.PartQuestBBeforeInjPrevConcusSportFreq | ||
| Outcomes.PartQuestBBeforeInjPrevConcusSportType | ||
| Outcomes.PartQuestBBeforeInjSubTrt | 0 == No 1 == Yes |
This variable describes if the subject has ever sought treatment for problems related to use of alcohol or drugs before the injury. |
| Outcomes.PartQuestBBeforeInjTreatMig | 0 == No 1 == Yes |
This variable describes if a subject ever sought treatment for migraine before the injury. |
| Outcomes.PartQuestBPerformed | 0 == Not performed 1 == Performed/Completed |
This variable describes if the questionnaire assessment has been performed. |
| Outcomes.PartQuestBQuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
This variable describes the mode in which the questionnaire was completed. |
| Outcomes.PCL5AngryOutburstInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much the subject was bothered by irritable behavior, angry outbursts, or acting aggressively. |
| Outcomes.PCL5AnswersRefTBIExp | 0 == No 1 == Yes |
This variable describes how much a subject is bothered when they responded to the questions in this questionnaire were the answers in reference to the stressful experience which caused the tramatic brain injury. |
| Outcomes.PCL5AvoidHavingFeelingInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much the subject was bothered by avoiding memories, thoughts, or feelings related to the stressful experience. |
| Outcomes.PCL5AvoidSituationInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much a subject is bothered by avoiding external reminders of the stressful experience (for example, people, places, conversations, activities, objects, or situations). |
| Outcomes.PCL5Blame | 0 == 0-Not at all 1 == 1-A little bit 2 == 2-Moderately 3 == 3-Quite a bit 4 == 4-Extremely |
This variable describes how much a subject is bothered by blaming themself or someone else strongly for the stressful experience or what happened after it. |
| Outcomes.PCL5Date | ||
| Outcomes.PCL5DifficultyConcentratingInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much a subject is bothered by having difficulty concentrating. |
| Outcomes.PCL5DreamsInd | 0 == 0-Not at all 1 == 1-A little bit 2 == 2-Moderately 3 == 3-Quite a bit 4 == 4-Extremely |
This variable describes how much a subject is bothered by repeated, disturbing dreams of the stressful experience. |
| Outcomes.PCL5EmotionallyNumbInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much a subject is bothered by trouble experiencing positive feelings (for example, being unable to feel happiness or have loving feelings for people close to them). |
| Outcomes.PCL5FallStayAsleepInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much a subject was bothered by trouble falling or staying asleep. |
| Outcomes.PCL5FeelDistantInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much the subject if bothered by feeling distant or cut off from other people. |
| Outcomes.PCL5HappenAgainInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
THis variable describes how much a subject is bothered by suddenly feeling or acting as if the stressful experience was actually happening again. |
| Outcomes.PCL5JumpyInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much the subject was bothered by feeling jumpy or easily startled. |
| Outcomes.PCL5LossInterestInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable described how much the subject was bothered by loss of interest in activities that they used to enjoy. |
| Outcomes.PCL5MemoriesInd | 0 == 0-Not at all 1 == 1-A little bit 2 == 2-Moderately 3 == 3-Quite a bit 4 == 4-Extremely |
This variable describes how much a subject is bothered by repeated, disturbing, and unwanted memories of the stressful experience. |
| Outcomes.PCL5NegBeliefsOfSelfOthersWorld | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much a subject is bothered by having strong negative beliefs about themself, other people, or the world. |
| Outcomes.PCL5NegFeelingsFearAngerGuiltShame | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable described how much the subject was bothered by having strong negative feelings such as fear, horror, anger, guilt, or shame. |
| Outcomes.PCL5Performed | 0 == Not performed 1 == Performed/Completed |
This variable describes if the questionnaire is completed. |
| Outcomes.PCL5PhysicalReactionsInd | 0 == not at all 1 == a little bit 2 == moderately 3 == quite a bit 4 == extremely |
This variable desribes how much the subject was bothered by having strong physical reactions when something reminded them of a stressful experience (for example, heart pounding, trouble breathing, sweating). |
| Outcomes.PCL5QuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
This variable describes in which mode the questionnaire was completed. |
| Outcomes.PCL5RememberImportantInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much a subject is bothered by trouble remembering important parts of the stressful experience. |
| Outcomes.PCL5Risk | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much a subject is bothered by taking too many risks or doing things that cause them harm. |
| Outcomes.PCL5SuperAlertInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
This variable describes how much a subject is bothered by being "super-alert", watchful or on guard. |
| Outcomes.PCL5TotalScore | Calculated centrally | |
| Outcomes.PCL5VeryUpsetInd | 0 == Not at all 1 == A little bit 2 == Moderately 3 == Quite a bit 4 == Extremely |
THis variable describes how much a subject is feeling very upset when something reminded them of the stressful experience. |
| Outcomes.PHQ9AppteIssueScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been bothered by abnormal diet/appetite in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9ConcntrtnProbScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been bothered with troubling concentrating in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9Date | ||
| Outcomes.PHQ9DthHrtThghtScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been suffering with the thoughts of that he/she would be better off dead to hurt, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9DwnDeprssnHopelssScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been feeling down and depressed in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9IntrstPleasrActScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been bothered by having little interest or pleasure in doing things in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9LowSlfEstmScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been feeling bad for himself/herself in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9Performed | 0 == Not performed 1 == Performed/Completed |
Responses for the PHQ-9 relate to how oftent the subject has been bothered in the last 2 weeks |
| Outcomes.PHQ9ProbsEffectOnDailyAct | 0 == Not difficult at all 1 == Somewhat difficult 2 == Very difficult 3 == Extremely difficult |
Only applicable if any of the 9 problem areas checked. The scale related to how difficult it is to do work, take care of things at home, or get along with other people for the subject, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9QuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
This reflects the mode in which the assessment was performed; this could be "personal interview", "postal questionnaire", "telephone interview" or web-based. |
| Outcomes.PHQ9SleepProbScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been bothered with troubling falling/staying asleep or sleeping too much in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9SpdMovmntSpchScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been suffering with moving or speaking too slowly in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9TirdLckEnrgyScre | 0 == 0 - Not at all 1 == 1 - Several days 2 == 2 - More than half the days 3 == 3 - Nearly every day |
Score of how much the subject has been feeling tired in the past two weeks, as part of the Patient Health Questionnaire (PHQ). |
| Outcomes.PHQ9TotlScre | Not scored by investigator, calculated score. Total score of the questionnaire, as the part of Patient Health Questionnaire Depression (PHQ-9). | |
| Outcomes.QoLIBRIAdlScore | QoLIBRI Daily Life Autonomy Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRICogScore | QoLIBRI Cognition Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRIDate | ||
| Outcomes.QoLIBRIEmoScore | QoLIBRI Emotional Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRIEmotAchievmnts | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with what they have achieved since the brain injury. |
| Outcomes.QoLIBRIEmotAppearnce | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIEmotEnergy | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
This variable describes how satisfied the subject is with their level of energy. |
| Outcomes.QoLIBRIEmotFuture | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIEmotMotivtn | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIEmotSelfEstm | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIEmotSelfPerceptn | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIFeelAngry | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIFeelAnxious | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIFeelBored | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIFeelLonely | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIFeelSad | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIIndpDomesticAct | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIIndpExtent | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIIndpOutAbout | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIIndpOwnLife | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIIndpPersonalFin | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIIndpSocAct | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIIndpWrkEd | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIOSBrainWorking | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIOSCompleteBy | 1 == Patient alone 2 == Relative or friend or carer alone 3 == Patient and relative, friend or carer together |
|
| Outcomes.QoLIBRIOSCurrSituationFutureProspects | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIOSDate | ||
| Outcomes.QoLIBRIOSDayToDay | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIOSFeelingsEmotions | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIOSPerformed | 0 == Not performed 1 == Performed/Completed |
This variable describes if the questionnaire assessment is performed. |
| Outcomes.QoLIBRIOSPersonalSocialLife | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
This variable described how satisfied a subject is with their personal and social life. |
