ID

27780

Description

Schwedisches Schlaganfallregister RIKSSTROKE Quelle: http://www.riksstroke.org/eng/ Riksstroke – a Swedish national quality register for stroke care primarily aimed at health professionals and decision makers in health care. We collect, analyze and follow-up data on morbidity and hospital stay. TIA

Link

http://www.riksstroke.org/eng/

Keywords

  1. 11/23/17 11/23/17 -
  2. 11/29/17 11/29/17 -
Copyright Holder

Riksstroke

Uploaded on

November 29, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Swedish Stroke Registry RIKSSTROKE

  1. StudyEvent: ODM
    1. TIA
TIA - Patient Information
Description

TIA - Patient Information

Alias
UMLS CUI-1
C0007787
UMLS CUI-2
C1955348
UMLS CUI-3
C0034975
Personal ID number
Description

Personal ID number

Data type

integer

Alias
UMLS CUI [1]
C2348585
Gender
Description

Gender

Data type

integer

Alias
UMLS CUI [1]
C0079399
Name
Description

Name

Data type

text

Alias
UMLS CUI [1]
C1299487
Date of onset TIA
Description

Date of onset TIA

Data type

date

Alias
UMLS CUI [1,1]
C0007787
UMLS CUI [1,2]
C0574845
Diagnosis Code (G)
Description

G 45 = TIA/cerebral ischemia/transient within 24 hours G (G45.4 transitory global amnesia is not registered)

Data type

float

Alias
UMLS CUI [1,1]
C1550350
UMLS CUI [1,2]
C0007787
Sequence of care
Description

Sequence of care

Alias
UMLS CUI-1
C0017313
UMLS CUI-2
C0679878
UMLS CUI-3
C0007787
Reporting hospital
Description

Reporting hospital

Data type

text

Alias
UMLS CUI [1,1]
C0019994
UMLS CUI [1,2]
C0700287
Reporting Ward/department
Description

Reporting Ward/department

Data type

text

Alias
UMLS CUI [1,1]
C0019961
UMLS CUI [1,2]
C0700287
Completed by (name of person completing this form)
Description

name of person completing this form

Data type

text

Alias
UMLS CUI [1,1]
C1550483
UMLS CUI [1,2]
C0027365
Has the patient been admitted for treatment for this TIA episode?
Description

admitted for treatment for this TIA episode

Data type

boolean

Alias
UMLS CUI [1,1]
C0007787
UMLS CUI [1,2]
C0332189
UMLS CUI [1,3]
C0087111
Did the patient arrive by ambulance?
Description

arrive by ambulance

Data type

integer

Alias
UMLS CUI [1,1]
C0002422
UMLS CUI [1,2]
C0150390
Number of hours from onset to arrival at hospital
Description

Number of hours from onset to arrival at hospital

Data type

integer

Alias
UMLS CUI [1,1]
C0007787
UMLS CUI [1,2]
C0449244
UMLS CUI [1,3]
C1320532
UMLS CUI [1,4]
C0449238
Thrombolysis alarm “save the brain/stroke alarm”
Description

(refers to the alarm for thrombolytic therapy if needed)

Data type

integer

Alias
UMLS CUI [1,1]
C0040044
UMLS CUI [1,2]
C2956061
UMLS CUI [2]
C0007787
Date of arrival at hospital
Description

(refers to date of arrival at the hospital where the patient initially received treatment for stroke)

Data type

date

Alias
UMLS CUI [1,1]
C3263562
UMLS CUI [1,2]
C0019994
UMLS CUI [1,3]
C0011008
UMLS CUI [2]
C0007787
Time of arrival at hospital
Description

(refers to time of arrival at the hospital where the patient initially received treatment for stroke)

Data type

time

Alias
UMLS CUI [1]
C1320532
UMLS CUI [2]
C0007787
Has the patient been admitted to the stroke unit for this episode?
Description

admitted to the stroke unit

Data type

integer

Alias
UMLS CUI [1,1]
C0587502
UMLS CUI [1,2]
C0030673
UMLS CUI [2]
C0007787
Risk Factors TIA
Description

