Age
Item
1. patient less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
Outpatient | Referral for Cardiac Catheterization Procedures elective | Coronary angiography | Percutaneous Coronary Intervention
Item
2. patient referred as an outpatient for elective cardiac catheterization with coronary angiography and ad hoc percutaneous coronary intervention (if coronary anatomy suitable)
boolean
C0029921 (UMLS CUI [1])
C2585524 (UMLS CUI [2,1])
C0018795 (UMLS CUI [2,2])
C0439608 (UMLS CUI [2,3])
C0085532 (UMLS CUI [3])
C1532338 (UMLS CUI [4])
Stable angina | Stress Test Suggestive of Ischemia | Myocardial Infarction
Item
3. patient has stable angina or a stress test suggestive of ischemia and/or prior myocardial infarction
boolean
C0340288 (UMLS CUI [1])
C3494508 (UMLS CUI [2,1])
C0332299 (UMLS CUI [2,2])
C0022116 (UMLS CUI [2,3])
C0027051 (UMLS CUI [3])
Femoral artery Approach Anticipated | Cardiac Catheterization Procedure
Item
4. anticipated femoral arterial approach for the cardiac catheterization procedure
boolean
C0015801 (UMLS CUI [1,1])
C0449445 (UMLS CUI [1,2])
C3840775 (UMLS CUI [1,3])
C0018795 (UMLS CUI [2])
Informed Consent
Item
5. patient provides written informed consent
boolean
C0021430 (UMLS CUI [1])
Criteria Fulfill
Item
patients will be excluded if any of the following are present:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Clopidogrel | Ticlopidine
Item
1. use of clopidogrel or ticlopidine during the 14 days prior to the scheduled procedure
boolean
C0070166 (UMLS CUI [1])
C0040207 (UMLS CUI [2])
Hypersensitivity Clopidogrel | Desensitization Independent of | Hypersensitivity Plavix Component
Item
2. known hypersensitivity to clopidogrel (regardless of desensitization) or to any other components of plavix
boolean
C0020517 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
C0178702 (UMLS CUI [2,1])
C0332291 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0633084 (UMLS CUI [3,2])
C1705248 (UMLS CUI [3,3])
Medical contraindication Clopidogrel
Item
3. contraindication to clopidogrel, including
boolean
C1301624 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
Blood Coagulation Disorder Pre-existing | Blood dyscrasia
Item
1. pre-existing bleeding disorder or hematological dyscrasia
boolean
C0005779 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
C0018939 (UMLS CUI [2])
INR
Item
2. inr >1.4 immediately prior to the scheduled procedure
boolean
C0525032 (UMLS CUI [1])
Platelet Count measurement
Item
3. platelet count <50 k/ul
boolean
C0032181 (UMLS CUI [1])
Hemorrhage
Item
4. significant bleeding during the 14 days prior to the scheduled procedure
boolean
C0019080 (UMLS CUI [1])
Operative Surgical Procedure Location Compressing Lacking | Invasive procedure Location Compressing Lacking
Item
5. surgery or invasive procedure at a non-compressible location during the 30 days prior to the scheduled procedure
boolean
C0543467 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
C0332260 (UMLS CUI [1,3])
C0332268 (UMLS CUI [1,4])
C4048276 (UMLS CUI [2,1])
C0450429 (UMLS CUI [2,2])
C0332260 (UMLS CUI [2,3])
C0332268 (UMLS CUI [2,4])
Operative Surgical Procedure Need Anticipated | Invasive procedure Need Anticipated
Item
6. anticipated need for surgery or other invasive procedure within 30 days following the scheduled procedure
boolean
C0543467 (UMLS CUI [1,1])
C0027552 (UMLS CUI [1,2])
C3840775 (UMLS CUI [1,3])
C4048276 (UMLS CUI [2,1])
C0027552 (UMLS CUI [2,2])
C3840775 (UMLS CUI [2,3])
Red Blood Cell Transfusion Unwilling | Relationship Hemorrhage Life Threatening
Item
7. patient states unwillingness to undergo transfusion of red blood cells even in the event of life threatening bleeding
boolean
C0086252 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0439849 (UMLS CUI [2,1])
C0019080 (UMLS CUI [2,2])
C2826244 (UMLS CUI [2,3])
Cardiac Status Unstable
Item
4. unstable cardiac status
boolean
C1999091 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
Patient Admission Cardiac problem | Inpatient Referral for Cardiac Catheterization
Item
1. patient was admitted for a cardiac condition and referred as an inpatient for cardiac catheterization
boolean
C0030673 (UMLS CUI [1,1])
C0262402 (UMLS CUI [1,2])
C0021562 (UMLS CUI [2,1])
C2585524 (UMLS CUI [2,2])
C0018795 (UMLS CUI [2,3])
Myocardial Infarction
Item
2. myocardial infarction diagnosed as occurring during the 30 days prior to the scheduled procedure
boolean
C0027051 (UMLS CUI [1])
Troponin T Assay
Item
3. pre-procedure troponin-t >0.01 ng/ml
boolean
C1141947 (UMLS CUI [1])
Angina, Unstable
Item
4. unstable angina
boolean
C0002965 (UMLS CUI [1])
Symptoms Ischemic At rest | Symptoms Ischemic Exertion Mild | Walking One Block | Climbing One Flight of Stairs | EKG ST segment changes | Myocardial injury | Myocardial Ischemia
