Coronary Artery Disease Symptomatic
Item
symptomatic coronary artery disease
boolean
C1956346 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
Informed Consent
Item
subject has signed informed consent for data release
boolean
C0021430 (UMLS CUI [1])
Study Subject Geographic Stable | Participation Follow-up Willing
Item
subject is geographically stable and willing to participate at all follow up assessments
boolean
C0681850 (UMLS CUI [1,1])
C1517526 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0679823 (UMLS CUI [2,1])
C3274571 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Age
Item
subject is≥18 years of age.
boolean
C0001779 (UMLS CUI [1])
Informed Consent Lacking
Item
subject did not sign informed consent for data release
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Intolerance to Aspirin | Intolerance to Clopidogrel | Intolerance to Ticlopidine | Intolerance to Heparin | Intolerance Anticoagulation Therapy | Intolerance Antiplatelet therapy | Antiplatelet therapy Requirement Percutaneous Coronary Intervention | Intolerance to Stainless Steel | Intolerance to Sirolimus | Intolerance to Contrast Media
Item
known intolerance to aspirin, clopidogrel, ticlopidine, heparin or any other anticoagulation, antiplatelet therapy required for pci, stainless steel, sirolimus or contrast media.
boolean
C1744706 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C1744706 (UMLS CUI [3,1])
C0040207 (UMLS CUI [3,2])
C1744706 (UMLS CUI [4,1])
C0019134 (UMLS CUI [4,2])
C0231199 (UMLS CUI [5,1])
C0003281 (UMLS CUI [5,2])
C0231199 (UMLS CUI [6,1])
C1096021 (UMLS CUI [6,2])
C1096021 (UMLS CUI [7,1])
C1514873 (UMLS CUI [7,2])
C1532338 (UMLS CUI [7,3])
C1744706 (UMLS CUI [8,1])
C0038126 (UMLS CUI [8,2])
C1744706 (UMLS CUI [9,1])
C0072980 (UMLS CUI [9,2])
C1744706 (UMLS CUI [10,1])
C0009924 (UMLS CUI [10,2])
Operative Surgical Procedures Planned | Exception Maintenance Antiplatelet therapy Dual
Item
planned surgery within 6 months after pci unless dual antiplatelet therapy will be maintained
boolean
C0543467 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0024501 (UMLS CUI [2,2])
C1096021 (UMLS CUI [2,3])
C0205173 (UMLS CUI [2,4])
Study Subject Participation Status | End Point Primary Lacking
Item
currently participating in another study and primary endpoint is not yet reached.
boolean
C2348568 (UMLS CUI [1])
C2349179 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])