Patient ID; Centre Number
Item
Patient ID, Centre No.
text
C1269815 (UMLS CUI [1,1])
C2825181 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
Patient ID; Envelope Number
Item
Patient ID, Envelope No.
text
C1269815 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
eligibility criteria fulfilled
Item
All eligibility criteria met
boolean
C1516637 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Interventional cardiologist; experience
Item
Interventional cardiologist meets minimum experience criteria
boolean
C0175906 (UMLS CUI [1,1])
C0184661 (UMLS CUI [1,2])
C0237607 (UMLS CUI [1,3])
written informed consent
Item
Written informed consent obtained
boolean
C0021430 (UMLS CUI [1,1])
C1547186 (UMLS CUI [1,2])
admission laboratory test; cardiac enzymes/markers
Item
Blood drawn for admission laboratory tests including cardiac enzymes/markers
boolean
C0022885 (UMLS CUI [1,1])
C0443763 (UMLS CUI [1,2])
C1271630 (UMLS CUI [1,3])
inflammatory and coagulation markers
Item
Additional blood drawn for central evaluation of inflammatory and coagulation markers
boolean
C0022885 (UMLS CUI [1,1])
C0005778 (UMLS CUI [1,2])
C3805088 (UMLS CUI [1,3])
Baseline ECG, before
Item
Baseline ECG within 24 hours prior to acute PCI or 1 week if elective PCI
boolean
C1623258 (UMLS CUI [1,1])
C1442488 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
Pretreatment, Percutaneous Coronary Intervention; clopidogrel, Dosage, Last
Item
Last Dose of Clopidogrel before PCI
float
C1532338 (UMLS CUI [1,1])
C3539076 (UMLS CUI [1,2])
C0070166 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,4])
C1517741 (UMLS CUI [1,5])
Pretreatment, Percutaneous Coronary Intervention; clopidogrel, Dosage, Last
Item
Last Dose of Clopidogrel before PCI, Date
date
C1532338 (UMLS CUI [1,1])
C3539076 (UMLS CUI [1,2])
C0070166 (UMLS CUI [1,3])
C1762893 (UMLS CUI [1,4])
Pretreatment, Percutaneous Coronary Intervention; clopidogrel, Time last dose
Item
Last Dose of Clopidogrel before PCI, Time
time
C1532338 (UMLS CUI [1,1])
C3539076 (UMLS CUI [1,2])
C0070166 (UMLS CUI [1,3])
C0946444 (UMLS CUI [1,4])
Pretreatment, Percutaneous Coronary Intervention; ASA, dosage, last
Item
Last Dose of ASA before PCI
float
C1532338 (UMLS CUI [1,1])
C3539076 (UMLS CUI [1,2])
C0004057 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,4])
C1517741 (UMLS CUI [1,5])
Pretreatment, Percutaneous Coronary Intervention; ASA, date last dose
Item
Last Dose of ASA before PCI, date
date
C1532338 (UMLS CUI [1,1])
C3539076 (UMLS CUI [1,2])
C0004057 (UMLS CUI [1,3])
C1762893 (UMLS CUI [1,4])
Pretreatment, Percutaneous Coronary Intervention; ASA, Time last dose
Item
Last Dose of ASA before PCI, time
time
C1532338 (UMLS CUI [1,1])
C3539076 (UMLS CUI [1,2])
C0004057 (UMLS CUI [1,3])
C0946444 (UMLS CUI [1,4])
Body Weight
Item
Weight in kilograms
float
C0005910 (UMLS CUI [1])
undefined item
Item
Investigator wishes to proceed with PCI
text
GPIIb/IIIa inhibitor
Item
Has patient received a GPIIb/IIIa inhibitor or is there a plan for upfront use?
boolean
C3640054 (UMLS CUI [1])
Randomization Date
Item
Date patient randomized
date
C0034656 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Randomization Time
Item
Time patient randomized
time
C0034656 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Study drug injection; date
Item
Date study drug injected
date
C3854006 (UMLS CUI [1,1])
C3469597 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Study drug injection; time
Item
Time study drug injected
time
C3854006 (UMLS CUI [1,1])
C3469597 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])