Item
i. ischemic symptoms at rest ii. ischemic symptoms with mild exertion (e.g., walking one to two level blocks or climbing one flight of stairs) e. pre-procedure electrocardiogram with st segment changes indicative of ongoing myocardial injury or ischemia
boolean
C1457887 (UMLS CUI [1,1])
C0475224 (UMLS CUI [1,2])
C0443144 (UMLS CUI [1,3])
C1457887 (UMLS CUI [2,1])
C0475224 (UMLS CUI [2,2])
C0015264 (UMLS CUI [2,3])
C2945599 (UMLS CUI [2,4])
C3827522 (UMLS CUI [3])
C3831081 (UMLS CUI [4])
C0232326 (UMLS CUI [5])
C0746730 (UMLS CUI [6])
C0151744 (UMLS CUI [7])
Kidney Failure, Chronic | Troponin T increased Possible
Item
5. chronic renal failure (which may raise troponin-t levels)
boolean
C0022661 (UMLS CUI [1])
C1142294 (UMLS CUI [2,1])
C0332149 (UMLS CUI [2,2])
Dialysis
Item
1. patient currently undergoing dialysis
boolean
C0011946 (UMLS CUI [1])
Creatinine measurement, serum
Item
2. serum creatinine >2 mg/dl
boolean
C0201976 (UMLS CUI [1])
eGFR MDRD
Item
3. estimated glomerular filtratation rate (egfr using the mdrd formula) <45 ml/min/1.73 m2
boolean
C3811844 (UMLS CUI [1,1])
C3839656 (UMLS CUI [1,2])
Procedure Factor
Item
6. procedural factors
boolean
C0184661 (UMLS CUI [1,1])
C1521761 (UMLS CUI [1,2])
Coronary angiography Redundant | Cardiac Catheterization Scheduled
Item
1. patient does not require coronary angiography as part of the scheduled cardiac catheterization
boolean
C0085532 (UMLS CUI [1,1])
C1313915 (UMLS CUI [1,2])
C0018795 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Patient Inappropriate Percutaneous Coronary Intervention | Coronary angiography
Item
2. patient is not a candidate for percutaneous coronary intervention during the same procedure as the diagnostic coronary angiography
boolean
C0030705 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C1532338 (UMLS CUI [1,3])
C0085532 (UMLS CUI [2])
Arterial Access Approach Brachial | Arterial Access Approach Radius | Arterial Access Approach Other | Exception Approach Femoral
Item
3. anticipated need for arterial access using brachial, radial or other non-femoral approach
boolean
C3272298 (UMLS CUI [1,1])
C0449445 (UMLS CUI [1,2])
C0445456 (UMLS CUI [1,3])
C3272298 (UMLS CUI [2,1])
C0449445 (UMLS CUI [2,2])
C0034627 (UMLS CUI [2,3])
C3272298 (UMLS CUI [3,1])
C0449445 (UMLS CUI [3,2])
C0205394 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0449445 (UMLS CUI [4,2])
C0015811 (UMLS CUI [4,3])
Access Femoral artery Femoral bypass graft
Item
4. anticipated need to access the femoral artery via a femoral bypass graft
boolean
C0444454 (UMLS CUI [1,1])
C0015801 (UMLS CUI [1,2])
C0850111 (UMLS CUI [1,3])
Other Coding | Aortic Stenosis Evaluation Planned | Hypertrophic Cardiomyopathy Evaluation Planned
Item
5. anticipated need for an arterial sheath 6 french in size or larger (e.g., planned evaluation of aortic stenosis or hypertrophic cardiomyopathy)
boolean
C3846158 (UMLS CUI [1])
C0003507 (UMLS CUI [2,1])
C1261322 (UMLS CUI [2,2])
C1301732 (UMLS CUI [2,3])
C0007194 (UMLS CUI [3,1])
C1261322 (UMLS CUI [3,2])
C1301732 (UMLS CUI [3,3])
Heparin | Cardiac Catheterization Procedures | Aortic Valve Stenosis Guide wire | Intravascular ultrasound | Intracoronary pressure guide wire
Item
6. anticipated need for heparin anticoagulation during the diagnostic cardiac catheterization procedure (e.g., crossing a stenosed aortic valve with a 0.035" wire, planned intra-vascular ultrasound or pressure wire study)
boolean
C0019134 (UMLS CUI [1])
C0018795 (UMLS CUI [2])
C0003507 (UMLS CUI [3,1])
C0181089 (UMLS CUI [3,2])
C1456025 (UMLS CUI [4])
C1299422 (UMLS CUI [5])
Childbearing Potential Pregnancy test negative Lacking
Item
7. woman of child-bearing potential who does not have a negative pregnancy test immediately prior to the scheduled procedure
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Study Subject Participation Status | Clinical Study Follow-up Incomplete
Item
8. participation in another non-observational clinical study that has not yet completed all mandatory follow-up (i.e., patients who are participating in a "natural history" observational registry where no active therapy is being investigated may participate)
boolean
C2348568 (UMLS CUI [1])
C3274571 (UMLS CUI [2,1])
C0205257 (UMLS CUI [2,2])
Study Subject Participation Status
Item
9. prior participation in this study
boolean
C2348568 (UMLS CUI [1])
Informed Consent Unable | Study Protocol Comprehension Unable
Item
10. inability to provide written informed consent or demonstrate understanding of the risks and benefits associated with participation in this study
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C2348563 (UMLS CUI [2,1])
C0162340 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])