Risk Factors TIA

Alias
UMLS CUI-1
C0035648
UMLS CUI-2
C0007787
Previous stroke
Description

Previous stroke

Data type

integer

Alias
UMLS CUI [1]
C0559159
Previous TIA / Amaurosis fugax?
Description

(Does not apply to G45.4 transitory global amnesia)

Data type

integer

Alias
UMLS CUI [1]
C0149793
UMLS CUI [2]
C0007787
Auricular fibrillation, previously diagnosed
Description

(Including intermittent fibrillation or flutter)

Data type

integer

Alias
UMLS CUI [1]
C0004238
Auricular fibrillation, recently identified on arrival at hospital or during treatment
Description

(Including intermittent fibrillation or flutter)

Data type

integer

Alias
UMLS CUI [1]
C0004238
Smoker (>1 cigarette/day, or quit during the last three months)
Description

Smoker

Data type

integer

Alias
UMLS CUI [1]
C0543414
Acute Care/Diagnosis TIA
Description

Acute Care/Diagnosis TIA

Alias
UMLS CUI-1
C0007787
UMLS CUI-2
C0679878
UMLS CUI-3
C0011900
CT brain scan during treatment
Description

CT brain scan

Data type

integer

Alias
UMLS CUI [1]
C0412585
MRI brain scan during treatment
Description

MRI brain scan

Data type

integer

Alias
UMLS CUI [1]
C0412675
If yes, MR brain scan during acute phase:
Description

MR brain scan result

Data type

integer

Alias
UMLS CUI [1,1]
C0412675
UMLS CUI [1,2]
C1274040
Carotid ultrasound performed
Description

Carotid ultrasound

Data type

integer

Alias
UMLS CUI [1]
C0948945
If yes, examination date
Description

Carotid ultrasound date

Data type

date

Alias
UMLS CUI [1,1]
C0948945
UMLS CUI [1,2]
C0011008
CT angiography performed
Description

(does not refer to CT perfusion)

Data type

integer

Alias
UMLS CUI [1]
C1536105
If yes, examination date
Description

CT angiography date

Data type

date

Alias
UMLS CUI [1,1]
C0085532
UMLS CUI [1,2]
C0011008
MR angiography performed
Description

MR angiography

Data type

integer

Alias
UMLS CUI [1]
C0002978
If yes, examination date
Description

MR angiography date

Data type

date

Alias
UMLS CUI [1,1]
C0002978
UMLS CUI [1,2]
C0011008
CT or MR angiography performed of vessels affected
Description

(always ask a doctor if uncertain about which vessels)

Data type

integer

Alias
UMLS CUI [1]
C0002978
Long term ECG (telemetry, Holter or equivalent) performed during period of treatment
Description

Long term ECG

Data type

integer

Alias
UMLS CUI [1]
C0430461
Has the patient been evaluated by an occupational therapist during the period of treatment?
Description

occupational therapist evaluate the patient

Data type

integer

Alias
UMLS CUI [1,1]
C1444296
UMLS CUI [1,2]
C0028807
Has the patient been evaluated by a physiotherapist during the period of treatment?
Description

physiotherapist evaluate the patient

Data type

integer

Alias
UMLS CUI [1,1]
C0679830
UMLS CUI [1,2]
C2362565
Pharmaceutical Treatment
Description

Pharmaceutical Treatment

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0087111
UMLS CUI-3
C0007787
Antihypertensive agents: At onset?
Description

(applies to all groups, independent of indication)

Data type

integer

Alias
UMLS CUI [1]
C0003364
Antihypertensive agents: At discharge?
Description

Antihypertensive agents

Data type

integer

Alias
UMLS CUI [1]
C0003364
Statins (e.g. Atorvastatin, Crestor, Lipitor, Pravastatin, Simvastatin): At onset?
Description

Statins

Data type

integer

Alias
UMLS CUI [1]
C0360714
Statins (e.g. Atorvastatin, Crestor, Lipitor, Pravastatin, Simvastatin): At discharge?
Description

