Age
Item
1. the patient must be ≥18 years and ≤75 of age.
boolean
C0001779 (UMLS CUI [1])
Chest Pain Prolonged Duration | Nitrate | ST segment elevation | ST segment elevation over precordial leads on ECG | Left Bundle-Branch Block New
Item
2. prolonged, continuous (≥ 30 min) chest pain despite nitrate and: (1) st-segment elevation ≥ at least 2 leads, with reciprocal st-segment elevation ≥ 0.05mv and precordial leads st-segment elevation ≥ 0.01mv, or (2) newly developed left bundle branch block
boolean
C0008031 (UMLS CUI [1,1])
C0439590 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0699857 (UMLS CUI [2])
C0520886 (UMLS CUI [3])
C4228865 (UMLS CUI [4])
C0023211 (UMLS CUI [5,1])
C0205314 (UMLS CUI [5,2])
Symptoms Duration
Item
3. symptoms ≥ 30 min and ≤12 hours
boolean
C1457887 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Informed Consent
Item
4. the patient has consented to participate and has authorized the collection and release of his medical information by signing the "patient informed consent form"
boolean
C0021430 (UMLS CUI [1])
Lesion Coronary artery Native Quantity | Requirement Intervention | Other Coding | Implantation Sirolimus drug-eluting stent | Other Coding | Implantation Zotarolimus Drug-Eluting Coronary Stents
Item
5. all lesions requiring interventions in one or more native coronary arteries are amendable for implantation of one or more cypher® sirolimus-eluting coronary stent system or endeavor® zotarolimus-eluting coronary stent
boolean
C0221198 (UMLS CUI [1,1])
C0205042 (UMLS CUI [1,2])
C0302891 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,4])
C1514873 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])
C3846158 (UMLS CUI [3])
C0021107 (UMLS CUI [4,1])
C2199093 (UMLS CUI [4,2])
C3846158 (UMLS CUI [5])
C0021107 (UMLS CUI [6,1])
C1700035 (UMLS CUI [6,2])
C1262327 (UMLS CUI [6,3])
Protocol Compliance | Protocol Compliance Guardian
Item
6. the patient or guardian is willing and able to cooperate with study procedures and required follow up visits.
boolean
C0525058 (UMLS CUI [1])
C0525058 (UMLS CUI [2,1])
C1274041 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Childbearing Potential Planned Pregnancy
Item
1. pregnant and breast-feeding female and female of childbearing potential, who possibly plan to become pregnant any time after enrollment into this study.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0032992 (UMLS CUI [3,2])
Sirolimus Intravenous Systemic
Item
2. systemic (intravenous) sirolimus use within 12 months.
boolean
C0072980 (UMLS CUI [1,1])
C1522726 (UMLS CUI [1,2])
C0205373 (UMLS CUI [1,3])
Pharmaceutical Preparations Use of Stent | Hypersensitivity Pharmaceutical Preparations Specified | Hypersensitivity Component Pharmaceutical Preparations Specified
Item
3. patients with hypersensitivity or allergies to one of the drugs or components indicated in the instructions for use of either stents.
boolean
C0013227 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
C0038257 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C0013227 (UMLS CUI [2,2])
C0205369 (UMLS CUI [2,3])
C0020517 (UMLS CUI [3,1])
C1705248 (UMLS CUI [3,2])
C0013227 (UMLS CUI [3,3])
C0205369 (UMLS CUI [3,4])
Bleeding tendency | Blood Coagulation Disorders | Heparin-induced thrombocytopenia | Transfusion blood refusal
Item
4. history of bleeding diathesis or known coagulopathy (including heparin-induced thrombocytopenia), or will refuse blood transfusions.
boolean
C1458140 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
C0272285 (UMLS CUI [3])
C0749628 (UMLS CUI [4])
Gastrointestinal Hemorrhage | Genitourinary tract hemorrhage | Major surgery
Item
5. gastrointestinal or genitourinary bleeding within the prior 3 months, or major surgery within 2 months.
