Acute coronary syndrome
Item
Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
boolean
C0948089 (UMLS CUI-1)
NSTEMI
Item
Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
boolean
C3537184 (UMLS CUI-1)
Troponin
Item
Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
boolean
C0523952 (UMLS CUI-1)
Coronary angiography
Item
Scheduled for coronary angiography greater than or equal to 2 and less than 24 hours from time of planned randomization, but no more than 48 hours from randomization
boolean
C0085532 (UMLS CUI-1)
PCI
Item
Scheduled for coronary PCI greater than or equal to 2 and less than 24 hours from time of planned randomization, but no more than 48 hours from randomization
boolean
C1532338 (UMLS CUI-1)
Prasugrel
Item
Must be eligible for treatment with prasugrel
boolean
C1620287 (UMLS CUI-1)
Aspirin
Item
Must be eligible for treatment with aspirin (ASA)
boolean
C0004057 (UMLS CUI-1)
GP IIb/IIIa antagonist
Item
Must be eligible for treatment with a glycoprotein IIb/IIIa receptor (GPIIb/IIIa) inhibitor
text
C3640054 (UMLS CUI-1)
Clopidogrel
Item
May be on a maintenance dose of clopidogrel 75 mg and must be able to switch to prasugrel
boolean
C0070166 (UMLS CUI-1)
Cardiac catheterization laboratory
Item
Must be enrolled at a cardiac catheterization laboratory hospital or at a hospital/ambulance service affiliated with a cardiac catheterization laboratory hospital
boolean
C0019994 (UMLS CUI [1,1])
C0018795 (UMLS CUI [1,2])
STEMI
Item
Present with ST-segment elevation myocardial infarction (STEMI) at the time of entry or randomization
boolean
C1536220 (UMLS CUI-1)
Cardiogenic shock
Item
Have cardiogenic shock
boolean
C0036980 (UMLS CUI-1)
Ventricular arrhythmia
Item
Have refractory ventricular arrhythmias
boolean
C0085612 (UMLS CUI-1)
Congestive heart failure
Item
Have New York Heart Association (NYHA) Class IV congestive heart failure (CHF)
text
C1319796 (UMLS CUI-1)
C0018802 (UMLS CUI-2)
Cardiac arrest
Item
Have had cardiac arrest within 1 week of entry or randomization into the study
boolean
C0018790 (UMLS CUI-1)