Statins

Data type

integer

Alias
UMLS CUI [1]
C0360714
ASA (e.g. Trombyl): At onset?
Description

ASA

Data type

integer

Alias
UMLS CUI [1]
C0004057
ASA (e.g. Trombyl): At discharge?
Description

ASA

Data type

integer

Alias
UMLS CUI [1]
C0004057
Clopidogrel (e.g. Plavix): At onset?
Description

Clopidogrel

Data type

integer

Alias
UMLS CUI [1]
C0070166
Clopidogrel (e.g. Plavix): At discharge?
Description

Clopidogrel

Data type

integer

Alias
UMLS CUI [1]
C0070166
ASA + dipyridamole (Asasantin): At onset?
Description

ASA + dipyridamole

Data type

integer

Alias
UMLS CUI [1]
C0626271
ASA + dipyridamole (Asasantin): At discharge?
Description

ASA + dipyridamole

Data type

integer

Alias
UMLS CUI [1]
C0626271
Dipyridamole (Persantin): At onset?
Description

Dipyridamole

Data type

integer

Alias
UMLS CUI [1]
C0012582
Dipyridamole (Persantin): At discharge?
Description

Dipyridamole

Data type

integer

Alias
UMLS CUI [1]
C0012582
Antithrombotic drugs other than ASA, clopidogrel and dipyradimole (e.g. Brilique, Efient, Pletal, Possia): At onset?
Description

Antithrombotic drugs

Data type

integer

Alias
UMLS CUI [1]
C1704311
Antithrombotic drugs other than ASA, clopidogrel and dipyradimole (e.g. Brilique, Efient, Pletal, Possia): At discharge?
Description

Antithrombotic drugs

Data type

integer

Alias
UMLS CUI [1]
C1704311
Warfarin (Waran): At onset?
Description

Warfarin

Data type

integer

Alias
UMLS CUI [1]
C0043031
If yes, treatment with warfarin at onset state PK (INR) value regardless of diagnosis
Description

9.9= not known

Data type

float

Alias
UMLS CUI [1]
C0525032
Apixaban (Eliquis): At onset?
Description

Apixaban

Data type

integer

Alias
UMLS CUI [1]
C1831808
Apixaban (Eliquis): At discharge?
Description

Apixaban

Data type

integer

Alias
UMLS CUI [1]
C1831808
Dabigatran (Pradaxa): At onset?
Description

Dabigatran

Data type

integer

Alias
UMLS CUI [1]
C2348066
Dabigatran (Pradaxa): At discharge?
Description

Dabigatran

Data type

integer

Alias
UMLS CUI [1]
C2348066
Rivaroxaban (Xarelto): At onset?
Description

Rivaroxaban

Data type

integer

Alias
UMLS CUI [1]
C1739768
Rivaroxaban (Xarelto): At discharge?
Description

Rivaroxaban

Data type

integer

Alias
UMLS CUI [1]
C1739768
Peroral anticoagulants other than the above: At onset?
Description

Peroral anticoagulants

Data type

integer

Alias
UMLS CUI [1]
C0354604
Peroral anticoagulants other than the above: At discharge?
Description

Peroral anticoagulants

Data type

integer

Alias
UMLS CUI [1]
C0354604
Main reason for non-intervention with peroral anticoagulants at time of discharge in the case of atrial fibrillation and diagnosis I63
Description

peroral anticoagulants

Data type

integer

Alias
UMLS CUI [1,1]
C0354604
UMLS CUI [1,2]
C0392360
PAP (physical activity on prescription)?
Description

physical activity on prescription

Data type

integer

Alias
UMLS CUI [1,1]
C0026606
UMLS CUI [1,2]
C0033080
Information and Follow-up
Description

Information and Follow-up

Alias
UMLS CUI-1
C1522577
UMLS CUI-2
C1533716
UMLS CUI-3
C1955348
UMLS CUI-4
C0007787
Smoker informed at onset of need to quit smoking
Description

Smoker informed of need to quit smoking

Data type

integer

Alias
UMLS CUI [1,1]
C1273715
UMLS CUI [1,2]
C1272683
Information provided regarding driving
Description

