Age
Item
Age > 18 years
boolean
C0001779 (UMLS CUI [1])
Gender
Item
Patient is male or un-pregnant female
boolean
C0079399 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Coronary stenosis
Item
Stenosis > 70% in one of the major epicardial coronary arteries
boolean
C0242231 (UMLS CUI [1,1])
C0442016 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
Contra-indications of stent implantation
Item
No contra-indications of stent implantation existing
boolean
C0521232 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Signed informed consent
Item
Patient signed the informed consent
boolean
C0021430 (UMLS CUI [1])
Acute myocardial infarction
Item
Did the Patient suffer from acute myocardial infarction within one week?
boolean
C0155626 (UMLS CUI [1])
Contra-indications of stent implantation or intolerance to dual antiplatlet therapy
Item
Patient has contra-indications of stent implantation or can not tolerate dual antiplatelet therapy
boolean
C1301624 (UMLS CUI [1,1])
C0521232 (UMLS CUI [1,2])
C0277585 (UMLS CUI [2,1])
C1096021 (UMLS CUI [2,2])
C1554184 (UMLS CUI [2,3])
History of stent implantation
Item
No history of stent implantation within last one-year
boolean
C0521232 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Other brand coronary stent
Item
Patient received other brand coronary stent during index procedure
boolean
C0592503 (UMLS CUI [1,1])
C0687568 (UMLS CUI [1,2])
Achievement of informed consent
Item
No achievement of informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])