Percutaneous Coronary Intervention Planned | Non ST segment elevation acute coronary syndrome | Percutaneous Coronary Intervention Primary ST segment elevation myocardial infarction | Percutaneous Coronary Intervention elective | Cardiac Catheterization Procedures
Item
scheduled for pci, including pci for non-st elevation acute coronary syndromes (acs), primary pci for st elevation myocardial infarction (mi) or elective pci (with planned overnight stay in hospital). (patients undergoing diagnostic heart catherization who are suitable candidates for "ad hoc" pci are also eligible).
boolean
C1532338 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C3160886 (UMLS CUI [2])
C1532338 (UMLS CUI [3,1])
C0205225 (UMLS CUI [3,2])
C1536220 (UMLS CUI [3,3])
C1532338 (UMLS CUI [4,1])
C0439608 (UMLS CUI [4,2])
C0018795 (UMLS CUI [5])
Age
Item
age < 21 years
boolean
C0001779 (UMLS CUI [1])
Activated clotting time measurement
Item
activated clotting time (act) > 200 seconds immediately prior to pci
boolean
C0427611 (UMLS CUI [1])
Heparin, Low-Molecular-Weight
Item
use of low molecular weight heparin (lmwh) in the previous 6 hours before pci
boolean
C0019139 (UMLS CUI [1])
oral anticoagulants | International Normalized Ratio
Item
currently receiving an oral anticoagulant (oac) agent with an inr > 1.8
boolean
C0354604 (UMLS CUI [1])
C0525032 (UMLS CUI [2])
Thrombolytic Therapy ST segment elevation myocardial infarction
Item
thrombolytic therapy for st elevation mi in the previous 24 hours before pci
boolean
C0040044 (UMLS CUI [1,1])
C1536220 (UMLS CUI [1,2])
Internal hemorrhage | Bleeding tendency
Item
active internal bleeding or history of hemorrhagic diathesis
boolean
C1390214 (UMLS CUI [1])
C1458140 (UMLS CUI [2])
Thrombocytopenia | Platelet Count measurement
Item
thrombocytopenia (platelet count < 100 x 10-9/l)
boolean
C0040034 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
Pregnancy | Childbearing Potential Contraceptive methods Lacking
Item
pregnant women or women of childbearing potential who are not using an effective method of contraception
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
Hypersensitivity Heparin | Hypersensitivity fondaparinux | Hypersensitivity Aspirin | Hypersensitivity clopidogrel
Item
known allergy to unfractionated heparin, fondaparinux, aspirin or clopidogrel
boolean
C0020517 (UMLS CUI [1,1])
C0019134 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1098510 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0004057 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0070166 (UMLS CUI [4,2])
Medical contraindication Absolute Anticoagulation Therapy
Item
absolute contra-indication to anticoagulation
boolean
C1301624 (UMLS CUI [1,1])
C0205344 (UMLS CUI [1,2])
C0003281 (UMLS CUI [1,3])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
participation in other clinical research studies involving the evaluation of other investigational drugs or devices within 30 days of enrollment or prior participation in this study.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])