Information provided regarding driving

Data type

integer

Alias
UMLS CUI [1,1]
C0004379
UMLS CUI [1,2]
C1533716
UMLS CUI [1,3]
C0038454
Has a follow-up appointment on the basis of this TIA episode been made with a nurse or doctor?
Description

follow-up appointment

Data type

integer

Alias
UMLS CUI [1,1]
C0007787
UMLS CUI [1,2]
C0589121
UMLS CUI [1,3]
C0586344
ABCD2 score
Description

ABCD2 score

Alias
UMLS CUI-1
C1518965
UMLS CUI-2
C0449821
UMLS CUI-3
C0007787
Age
Description

Age

Data type

integer

Alias
UMLS CUI [1]
C0001779
Blood pressure
Description

Blood pressure

Data type

integer

Alias
UMLS CUI [1]
C0005823
Clinical picture for this TIA episode
Description

(Many different symptoms are associated with a TIA. The ABCD2 score applies to only two groups of symptoms)

Data type

integer

Alias
UMLS CUI [1,1]
C0007787
UMLS CUI [1,2]
C1457887
Duration of symptoms
Description

Duration of symptoms

Data type

integer

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C0007787
Diabetes
Description

Diabetes

Data type

integer

Alias
UMLS CUI [1]
C0011849

Similar models

  1. StudyEvent: ODM
    1. TIA
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
TIA - Patient Information
C0007787 (UMLS CUI-1)
C1955348 (UMLS CUI-2)
C0034975 (UMLS CUI-3)
Personal ID number
Item
Personal ID number
integer
C2348585 (UMLS CUI [1])
Item
Gender
integer
C0079399 (UMLS CUI [1])
Code List
Gender
CL Item
male (1)
CL Item
female (2)
Name
Item
Name
text
C1299487 (UMLS CUI [1])
Date of onset TIA
Item
Date of onset TIA
date
C0007787 (UMLS CUI [1,1])
C0574845 (UMLS CUI [1,2])
Diagnosis Code
Item
Diagnosis Code (G)
float
C1550350 (UMLS CUI [1,1])
C0007787 (UMLS CUI [1,2])
Item Group
Sequence of care
C0017313 (UMLS CUI-1)
C0679878 (UMLS CUI-2)
C0007787 (UMLS CUI-3)
Reporting hospital
Item
Reporting hospital
text
C0019994 (UMLS CUI [1,1])
C0700287 (UMLS CUI [1,2])
Reporting Ward/department
Item
Reporting Ward/department
text
C0019961 (UMLS CUI [1,1])
C0700287 (UMLS CUI [1,2])
name of person completing this form
Item
Completed by (name of person completing this form)
text
C1550483 (UMLS CUI [1,1])
C0027365 (UMLS CUI [1,2])
admitted for treatment for this TIA episode
Item
Has the patient been admitted for treatment for this TIA episode?
boolean
C0007787 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
Item
Did the patient arrive by ambulance?
integer
C0002422 (UMLS CUI [1,1])
C0150390 (UMLS CUI [1,2])
Code List
Did the patient arrive by ambulance?
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item
Number of hours from onset to arrival at hospital
integer
C0007787 (UMLS CUI [1,1])
C0449244 (UMLS CUI [1,2])
C1320532 (UMLS CUI [1,3])
C0449238 (UMLS CUI [1,4])
Code List
Number of hours from onset to arrival at hospital
CL Item
< 3 hrs  (1)
CL Item
< 4.5 hrs  (2)
CL Item
< 24 hrs  (3)
CL Item
> 24 hrs (4)
CL Item
not known (5)
CL Item
 (6)
Item
Thrombolysis alarm “save the brain/stroke alarm”
integer
C0040044 (UMLS CUI [1,1])
C2956061 (UMLS CUI [1,2])
C0007787 (UMLS CUI [2])
Code List
Thrombolysis alarm “save the brain/stroke alarm”
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Date of arrival at hospital
Item
Date of arrival at hospital
date
C3263562 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0007787 (UMLS CUI [2])
Time of arrival at hospital
Item
Time of arrival at hospital
time
C1320532 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Item
Has the patient been admitted to the stroke unit for this episode?
integer
C0587502 (UMLS CUI [1,1])
C0030673 (UMLS CUI [1,2])
C0007787 (UMLS CUI [2])
Code List
Has the patient been admitted to the stroke unit for this episode?
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item Group
Risk Factors TIA
C0035648 (UMLS CUI-1)
C0007787 (UMLS CUI-2)
Item
Previous stroke
integer
C0559159 (UMLS CUI [1])
Code List
Previous stroke
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item
Previous TIA / Amaurosis fugax?
integer