| Outcomes.QoLIBRIOSPhysCondition | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRIOSQuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
This variable informs how the assessment was performed. Could be "Personal interview", "Postal questionnaire", "Telephone interview" or "Web-based completion". |
| Outcomes.QoLIBRIOStartTime | ||
| Outcomes.QoLIBRIOStopTime | ||
| Outcomes.QoLIBRIOSTotalScore | Total score for Qolibri-OS | |
| Outcomes.QoLIBRIOTimeSpent | ||
| Outcomes.QoLIBRIPerformed | 0 == Not performed 1 == Performed/Completed |
This variable informs if the assessment was performed or not |
| Outcomes.QoLIBRIPhysProbBrainInj | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIPhysProbInjs | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIPhysProbPain | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIPhysProbSeeHear | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIPhysProbSlow | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIPhysScore | QoLIBRI Physical Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRIQuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
The mode in which the assessment was performed |
| Outcomes.QoLIBRISelfScore | QoLIBRI Self Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRISocRelAffectn | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRISocRelAttitudes | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRISocRelFamily | 1 == Not at all 2 == Slightly 3 == Moderately 4 == Quite 5 == Very |
|
| Outcomes.QoLIBRISocRelFriends | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRISocRelPartner | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRISocRelSexLife | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRISocScore | QoLIBRI Social Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.QoLIBRIThnkConcentrate | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
Questions relate to how the subject feels now (including last week) |
| Outcomes.QoLIBRIThnkDecisions | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIThnkExpress | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIThnkMemory | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIThnkNavigate | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIThnkSolns | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRIThnkSpeed | 1 == 1- Not at all 2 == 2- Slightly 3 == 3- Moderately 4 == 4- Quite 5 == 5- Very |
|
| Outcomes.QoLIBRITotalScore | QoLIBRI Total Score. Calculation of QOLIBRI subscale and total scores allowed up to 1/3 of items to be missing (details at http://qolibrinet.com/scoring/). | |
| Outcomes.RAVLT20MinDelayPrincipalList7 | ||
| Outcomes.RAVLTCompletionCode | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logstical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Other |
|
| Outcomes.RAVLTDate | ||
| Outcomes.RAVLTInterferenceList1 | ||
| Outcomes.RAVLTNeuroPsychCompCode | 1.0 == 1.0 Test not done 2.0 == 2.0 Test attempted but not completed 3.0 == 3.0 Test completed |
|
| Outcomes.RAVLTPrincipalList1 | ||
| Outcomes.RAVLTPrincipalList2 | ||
| Outcomes.RAVLTPrincipalList3 | ||
| Outcomes.RAVLTPrincipalList4 | ||
| Outcomes.RAVLTPrincipalList5 | ||
| Outcomes.RAVLTPrincipalListRecall6 | ||
| Outcomes.RAVLTTestAttemptdNotCompOptions | 2.1 == Not completed - Cognitive/neurological deficits 2.2 == Not completed - Non-neurological/physical reason 2.3 == Not completed - Lack of effort/uncooperative 2.4 == Not completed - Language 2.5 == Not completed - Illness/fatigue 2.6 == Not completed - Logistical reasons, other reasons 2.7 == Not completed - Examiner error |
If the test was attempted but not completed, this variable specifies the reason. |
| Outcomes.RAVLTTestAttemptdNotCompOptionsOTHER | If the reason why the test was attempted but not completed, was another reason than pre-defined, the other reason must be specified here. | |
| Outcomes.RAVLTTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
If the Test was completed, this variable was to specify how it was completed. |
| Outcomes.RAVLTTestComplNonStandAdminOTHER | ||
| Outcomes.RAVLTTestNotDoneOptions | 1.1 == Not attempted - Cognitive/neurological deficits 1.2 == Not attempted - Non-neurological/physical reasons 1.3 == Not attempted - Lack of effort/uncooperative 1.4 == Not attempted - Language 1.5 == Not attempted - Illness/fatigue 1.6 == Not attempted - Logistical reasons, other reasons 1.7 == Not attempted - Examiner error 1.8 == Not attempted - Patient not available |
This variable described why the test is not done. |
| Outcomes.RAVLTTestNotDoneOptionsOTHER | ||
| Outcomes.RAVLTTotalScorePrincipal | Rey Auditory Verbal Learning Test Total Score. Calculated centrally. | |
| Outcomes.RAVLTWordListNum | 1 == 1 2 == 2 3 == 3 |
Indicates which RAVLT Word List Form was used for the asessment |
| Outcomes.RPQ13Score | Not scored by investigator, calculated score | |
| Outcomes.RPQ3Score | Not scored by investigator, calculated score | |
| Outcomes.RPQBlurredVision | 0 == Not experienced at all 1 == No more of a problem 2 == A mild problem 3 == A moderate problem 4 == A severe problem |
|
| Outcomes.RPQDate | Baseline RPQ documents complaints and symptoms commonly reported after TBI. Baseline RPQ can only be assessed in conscious subjects who are out of PTA. Provides further details on AOC. | |
| Outcomes.RPQDepressed | 0 == Not experienced at all 1 == No more of a problem 2 == A mild problem 3 == A moderate problem 4 == A severe problem |
|
| Outcomes.RPQDizziness | 0 == Not experienced at all 1 == No more of a problem 2 == A mild problem 3 == A moderate problem 4 == A severe problem |
|
| Outcomes.RPQDoubleVision | 0 == Not experienced at all 1 == No more of a problem 2 == A mild problem 3 == A moderate problem 4 == A severe problem |
|
| Outcomes.RPQFatigue | 0 == Not experienced at all 1 == No more of a problem 2 == A mild problem 3 == A moderate problem 4 == A severe problem |
|
| Outcomes.RPQForgetful | 0 == Not experienced at all 1 == No more of a problem 2 == A mild problem 3 == A moderate problem 4 == A severe problem |
|
| Outcomes.RPQFrustrated | 0 == Not experienced at all 1 == No more of a problem 2 == A mild problem 3 == A moderate problem 4 == A severe problem |
|
| Outcomes.RPQHeadaches | 0 == 0-Not experienced at all 1 == 1- No more of a problem 2 == 2- A mild problem 3 == 3- A moderate problem 4 == 4- A severe problem |
Scoring of symptoms in RPQ: 0=none; 1=no more of a problem; 2=a mild problem; 3= a moderate problem; 4= a severe problem. |
| Outcomes.RPQIrritable | 0 == Not experienced at all 1 == No more of a problem 2 == A mild problem 3 == A moderate problem 4 == A severe problem |
|
| Outcomes.RPQLightSensitivity | 0 == 0-Not experienced at all 1 == 1- No more of a problem 2 == 2- A mild problem 3 == 3- A moderate problem 4 == 4- A severe problem |
|
| Outcomes.RPQLongerToThink | 0 == NotĀ experiencedĀ atĀ all 1 == NoĀ moreĀ ofĀ aĀ problem 2 == AĀ mildĀ problem 3 == AĀ moderateĀ problem 4 == AĀ severeĀ problem |
|
| Outcomes.RPQNausea | 0 == NotĀ experiencedĀ atĀ all 1 == NoĀ moreĀ ofĀ aĀ problem 2 == AĀ mildĀ problem 3 == AĀ moderateĀ problem 4 == AĀ severeĀ problem |
|
| Outcomes.RPQNoiseSensitivity | 0 == NotĀ experiencedĀ atĀ all 1 == NoĀ moreĀ ofĀ aĀ problem 2 == AĀ mildĀ problem 3 == AĀ moderateĀ problem 4 == AĀ severeĀ problem |
|
| Outcomes.RPQOther1 | 0 == 0-Not experienced at all 1 == 1-No more of a problem 2 == 2-A mild problem 3 == 3-A moderate problem 4 == 4-A severe problem |
|
| Outcomes.RPQOther1Text | ||
| Outcomes.RPQOther2 | 0 == 0-Not experienced at all 1 == 1-No more of a problem 2 == 2-A mild problem 3 == 3-A moderate problem 4 == 4-A severe problem |
|
| Outcomes.RPQOther2Text | ||
| Outcomes.RPQPerformed | 0 == Not performed 1 == Performed/Completed |
Reflects is the assessment was performed or not |
| Outcomes.RPQPoorConcentration | 0 == 0-Not experienced at all 1 == 1- No more of a problem 2 == 2- A mild problem 3 == 3- A moderate problem 4 == 4- A severe problem |
|
| Outcomes.RPQQuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
The mode in which the assessment was performed; could be "Personal interview", "Postal questionnaire", "Telephone interview", "Web-based completion" |
| Outcomes.RPQRestless | 0 == 0-Not experienced at all 1 == 1- No more of a problem 2 == 2- A mild problem 3 == 3- A moderate problem 4 == 4- A severe problem |
|
| Outcomes.RPQSleepDisturbance | 0 == 0-Not experienced at all 1 == 1- No more of a problem 2 == 2- A mild problem 3 == 3- A moderate problem 4 == 4- A severe problem |
|
| Outcomes.RPQTime | ||
| Outcomes.RPQTotalScore | RPQ(Rivermead post-concussion symptoms questionnaire) Total Score. Calculated centrally. | |
| Outcomes.SF12Date | ||
| Outcomes.SF12EmotProbLessAccomp | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF12EmotProbWkLessCare | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks; Please note: This question appears to have been mis-phrased" in the English version of the e-CRF but was correct on the pdf questionnaires used by the outcome assessors. |
| Outcomes.SF12GenHlth | 1 == 1 - Excellent 2 == 2 - Very Good 3 == 3 - Good 4 == 4 - Fair 5 == 5 - Poor |
|
| Outcomes.SF12HlthLmtClmbSvrlFlStair | 1 == 1 - Yes, Limited A Lot 2 == 2 - Yes, Limited A Little 3 == 3 - No, Not Limited At All |
|
| Outcomes.SF12HlthLmtModAct | 1 == 1 - Yes, Limited A Lot 2 == 2 - Yes, Limited A Little 3 == 3 - No, Not Limited At All |
|
| Outcomes.SF12PainInterfWrk | 1 == 1 - Not At All 2 == 2 - A Little Bit 3 == 3 - Moderately 4 == 4 - Quite A Bit 5 == 5 - Extremely |
Question relates to the past 4 weeks |
| Outcomes.SF12Performed | 0 == Not performed 1 == Performed/Completed |
|
| Outcomes.SF12PhyEmotInterfSoc | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF12PhyHlthLessAccomp | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF12PhyHlthLmtWrkAct | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF12QuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
This variable reflects the mode of the assessment: it could be "Personal interview", "Postal questionnaire", "Telephone interview" or "Web-based completion" |
| Outcomes.SF12ScoreBP | SF-12v2. Bodily Pain - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreBPNBS | SF-12v2. Bodily Pain Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreGH | SF-12v2. General Health (GH) - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreGHNBS | SF-12v2. General Health (GH) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreHMNBS | SF-12v2. Mental Health (MH) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreMCS | SF-12v2. Mental Component Summary - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreMH | SF-12v2. Mental Health (MH) - Scored on a 0-100 scale | |
