Informed consent
Item
Willing and able to give informed consent and comply with study procedures and follow-up through 1 year.
boolean
C0021430 (UMLS CUI-1)
Myocardial Ischemia
Item
symptoms of cardiac ischemia
boolean
C0151744 (UMLS CUI-1)
Age
Item
60 years of age or more
boolean
C0001779 (UMLS CUI-1)
Electrocardiogram change
Item
Electrocardiogram changes
boolean
C0855329 (UMLS CUI-1)
Troponin
Item
Elevated troponin levels
boolean
C0523952 (UMLS CUI-1)
CK-MB
Item
Elevated CK-MB levels
boolean
C0523584 (UMLS CUI-1)
History of cardiovascular disease
Item
Prior history of cardiovascular disease
boolean
C0455539 (UMLS CUI-1)
Pregnancy
Item
pregnancy (known or suspected)
boolean
C0549206 (UMLS CUI-1)
Hemodialysis
Item
renal dialysis within 30 days prior to randomizing in study
boolean
C0019004 (UMLS CUI-1)
Stroke
Item
Stroke
boolean
C0038454 (UMLS CUI-1)
CNS disorder
Item
central nervous system damage
boolean
C0007682 (UMLS CUI-1)
Bleeding risk
Item
bleeding disorders
boolean
C3251812 (UMLS CUI-1)
major surgery
Item
major surgery
boolean
C0679637 (UMLS CUI-1)
major injury
Item
major trauma
boolean
C0332677 (UMLS CUI-1)
Heparin
Item
treatment with heparin
boolean
C2825026 (UMLS CUI-1)
Eptifibatide
Item
Treatment with eptifibatide
boolean
C0253563 (UMLS CUI-1)