Long-Term Effects of Percutaneous Coronary Intervention of the Totally Occluded Infarct-Related Artery in the Subacute Phase After Myocardial Infarction

Author:

Hochman Judith S.1,Reynolds Harmony R.1,Džavík Vladimír1,Buller Christopher E.1,Ruzyllo Witold1,Sadowski Zygmunt P.1,Maggioni Aldo P.1,Carvalho Antonio C.1,Rankin James M.1,White Harvey D.1,Goldberg Suzanne1,Forman Sandra A.1,Mark Daniel B.1,Lamas Gervasio A.1

Affiliation:

1. From the New York University Cardiovascular Clinical Research Center, New York (J.S.H., H.R.R.); Peter Munk Cardiac Centre, University Health Network, Toronto, ON, Canada (V.D.); Division of Cardiology, St. Michael's Hospital and Department of Medicine, University of Toronto, Toronto, Ontario, Canada (C.E.B.); National Institute of Cardiology, Warsaw, Poland (W.R., Z.P.S.); Italian Association of Hospital Cardiologist (ANMCO) Research Center, Florence, Italy (A.P.M.); Hospital São Paulo, Moema–Sao...

Abstract

Background— Despite observations suggesting a benefit for late opening of totally occluded infarct-related arteries after myocardial infarction, the Occluded Artery Trial (OAT) demonstrated no reduction in the composite of death, reinfarction, and class IV heart failure over a 2.9-year mean follow-up. Follow-up was extended to determine whether late trends would favor either treatment group. Methods and Results— OAT randomized 2201 stable patients with infarct-related artery total occlusion >24 hours (calendar days 3–28) after myocardial infarction. Patients with severe inducible ischemia, rest angina, class III-IV heart failure, and 3-vessel/left main disease were excluded. We conducted extended follow-up of enrolled patients for an additional 3 years for the primary end point and angina (6-year median survivor follow-up; longest, 9 years; 12 234 patient-years). Rates of the primary end point (hazard ratio, 1.06; 95% confidence interval, 0.88–1.28), fatal and nonfatal myocardial infarction (hazard ratio, 1.25; 95% confidence interval, 0.89–1.75), death, and class IV heart failure were similar for the percutaneous coronary intervention (PCI) and medical therapy alone groups. No interactions between baseline characteristics and treatment group on outcomes were observed. The vast majority of patients at each follow-up visit did not report angina. There was less angina in the PCI group through early in follow-up; by 3 years, the between group difference was consistently <4 patients per 100 treated and not significantly different, although there was a trend toward less angina in the PCI group at 3 and 5 years. The 7-year rate of PCI of the infarct-related artery during follow-up was 11.1% for the PCI group compared with 14.7% for the medical therapy alone group (hazard ratio, 0.79; 95% confidence interval, 0.61–1.01; P =0.06). Conclusions— Extended follow-up of the OAT cohort provides robust evidence for no reduction of long-term rates of clinical events after routine PCI in stable patients with a totally occluded infarct-related artery and without severe inducible ischemia in the subacute phase after myocardial infarction. Clinical Trial Registration— http://www.clinicaltrials.gov . Unique identifier: NCT00004562.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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