boolean
C0017181 (UMLS CUI [1])
C0919591 (UMLS CUI [2])
C0679637 (UMLS CUI [3])
Platelet Count measurement | Hemoglobin measurement
Item
6. current platelet count <100 x 10^9cells/l or hgb <10 g/dl.
boolean
C0032181 (UMLS CUI [1])
C0518015 (UMLS CUI [2])
Thrombolytic Therapy Myocardial Infarction
Item
7. fibrinolytic therapy for current mi treatment
boolean
C0040044 (UMLS CUI [1,1])
C0027051 (UMLS CUI [1,2])
Intervention Coronary Target vessel | Vascular Disease Post Coronary Artery Bypass Surgery
Item
8. previous coronary intervention on target vessel or post-cabg vessel disease
boolean
C0184661 (UMLS CUI [1,1])
C1522318 (UMLS CUI [1,2])
C0449618 (UMLS CUI [1,3])
C0042373 (UMLS CUI [2,1])
C0687676 (UMLS CUI [2,2])
C0010055 (UMLS CUI [2,3])
Transplantation
Item
9. transplant patients
boolean
C0040732 (UMLS CUI [1])
Cardiac ejection fraction
Item
10. patients with ef<25%
boolean
C0232174 (UMLS CUI [1])
Shock, Cardiogenic | Life Expectancy
Item
11. patients with cardiogenic shock; with a life expectancy shorter than 12 months
boolean
C0036980 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
Renal dysfunction Severe | Creatinine measurement, serum | Dependence on renal dialysis
Item
12. severe kidney dysfunction: creatinine level ≥2.0mg/dl or dependence on dialysis.
boolean
C3279454 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0201976 (UMLS CUI [2])
C0524376 (UMLS CUI [3])
Liver Dysfunction Severe | Aspartate aminotransferase increased | Alanine aminotransferase increased
Item
13. severe hepatic dysfunction (ast and alt ≥ 3 times upper normal reference values).
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0151904 (UMLS CUI [2])
C0151905 (UMLS CUI [3])
Study Subject Participation Status | Investigational Medical Device | Investigational New Drugs | Interference Endpoints Current | Patient need for Coronary angiography | Patient need for Coronary artery Imaging Procedure
Item
14. the patient is currently, and during the crest-mi study, participating in another investigational device or drug study that clinically interferes with the crest-mi study endpoints; or requires coronary angiography or other coronary artery imaging procedures. the patient may only be enrolled in the crest-mi study once.
boolean
C2348568 (UMLS CUI [1])
C2346570 (UMLS CUI [2])
C0013230 (UMLS CUI [3])
C0521102 (UMLS CUI [4,1])
C2349179 (UMLS CUI [4,2])
C0521116 (UMLS CUI [4,3])
C0686904 (UMLS CUI [5,1])
C0085532 (UMLS CUI [5,2])
C0686904 (UMLS CUI [6,1])
C0205042 (UMLS CUI [6,2])
C0079595 (UMLS CUI [6,3])
Blood Vessel Tortuous Severe | Blood Vessel Calcified Severe | Stent Problem | Blood Vessel Diameter Inappropriate Stent | Patient Inappropriate Placement of stent
Item
15. severe tortuous or calcified vessel; stent can not or has difficulty to go through; blood vessel diameter is smaller than the minimum stent diameter available; patients unsuitable for stent implantation.
boolean
C0005847 (UMLS CUI [1,1])
C4068863 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C0005847 (UMLS CUI [2,1])
C0175895 (UMLS CUI [2,2])
C0205082 (UMLS CUI [2,3])
C0038257 (UMLS CUI [3,1])
C0033213 (UMLS CUI [3,2])
C0005847 (UMLS CUI [4,1])
C1301886 (UMLS CUI [4,2])
C1548788 (UMLS CUI [4,3])
C0038257 (UMLS CUI [4,4])
C0030705 (UMLS CUI [5,1])
C1548788 (UMLS CUI [5,2])
C0522776 (UMLS CUI [5,3])