| Outcomes.SF12ScorePCS | SF-12v2. Physical Component Summary - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScorePF | SF-12v2. Physical Functioning - Scored on a 0-100 scale | |
| Outcomes.SF12ScorePFNBS | SF-12v2. Physical Functioning Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreRE | SF-12v2. Role-Emotional (RE) - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreRENBS | SF-12v2. Role-Emotional (RE) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreRP | SF-12v2. Role-Physical (RP) - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreRPNBS | SF-12v2. Role-Physical (RP) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreSF | SF-12v2. Social Functioning - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreSFNBS | SF-12v2. Social Functioning Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12ScoreVT | SF-12v2. Vitality - Scored on a 0-100 scale | |
| Outcomes.SF12ScoreVTNBS | SF-12v2. Vitality Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF12TimesFeelCalmPcful | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF12TimesFeelDown | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF12TimesFeelEnergetic | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36AsHlthy | 1 == 1 - Definitely true 2 == 2 - Mostly true 3 == 3 - Don't know 4 == 4 - Mostly false 5 == 5 - Definitely false |
|
| Outcomes.SF36Date | ||
| Outcomes.SF36EmotProbLessAccomp | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36EmtProbCutTimeWrk | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36EmtProbLessCare | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36ExpctWrseHlth | 1 == 1 - Definitely true 2 == 2 - Mostly true 3 == 3 - Don't know 4 == 4 - Mostly false 5 == 5 - Definitely false |
|
| Outcomes.SF36GenHlth | 1 == 1 - Excellent 2 == 2 - Very good 3 == 3 - Good 4 == 4 - Fair 5 == 5 - Poor |
|
| Outcomes.SF36HlthExcllnt | 1 == 1 - Definitely true 2 == 2 - Mostly true 3 == 3 - Don't know 4 == 4 - Mostly false 5 == 5 - Definitely false |
|
| Outcomes.SF36HlthLmtBathDress | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtBendKneel | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtClmbOneFlStair | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtClmbSvrlFlStair | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtLiftCarry | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtModAct | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtVigAct | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtWalkHndrdYards | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtWalkMile | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthLmtWalkSvrlHndrdYards | 1 == 1 - Yes, limited a lot. 2 == 2 - Yes, limited a little. 3 == 3 - No, not limited at all. |
|
| Outcomes.SF36HlthOneYrAgo | 1 == 1 - Much better now than a year ago 2 == 2 - Somewhat better now than a year ago 3 == 3 - About the same as one year ago 4 == 4 - Somewhat worse now than one year ago 5 == 5 - Much worse now than one year ago |
|
| Outcomes.SF36IllMoreEasily | 1 == 1 - Definitely true 2 == 2 - Mostly true 3 == 3 - Don't know 4 == 4 - Mostly false 5 == 5 - Definitely false |
|
| Outcomes.SF36LvlBodPain | 1 == 1 - None 2 == 2 - Very mild 3 == 3 - Mild 4 == 4 - Moderate 5 == 5 - Severe 6 == 6 - Very severe |
Question relates to the past 4 weeks |
| Outcomes.SF36PainInterfWrk | 1 == 1 - Not at all 2 == 2 - A little bit 3 == 3 - Moderately 4 == 4 - Quite a bit 5 == 5 - Extremely |
Question relates to the past 4 weeks |
| Outcomes.SF36Performed | 0 == Not performed 1 == Performed/Completed |
Indicates if the SF-36 assessment was performed or not |
| Outcomes.SF36PhysEmotInterfNormSoc | 1 == 1 - Not at all 2 == 2 - Slightly 3 == 3 - Moderately 4 == 4 - Quite a bit 5 == 5 - Extremely |
Question relates to the past 4 weeks |
| Outcomes.SF36PhysEmotInterfSoc | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36PhysHlthCutTimeWrk | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36PhysHlthDiffWrkAct | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36PhysHlthLessAccomp | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36PhysHlthLmtWrkAct | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36QuestionnaireMode | 1 == Telephone interview 2 == Postal questionnaire 3 == Web-based completion 4 == Personal interview |
The mode of assessment ; this could be "Personal interview", "Postal questionnaire", "Telephone interview" or "Web-based completion" |
| Outcomes.SF36ScoreBP | SF-36v2. Bodily Pain - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreBPNBS | SF-36v2. Bodily Pain Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreGH | SF-36v2. General Health (GH) - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreGHNBS | SF-36v2. General Health (GH) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreHMNBS | SF-36v2. Mental Health (MH) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreMCS | SF-36v2. Mental Component Summary - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreMH | SF-36v2. Mental Health (MH) - Scored on a 0-100 scale | |
| Outcomes.SF36ScorePCS | SF-36v2. Physical Component Summary - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScorePF | SF-36v2. Physical Functioning - Scored on a 0-100 scale | |
| Outcomes.SF36ScorePFNBS | SF-36v2. Physical Functioning Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreRE | SF-36v2. Role-Emotional (RE) - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreRENBS | SF-36v2. Role-Emotional (RE) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreRP | SF-36v2. Role-Physical (RP) - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreRPNBS | SF-36v2. Role-Physical (RP) Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreSF | SF-36v2. Social Functioning - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreSFNBS | SF-36v2. Social Functioning Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36ScoreVT | SF-36v2. Vitality - Scored on a 0-100 scale | |
| Outcomes.SF36ScoreVTNBS | SF-36v2. Vitality Norm-Based Score - T-score using 1998 norms and maximum data recovery (Acute at 2 weeks and standard at other timepoints) | |
| Outcomes.SF36TimesFeelCalmPcful | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36TimesFeelDown | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36TimesFeelDumps | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36TimesFeelEnergetic | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36TimesFeelFullLife | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36TimesFeelHappy | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36TimesFeelNerv | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36TimesFeelTired | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.SF36TimesFeelWornOut | 1 == 1 - All of the time 2 == 2 - Most of the time 3 == 3 - Some of the time 4 == 4 - A little of the time 5 == 5 - None of the time |
Question relates to the past 4 weeks |
| Outcomes.Timepoint | Base == Baseline 2wk == 2 weeks 3mo == 3 months 6mo == 6 months 12mo == 12 months 24mo == 24 months |
Outcome timepoints are 2-3 weeks, 3 months, 6 months, 12 months and 24 months. Depending on the stratum and sub-studies of a patient, follow up was performed at some of these time points or at all timepoints. For an overview, please check the SOP Manual. |
| Outcomes.TMTCompletionCode | 1.0 == 1.0 Test completed in full 1.1 == 1.1 Non-standard adm - written 1.2 == 1.2 Non-standard adm - other 1.3 == 1.3 Test completed over the phone 2.1 == 2.1 Not completed - Cognitive/neuro 2.2 == 2.2 Not completed - Non-neuro/phys 2.3 == 2.3 Not completed - Poor effort 2.4 == 2.4 Not completed - Language 2.5 == 2.5 Not completed - Illness 2.6 == 2.6 Not completed - Logstical 3.1 == 3.1 Not attempted - Cognitive/neuro 3.2 == 3.2 Not attempted - Non-neuro/phys 3.3 == 3.3 Not attempted - Poor effort 3.4 == 3.4 Not attempted - Language 3.5 == 3.5 Not attempted - Illness 3.6 == 3.6 Not attempted - Logistical 4.0 == 4.0 Not attempted - Examiner error 5.0 == 5.0 Other |
|
| Outcomes.TMTDate | ||
| Outcomes.TMTHandedness | 1 == Dominant 2 == Non-Dominant |
This variable reflects if the patient used his dominant or non-dominant hand to perform the test |
| Outcomes.TMTNeuroPsychCompCode | 1.0 == 1.0 Test not done 2.0 == 2.0 Test attempted but not completed 3.0 == 3.0 Test completed |
|
| Outcomes.TMTPartATime | ||
| Outcomes.TMTPartBTime | ||
| Outcomes.TMTTestAttemptdNotCompOptions | 2.1 == Not completed - Cognitive/neurological deficits 2.2 == Not completed - Non-neurological/physical reason 2.3 == Not completed - Lack of effort/uncooperative 2.4 == Not completed - Language 2.5 == Not completed - Illness/fatigue 2.6 == Not completed - Logistical reasons, other reasons 2.7 == Not completed - Examiner error |
|
| Outcomes.TMTTestAttemptdNotCompOptionsOTHER | ||
| Outcomes.TMTTestCompletedOptions | 3.0 == Test completed in full - results valid 3.1 == Test completed - Non-standard, results valid 3.2 == Non-standard administration - Other |
|
| Outcomes.TMTTestComplNonStandAdminOTHER | ||
| Outcomes.TMTTestNotDoneOptions | 1.1 == Not attempted - Cognitive/neurological deficits 1.2 == Not attempted - Non-neurological/physical reasons 1.3 == Not attempted - Lack of effort/uncooperative 1.4 == Not attempted - Language 1.5 == Not attempted - Illness/fatigue 1.6 == Not attempted - Logistical reasons, other reasons 1.7 == Not attempted - Examiner error 1.8 == Not attempted - Patient not available |
This variable needs to be completed when TMT completion code is set to 1.0 Test not done. |
| Outcomes.TMTTestNotDoneOptionsOTHER | ||
| Outcomes.TUGDate | ||
| Outcomes.TUGTimedResult | Interpretation: < 10 sec = normal; < 20 sec: good mobility, can go out alone, mobile without gait aid; < 30 sec: problems, cannot go outside alone, requires a gait aid | |
| PriorMeds.PmMedicalCode | Medical History of patients has been recorded under MedHx.MedHx* A number of predefined medical conditions were coded in the e-CRF. If the patient was taking medication for this predefined medical condition, the same code needed to be entered here. An option other was also available for conditions not listed. Please check MedHx.MedHx* for the information on the medical condition(s) corresponding to this variable. | |
| PriorMeds.PmMedicationName | These fields capture information on medication taken pre-injury. For each medication taken, the corresponding Medical History code is listed to document the reason for which this med was taken. If the medication taken was not linked to one of the recorded medication history codes, Investigators were asked to enter "777" as related history code. | |
| Registry.AbdomenPelvicContentsAIS | 0 1 2 3 4 5 6 |
|
| Registry.AbdomenPelvicContentsISS | ||
