Age
Item
male or female patients aged >=18 years
boolean
C0001779 (UMLS CUI [1])
Atrial Fibrillation
Item
patients with non valvular atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
Patient Finding
Item
patient presenting with:
boolean
C0030705 (UMLS CUI [1,1])
C0243095 (UMLS CUI [1,2])
Acute Coronary Syndrome | ST segment elevation myocardial infarction | Non-ST elevation (NSTEMI) myocardial infarction | Angina, Unstable | Percutaneous Coronary Intervention | Stenting Bare metal stent | Stenting Drug-Eluting Stents | Coronary Artery Disease Stable | Lesion Quantity Eligible PCI
Item
an acs (stemi, nonstemi [nstemi] or unstable angina [ua]) that was successfully treated by pci and stenting (either bare metal stent or drug eluting stent) or stable coronary artery disease with at least one lesion eligible for pci that was successfully treated by elective pci and stenting (either bms or des)
boolean
C0948089 (UMLS CUI [1])
C1536220 (UMLS CUI [2])
C1561921 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C1532338 (UMLS CUI [5])
C2348535 (UMLS CUI [6,1])
C2825200 (UMLS CUI [6,2])
C2348535 (UMLS CUI [7,1])
C1322815 (UMLS CUI [7,2])
C1956346 (UMLS CUI [8,1])
C0205360 (UMLS CUI [8,2])
C0221198 (UMLS CUI [9,1])
C1265611 (UMLS CUI [9,2])
C1548635 (UMLS CUI [9,3])
C1532338 (UMLS CUI [9,4])
Informed Consent
Item
the patient must be able to give informed consent in accordance with international conference on harmonisation good clinical practice guidelines and local legislation and/or regulations.
boolean
C0021430 (UMLS CUI [1])
Mechanical heart valve prosthesis | Heart Valve Prosthesis biological
Item
patients with a mechanical or biological heart valve prosthesis
boolean
C3873910 (UMLS CUI [1])
C0018825 (UMLS CUI [2,1])
C0205460 (UMLS CUI [2,2])
Shock, Cardiogenic
Item
cardiogenic shock during current hospitalisation
boolean
C0036980 (UMLS CUI [1])
Cerebrovascular accident
Item
stroke within 1 month prior to screening visit
boolean
C0038454 (UMLS CUI [1])
Major surgery
Item
patients who have had major surgery within the month prior to screening
boolean
C0679637 (UMLS CUI [1])
Gastrointestinal Hemorrhage | Exception Cause eliminated
Item
gastrointestinal haemorrhage within one month prior to screening, unless, in the opinion of the investigator, the cause has been permanently eliminated
boolean
C0017181 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0015127 (UMLS CUI [2,2])
C0849355 (UMLS CUI [2,3])
Hemorrhage Episode Major | Hemorrhage Episode Life Threatening
Item
major bleeding episode including life-threatening bleeding episode in one month prior to screening visit
boolean
C0019080 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
C0019080 (UMLS CUI [2,1])
C0332189 (UMLS CUI [2,2])
C2826244 (UMLS CUI [2,3])
Anemia | Hemoglobin measurement | Thrombocytopenia | Heparin-induced thrombocytopenia | Platelet Count measurement
Item
anaemia (haemoglobin <10g/dl) or thrombocytopenia including heparin-induced thrombocytopenia (platelet count <100 x 109/l) at screening
boolean
C0002871 (UMLS CUI [1])
C0518015 (UMLS CUI [2])
C0040034 (UMLS CUI [3])
C0272285 (UMLS CUI [4])
C0032181 (UMLS CUI [5])
Renal Insufficiency Severe | Estimation of creatinine clearance by Cockcroft-Gault formula
Item
severe renal impairment (estimated crcl calculated by cockcroft-gault equation) <30ml/min at screening
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2711451 (UMLS CUI [2])
Liver disease
Item
active liver disease
boolean
C0023895 (UMLS CUI [1])