Occlusion Duration Estimated
Item
the estimated duration of the occlusion is at least 2 weeks.
boolean
C1947917 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0750572 (UMLS CUI [1,3])
Signs Ischemia | Relationship Coronary Occlusion
Item
signs of ischemia related to the occluded coronary artery.
boolean
C0311392 (UMLS CUI [1,1])
C0022116 (UMLS CUI [1,2])
C0439849 (UMLS CUI [2,1])
C0151814 (UMLS CUI [2,2])
Coronary Occlusion Recanalization Successful
Item
successful recanalization of the occluded artery is achieved.
boolean
C0151814 (UMLS CUI [1,1])
C0034771 (UMLS CUI [1,2])
C1272703 (UMLS CUI [1,3])
Reference Diameter Size
Item
reference diameter is > 2.5 mm.
boolean
C1706462 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
Informed Consent
Item
written informed consent obtained.
boolean
C0021430 (UMLS CUI [1])
Percutaneous Coronary Intervention Primary Myocardial Infarction | Emergency Percutaneous Coronary Intervention Myocardial Infarction
Item
primary or rescue pci for acute myocardial infarction
boolean
C1532338 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0027051 (UMLS CUI [1,3])
C0013956 (UMLS CUI [2,1])
C1532338 (UMLS CUI [2,2])
C0027051 (UMLS CUI [2,3])
Lesion Crossed Unsuccessful
Item
the lesion could not be crossed.
boolean
C0221198 (UMLS CUI [1,1])
C0205203 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Lesion Anatomy Complex | Placement of stent Unlikely
Item
lesions with complex anatomy making successful stent deployment unlikely.
boolean
C0221198 (UMLS CUI [1,1])
C0700276 (UMLS CUI [1,2])
C0439855 (UMLS CUI [1,3])
C0522776 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
Guide wire Lumen Relationship Inappropriate | Lumen Distal Occlusion
Item
the guide wire is not in the true lumen distal to the occlusion.
boolean
C0181089 (UMLS CUI [1,1])
C0225997 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C1548788 (UMLS CUI [1,4])
C0225997 (UMLS CUI [2,1])
C0205108 (UMLS CUI [2,2])
C1947917 (UMLS CUI [2,3])
Hypersensitivity Sirolimus | Hypersensitivity Zotarolimus
Item
sirolimus or zotarolimus allergy
boolean
C0020517 (UMLS CUI [1,1])
C0072980 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1700035 (UMLS CUI [2,2])
Vein Bypass Graft Procedures | Bypass graft Arterial
Item
venous or arterial bypass grafts
boolean
C0519413 (UMLS CUI [1])
C0185098 (UMLS CUI [2,1])
C0221464 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant or nursing women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
participation in an other trial.
boolean
C2348568 (UMLS CUI [1])
Factor Long-term Follow-up Difficult | Factor Long-term Follow-up Unlikely
Item
factors making long-term follow-up difficult or unlikely.
boolean
C1521761 (UMLS CUI [1,1])
C1517942 (UMLS CUI [1,2])
C0332218 (UMLS CUI [1,3])
C1521761 (UMLS CUI [2,1])
C1517942 (UMLS CUI [2,2])
C0750558 (UMLS CUI [2,3])
Life Expectancy
Item
life expectancy <1 year.
boolean
C0023671 (UMLS CUI [1])
Medical contraindication Aspirin | Medical contraindication Clopidogrel | Medical contraindication Heparin
Item
contraindications for asa or clopidogrel or heparin.
boolean
C1301624 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C1301624 (UMLS CUI [3,1])
C0019134 (UMLS CUI [3,2])
Coumadin Discontinuation Unsuccessful
Item
use of coumadins that could not be stopped before the procedure.
boolean
C0699129 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])