| Registry.AbdomenPelvicLumbarRegionAIS | ||
| Registry.Age | Recorded in years. | |
| Registry.Anticoagulants | 0 = No 1 = Yes 88 = Unknown |
|
| Registry.BrainInjuryAIS | 0 1 2 3 4 5 6 |
|
| Registry.BrainInjuryISS | ||
| Registry.CervicalSpineAIS | 0 1 2 3 4 5 6 |
|
| Registry.CervicalSpineISS | ||
| Registry.ChestSpineRegionAIS | ||
| Registry.CraniotomyForHaematoma | ||
| Registry.CraniotomyForHaematomaDate | ||
| Registry.CraniotomyForHaematomaDateTime | Calculated from Registry.CraniotomyForHaematomaDate and Registry.CraniotomyForHaematomaTime | |
| Registry.CraniotomyForHaematomaTime | ||
| Registry.CT1Date | Date of the first Brain CT | |
| Registry.CT1DateTime | Calculated value from Registry.CT1Date and Registry.CT1Time | |
| Registry.CT1Time | Time of the first Brain CT | |
| Registry.CT1TimeSinceInj | Calculated value from Registry.CT1Date, Registry.CT1Time and Registry.DateInj, Registry.TimeInj | |
| Registry.CTAbnormalBasalCisterns | 1 = Open 2 = Compressed/obliterated 88 = Unknown |
These details record the investigators score of the first CT brain. |
| Registry.CTIntracranialLesions | 0 = No 1 = Yes 88 = Unknown |
These details record the investigators score of the first or subsequent CT brain scans as to whether or not TBI or intracranial bleeding is visible. |
| Registry.CTIntracranialLesionsPresentASDH | 0 = No 1 = Small 2 = Large (mass) 88 = Unknown |
These details record the investigators score of the first CT brain. |
| Registry.CTIntracranialLesionsPresentContusions | 0 = No 1 = Small 2 = Large (mass) 88 = Unknown |
These details record the investigators score of the first CT brain. |
| Registry.CTIntracranialLesionsPresentEDH | 0 = No 1 = Small 2 = Large (mass) 88 = Unknown |
These details record the investigators score of the first CT brain. |
| Registry.CTResult | 0 = Normal 1 = Abnormal |
These details record the investigators score of the first CT brain. |
| Registry.CTShift | 0 = No 1 = 0-4mm 2 = ā„5mm 88 = Unknown |
These details record the investigators score of the first CT brain. |
| Registry.CTtSAH | 0 = No 1 = Yes 88 = Unknown |
These details record the investigators score of the first CT brain. |
| Registry.DamageControlLaparotomy | ||
| Registry.DamageControlLaparotomyDate | ||
| Registry.DamageControlLaparotomyDateTime | Calculated from Registry.DamageControlLaparotomyDate and Registry.DamageControlLaparotomyTime | |
| Registry.DamageControlLaparotomyTime | ||
| Registry.DamageControlThoracotomy | ||
| Registry.DamageControlThoracotomyDate | ||
| Registry.DamageControlThoracotomyDateTime | Calculated from Registry.DamageControlThoracotomyDate and Registry.DamageControlThoracotomyTime | |
| Registry.DamageControlThoracotomyTime | ||
| Registry.DateInj | ||
| Registry.DateTimeInj | ||
| Registry.DateTimeInjReliable | 1 = Verified 2 = Estimate |
This variable documents if the time of injury is accurate, or is based on "best possible estimate", in case exact time of injury not known. |
| Registry.DayInjury | 0 == Sunday 1 == Monday 2 == Tuesday 3 == Wednesday 4 == Thursday 5 == Friday 6 == Saturday |
Day of injury. (Sunday - Saturday) |
| Registry.DeathCause | 1 = Head injury/initial injury 2 = Head injury/secondary intracranial damage 3 = Systemic trauma 4 = Medical complications 88 = Unknown 99 = Other |
Principle cause of death |
| Registry.DeathDate | ||
| Registry.DeathDateTime | Calculated from Registry.DeathDate and Registry.DeathTime | |
| Registry.DeathTime | Time of death | |
| Registry.DeathTimeSinceInj | ||
| Registry.DecompressionCraniectomy | ||
| Registry.DecompressionCraniectomyDate | ||
| Registry.DecompressionCraniectomyDateTime | ||
| Registry.DecompressionCraniectomyTime | ||
| Registry.DischargeDate | ||
| Registry.DischargeDateTime | ||
| Registry.DischargeDestination | 1=Discharged to other hospital 2=Discharged to rehabilitation 3=Discharged to nursing home 5=Discharged to home with carer 6=Discharged to home and self-care but judged unfit for work 7=Discharged to home and self-care without reservations 8=Discharged to home and self-care with some reservations 88= Unknown |
Documents destination upon hospital discharge |
| Registry.DischargeTime | ||
| Registry.EDArrDBP | ||
| Registry.EDArrivalBloodPressureUnknown | ||
| Registry.EDArrivalOxygenSatUnknown | ||
| Registry.EDArrivedIntubated | This variable should have been checked if the patient already arrived intubated. | |
| Registry.EDArrPupilLftEyeMeasr | ||
| Registry.EDArrPupilLftEyeMeasrUnkUnt | 66 = Untestable 88 = Unknown |
|
| Registry.EDArrPupilRtEyeMeasr | ||
| Registry.EDArrPupilRtEyeMeasrUnkUnt | 66 = Untestable 88 = Unknown |
|
| Registry.EDArrSBP | ||
| Registry.EDArrSpO2 | ||
| Registry.EDCTBrain | 0 = No 1 = Yes 88 = Unknown |
Indication for CT was an inclusion criterium for the Core study - thus, nearly all patients in Core will have had a CT brain. |
| Registry.EDIntubation | 0 = No 1 = Yes 88 = Unknown |
|
| Registry.EnrollDate | Records the date of enrollment to the Registry Data Collection. | |
| Registry.ExternaAIS | 0 1 2 3 4 5 6 |
|
| Registry.ExternaISS | ||
| Registry.ExternalFixationLimb | ||
| Registry.ExternalFixationLimbDate | ||
| Registry.ExternalFixationLimbDateTime | Calculated from Registry.ExternalFixationLimbDate and Registry.ExternalFixationLimbTime | |
| Registry.ExternalFixationLimbTime | ||
| Registry.ExternalVentricularCSFDrainage | ||
| Registry.ExternalVentricularCSFDrainageDate | ||
| Registry.ExternalVentricularCSFDrainageDateTime | Calculated from Registry.ExternalVentricularCSFDrainageDate and Registry.ExternalVentricularCSFDrainageTime | |
| Registry.ExternalVentricularCSFDrainageTime | ||
| Registry.ExternaRegionAIS | ||
| Registry.ExtraperitonealPelvicPacking | ||
| Registry.ExtraperitonealPelvicPackingDate | ||
| Registry.ExtraperitonealPelvicPackingDateTime | Calculated from Registry.ExtraperitonealPelvicPackingDate and Registry.ExtraperitonealPelvicPackingTime | |
| Registry.ExtraperitonealPelvicPackingTime | ||
| Registry.ExtremitiesRegionAIS | ||
| Registry.FaceAIS | 0 1 2 3 4 5 6 |
|
| Registry.FaceISS | ||
| Registry.FaceRegionAIS | ||
| Registry.GcsEDArrEyes | 1 = 1-None 2 = 2-To pain 3 = 3-To speech 4 = 4-Spontaneously S = Untestable (swollen) O = Untestable (other) UN = Unknown |
In the Core data,the initial GCS and pupillary reactivity can be scored at 4 pre-defined moments in the pre-hospital/presentation phase: 1.: scene of accident; 2: first hospital (in case of secondary regerral; 3.: arrival to Er of study hospital; 4.: post-stabilization; In addition, assessment at a different time point is possible (designated as other). A derived variable captures the highest available GCS score across these time periods. |
| Registry.GcsEDArrMotor | 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 |
|
| Registry.GcsEDArrPupils | 0 = None reacting 1 = One reacting 2 = Both reacting |
|
| Registry.GcsEDArrScore | score by investigators in case component scores not available, but GCS sum score available | |
| Registry.GcsEDArrVerbal | 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 |
|
| Registry.HeadBrainCervicalRegionAIS | ||
| Registry.HeadNeckAIS | 0 1 2 3 4 5 6 |
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. |
| Registry.HeadNeckISS | ||
| Registry.HospitalAdm | 0 = No 1 = Yes 88 = Unknown |
|
| Registry.ICPDeviceInsertion | ||
| Registry.ICPDeviceInsertionDate | ||
| Registry.ICPDeviceInsertionDateTime | Calculated from Registry.ICPDeviceInsertionDate and Registry.ICPDeviceInsertionTime | |
| Registry.ICPDeviceInsertionTime | ||
| Registry.ICUAdm | 0 = No 1 = Yes 88 = Unknown |
|
| Registry.ICUAdmDate | ||
| Registry.ICUAdmDateTime | Calculated from Registry.ICUAdmDate and Registry.ICUAdmTime | |
| Registry.ICUAdmTime | ||
| Registry.ICUAdmTimeSinceInj | ||
| Registry.ICUDischDate | ||
| Registry.ICUDischDateTime | Calculated from Registry.ICUDischDate and Registry.ICUDischTime | |
| Registry.ICUDischTime | ||
| Registry.ICUDishcTimeSinceInj | ||
| Registry.InjMech | 1 = RTA Pedestrian 2 = RTA Cyclist 3 = RTA Motorcyclist 4 = RTA Driver 5 = RTA Other vehicle occupant 6 = Fall standing height 7 = Fall from height 8 = Assault fists 9 = Assault blunt instrument 10 = Assault knife 11 = Assault firearm 12 = Self Harm 13 = Sport/recreational activity 14 = Other, please specify 99 = Other violence 88 = Unknown |
|
| Registry.InjPlace | 1 = Street/traffic 2 = Home 3 = Work 4 = Sports field/hall 6 = Public place 99 = Other 88 = Unknown |
|
| Registry.InjType | 1 = Blunt/closed 2 = Blast 3 = Crush 4 = Penetrating 88 = Unknown |
|
| Registry.InterventionalRadiology | ||
| Registry.InterventionalRadiologyDate | ||
| Registry.InterventionalRadiologyDateTime | Calculated from Registry.InterventionalRadiologyDate and Registry.InterventionalRadiologyTime | |
| Registry.InterventionalRadiologyTime | ||
| Registry.InterventionsOther | ||
| Registry.InterventionsOtherDate | ||
| Registry.InterventionsOtherDateTime | Calculated from Registry.InterventionsOtherDate and Registry.InterventionsOtherTime | |
| Registry.InterventionsOtherTime | ||
| Registry.KeyEmergencyInterventions | 0 = No 1 = Yes 88 = Unknown |
|
| Registry.LowerExtremitiesAIS | 0 1 2 3 4 5 6 |
|
| Registry.LowerExtremitiesISS | ||
| Registry.LumbarSpineAIS | 0 1 2 3 4 5 6 |
|
| Registry.LumbarSpineISS | ||
| Registry.MonthInjury | 1 == January 2 == February 3 == March 4 == April 5 == May 6 == June 7 == July 8 == August 9 == September 10 == October 11 == November 12 == December |
Month of Injury (January - December) |
| Registry.PatientType | 1 == ER 2 == Admission 3 == ICU |
Stratum coded from ICUAdm, ERAdm, HospitalAdm |
| Registry.PelvicGirdleAIS | 0 1 2 3 4 5 6 |
|
| Registry.PelvicGirdleISS | ||
| Registry.PlateletAggregInhibitors | 0 = No 1 = Yes 88 = Unknown |
|
| Registry.PreInjuryASAPSClassification | 1 = A normal healthy patient 2 = A patient with mild systemic disease 3 = A patient with severe systemic disease 4 = A patient with severe systemic disease that is a constant threat to life 88 = Unknown |
Common classification system used in anaesthesia; denotes overall health |
| Registry.PresCTBrain | 0 = No 1 = Yes 88 = Unknown |
only applicable in case of secondary referral. Procedure performed at first hospital (not study hospital). |
| Registry.PresEmergencyCare | 0 = No professional care 1 = Ambulance service (no physician) 2 = Helicopter service 3 = Medical mobile team 98 = N/A (for example injury in hospital) |
|
| Registry.PresEmergencyCareIntubation | 0 = No 1 = Yes 88 = Unknown |
|
| Registry.PresEmergencyCareVentilation | 0 = No 1 = Yes 88 = Unknown |
|
| Registry.PresERExtracranialSurg | 0 = No 1 = Yes 88 = Unknown |
only applicable in case of secondary referral. Procedure performed at first hospital (not study hospital). |
