Myocardial Infarction Report Form PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

Myocardial Infarction Report Form
Beskrivning

Myocardial Infarction Report Form

Alias
UMLS CUI-1
C0027051
UMLS CUI-2
C1516308
1. Date of MI event (dd mon yy)
Beskrivning

Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0027051
2. Chest pain?
Beskrivning

Chest Pain

Datatyp

boolean

Alias
UMLS CUI [1]
C0008031
If `YES` please indicate whether typical or atypical chest pain
Beskrivning

If Yes

Datatyp

integer

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C1521902
3. Was the patient on study medication within the 7 days prior to event?
Beskrivning

Patient on study medication

Datatyp

boolean

Alias
UMLS CUI [1]
C0013227
If no indicate which medication the patient was not taking (Please indicate all that apply)
Beskrivning

if NO

Datatyp

integer

Alias
UMLS CUI [1]
C2348235
Assessments
Beskrivning

Assessments

Alias
UMLS CUI-1
C0220825
4. is infarction documented by ECG changes.
Beskrivning

ECG Changes

Datatyp

boolean

Alias
UMLS CUI [1]
C0855329
If Yes, please provide details of ECG
Beskrivning

details of ECG

Datatyp

text

Alias
UMLS CUI [1]
C1522508
Q Waves
Beskrivning

Q waves

Datatyp

integer

Alias
UMLS CUI [1]
C1305738
ST elevation
Beskrivning

ST elevation

Datatyp

integer

Alias
UMLS CUI [1]
C0520886
ST depression >2mm
Beskrivning

ST depression >2mm

Datatyp

integer

Alias
UMLS CUI [1]
C0520887
T inversion >3mm
Beskrivning

T inversion >3mm

Datatyp

integer

Alias
UMLS CUI [1]
C0520888
5. New bundle branch block (BBB)?
Beskrivning

bundle branch block

Datatyp

boolean

If Yes specify type
Beskrivning

If Yes

Datatyp

integer

6. Rhythm:
Beskrivning

Rhythm

Datatyp

integer

7. Was coronary intervention done within the 3 days prior to the event?
Beskrivning

Coronary Intervention

Datatyp

boolean

8. Was myocardial infarction confirmed by enzymes or biomarkers?
Beskrivning

Myocardial Infarction

Datatyp

boolean

Details for myocardial infarction
Beskrivning

Details for myocardial infarction

Value
Beskrivning

Value

Datatyp

text

Alias
UMLS CUI [1]
C1522609
Local Lab ranges Upper Limit Of Normal
Beskrivning

Local Lab ranges Upper Limit Of Normal

Datatyp

text

Hospitalization
Beskrivning

Hospitalization

Alias
UMLS CUI-1
C0019993
1. Did the vent lead to hospitalization. If yes please complete the Hospitalization Report Form.
Beskrivning

Hospitalization

Datatyp

boolean

Alias
UMLS CUI [1]
C0019993
Fatal Outcome
Beskrivning

Fatal Outcome

2. Was the event fatal (death within 28days). If yes please complete Death Report Form
Beskrivning

Fatal Event

Datatyp

boolean

Please remember to fax Supporting Documentation clearly identified with the patient number
Beskrivning

Please remember to fax Supporting Documentation clearly identified with the patient number

3. Please indicate which supporting documentation has been supplied:
Beskrivning

Fax Supporting Documentation

Datatyp

integer

Invenstigator´s Declaration
Beskrivning

Invenstigator´s Declaration

3. Invenstigator´s Declaration By signing and dating this page, I declare that I have reviewed for accuracy all case report form pages for this patient; the information contained on these pages accurately reflects the medical record including the results of tests and evaluations performed in the dates specified.
Beskrivning

