Date of myocardial infarction
Item
Date of myocardial infarction
date
C0011008 (UMLS CUI [1,1])
C0027051 (UMLS CUI [1,2])
Item
Cardiac marker enzymes used for laboratory verification
text
C0443763 (UMLS CUI [1])
Code List
Cardiac marker enzymes used for laboratory verification
CL Item
Creatine Kinase (3)
CL Item
Creatine Kinase MB (4)
Highest level of cardiac marker enzyme
Item
Highest level of cardiac marker enzyme
float
C0741921 (UMLS CUI [1])
Units used for measurement
Item
Units used for measurement of cardiac marker enzymes
text
C1519795 (UMLS CUI [1])
Upper Limit of Normal
Item
Upper Limit of Normal for this marker enzyme
float
C1519815 (UMLS CUI [1])
Unit of measure
Item
Unit of measure for ULN
text
C1519795 (UMLS CUI [1])
Item
Clinical symptoms of cardiac ischemia
integer
C0151744 (UMLS CUI [1])
Code List
Clinical symptoms of cardiac ischemia
Item
ST elevation in ECG
integer
C0520886 (UMLS CUI [1])
Code List
ST elevation in ECG
Item
Development of pathological Q waves in the ECG
integer
C0429090 (UMLS CUI [1])
Code List
Development of pathological Q waves in the ECG
Item
Cardiac dyskinesia or ventricular asynergy
integer
C0232168 (UMLS CUI [1])
C0232171 (UMLS CUI [2])
Code List
Cardiac dyskinesia or ventricular asynergy
Other relevant information
Item
Other relevant information,please specify
text
C0517287 (UMLS CUI [1])
Item
Correlation with trial procedure CABG +/- CEA
integer
C1707520 (UMLS CUI [1])
Code List
Correlation with trial procedure CABG +/- CEA
CL Item
no correlation (5)
CL Item
can not be assessed (6)
Item
Outcome
integer
C1705586 (UMLS CUI [1])
CL Item
not yet recovered (2)
CL Item
recovered with sequelae (4)
Date of death
Item
If myocardial infarction was fatal,please specify the date of death
date
C0011008 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
Date of completion
Item
Date of completion of this form
date
C0011008 (UMLS CUI [1])
Signature
Item
Signature by investigator
text
C1519316 (UMLS CUI [1])
Name of Investigator
Item
Name of Investigator
text
C0008961 (UMLS CUI [1])