| Registry.PresERIntracranialSurg | 0 = No 1 = Yes 88 = Unknown |
only applicable in case of secondary referral. Procedure performed at first hospital (not study hospital). |
| Registry.PresFHospDate | First hospital is defined as the initial hospital to which the patient was brought before being transferred to Study hospital. Consequently, only applicable in case of secondary transferral. However, in some sites data for first hospital may have been entered also when the patient was brought directly to the study hospital. | |
| Registry.PresFHospDateTime | Calculated from Registry.PresFHospDate and Registry.PresFHospTime | |
| Registry.PresFHospTime | only applicable in case of secondary referral | |
| Registry.PresFHospTimeSinceInj | ||
| Registry.PresIntubation | 0 = No 1 = Yes 88 = Unknown |
only applicable in case of secondary referral. Procedure performed at first hospital (not study hospital). |
| Registry.PresSTHospDate | ||
| Registry.PresSTHospDateTime | Calculated from Registry.PresSTHospDate and Registry.PresSTHospTime | |
| Registry.PresSTHospTime | ||
| Registry.PresSTHospTimeSinceInj | ||
| Registry.PresTBIRef | 1 = Primary referral 2 = Secondary referral from other hospital |
|
| Registry.RegistryCompleteStatus | ||
| Registry.Sex | M = Male F = Female |
The difference between male and female, based upon the interactions between genes and between the genotype and the environment. Gender of Subject. |
| Registry.SiteCode | ||
| Registry.StatusOnDischarge | 0 = Dead 1 = Alive |
Assessment by investigator |
| Registry.ThoracicSpineAIS | 0 1 2 3 4 5 6 |
|
| Registry.ThoracicSpineISS | ||
| Registry.ThoraxChestAIS | 0 1 2 3 4 5 6 |
|
| Registry.ThoraxChestISS | ||
| Registry.TimeInj | ||
| Registry.TotalISS | 0 1 2 3 4 5 6 |
Represents the quadratic sum of the three AIS regions with the highest score. |
| Registry.UpperExtremitiesAIS | 0 1 2 3 4 5 6 |
|
| Registry.UpperExtremitiesISS | ||
| Registry.WardAdm | 0 = No 1 = Yes 88 = Unknown |
The intent here was to record direct admission to the ward versus direct admission to the ICU (Registry.ICUAdm). However, the possibility that this variable was also checked for patients discharged from the ICU to the Ward cannot be excluded. |
| Registry.WardAdmDate | ||
| Registry.WardAdmDateTime | Calculated from Registry.WardAdmDate and Registry.WardAdmTime | |
| Registry.WardAdmTime | ||
| Registry.WardAdmTimeSinceInj | ||
| Subject.Age | Age in years | |
| Subject.AnytimeGOSECompleteStatus | ||
| Subject.AnytimeGOSEDate | ||
| Subject.AnytimeGOSEMethod | ||
| Subject.AnytimeGOSEPtAlive | ||
| Subject.AnytimeGOSEScore | ||
| Subject.ApptPtShowOutcomes12Mo | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptPtShowOutcomes24mo | 0 == No 1 == Yes |
|
| Subject.ApptPtShowOutcomes2Wk | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptPtShowOutcomes3Mo | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptPtShowOutcomes6Mo | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptQuestComplOutcomes12Mo | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptQuestComplOutcomes24Mo | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptQuestComplOutcomes2Wk | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptQuestComplOutcomes3Mo | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptQuestComplOutcomes6Mo | 0 == No 1 == Yes 77 == N/A |
|
| Subject.ApptQuestLangUsed12Mo | SWE == Swedish ARA == Arabic HEB == Hebrew RUS == Russian SPA == Spanish SLO == Slovakian SER == Serbian ROM == Romanian NOR == Norwegian LIT == Lithuanian ITA == Italian HUN == Hungarian FIN == Finnish DAN == Danish DUT == Dutch FRE == French GER == German ENG == English |
|
| Subject.ApptQuestLangUsed24Mo | SWE == Swedish ARA == Arabic HEB == Hebrew RUS == Russian SPA == Spanish SLO == Slovakian SER == Serbian ROM == Romanian NOR == Norwegian LIT == Lithuanian ITA == Italian HUN == Hungarian FIN == Finnish DAN == Danish DUT == Dutch FRE == French GER == German ENG == English |
|
| Subject.ApptQuestLangUsed2Wk | SWE == Swedish ARA == Arabic HEB == Hebrew RUS == Russian SPA == Spanish SLO == Slovakian SER == Serbian ROM == Romanian NOR == Norwegian LIT == Lithuanian ITA == Italian HUN == Hungarian GER == German FIN == Finnish DAN == Danish FRE == French DUT == Dutch ENG == English |
|
| Subject.ApptQuestLangUsed3Mo | SWE == Swedish ARA == Arabic HEB == Hebrew RUS == Russian SPA == Spanish SLO == Slovakian SER == Serbian ROM == Romanian NOR == Norwegian LIT == Lithuanian ITA == Italian HUN == Hungarian FIN == Finnish DAN == Danish DUT == Dutch FRE == French GER == German ENG == English |
|
| Subject.ApptQuestLangUsed6Mo | SWE == Swedish ARA == Arabic HEB == Hebrew RUS == Russian SPA == Spanish SLO == Slovakian SER == Serbian ROM == Romanian NOR == Norwegian LIT == Lithuanian ITA == Italian HUN == Hungarian FIN == Finnish DAN == Danish DUT == Dutch FRE == French GER == German ENG == English |
|
| Subject.ApptQuestLocLang12Mo | 0 == No 1 == Yes 99 == Unknown |
|
| Subject.ApptQuestLocLang24Mo | 0 == No 1 == Yes 99 == Unknown |
|
| Subject.ApptQuestLocLang2Wk | 0 == No 1 == Yes 99 == Unknown |
|
| Subject.ApptQuestLocLang3Mo | 0 == No 1 == Yes 99 == Unknown |
|
| Subject.ApptQuestLocLang6Mo | 0 == No 1 == Yes 99 == Unknown |
|
| Subject.ApptScheduledDateOutcomes12mo | Milestone Window: 12month outcomes must be completed 10 - 14 months from DOI. | |
| Subject.ApptScheduledDateOutcomes24mo | Milestone Window: 24month outcomes must be completed 22 - 28 months from DOI | |
| Subject.ApptScheduledDateOutcomes2wk | Milestone window: 2week outcomes must be completed 10 - 27 days from DOI (Date Of Injury) | |
| Subject.ApptScheduledDateOutcomes3mo | Milestone Window: 3month outcomes must be completed 11 - 18 weeks from DOI (Date of Injury). | |
| Subject.ApptScheduledDateOutcomes6mo | Milestone Window: 6month outcomes must be completed 5 - 8 months from DOI (Date of Injury). | |
| Subject.ApptScheduledTimeOutcomes12mo | ||
| Subject.ApptScheduledTimeOutcomes24mo | ||
| Subject.ApptScheduledTimeOutcomes2wk | ||
| Subject.ApptScheduledTimeOutcomes3mo | ||
| Subject.ApptScheduledTimeOutcomes6mo | ||
| Subject.ApptTargetDateOutcomes12Mo | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.ApptTargetDateOutcomes24mo | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.ApptTargetDateOutcomes2Wk | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.ApptTargetDateOutcomes3Mo | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.ApptTargetDateOutcomes6Mo | The variables on the forms follow-up appointments document the prefered appointment date, the actually scheduled date and time and provide general informatoin if the patient completed the follow-up or not. Forms are available for all possible follow-up moments, please note that not all these times may be applicable, for example the details for 24 months outcome would only apply to patients in the ICU stratum who underwent MR imaging | |
| Subject.AssociatedStudy | 1 == RESCUE-ASDH 2 == TAHITI-B 3 == PROLABI |
Documents if a subject was enrolled in an associated CENTER-TBI study: RESCUE ASDH/Tahiti/Prolabi |
| Subject.Comments | ||
| Subject.ConsentWithdrawn | ||
| Subject.ConsentWithdrawnDate | ||
| Subject.ConsentWithdrawnReason | WHY Question: documents the reason for withdrawing subject | |
| Subject.ConsentWithdrawnTime | ||
| Subject.DateInj | Date of Injury. Anonymised and saved as 1970-01-01 for all patients. All other dates are converted relative to date of Injury. | |
| Subject.DateOfAdmission | This variable denotes date of admission to hospital; Therefore not applicable to subjects in ER stratum. In principle the date of injury; date of enrollment and Date of Admission to ICU or Ward will match, but in some cases there can be a difference of 1 or 2 days. For example when a patient was injured late at night, it is possible that the consent was only obtained in the morning, hence the date of Study Enrollment will be 1 day later than the date of injury. Or in some hospitals a patient is kept for 24 hours in observation at the ER in a specific unit before being transferred to ICU or Ward. Hence the Date of Admission to ICU or Ward can be 1 or 2 days later. Or if there is no bed available on ICU or Ward for a patient being injured late at night, there can be a delay in admitting the patient. Also, in some countries, Enrollment Date > 24h was accepted according to local regulations and IRB. | |
| Subject.DateTimeInjReliable | 1 == Verified 2 == Estimated |
This variable documents if the time of injury is accurate, or is based on "best possible estimate", in case exact time of injury not known. |
| Subject.DayInjury | 0 == Sunday 1 == Monday 2 == Tuesday 3 == Wednesday 4 == Thursday 5 == Friday 6 == Saturday |
Day of injury. (Sunday - Saturday) |
| Subject.DeathCause | 1 == Head injury/initial injury 2 == Head injury/secondary intracranial damage 3 == Systemic trauma 4 == Medical complications 88 == Unknown 99 == Other |
Cause of death in or outside the hospital |
| Subject.DeathCauseOther | ||
| Subject.DeathDate | Date of death also recorded on hospital discharge and at followup: FollowUp.FUPrincipalDeathCause;Death may also have been recorded in the ER forms: Subject.DeathDate | |
| Subject.DeathERDeclaredBrainDeadFollowingNationalCriteria | 0 == No 1 == Yes 88 == Unknown |
Only applicable if patient declared "dead" on the ER |
| Subject.DeathERDOA | 0 == No 1 == Yes 88 == Unknown |
Only applicable if patient declared "dead" on the ER |
| Subject.DeathERUnsuccResusForExtraCranInj | 0 == No 1 == Yes 88 == Unknown |
Only applicable if patient declared "dead" on the ER |
| Subject.DeathERWithdrawalLifeSuppForSeverityOfTBI | 0 == No 1 == Yes 88 == Unknown |
Only applicable if patient declared "dead" on the ER |
| Subject.DeathTime | Time of death | |
| Subject.DerivedImputed180DaysGOSE | ā1ā= Dead ā2_or_3ā= VS / Lower Severe Disability ā4ā= Upper Severe Disability ā5ā = Lower Moderate Disability ā6ā = Upper Moderate Disability ā7ā = Lower Good Recovery ā8ā =Upper Good Recovery |
