Occluded Artery Trial (OAT) (OAT)
Cardiovascular Diseases, Heart Diseases, Myocardial Infarction
About this trial
This is an interventional treatment trial for Cardiovascular Diseases
Eligibility Criteria
Inclusion Criteria: Recent MI (3-28 days) (Day 1 is the calendar day of the MI system onset) MI is defined based on at least 2 of 3 MI criteria confirmed by: 1) ischemic symptoms ≥30 minutes, 2) cardiac serum marker elevation (creatine kinase (CK) ≥2x upper limit of normal and CK-MB elevated above the upper limit of the laboratory normal) or troponin T, or troponin I elevated at least twice the upper limit of normal, 3) EKG: New Q-waves of ≥0.03 sec and/or 1/3 of QRS complex in ≥2 related EKG leads. If cardiac serum markers are elevated (2), any one of the following EKG findings satisfy inclusion criteria; new ST-T changes (ST elevation or depression), new left bundle-branch block (LBBB), loss of R-wave voltage ≥50% in ≥2 related leads or deep T wave inversions ≥3mm in ≥2 leads. TIMI flow 0 or 1 in infarct related artery (IRA) Meets criteria for high risk: EF <50% or site of occlusion is proximal, in left anterior descending (proximal to the second major diagonal branch); large right coronary artery; or circumflex, if supplying large obtuse marginal, and part of inferior wall (i.e., large dominant or co-dominant vessel). Exclusion Criteria: Age <18 y Clinical indication for revascularization defined as follows: rest or low-threshold angina after MI; severe inducible ischemia on low level exercise or pharmacological stress testing (ST decreased ≥2 mm or inability to complete stage 1 or achieve 3-4 metabolic equivalents without angina, hypotension, or reversible perfusion defects in multiple territories or decreased wall motion thickening in >2 segments on echocardiogram); left main coronary disease (≥50% stenosis); or triple-vessel disease (3 major epicardial coronaries with >70% stenoses) Serious illness such as cancer or pulmonary disease that limits 3-year survival Severe renal disease defined as serum creatinine >3.0 mg/dL that markedly increases risk of radiographic contrast Severe valvular disease History of anaphylaxis to radiographic contrast Infarct artery too small (reference segment diameter <2.5 mm), target segment within or beyond extreme tortuosity (>90° angulation), or otherwise technically a poor candidate for PCI Chronic occlusion of IRA (seen on angiogram obtained before index MI or angiographic evidence of chronicity, e.g., presence of bridging collaterals) NYHA classes III-IV CHF; patients may be treated for acute heart failure complicating MI and rescreened Cardiogenic shock or sustained hypotension: systolic BP <90 mm Hg or cardiac index <2.2 L/min per m^2 LV aneurysm in the same location as index MI and present before index MI Inability to cooperate with the protocol Patient refusal or inability to give informed consent Refusal of patient's physician to allow patient to participate Pregnancy Contraindication to anticoagulation during PCI or to routine antiplatelet therapy after stent implantation Qualifying IRA that has been grafted previously; patients with prior CABG may be enrolled if the IRA was not previously grafted Dilated or hypertrophic cardiomyopathy
Sites / Locations
- New York University School of Medicine
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Optimal Medical Therapy Only (MED)
Percutaneous Coronary Intervention (PCI)
Conventional medical management, including aspirin, beta blockers, angiotensin converting enzyme (ACE) inhibitors, and risk factor modification
Conventional medical management, including aspirin, beta blockers, angiotensin converting enzyme (ACE) inhibitors, and risk factor modification, plus percutaneous coronary intervention and coronary stenting