Coronary angiography Willing | Percutaneous Coronary Intervention potential Willing
Item
willing to receive the coronary angiography and potential pci therapy
boolean
C0085532 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2,1])
C3245505 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Statins
Item
patients was treated by statins before randomization
boolean
C0360714 (UMLS CUI [1])
Coronary Stenosis Percentage | Target Lesion
Item
patient with ≤ 20% and ≥ 70% coronary narrowing and target lesion
boolean
C0242231 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C2986546 (UMLS CUI [2])
ST elevation myocardial infarction Duration
Item
st elevation myocardial infarction less than 7 days
boolean
C1536220 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Informed Consent Lacking
Item
without informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Liver Dysfunction | Aspartate aminotransferase measurement | Alanine aminotransferase measurement
Item
abnormal liver function before randomization, (ast, alt ≥uln)
boolean
C0086565 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
Hepatitis | Myopathy
Item
active hepatitis or muscular disease
boolean
C0019158 (UMLS CUI [1])
C0026848 (UMLS CUI [2])
Renal Insufficiency | Creatinine measurement, serum
Item
impaired renal function with serum creatinine level > 3mg/dl
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Impaired left ventricular function | Left ventricular ejection fraction
Item
impaired left ventricular function with lvef > 30%
boolean
C0242698 (UMLS CUI [1])
C0428772 (UMLS CUI [2])
Study Subject Participation Status
Item
participate in other studies
boolean
C2348568 (UMLS CUI [1])