This variable contains a GOSE that has been imputed at exactly 180 days after injury. Imputation is based on the composite GOSE recorded at different timepoints 2 weeks to one year. The imputation of the GOSE uses a multi-state model. The model does not include any baseline covariates. Since the imputation uses GOSE information across time points, the imputed 6 month GOSE does not necessarily correspond to outcomes that are observed at 6 months. Apart from deaths, imputed values of the GOSE are subject to uncertainty, and this is reflected in the companion variables that give the probabilities that a given outcome is in each of the GOSE categories 1 to 8. (Subject.DerivedImputed180DaysGOSE_1_probability, Subject.DerivedImputed180DaysGOSE_2_3_probability, Subject.DerivedImputed180DaysGOSE_4_probability, Subject.DerivedImputed180DaysGOSE_5_probability, Subject.DerivedImputed180DaysGOSE_6_probability, Subject.DerivedImputed180DaysGOSE_7_probability, Subject.DerivedImputed180DaysGOSE_8_probability). The category with the highest probability is taken as the final imputed value. Deaths have been added to this variable where a date of death is recorded on or before 180 days. The GOSE is a character/ string variable (not numeric) with the following categories: ā1ā= Dead, ā2_or_3ā= VS / Lower Severe Disability, ā4ā= Upper Severe Disability, ā5ā = Lower Moderate Disability, ā6ā = Upper Moderate Disability, ā7ā = Lower Good Recovery, ā8ā =Upper Good Recovery. |
| Subject.DerivedImputed180DaysGOSE_1_probability | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_2_or_3_probability | ||
| Subject.DerivedImputed180DaysGOSE_2_probability | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_3_probability | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_4_probability | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_5_probability | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_6_probability | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_7_probability | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DerivedImputed180DaysGOSE_8_probability | See "Subject.DerivedImputed180DaysGOSE" | |
| Subject.DNRDateTime | ||
| Subject.EduLvlEUROFather | 0 == None, not currently in school 1 == Currently in diploma or degree-oriented program 2 == Primary school 3 == Secondary school / High school 4 == Post-high school training (e.g. trade/technical certificate) 5 == College / University (diploma or degree) 88 == Unknown |
Only if age <18 |
| Subject.EduLvlEUROMother | 0 == None not currently in school 1 == Currently in diploma or degree-oriented program 2 == Primary school 3 == Secondary school / High school 4 == Post-high school training (e.g. trade/technical certificate) 5 == College / University (diploma or degree) 88 == Unknown |
Only if age <18 |
| Subject.EduLvlUSATyp | 0 == None, not currently in school 1 == Currently in diploma or degree-oriented program 2 == Primary school 3 == Secondary school / High school 4 == Post-high school training (e.g. trade/technical certificate) 5 == College / University (diploma or degree) 88 == Unknown |
|
| Subject.EduYrCt | Number of years of education completed | |
| Subject.EmplmtStatus | 1 == Working (35 hours or more per week) 2 == Working (20-34 hours per week) 3 == Working (less than 20 hours per week) 4 == In working force, but currently on sick leave 5 == Special employment / sheltered employment 6 == Looking for work, unemployed 7 == Unable to work 8 == Retired 9 == Student / schoolgoing 10 == Homemaker, keeping house 88 == Unknown |
|
| Subject.EnrollDate | Date of Study Enrollment. In principle the date of injury and date of enrollment will match, but in some cases there can be a difference of 1 or 2 days. For example when a patient was injured late at night, it is possible that the consent was only obtained in the morning, hence the date of Study Enrollment will be 1 day later than the date of injury. | |
| Subject.EnrolledInOtherStudy | 0 == No 1 == Yes 99 == Unknown |
Denotes if a subject was also enrolled in a concomitant study |
| Subject.EOSDate | ||
| Subject.EOSFormCompletion | 0 == No 1 == Yes |
|
| Subject.EOSFormNotCompleteOtherReasonTxt | ||
| Subject.EOSFormNotCompletePrimReason | 1 == Consent withdrawn 2 == Violation study conduct 99 == Other |
|
| Subject.EOSFormNotCompleteViolateStudyConductTxt | ||
| Subject.EOSReason | 1 == Completion of study 2 == Inability to obtain follow-up 3 == Withdrawal from study (by patient or representative) 4 == Adverse event(s) 5 == Decision for DNR*: 6 == Withdrawal of support 7 == Death 99 == Other |
|
| Subject.EOSReasonOtherTxt | ||
| Subject.FUConsentForContStudyPart | This variable documents written consent obtained from the patient for continued study participation | |
| Subject.FUConsentForContStudyPartDate | ||
| Subject.GOSE6monthEndpointDerived | ā1ā= Dead ā2_or_3ā= VS / Lower Severe Disability ā4ā= Upper Severe Disability ā5ā = Lower Moderate Disability ā6ā = Upper Moderate Disability ā7ā = Lower Good Recovery ā8ā =Upper Good Recovery. |
A six month GOSE endpoint that uses both observed ratings and imputed values. The variable is constructed as follows: (1) āDeadā is recorded for those with a date of death on or before 180 days post injury. (2) If there is an observed GOSE in the range 150 to 240 days (i.e. in the per protocol time window for six month assessment) then this rating is used. (3) If there is no per-protocol rating, then then an imputed 180 day GOSE is used where available. For a description of the imputation method see the variable āSubject.DerivedImputed180DaysGOSEā. The GOSE is a character/ string variable (not numeric) with the following categories: ā1ā= Dead, ā2_or_3ā= VS / Lower Severe Disability, ā4ā= Upper Severe Disability, ā5ā = Lower Moderate Disability, ā6ā = Upper Moderate Disability, ā7ā = Lower Good Recovery, ā8ā =Upper Good Recovery. |
| Subject.GOSE6month_probability_1 | Superseded variable. | |
| Subject.GOSE6month_probability_2 | Superseded variable | |
| Subject.GOSE6month_probability_3 | Superseded variable | |
| Subject.GOSE6month_probability_4 | Superseded variable | |
| Subject.GOSE6month_probability_5 | Superseded variable | |
| Subject.GOSE6month_probability_6 | Superseded variable | |
| Subject.GOSE6month_probability_7 | Superseded variable | |
| Subject.GOSE6month_probability_8 | Superseded variable | |
| Subject.GUPI | The Global Unique Patient Identifier (GUPI) is a unique identifier that meets protection requirements in the EU and in Member States. This process takes patient specific characteristics (such as the first name, middle name, last name, place of birth, country of birth, date of birth, and gender) to generate a unique GUPI for each patient using an irreversible process, referred to as a āone way hashā. This process replicates an approach taken by the Federal Inter-agency Traumatic Brain Injury Research initiative (FITBIR; https://fitbir.nih.gov/) in the USA to create a similar construct, which they term a Global Unique Identifier (GUID; see https://fitbir.nih.gov/jsp/contribute/guid-overview.jsp). This process is one of the options considered by rulings on EU Data Protection requirements at the start of the study (see http://ec.europa.eu/justice/data-protection/article-29/documentation/opinion-recommendation/files/2014/wp216_en.pdf). | |
| Subject.InfConsBy | 1 == Doctor (MD) 2 == Nurse 4 == Research assistant 99 == Other |
Type of health care professional who requested and obtained consent |
| Subject.InfConsDate | Confirmation of consent date; denotes written confirmation | |
| Subject.InfConsentBlood | ||
| Subject.InfConsentData | Explicit consent was requested for broad use and possible transfer of clinical data, blood samples, genetics, MRI and outcome. | |
| Subject.InfConsentDNA | ||
| Subject.InfConsentMRI | ||
| Subject.InfConsentOutcomeAssmts | ||
| Subject.InfConsInitialDate | ||
| Subject.InfConsInitialTime | ||
| Subject.InfConsTime | Confirmation of consent time; denotes written confirmation | |
| Subject.InfConsTyp | 1 == Informed consent (by subject) oral 2 == Informed consent (by subject) written 3 == Proxy consent verbal 4 == Proxy consent written 5 == Deferred consent 6 == Waiver of consent |
Designates the initial form of consent used |
| Subject.InfConsWhen | 1 == Written proxy consent BEFORE enrolment 2 == Written proxy consent AFTER enrolment 3 == Written informed consent by patient |
|
| Subject.JobclassCat | 0 == None 1 == Manager / Professional 2 == Technician / Supervisor / Associate Professional 3 == Clerk / Sales 4 == Skilled manual worker 5 == Manual worker 99 == Other |
Only displayed if employment status is 1-4 |
| Subject.JobclassCatOther | ||
| Subject.LengthOfStay | This variable reflects the length of stay of the patient at the study hospital. It has been derived using the information of the date and time of arrival at the study hospital and date and time of (study) hospital discharge. | |
| Subject.MartlPartnerStatus | 1 == Never been married 2 == Married 3 == Living together/common law 4 == Divorced 5 == Separated 6 == Widowed 88 == Unknown 99 == Other |
|
| Subject.MonthInjury | 1 == January 2 == February 3 == March 4 == April 5 == May 6 == June 7 == July 8 == August 9 == September 10 == October 11 == November 12 == December |
Month of Injury (January - December) |
| Subject.ObservStudyOtherObservStudy | ||
| Subject.ObservStudyOtherRegistry | ||
| Subject.ObservStudyRegistry | 1 == CREACTIVE 2 == TARN or EuroTARN registry 3 == German Trauma registry 4 == Net-QuRe 98 == Other Registry 99 == Other Observational Study |
Specifies if subject is also enrolled in another observational study/registry |
| Subject.PatientType | 1 == ER 2 == Admission 3 == ICU |
Subjects enrolled in the Core data collection of CENTER are differentiated by stratum (3 strata): ER: discharged directly from ER (dead or alive); Adm: admitted to hospital ward from the ER (may be transferred later to ICU); ICU: directly admitted from ER (or other hospital) to ICU. Patients remain in the stratum allocated, even though they may be internally transferred after admission. This means that the stratum is allocated at presentation based on planned care paths. But possibility exists that a patient allocated to for example the ER stratum, was still admitted to WARD or ICU in a later stage of his care path due to worsening. General enrollment criteria for Core study: Patients with a clinical diagnosis of TBI and clinical indication for CT scan. |
| Subject.Race | Race of Subject | |
| Subject.RandomizedControlTrial | 1 == CRASH-3 2 == EPO-TBI 3 == Eurotherm 4 == POLAR (Oxy-TC) 5 == NOSTRA 99 == Other Randomized Clinical Trial |
This variables is to ask if the patient is enrolled in another randomized controlled trial |
| Subject.RandomizedControlTrialOther | ||
| Subject.SesEduNoFather | Only if age <18 | |
| Subject.SesEduNoMother | Only if age <18 | |
| Subject.SesNumberPeopleLivingWith | Living together and number of people living with provides an indication of "social support" - important to recovery and social re-integration. | |
| Subject.SESPrimAdultAlone | ||
| Subject.SESPrimAdultChildren | ||
| Subject.SESPrimAdultParents | ||
| Subject.SESPrimAdultSiblings | ||
| Subject.SESPrimAdultSignOther | ||
| Subject.SESPrimAdultSpousePartner | ||
| Subject.SESPrimAdultUnknown | ||
| Subject.Sex | M == Male F == Female |