Invenstigator´s Declaration

Datatyp

text

Investigator´s signature
Beskrivning

Investigator´s signature

Datatyp

text

Alias
UMLS CUI [1]
C2346576
Date of Signature
Beskrivning

Date of Signature

Datatyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1519316

Similar models

Myocardial Infarction Report Form PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Myocardial Infarction Report Form
C0027051 (UMLS CUI-1)
C1516308 (UMLS CUI-2)
Date
Item
1. Date of MI event (dd mon yy)
date
C0011008 (UMLS CUI [1,1])
C0027051 (UMLS CUI [1,2])
Chest Pain
Item
2. Chest pain?
boolean
C0008031 (UMLS CUI [1])
Item
If `YES` please indicate whether typical or atypical chest pain
integer
C0027051 (UMLS CUI [1,1])
C1521902 (UMLS CUI [1,2])
Code List
If `YES` please indicate whether typical or atypical chest pain
CL Item
Typical (1)
CL Item
Atypical (2)
Patient on study medication
Item
3. Was the patient on study medication within the 7 days prior to event?
boolean
C0013227 (UMLS CUI [1])
Item
If no indicate which medication the patient was not taking (Please indicate all that apply)
integer
C2348235 (UMLS CUI [1])
Code List
If no indicate which medication the patient was not taking (Please indicate all that apply)
CL Item
Bottle A (1)
CL Item
Bottle B (2)
CL Item
Blister Card C (3)
CL Item
Blister Card D (4)
Item Group
Assessments
C0220825 (UMLS CUI-1)
ECG Changes
Item
4. is infarction documented by ECG changes.
boolean
C0855329 (UMLS CUI [1])
details of ECG
Item
If Yes, please provide details of ECG
text
C1522508 (UMLS CUI [1])
Item
Q Waves
integer
C1305738 (UMLS CUI [1])
Code List
Q Waves
CL Item
Anterior (1)
CL Item
Inferior (2)
CL Item
Lateral (3)
CL Item
Anterolateral (4)
CL Item
Posterior (5)
CL Item
None (6)
Item
ST elevation
integer
C0520886 (UMLS CUI [1])
Code List
ST elevation
CL Item
Anterior (1)
CL Item
Inferior (2)
CL Item
Lateral (3)
CL Item
Anterolateral (4)
CL Item
Posterior (5)
CL Item
None (6)
Item
ST depression >2mm
integer
C0520887 (UMLS CUI [1])
Code List
ST depression >2mm
CL Item
Anterior (1)
CL Item
Inferior (2)
CL Item
Lateral (3)
CL Item
Anterolateral (4)
CL Item
Posterior (5)
CL Item
None (6)
Item
T inversion >3mm
integer
C0520888 (UMLS CUI [1])
Code List
T inversion >3mm
CL Item
Anterior (1)
CL Item
Inferior (2)
CL Item
Lateral (3)
CL Item
Anterolateral (4)
CL Item
Posterior (5)
CL Item
None (6)
bundle branch block
Item
5. New bundle branch block (BBB)?
boolean
Item
If Yes specify type
integer
Code List
If Yes specify type
CL Item
Right BBB (1)
CL Item
Left BBB (2)
Item
6. Rhythm:
integer
Code List
6. Rhythm:
CL Item
Sinus (1)
CL Item
Atrial fib/flutter (2)
CL Item
Other (specify) (3)
Coronary Intervention
Item
7. Was coronary intervention done within the 3 days prior to the event?
boolean
Myocardial Infarction
Item
8. Was myocardial infarction confirmed by enzymes or biomarkers?
boolean
Item Group
Details for myocardial infarction
Item
Value
text
C1522609 (UMLS CUI [1])
Code List
Value
CL Item
Peak CK (9)
CL Item
Peak CK-MB (10)
CL Item
Peak LDH (11)
CL Item
Peak AST (12)
CL Item
Troponin T (13)
CL Item
Troponin I (14)
Item
Local Lab ranges Upper Limit Of Normal
text
Code List
Local Lab ranges Upper Limit Of Normal
CL Item
Peak CK (9)
CL Item
Peak CK-MB (10)
CL Item
Peak LDH (11)
CL Item
Peak AST (12)
CL Item
Troponin T (13)
CL Item
Troponin I (14)
Item Group
Hospitalization
C0019993 (UMLS CUI-1)
Hospitalization
Item
1. Did the vent lead to hospitalization. If yes please complete the Hospitalization Report Form.
boolean
C0019993 (UMLS CUI [1])
Item Group
Fatal Outcome
Fatal Event
Item
2. Was the event fatal (death within 28days). If yes please complete Death Report Form
boolean
Item Group
Please remember to fax Supporting Documentation clearly identified with the patient number
Item
3. Please indicate which supporting documentation has been supplied:
integer
Code List
3. Please indicate which supporting documentation has been supplied:
CL Item
ECGs (1)
CL Item
Hospital discharge summaries (2)
CL Item
Clinical description of event (3)
CL Item
Other (4)
Item Group
Invenstigator´s Declaration
Invenstigator´s Declaration
Item
3. Invenstigator´s Declaration By signing and dating this page, I declare that I have reviewed for accuracy all case report form pages for this patient; the information contained on these pages accurately reflects the medical record including the results of tests and evaluations performed in the dates specified.
text
Investigator´s signature
Item
Investigator´s signature
text
C2346576 (UMLS CUI [1])
Date of Signature
Item
Date of Signature
date
C0011008 (UMLS CUI [1,1])
C1519316 (UMLS CUI [1,2])