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Late Intervention on an Occluded Infarct-Related Artery: A Meta-analysis of The Randomized Controlled Trials

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Publication Date: 13 Dec 2007

Journal: Clinical Medicine Insights: Cardiology Clinical Medicine: Cardiology 2007:1 25-32

CMIcar
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Abstract Axel Zagler1, Todd B. Heimowitz1, Esteban Escolar1, Steven J. Hussein1, Zaheer R. Yousef2, Philippe Gabriel Steg3, Vladimir Dzavik4, Judith S. Hochman5, Paul A. Vignola1, Gervasio A. Lamas1

1Mount Sinai Medical Center, Miami Beach, FL. 2University Hospital of Wales, UK. 3Department of Cardiology, Hôpital Bichat-Claude Bernard, Paris. 4University Health Network, Toronto General Hospital, Toronto. 5Cardiovascular Clinical Research Center, New York University School of Mdeicine, New York, NY

Abstract

Context: Late intervention to open an occluded infarct-related artery (IRA) after initial acute myocardial infarction was postulated to lead to clinical benefit.

Objective: To conduct a meta-analysis of the randomized trials.

Study selection: Eligibility criteria were: 1) randomized trials comparing percutaneous coronary intervention (PCI) in a totally occluded artery (TIMI flow 0-1) versus medical therapy, 2) in stable post myocardial infarction (MI) patients without spontaneous or low level exercise induced ischemia, 3) trials with a time from the onset of symptoms to randomization >24 hours, but <6 weeks, and 4) trials reporting mortality and recurrent MI as an endpoint. Of 961 citations reviewed, 3 disagreements were easily resolved by discussion and 6 trials were selected for inclusion.

Data synthesis: The primary endpoint was the composite of recurrent MI or death. The secondary endpoints were the development of heart failure or recurrent myocardial infarction. In a meta-analysis of the 6 trials, which included 2642 patients, late intervention of an IRA had a RR of death or recurrent MI of 1.12 (95% CI 0.91–1.38). Data regarding the development of heart failure was available for 4 trials. In a meta-analysis of these 4 trials, which included 2527 patients, late intervention of an IRA had a RR of 0.79 (95% CI 0.58–1.08). Data regarding the occurrence of recurrent MI was available for 5 trials. In a meta-analysis of these 5 trials, which included 2598 patients, late intervention of an IRA had a RR of 1.28 (95% CI 0.91–1.79).

Conclusions: Our meta-analysis of the currently available randomized data addressing late intervention of an occluded IRA failed to reveal clinical benefit with regard to the clinical endpoints of death, heart failure or reinfarction. The trend towards an increase in reinfarction among the PCI treated patients suggested by the Open Artery Trial (OAT) investigators persisted, but did not achieve statistical significance.


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