The difference between male and female, based upon the interactions between genes and between the genotype and the environment. Gender of Subject. |
| Subject.SiteCode | ||
| Subject.StudentStatus | 0 == None 1 == Full time, diploma / degree oriented 2 == Part time, diploma / degree oriented 3 == Other school 88 == Unknown |
Only displayed if employment status is student/school going |
| Subject.SurgeriesNotes | ||
| Subject.TimeInj | If exact time of injury is unknown, Investigators were asked to approximate the closest time and code "estimation" in the following variable: Subject.DateTimeInjReliable | |
| Subject.TransOfCareCompleteStatusNotes | ||
| Subject.ValidGUPI | ||
| Subject.WithdrawalOption | 1 == Complete Withdrawal (no further contact, destruction of all data and samples collected up to that point) 2 == No further study related activities, but consent to access of clinical notes and use of existing data |
In case of complete withdrawal, all data have been deleted from the database |
| Subject.WithdrawSuppDateTime | ||
| Surgeries.CranialSurgDone | 0 == No 1 == Yes 88 == Unknown |
These variables document cranial surgical procedures performed during the hospital stay. Up to 5 different surgical sessions can be recorded; Start date/time, stop date/time, reason for surgery and any delays in starting surgery are recorded. Life-saving emergency procedures performed immediately after presentation are recorded in the ER section: InjuryHx.EmergSurgInterventionsIntraCran. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERIntracranialSurg. |
| Surgeries.DecompressiveCran | 0 == No 1 == Yes |
These variables specifically focus on decompressive craniectomy (DC). Considerable uncertainty exists on which patients may benefit from DC, as well as on the timing. Previous studies have shown that in approximately one third of cases the DC was too small in size. |
| Surgeries.DecompressiveCranLocation | 1 == Bifrontal 2 == Hemicraniectomy- left side 3 == Hemicraniectomy- right side 4 == Posterior fossa |
Documents type of decompressive craniectomy. |
| Surgeries.DecompressiveCranReason | 1 == Pre-emptive approach to treatment of (suspected) raised ICP (not last resort) 2 == Raised ICP, refractory to medical management (last resort) 3 == ICP not monitored, but CT evidence of raised ICP 4 == Not directly planned, but decided on because of intra-operative brain swelling 5 == Routinely performed with every ASDH or Contusion evacuation 6 == Development of cerebral infarction |
WHY question: documents main reason for performing DC |
| Surgeries.DecompressiveCranType | 1 == Isolated procedure 2 == In association with ASDH removal 3 == In association with contusion/ICH removal 4 == In association with ASDH and contusion/ICH removal |
The indications for the decompressive craniectomy can be documented here. |
| Surgeries.DecompressiveSize | In some sites, the size of DC was recorded by Investigators. No generable way of calculating was proposed. | |
| Surgeries.ExtraCranialSurgDone | 0 == No 1 == Yes 88 == Unknown |
These variables document extracranial surgical procedures performed during the hospital stay. Up to 5 different surgical sessions can be recorded; Start date/time, stop date/time, reason for surgery and any delays in starting surgery are recorded. Life-saving emergency procedures performed immediately after presentation are recorded in the ER section: InjuryHx.EmergSurgInterventionsExtraCran. Procedures performed in "first" hospital (in case of secondary referral) are documented at: InjuryHx.PresERExtracranialSurg. |
| Surgeries.SurgIntervenAppro | 0 == 0 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| SurgeriesCranial.ShortTermSurvivalNoSurg | 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. | |
| SurgeriesCranial.ShortTermSurvivalYesSurg | 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. | |
| SurgeriesCranial.SurgeryCranialDelay | 1 == Transferral from other hospital 2 == Haemodynamic instability 3 == No OR available 4 == Surgeon delayed 5 == No delay 99 == Other |
|
| SurgeriesCranial.SurgeryCranialReason | 1 == Emergency/Life saving 2 == Clinical deterioration 3 == Mass effect on CT 4 == Radiological progression 5 == suspicion of) raised ICP 6 == Guideline adherence 7 == To prevent deterioration |
WHY Question: aims to document the reason for intracranial surgery |
| SurgeriesCranial.SurgeryDescCranial | 01 == Aneurysm (non trauma) 02 == Acute subdural hematoma 03 == Contusion 04 == Craniofacial surgery 05 == CSF shunt 06 == Chronic subdural hematoma 07 == Decompressive craniectomy-hemicraniectomy 08 == Depressed skull fracture 09 == Epidural hematoma 10 == Intracerebral hematoma 11 == Infection 12 == Optic nerve decompression 13 == Posterior fossa surgery 14 == Skull base fracture 15 == Ventriculostomy for CSF drainage 16 == Debridement -minimal for penetrating injuries 17 == Debridement - extensive for penetrating injuries 18 == Foreign body removal 19 == Bone flap replacement 20 == Cranioplasty 21 == Other 071 == Decompressive craniectomy - bifrontal 072 == Decompressive craniectomy - removal previous bone flap |
Up to 3 different surgical codes can be entered per surgical session |
| SurgeriesCranial.SurgeryEndDate | ||
| SurgeriesCranial.SurgeryEndTime | ||
| SurgeriesCranial.SurgeryStartDate | ||
| SurgeriesCranial.SurgeryStartTime | ||
| SurgeriesExtraCranial.SurgeryDescExtraCranial | 22 == Maxillofacial 23 == Extremity fracture lower limb (internal fixation) 24 == Extremity fracture lower limb (external fixation) 25 == Extremity fracture upper limb (internal fixation) 26 == Extremity fracture upper limb (external fixation) 27 == Fasciotomy 28 == Laparotomy (abdomen) 29 == Pelvic fracture (internal fixation) 30 == Pelvic fracture (external fixation) 31 == Spinal stabilisation/cervical 32 == Spinal stabilisation/thoracic 33 == Spinal stabilisation/lumbar 34 == Thoracotomy 35 == Tracheostomy 36 == Vascular (operative) 37 == Vascular (endovascular treatment) 38 == Wound closure/graft 39 == Other |
|
| SurgeriesExtraCranial.SurgeryEndDate | ||
| SurgeriesExtraCranial.SurgeryEndTime | ||
| SurgeriesExtraCranial.SurgeryExtraCranialDelay | 1 == Transferral from other hospital 2 == Haemodynamic instability 3 == No OR available 4 == Surgeon delayed 5 == No Delay 99 == Other |
|
| SurgeriesExtraCranial.SurgeryExtraCranialReason | 1 == Emergency/Lifesaving 2 == Elective 3 == Treatment of complication 4 == Airway management 99 == Other |
|
| SurgeriesExtraCranial.SurgeryStartDate | ||
| SurgeriesExtraCranial.SurgeryStartTime | ||
| TransitionsOfCare.CauseOfDelay | 1 == Unavailability of beds in the receiving unit 2 == Unavailability of transport 3 == Wish of patient/proxies 4 == Need for isolation due to multi resistant bacteria 5 == Funding issues 6 == Bureaucratic causes 99 == Other |
WHY question: documents reason for delayed transition of care |
| TransitionsOfCare.CauseOfDelayOther | ||
| TransitionsOfCare.DateClinReadyForTransfer | This variable documents the date at which the patient is considered ready for transfer; the date of "effective" transfer documents the date to which this transfer actually occured. In case of a substantial difference, the cause of delay should be recorded | |
| TransitionsOfCare.DateEffectiveTransfer | ||
| TransitionsOfCare.Location | InHosp == In Hospital PostDisch == Post Discharge |
|
| TransitionsOfCare.TransFrom | RSHICU == Readmission Study Hosp - ICU RSH == Readmission Study Hospital SMCH == Substance misuse Care Unit PSY == Psychiatric Unit ER == ER NH == Nursing Home NSRU == Non-specialized rehab unit SRU == Rehab Unit, specialized in Brain Injury HOME == Home IHR == In-hospital Rehab MRI == MRI CT == CT OR == OR ICU == ICU WO == Ward - Other WS == Ward - Surgery WN == Ward - Neurology WNS == Ward - Neurosurgery HCU == High Care Unit RU == Rehab Unit 98 == Other Hospital 99 == Other |
This informs on the care pathway of the patient. It is important to also check the ER, ADM and/or ICU admission and discharge forms for information on the care pathway. |
| TransitionsOfCare.TransReason | 1 == Mechanical ventilation 2 == Frequent neurological observations 3 == Haemodynamic invasive monitoring 4 == Extracranial injuries 5 == Neurological operation 6 == Clinical deterioration 7 == CT abnormalities 8 == Clinical observation for TBI 9 == No ICU bed available 10 == Could be discharged home, but no adequate supervision 11 == Improvement 12 == Neurological deterioration 13 == Systemic compilation 14 == CT progression 15 == Planned surgery 16 == Condition stable 17 == (acute) Treatment goals accomplished 18 == Need to free a bed 19 == Further improvement 20 == Clinical rehab completed 21 == Lack of improvement 22 == Late neurological deterioration 23 == Problems unrelated to trauma 24 == Post operative care 25 == Neurological complication 99 == Other |
WHY question: documents reason for transition of care |
| TransitionsOfCare.TransTiming | PRE == Premature APP == Appropriate DEL == Delayed |
Transitions of care may be premature or delayed because of logistic problems. This variable aims to capture such information. |
| TransitionsOfCare.TransTo | NSRU == Non-specialized rehab unit SRU == Rehab Unit, specialized in Brain Injury ER == ER RSHICU == Readmission Study Hosp - ICU RSH == Readmission Study Hospital SMCH == Substance misuse Care Unit PSY == Psychiatric Unit NH == Nursing Home RU == Rehab Unit HOME == Home IHR == In-hospital Rehab MRI == MRI CT == CT OR == OR ICU == ICU WO == Ward - Other WS == Ward - Surgery WN == Ward - Neurology WNS == Ward - Neurosurgery HCU == High Care Unit 98 == Other Hospital 99 == Other |
|
| Vitals.DailyGCSTime | For each Day of assessment, a Best and Worst score of GCS and pupillary reactivity is requested. If both scores are the same, only the Worst is reported. | |
| Vitals.DVAssmtConditions | 0 == No sedation or paralysis 1 == Sedated 2 == Paralyzed 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
|
| Vitals.DVAssmtConditionsWorst | 0 == No sedation or paralysis 1 == Sedated 2 == Paralyzed 3 == Temporary stop of sedation/paralysis 4 == Reversal of sedation/paralysis 5 == Active reversal (pharmacologic) of sedation/paralysis 99 == Other |
Only applicable to ICU stratum |
| Vitals.DVBestPupilSymmetry | 1 == Equal 2 == Unequal R>L 3 == Unequal L>R |
The pupil are of equal size (symmetry) during the day |
| Vitals.DVBloodGasNotDone | ||
| Vitals.DVBloodOxySatHigh | As determined from Arterial Blood Gas | |
| Vitals.DVBloodOxySatHighNotDone | As determined from Arterial Blood Gas | |
| Vitals.DVBloodOxySatLow | As determined from Arterial Blood Gas | |
| Vitals.DVBloodOxySatLowNotDone | As determined from Arterial Blood Gas | |
| Vitals.DVBrainTempCLow | Brain temperature at the timepoint of the lowest body temperature of the day, degrees Celsius. | |
