Age | Percutaneous Coronary Intervention
Item
1. patients older than 18 years undergoing a pci procedure
boolean
C0001779 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
Pretreatment Intervention | Clopidogrel Dosage
Item
2. pretreatment with 600mg clopidogrel at least 2 hours before the intervention
boolean
C3539076 (UMLS CUI [1,1])
C0184661 (UMLS CUI [1,2])
C0070166 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
Informed Consent | Informed Consent Patient Representative
Item
3. informed, written consent by the patient or her/his legally-authorized representative for participation in the study.
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
ST segment elevation myocardial infarction
Item
1. recent st-elevation myocardial infarction within the last 48 hours
boolean
C1536220 (UMLS CUI [1])
Acute Coronary Syndrome | Biological Markers Positive | Troponin T Assay | Creatine kinase MB measurement
Item
2. acute coronary syndromes with positive biomarkers (troponin t > 0.03 μg/l or ck-mb > uln)
boolean
C0948089 (UMLS CUI [1])
C0005516 (UMLS CUI [2,1])
C1514241 (UMLS CUI [2,2])
C1141947 (UMLS CUI [3])
C0523584 (UMLS CUI [4])
Shock, Cardiogenic
Item
3. cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
Malignant Neoplasms Protocol Compliance Lacking | Life Expectancy | Comorbidity Protocol Compliance Lacking | Liver disease Severe | Kidney Disease Severe | Pancreatic Disease Severe
Item
4. malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than one year or that may result in protocol non-compliance
boolean
C0006826 (UMLS CUI [1,1])
C0525058 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
C0023671 (UMLS CUI [2])
C0009488 (UMLS CUI [3,1])
C0525058 (UMLS CUI [3,2])
C0332268 (UMLS CUI [3,3])
C0023895 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0022658 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C0030286 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
Hemorrhage | Bleeding tendency
Item
5. active bleeding; bleeding diathesis
boolean
C0019080 (UMLS CUI [1])
C1458140 (UMLS CUI [2])
Gastrointestinal Hemorrhage | Genitourinary tract hemorrhage
Item
6. history of gastrointestinal or genitourinary bleeding within the last 6 weeks
boolean
C0017181 (UMLS CUI [1])
C0919591 (UMLS CUI [2])
Disease Probability High Vascular lesions | Disease Probability High Hemorrhage | Gastric ulcer | Ulcerative Colitis
Item
7. presence of diseases which have a high probability of vascular lesions and subsequent bleeding such as active gastric ulcer or active ulcerous colitis
boolean
C0012634 (UMLS CUI [1,1])
C0033204 (UMLS CUI [1,2])
C0205250 (UMLS CUI [1,3])
C1402315 (UMLS CUI [1,4])
C0012634 (UMLS CUI [2,1])
C0033204 (UMLS CUI [2,2])
C0205250 (UMLS CUI [2,3])
C0019080 (UMLS CUI [2,4])
C0038358 (UMLS CUI [3])
C0009324 (UMLS CUI [4])
Trauma | Major surgery
Item
8. recent trauma or major surgery in the last month
boolean
C3714660 (UMLS CUI [1])
C0679637 (UMLS CUI [2])
Ophthalmologic Surgical Procedures | Operation on brain
Item
9. ophthalmic surgery or brain surgery in the last month
boolean
C0038901 (UMLS CUI [1])
C0195775 (UMLS CUI [2])
Retinal Diseases | Vitreous Hemorrhage
Item
10. retinopathies or vitreous body bleeding in the last month
boolean
C0035309 (UMLS CUI [1])
C0042909 (UMLS CUI [2])
Intracranial Hemorrhage | Abnormality structural | Cerebral arterial aneurysm
Item
11. history of intracranial bleeding or structural abnormalities (for example aneurysm of cerebral arteries)
boolean
C0151699 (UMLS CUI [1])
C1704258 (UMLS CUI [2,1])
C0678594 (UMLS CUI [2,2])
C1290398 (UMLS CUI [3])
Dissection of aorta Suspected | Pericarditis | Subacute Bacterial Endocarditis
Item
12. suspected aortic dissection; pericarditis and subacute bacterial endocarditis
boolean
C0340643 (UMLS CUI [1,1])
C0750491 (UMLS CUI [1,2])
C0031046 (UMLS CUI [2])
C0014122 (UMLS CUI [3])
Blood Transfusion Refused
Item
13. patient's refusal to blood transfusion.