C0149793 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Code List
Previous TIA / Amaurosis fugax?
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item
Auricular fibrillation, previously diagnosed
integer
C0004238 (UMLS CUI [1])
Code List
Auricular fibrillation, previously diagnosed
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item
Auricular fibrillation, recently identified on arrival at hospital or during treatment
integer
C0004238 (UMLS CUI [1])
Code List
Auricular fibrillation, recently identified on arrival at hospital or during treatment
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item
Smoker (>1 cigarette/day, or quit during the last three months)
integer
C0543414 (UMLS CUI [1])
Code List
Smoker (>1 cigarette/day, or quit during the last three months)
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item Group
Acute Care/Diagnosis TIA
C0007787 (UMLS CUI-1)
C0679878 (UMLS CUI-2)
C0011900 (UMLS CUI-3)
Item
CT brain scan during treatment
integer
C0412585 (UMLS CUI [1])
Code List
CT brain scan during treatment
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item
MRI brain scan during treatment
integer
C0412675 (UMLS CUI [1])
Code List
MRI brain scan during treatment
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item
If yes, MR brain scan during acute phase:
integer
C0412675 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Code List
If yes, MR brain scan during acute phase:
CL Item
shows new cerebral infarction  (1)
CL Item
shows no new cerebral infarction (2)
CL Item
examination result uncertain or not known (3)
Item
Carotid ultrasound performed
integer
C0948945 (UMLS CUI [1])
Code List
Carotid ultrasound performed
CL Item
yes  (1)
CL Item
no  (2)
CL Item
examination performed no more than 28 days before onset (3)
CL Item
not known (4)
Carotid ultrasound date
Item
If yes, examination date
date
C0948945 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
CT angiography performed
integer
C1536105 (UMLS CUI [1])
Code List
CT angiography performed
CL Item
yes  (1)
CL Item
no  (2)
CL Item
not examined due to patient's reduced consciousness  (3)
CT angiography date
Item
If yes, examination date
date
C0085532 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
MR angiography performed
integer
C0002978 (UMLS CUI [1])
Code List
MR angiography performed
CL Item
yes  (1)
CL Item
no  (2)
CL Item
examination performed no more than 28 days before onset (3)
CL Item
not known (4)
MR angiography date
Item
If yes, examination date
date
C0002978 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
CT or MR angiography performed of vessels affected
integer
C0002978 (UMLS CUI [1])
Code List
CT or MR angiography performed of vessels affected
CL Item
carotid vessels  (1)
CL Item
intracranial vessels  (2)
CL Item
both carotid and intracranial vessels  (3)
CL Item
not known (4)
Item
Long term ECG (telemetry, Holter or equivalent) performed during period of treatment
integer
C0430461 (UMLS CUI [1])
Code List
Long term ECG (telemetry, Holter or equivalent) performed during period of treatment
CL Item
yes  (1)
CL Item
no  (2)
CL Item
no, but arranged for period after discharge  (3)
CL Item
not known (4)
Item
Has the patient been evaluated by an occupational therapist during the period of treatment?
integer
C1444296 (UMLS CUI [1,1])
C0028807 (UMLS CUI [1,2])
Code List
Has the patient been evaluated by an occupational therapist during the period of treatment?
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item
Has the patient been evaluated by a physiotherapist during the period of treatment?
integer
C0679830 (UMLS CUI [1,1])
C2362565 (UMLS CUI [1,2])
Code List
Has the patient been evaluated by a physiotherapist during the period of treatment?
CL Item
yes (1)
CL Item
no (2)
CL Item
not known (3)
Item Group
Pharmaceutical Treatment
C0013227 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0007787 (UMLS CUI-3)
Item
Antihypertensive agents: At onset?