| Vitals.DVBrainTempLowNotDone | ||
| Vitals.DVBrainTempUnit | C == C F == F |
|
| Vitals.DVChangeCauseWorst | 1 == Mainly intracranial 2 == Mainly extracranial 3 == Both to an equal extent 88 == Unknown |
|
| Vitals.DVChangeInOneDay | 0 == No change 1 == Improving 2 == Episode of deterioration 3 == Sustained deterioration 4 == Fluctuating |
|
| Vitals.DVChangeInOneDayWorst | 0 == No change 1 == Improving 2 == Episode of deterioration 3 == Sustained deterioration 4 == Fluctuating |
|
| Vitals.DVDate | Daily vitals are documented in both the adm and ICU strata on Day 1-7, Day 10, Day 14, Day 21 and Day 28. Note: FOUR score only applicable to patients in the ICU. | |
| Vitals.DVDBP | The diastolic blood pressure at the timepoint of the highest systolic blood pressure. | |
| Vitals.DVDBPLow | The diastolic blood pressure at the timepoint of the lowest systolic blood pressure. | |
| Vitals.DVFiO2AtHighPaO2 | ||
| Vitals.DVFiO2AtHighPaO2NotDone | ||
| Vitals.DVFiO2AtLowPaO2 | ||
| Vitals.DVFiO2AtLowPaO2NotDone | ||
| Vitals.DVFourScoreBraintstem | 0 == Absent pupil, corneal, and cough reflex 1 == Pupil and corneal reflexes absent 2 == Pupil or corneal reflexes absent 3 == One pupil wide and fixed 4 == Pupil and corneal reflexes present 88 == Unknown |
|
| Vitals.DVFourScoreEye | 0 == Eyelids remain closed with pain 1 == Eyelids closed but opens to pain 2 == Eyelids closed but opens to loud voice 3 == Eyelids open but not tracking 4 == Eyelids open or opened tracking or blinking to command 88 == Unknown |
|
| Vitals.DVFourScoreMotor | 0 == No response to pain or generalized myoclonus status epilepticus 1 == Extensor posturing 2 == Flexion response to pain 3 == Localizing to pain 4 == Thumbs up, fist, or peace sign to command 88 == Unknown |
|
| Vitals.DVFourScoreNotDone | ||
| Vitals.DVFourScoreRespiration | 0 == Breathes at ventilator rate or apnea 1 == Breathes above ventilator rate 2 == Not intubated, irregular breathing pattern 3 == Not intubated, Cheyne- Stokes breathing pattern 4 == Not intubated, regular breathing pattern 88 == Unknown |
|
| Vitals.DVFourScoreTotal | DVFourScoreEye + DVFourScoreMotor + DVFourScoreBraintstem + DVFourScoreRespiration. No score if any of the components =88 (unknown) or NULL | |
| Vitals.DVGCSBest | 0 == No 1 == Yes |
|
| Vitals.DVGCSBestChangeCause | 1 == Mainly intracranial 2 == Mainly extracranial 3 == Both to an equal extent 88 == Unknown |
|
| Vitals.DVGCSBestTime | ||
| Vitals.DVGCSEyes | S == Untestable (swollen) UN == Unknown O == Untestable (Other) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously |
|
| Vitals.DVGCSMotor | O == Untestable (Other) UN == Unknown P == Untestable (Deep sedation/paralyzed) 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 |
|
| Vitals.DVGCSPupilsNotDone | ||
| Vitals.DVGCSScore | Best GCS Score: DVGCSEyes + DVGCSMotor + DVGCSVerbal. If one or more of these is Untestable or unknown then = "No Sum" | |
| Vitals.DVGCSVerbal | T == Untestable (Tracheotomy/endotracheal tube) O == Untestable (Other) UN == Unknown 1 == 1-None 2 == 2- Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
|
| Vitals.DVGCSWorstEyes | UNK == Unknown O == Untestable (Other) S == Untestable (swollen) 1 == 1-None 2 == 2-To pain 3 == 3-To speech 4 == 4-Spontaneously |
|
| Vitals.DVGCSWorstMotor | UN == Unknown O == Untestable (Other) P == Untestable (Deep sedation/paralyzed) 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 |
|
| Vitals.DVGCSWorstScore | Worst GCS: DVGCSWorstEyes + DVGCSWorstMotor + DVGCSWorstVerbal. If one or more of these is Untestable or unknown then = "No Sum" | |
| Vitals.DVGCSWorstVerbal | O == Untestable (Other) T == Untestable (Tracheotomy/endotracheal tube) UN == Unknown 1 == 1-None 2 == 2- Incomprehensible sound 3 == 3-Inappropriate words 4 == 4-Confused 5 == 5-Oriented |
|
| Vitals.DVHighestPaCO2 | Highest PaCO2 on a day, in mmHg. | |
| Vitals.DVHighestPaCO2kPa | The highest value of PaCO2 measured on each day, in kPa. | |
| Vitals.DVHighestPaCO2NotDone | ||
| Vitals.DVHighestPaCO2Unit | mmHg == mmHg kPa == kPa |
The unit in which the highest PaCO2 on a day is measured. |
| Vitals.DVHighestPaO2 | ||
| Vitals.DVHighestPaO2kPa | ||
| Vitals.DVHighestPaO2NotDone | ||
| Vitals.DVHighestPaO2OverHighestFiO2 | ||
| Vitals.DVHighestPaO2Unit | mmHg == mmHg kPa == kPa |
|
| Vitals.DVHighestpH | ||
| Vitals.DVHighestpHNotDone | ||
| Vitals.DVHR | The highest heart rate during the day. | |
| Vitals.DVHRHighTime | The timepoint for the highest heart rate of a day. | |
| Vitals.DVHRLow | The lowest heart rate of a day. | |
| Vitals.DVHRLowTime | The time of the lowest heart rate of a day | |
| Vitals.DVIntracranialSecondInsultsNotDone | ||
| Vitals.DVLowestPaCO2 | The lowest value of PaCO2 measured on each day, in mmHg. | |
| Vitals.DVLowestPaCO2kPa | The lowest value of PaCO2 measured on each day, in kPa. | |
| Vitals.DVLowestPaCO2NotDone | ||
| Vitals.DVLowestPaCO2Unit | mmHg == mmHg kPa == kPa |
The unit in which PaCO2 is measured. |
| Vitals.DVLowestPaO2 | ||
| Vitals.DVLowestPaO2kPa | ||
| Vitals.DVLowestPaO2NotDone | ||
| Vitals.DVLowestPaO2OverLowestFiO2 | ||
| Vitals.DVLowestPaO2Unit | mmHg == mmHg kPa == kPa |
|
| Vitals.DVLowestpH | ||
| Vitals.DVLowestpHNotDone | ||
| Vitals.DVPupilLftEyeMeasr | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| Vitals.DVPupilLftEyeMeasrUnkUnt | 66 == Untestable 88 == Unknown |
Only applicable to size |
| Vitals.DVPupilReactivityLghtLftEyeReslt | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
The best pupillary reactivity of the left eye during the day |
| Vitals.DVPupilReactivityLghtRtEyeReslt | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
Best pupillary reactivity of the right eye during the day |
| Vitals.DVPupilRtEyeMeasr | 1 == 1 2 == 2 3 == 3 4 == 4 5 == 5 6 == 6 7 == 7 8 == 8 9 == 9 10 == 10 |
|
| Vitals.DVPupilRtEyeMeasrUnkUnt | 66 == Untestable 88 == Unknown |
Only applicable to size |
| Vitals.DVSBP | The highest systolic blood pressure for each day where vitals are recorded. | |
| Vitals.DVSBPHighTime | ||
| Vitals.DVSBPLow | The lowest systolic blood pressure for each day. | |
| Vitals.DVSBPLowTime | The time at which the lowest systolic blood pressure and its associated diastolic blood pressure is recorded. | |
| Vitals.DVSpO2 | ||
| Vitals.DVSpO2HighTime | ||
| Vitals.DVSpO2Low | ||
| Vitals.DVSpO2LowTime | ||
| Vitals.DVTempBrainC | Brain temperature at the timepoint of the highest body temperature of the day, degrees Celsius. | |
| Vitals.DVTempBrainNotDone | ||
| Vitals.DVTempBrainUnit | F == F C == C |
|
| Vitals.DVTempHighC | The highest body temperature of the day in degrees Celsius. For the associated time point, see Vitals.DVTempHighDateTime. For location of where the temperature was measured, see Vitals.DVTempLocation. | |
| Vitals.DVTempHighTime | Time when the highest temp of the day was recorded. | |
| Vitals.DVTempLocation | 1 == External-axillary 2 == External-skin 3 == Core- rectal 4 == Core-bladder 5 == Core- oesophageal 6 == Core- tympanic 7 == Core- nasopharynx |
Location of thermometer probe |
| Vitals.DVTempLowC | The lowest temperature of a day in degrees Celsius. For the timepoint, see Vitals.DVTempLowDateTime. For location of where the temperature was measured, see Vitals.DVTempLocation. | |
| Vitals.DVTempLowTime | Time when the lowest temp of the day was recorded. | |
| Vitals.DVTempNotDone | ||
| Vitals.DVTempUnitHigh | C == C F == F |
The unit in which the temperature is measured |
| Vitals.DVTempUnitLow | C == C F == F |
The unit in which the lowest body temperature of the day is measured. |
| Vitals.DVTimepoint | 1 == Day 1 2 == Day 2 3 == Day 3 4 == Day 4 5 == Day 5 6 == Day 6 7 == Day 7 10 == Day 10 14 == Day 14 21 == Day 21 28 == Day 28 |
Intended day after injury when the vitals are recorded |
| Vitals.DVVitalsNotDone | ||
| Vitals.DVWorstPupilLftEyeMeasr | ||
| Vitals.DVWorstPupilLftEyeMeasrUnkUnt | 66 == Untestable 88 == Unknown |
Only applicable to size |
| Vitals.DVWorstPupilReactivityLghtLftEyeResult | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
|
| Vitals.DVWorstPupilReactivityLghtRghtEyeResult | 1 == + (Brisk) 2 == + (Sluggish) 3 == - (Negative) |
|
| Vitals.DVWorstPupilRghtEyeMeasr | ||
| Vitals.DVWorstPupilRghtEyeMeasrUnkUnt | 66 == Untestable 88 == Unknown |
Only applicable to size |
| Vitals.DVWorstPupilSymmetry | 1 == Equal 2 == Unequal R>L 3 == Unequal L>R |
|
| Vitals.HosComplEventHypocapnia | 0 == No 1 == Single episode, short duration 2 == Multiple episodes or prolonged duration 88 == Unknown |
Second Insults reported here relate to the the hospital phase (both ward and ICU). Definite hypocapnia is defined as a PaCO2 <=3.3 kPa (25 mmHg) |
| Vitals.HosComplEventHypotension | 0 == No 1 == Single episode, short duration 2 == Multiple episodes or prolonged duration 88 == Unknown |
Second Insults reported here relate to the the hospital phase (both ward and ICU). Pre-hospital hypoxia is documented at: InjuryHx.EDComplEventHypotension. Definite hypotension is defined as a documented systolic BP < 90 mm Hg (adults) |
| Vitals.HosComplEventHypoxia | 0 == No 1 == Single episode, short duration 2 == Multiple episodes or prolonged duration 88 == Unknown |
Second Insults reported here relate to the hospital phase (both ward and ICU). Pre-hospital hypoxia is documented at: InjuryHx.EDComplEventHypoxia. Definite hypoxia is defined as a documented PaO2 <8 kPa (60 mm Hg) and/or SaO2<90% |
| Vitals.HosComplEventSeizures | 0 == No 1 == Single episode, short duration 2 == Partial/Focal 3 == Generalized 4 == Status epilepticus 5 == Silent seizure activity (only electrical, no clinical manifestation) 88 == Unknown |
|
| Vitals.HospSecondInsultsNeuroWorse | 0 == No 1 == Yes 88 == Unknown |
The importance of Neuroworsening was first described by Morris and Marshall. The occurrence of neuroworsening is related to poorer outcome in subjects with moderate to severe TBI. Neuroworsening is defined as 1) a decrease in GCS motor score of 2 or more points; 2) a new loss of pupillary reactivity or development of pupillary assymmetry >= 2mm; 3) deterioration in neurological or CT status sufficient to warrant immediate medical or surgical intervention |
| Vitals.HospSecondInsultsNeuroWorseAction | 1 == None 2 == Unscheduled CT scan 3 == Change in medical therapy 4 == Surgical intervention |
|
| Vitals.HospSecondInsultsNeuroWorseYes | 1 == Decrease in motor score >= 2 points 2 == Development of pupillary abnormalities 3 == Other neurological and/or CT deterioration |
This variable provides a specification of the type of neuroworsening if it occurs. |
| Vitals.PatientLocation | Ward == Ward ICU == ICU |
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