boolean
C0005841 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
Anticoagulation Therapy Oral | Coumadin Derivative
Item
14. oral anticoagulation therapy with coumarin derivative within the last 7 days
boolean
C0003281 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0699129 (UMLS CUI [2,1])
C1527240 (UMLS CUI [2,2])
Unfractionated Heparin | Exception Activated clotting time measurement | Heparin, Low-Molecular-Weight
Item
15. treatment with ufh within 6 hours unless an act is less than 150 sec or low-molecular weight heparin within 8 hours before enrollment
boolean
C2825026 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0427611 (UMLS CUI [2,2])
C0019139 (UMLS CUI [3])
bivalirudin
Item
16. treatment with bivalirudin within 24 hours before enrollment
boolean
C0168273 (UMLS CUI [1])
Uncontrolled hypertension Severe Unresponsive to Treatment
Item
17. severe uncontrolled hypertension >180/110 mmhg unresponsive to therapy
boolean
C1868885 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205269 (UMLS CUI [1,3])
Staged Percutaneous Coronary Intervention Planned | Percutaneous Coronary Intervention Recent
Item
18. planned staged pci procedure within 30 days from index procedure or prior pci within the last 30 days.
boolean
C3272260 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
Hematology finding abnormal | Hemoglobin measurement | Platelet Count measurement
Item
19. relevant hematologic deviations: hemoglobin < 100 g/l, platelet count < 100 x 109 /l.
boolean
C0475182 (UMLS CUI [1])
C0518015 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
Glomerular Filtration Rate | Creatinine measurement, serum | Dependence on renal dialysis
Item
20. glomerular filtration rate (gfr) < 30 ml/min or serum creatinine > 30 mg/l or dependence on renal dialysis.
boolean
C0017654 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0524376 (UMLS CUI [3])
Hypersensitivity Investigational New Drugs | Aspirin allergy | Hypersensitivity Clopidogrel | Hypersensitivity Unfractionated Heparin | Anaphylaxis Post Exposure to Contrast Media
Item
21. known allergy to the study medications: aspirin, clopidogrel, ufh, true anaphylaxis after prior exposure to contrast media.
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0004058 (UMLS CUI [2])
C0020517 (UMLS CUI [3,1])
C0070166 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C2825026 (UMLS CUI [4,2])
C0002792 (UMLS CUI [5,1])
C0687676 (UMLS CUI [5,2])
C0332157 (UMLS CUI [5,3])
C0009924 (UMLS CUI [5,4])
Heparin-induced thrombocytopenia type II
Item
22. known heparin-induced thrombocytopenia (typ ii)
boolean
C0272275 (UMLS CUI [1])
Study Subject Participation Status
Item
23. previous enrollment in this trial.
boolean
C2348568 (UMLS CUI [1])
Pregnancy | Pregnancy Suspected | Pregnancy, Planned | Pregnancy test positive
Item
24. pregnancy (present, suspected or planned) or positive pregnancy test.
boolean
C0032961 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0032992 (UMLS CUI [3])
C0240802 (UMLS CUI [4])
Spinal Anesthesia | Peridural Anesthesia
Item
25. spinal, peridural and epidural anesthesia
boolean
C0002928 (UMLS CUI [1])
C0002913 (UMLS CUI [2])
Protocol Compliance Unable
Item
26. patient's inability to fully cooperate with the study protocol.
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])