integer
C0003364 (UMLS CUI [1])
Code List
Antihypertensive agents: At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Antihypertensive agents: At discharge?
integer
C0003364 (UMLS CUI [1])
Code List
Antihypertensive agents: At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Statins (e.g. Atorvastatin, Crestor, Lipitor, Pravastatin, Simvastatin): At onset?
integer
C0360714 (UMLS CUI [1])
Code List
Statins (e.g. Atorvastatin, Crestor, Lipitor, Pravastatin, Simvastatin): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Statins (e.g. Atorvastatin, Crestor, Lipitor, Pravastatin, Simvastatin): At discharge?
integer
C0360714 (UMLS CUI [1])
Code List
Statins (e.g. Atorvastatin, Crestor, Lipitor, Pravastatin, Simvastatin): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
ASA (e.g. Trombyl): At onset?
integer
C0004057 (UMLS CUI [1])
Code List
ASA (e.g. Trombyl): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
ASA (e.g. Trombyl): At discharge?
integer
C0004057 (UMLS CUI [1])
Code List
ASA (e.g. Trombyl): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Clopidogrel (e.g. Plavix): At onset?
integer
C0070166 (UMLS CUI [1])
Code List
Clopidogrel (e.g. Plavix): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Clopidogrel (e.g. Plavix): At discharge?
integer
C0070166 (UMLS CUI [1])
Code List
Clopidogrel (e.g. Plavix): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
ASA + dipyridamole (Asasantin): At onset?
integer
C0626271 (UMLS CUI [1])
Code List
ASA + dipyridamole (Asasantin): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
ASA + dipyridamole (Asasantin): At discharge?
integer
C0626271 (UMLS CUI [1])
Code List
ASA + dipyridamole (Asasantin): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Dipyridamole (Persantin): At onset?
integer
C0012582 (UMLS CUI [1])
Code List
Dipyridamole (Persantin): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Dipyridamole (Persantin): At discharge?
integer
C0012582 (UMLS CUI [1])
Code List
Dipyridamole (Persantin): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Antithrombotic drugs other than ASA, clopidogrel and dipyradimole (e.g. Brilique, Efient, Pletal, Possia): At onset?
integer
C1704311 (UMLS CUI [1])
Code List
Antithrombotic drugs other than ASA, clopidogrel and dipyradimole (e.g. Brilique, Efient, Pletal, Possia): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Antithrombotic drugs other than ASA, clopidogrel and dipyradimole (e.g. Brilique, Efient, Pletal, Possia): At discharge?
integer
C1704311 (UMLS CUI [1])
Code List
Antithrombotic drugs other than ASA, clopidogrel and dipyradimole (e.g. Brilique, Efient, Pletal, Possia): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Warfarin (Waran): At onset?
integer
C0043031 (UMLS CUI [1])
Code List
Warfarin (Waran): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
PK (INR) value
Item
If yes, treatment with warfarin at onset state PK (INR) value regardless of diagnosis
float
C0525032 (UMLS CUI [1])
Item
Apixaban (Eliquis): At onset?
integer
C1831808 (UMLS CUI [1])
Code List
Apixaban (Eliquis): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Apixaban (Eliquis): At discharge?
integer
C1831808 (UMLS CUI [1])
Code List
Apixaban (Eliquis): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Dabigatran (Pradaxa): At onset?
integer
C2348066 (UMLS CUI [1])
Code List
Dabigatran (Pradaxa): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Dabigatran (Pradaxa): At discharge?
integer
C2348066 (UMLS CUI [1])
Code List
Dabigatran (Pradaxa): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Rivaroxaban (Xarelto): At onset?
integer
C1739768 (UMLS CUI [1])
Code List
Rivaroxaban (Xarelto): At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Rivaroxaban (Xarelto): At discharge?
integer
C1739768 (UMLS CUI [1])
Code List
Rivaroxaban (Xarelto): At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Peroral anticoagulants other than the above: At onset?
integer
