Age
Item
1. patients with age of ≥18 and ≤80 years old.
boolean
C0001779 (UMLS CUI [1])
Stable angina | Angina, Unstable | NSTEMI
Item
2. patients with stable or unstable angina, or nstemi.
boolean
C0340288 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C1561921 (UMLS CUI [3])
Bifurcation lesion of coronary artery de novo Classification | Vessel Main Diameter | Side Branch Diameter
Item
3. de novo true bifurcation lesions (medina 0,1,1/1,1,1/1,0,1); mv diameter ≥2.5mm and sb diameter ≥2.25.
boolean
C1299363 (UMLS CUI [1,1])
C1515568 (UMLS CUI [1,2])
C0008902 (UMLS CUI [1,3])
C0005847 (UMLS CUI [2,1])
C1542147 (UMLS CUI [2,2])
C1301886 (UMLS CUI [2,3])
C0441987 (UMLS CUI [3,1])
C1253959 (UMLS CUI [3,2])
C1301886 (UMLS CUI [3,3])
Lesion Amenable Percutaneous Coronary Intervention | Score Angiography | Lesion Location Left Main Coronary Artery Bifurcation
Item
4. lesions suitable for pci (the syntax score <32 if lesions located at lm bifurcation).
boolean
C0221198 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C1532338 (UMLS CUI [1,3])
C0449820 (UMLS CUI [2,1])
C0002978 (UMLS CUI [2,2])
C0221198 (UMLS CUI [3,1])
C1515974 (UMLS CUI [3,2])
C3898614 (UMLS CUI [3,3])
Protocol Compliance
Item
5. patients willing to receive all protocol-required evaluations.
boolean
C0525058 (UMLS CUI [1])
Comprehension Study Protocol | Informed Consent
Item
6. patients completely understand the trial requirements and treatment procedures and provide written informed consent before any trial-specific tests or procedures are performed.
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
ST segment elevation myocardial infarction
Item
1. patients with stemi (within 24-hour from the onset of chest pain to admission).
boolean
C1536220 (UMLS CUI [1])
Lesion Inappropriate Percutaneous Coronary Intervention | Score Angiography | Lesion Location Left Main Coronary Artery Bifurcation | Medical contraindication Relationship Percutaneous Coronary Intervention | Patient condition | Lesion Characteristics
Item
2. lesions not suitable for pci (the syntax score ≥32 if lesions located at lm bifurcation, or any pci-related contraindications including patient conditions and/or lesion characteristics).
boolean
C0221198 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C1532338 (UMLS CUI [1,3])
C0449820 (UMLS CUI [2,1])
C0002978 (UMLS CUI [2,2])
C0221198 (UMLS CUI [3,1])
C1515974 (UMLS CUI [3,2])
C3898614 (UMLS CUI [3,3])
C1301624 (UMLS CUI [4,1])
C0439849 (UMLS CUI [4,2])
C1532338 (UMLS CUI [4,3])
C0683521 (UMLS CUI [5])
C0221198 (UMLS CUI [6,1])
C1521970 (UMLS CUI [6,2])
Chronic total occlusion Lesion | Involvement with Bifurcation
Item
3. a chronic total occlusion lesion involved in bifurcation
boolean
C1955779 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C1314939 (UMLS CUI [2,1])
C3146289 (UMLS CUI [2,2])
Lesion Calcification Severe | Requirement Rotational Atherectomy
Item
4. lesion with severe calcification that required for rotational atherectomy.
boolean
C0221198 (UMLS CUI [1,1])
C0175895 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C1514873 (UMLS CUI [2,1])
C0162655 (UMLS CUI [2,2])
Antiplatelet therapy Dual Long-term Unable
Item
5. patients intolerable to long-term dual anti-platelet therapy.
boolean
C1096021 (UMLS CUI [1,1])
C0205173 (UMLS CUI [1,2])
C0443252 (UMLS CUI [1,3])
C1299582 (UMLS CUI [1,4])
Disease Hematopoietic | Platelet Count measurement | White Blood Cell Count procedure
Item
6. patients with obvious hematopoietic disorders (e.g., platelet count< 100×10^9/l or >700×10^9/l, leukocyte count<3×10^9/l).
boolean
C0012634 (UMLS CUI [1,1])
C0229601 (UMLS CUI [1,2])
C0032181 (UMLS CUI [2])
C0023508 (UMLS CUI [3])
Hemorrhage | Bleeding tendency | Ulcer | Ischemic stroke | Brain hemorrhage | Malignant Intracranial Neoplasm | Craniocerebral Trauma | Hemostasis Difficult
Item
7. patients with active bleeding and obviously hemorrhagic tendency (e.g., active ulcer, recent ischemic stroke, previous hemorrhagic stroke, intracranial malignant tumors, recent craniocerebral trauma, or any other active bleeding or hemorrhagic tendency with difficult hemostasis
boolean
C0019080 (UMLS CUI [1])
C1458140 (UMLS CUI [2])
C0041582 (UMLS CUI [3])
C0948008 (UMLS CUI [4])
C0553692 (UMLS CUI [5])
C1334593 (UMLS CUI [6])
C0018674 (UMLS CUI [7])
C0019116 (UMLS CUI [8,1])
C0332218 (UMLS CUI [8,2])
Renal Insufficiency Serious | Creatinine measurement, serum | Hepatic Insufficiency | Alanine aminotransferase increased | Heart failure New York Heart Association Classification
Item
8. patients with serious renal insufficiency (scr<30ml/min) or hepatic insufficiency (alt≧3 times of normal upper limit), heart failure (nyha class >iii class).
boolean
C1565489 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0201976 (UMLS CUI [2])
C1306571 (UMLS CUI [3])
C0151905 (UMLS CUI [4])
C0018801 (UMLS CUI [5,1])
C1275491 (UMLS CUI [5,2])
Illness Serious | Life Expectancy
Item
9. patients with any other serious medical illness that life expectancy is less than 12 months.
boolean
C0221423 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0023671 (UMLS CUI [2])
Pregnancy | Pregnancy, Planned
Item
10. woman with pregnancy or planning to pregnancy
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Hypersensitivity Stenting Investigational | Hypersensitivity Sirolimus | Hypersensitivity Everolimus | Hypersensitivity Zotarolimus | Hypersensitivity Investigational New Drugs
Item
11. patients with known allergy to the study stent system (sirolimus, everolimus, zotarolimus) or to protocol-required concomitant medications
boolean
C0020517 (UMLS CUI [1,1])
C2348535 (UMLS CUI [1,2])
C1517586 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C0072980 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0541315 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C1700035 (UMLS CUI [4,2])
C0020517 (UMLS CUI [5,1])
C0013230 (UMLS CUI [5,2])
Procedure Planned | Protocol Compliance Lacking | Interference Interpretation Research data
Item
12. patients with a planned or planning procedure that may cause non-compliance with the present protocol or confound data interpretation.
boolean
C0184661 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0521102 (UMLS CUI [3,1])
C0459471 (UMLS CUI [3,2])
C0681873 (UMLS CUI [3,3])