C0354604 (UMLS CUI [1])
Code List
Peroral anticoagulants other than the above: At onset?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Peroral anticoagulants other than the above: At discharge?
integer
C0354604 (UMLS CUI [1])
Code List
Peroral anticoagulants other than the above: At discharge?
CL Item
yes (1)
CL Item
no (2)
CL Item
no, intervention planned at time of follow-up appointment within two weeks after discharge (3)
CL Item
not known (4)
Item
Main reason for non-intervention with peroral anticoagulants at time of discharge in the case of atrial fibrillation and diagnosis I63
integer
C0354604 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
Main reason for non-intervention with peroral anticoagulants at time of discharge in the case of atrial fibrillation and diagnosis I63
CL Item
insertion planned after discharge 2= contraindications (in accordance with FASS) (1)
CL Item
interactions with other drugs/neuropathy (in accordance with FASS) (3)
CL Item
caution (in accordance with FASS) (4)
CL Item
fall-prone  (5)
CL Item
dementia  (6)
CL Item
patient refuses treatment  (7)
CL Item
other reason  (8)
CL Item
not known (9)
CL Item
kontraindicerat (enl. FASS) (2)
Item
PAP (physical activity on prescription)?
integer
C0026606 (UMLS CUI [1,1])
C0033080 (UMLS CUI [1,2])
Code List
PAP (physical activity on prescription)?
CL Item
yes  (1)
CL Item
no  (2)
CL Item
no, the need for physical activity is already being met (3)
CL Item
patient declined  (4)
CL Item
not known (5)
Item Group
Information and Follow-up
C1522577 (UMLS CUI-1)
C1533716 (UMLS CUI-2)
C1955348 (UMLS CUI-3)
C0007787 (UMLS CUI-4)
Item
Smoker informed at onset of need to quit smoking
integer
C1273715 (UMLS CUI [1,1])
C1272683 (UMLS CUI [1,2])
Code List
Smoker informed at onset of need to quit smoking
CL Item
yes  (1)
CL Item
no  (2)
CL Item
not relevant given patient's condition  (3)
CL Item
not known (4)
Item
Information provided regarding driving
integer
C0004379 (UMLS CUI [1,1])
C1533716 (UMLS CUI [1,2])
C0038454 (UMLS CUI [1,3])
Code List
Information provided regarding driving
CL Item
yes  (1)
CL Item
no  (2)
CL Item
not relevant/no driving licence  (3)
CL Item
not known (4)
Item
Has a follow-up appointment on the basis of this TIA episode been made with a nurse or doctor?
integer
C0007787 (UMLS CUI [1,1])
C0589121 (UMLS CUI [1,2])
C0586344 (UMLS CUI [1,3])
Code List
Has a follow-up appointment on the basis of this TIA episode been made with a nurse or doctor?
CL Item
yes, at a special stroke unit (at or outside the hospital)  (1)
CL Item
yes, at another hospital admissions ward/department  (2)
CL Item
yes, at a health centre/equivalent (3)
CL Item
yes, at arranged accommodation (4)
CL Item
yes, at day rehab  (5)
CL Item
not known (7)
CL Item
 (6)
Item Group
ABCD2 score
C1518965 (UMLS CUI-1)
C0449821 (UMLS CUI-2)
C0007787 (UMLS CUI-3)
Item
Age
integer
C0001779 (UMLS CUI [1])
Code List
Age
CL Item
under 60 years (1)
CL Item
over 60 years (0)
Item
Blood pressure
integer
C0005823 (UMLS CUI [1])
Code List
Blood pressure
CL Item
over 140/90 at time of examination  (1)
CL Item
under 140/90 at time of examination (0)
Item
Clinical picture for this TIA episode
integer
C0007787 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
Code List
Clinical picture for this TIA episode
CL Item
speech difficulties without weakness (1)
CL Item
weakness on one side (unilaterally) could be combined with other symptoms  (2)
CL Item
other symptoms (0)
Item
Duration of symptoms
integer
C1457887 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0007787 (UMLS CUI [1,3])
Code List
Duration of symptoms
CL Item
symptoms lasted 10-59 minutes (1)
CL Item
symptoms lasted over 60 minutes  (2)
CL Item
symptoms lasted under 10 minutes (0)
Item
Diabetes
integer
C0011849 (UMLS CUI [1])
Code List
Diabetes
CL Item
diabetes, previously diagnosed or recently identified (1)
CL Item
no diabetes (0)

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