Impact of Left Ventricular Ejection Fraction on Clinical Outcomes Over Five Years After Infarct-Related Coronary Artery Recanalization (from the Occluded Artery Trial [OAT]) - 05/08/11

Résumé |
In the Occluded Artery Trial (OAT), percutaneous coronary intervention (PCI) of an infarct-related artery on days 3 to 28 after acute myocardial infarction was of no benefit compared to medical therapy alone. The present analysis was conducted to determine whether PCI might provide benefit to the subgroup of higher risk patients with a depressed ejection fraction (EF). Of 2,185 analyzed patients (age 58.6 ± 11.0 years) with infarct-related artery occlusion on days 3 to 28 after acute myocardial infarction in the Occluded Artery Trial, 1,094 were assigned to PCI and 1,091 to medical therapy. The primary end point was a composite of death, reinfarction, and New York Heart Association class IV heart failure. The outcomes were analyzed by EF (first tertile, EF ≤44%, vs second and third tertiles combined, EF >44%). Interaction of the treatment effect with EF on the study outcomes were examined using the Cox survival model. The 5-year rates of the primary end point (death, reinfarction, or New York Heart Association class IV heart failure) were not different in either subgroup (PCI vs medical therapy, hazard ratio 1.25, 99% confidence interval 0.83 to 1.88, for EF ≤44%; hazard ratio 0.98, 99% confidence interval 0.64 to 1.50, for EF >44%). However, in patients with an EF >44%, PCI reduced the rate of subsequent revascularization (p = 0.004, interaction p = 0.05). In conclusion, optimal medical therapy remains the overall treatment of choice for stable patients with a persistent total occlusion of the infarct-related artery after acute myocardial infarction, irrespective of the baseline EF. In patients with normal or moderately impaired left ventricular contractility, PCI reduced the need for subsequent revascularization but did not otherwise improve outcomes.
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| This work was supported by grants U01 HL062509 and U01 HL062511 from the National Heart, Lung, and Blood Institute, Bethesda, Maryland. Supplemental grant funds and product donations equivalent to 6% of the total study cost were provided by Eli Lilly (Indianapolis, Indiana), Millennium Pharmaceuticals (Cambridge, Massachusetts) and Schering Plough (Kenilworth, New Jersey), Guidant (Indianapolis, Indiana), Cordis/Johnson & Johnson (Bridgewater, New Jersey), Medtronic (Minneapolis, Minnesota), Merck (Whitehouse Station, New Jersey), and Bristol Myers Squibb Medical Imaging (New York, New York). |
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| The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Heart, Lung, and Blood Institute or the National Institutes of Health. |
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| Dr. Hochman received grant support to her institution from Eli Lilly (Indianapolis, Indiana) and Bristol Myers Squibb Medical Imaging (New York, New York) and product donation from Millennium Pharmaceuticals (Cambridge, Massachusetts), Schering Plough (Kenilworth, New Jersey), Guidant (Indianapolis, Indiana), and Merck (Whitehouse Station, NJ) for OAT and received consultation fees from Bristol Myers Squibb (New York, New York), honoraria for Steering Committee service from CV Therapeutics (Palo Alto, California), Eli Lilly (Indianapolis, Indiana), and GlaxoSmithKline (Brentford, London, United Kingdom), and honoraria for serving on the Data Safety Monitoring Board of a trial supported by Schering Plough (Kenilworth, New Jersey). Dr. Mancini received a research grant from Cordis (Bridgewater, New Jersey) and honoraria of <$10,000/yr from Pfizer (New York, New York), Merck Frosst Canada (Kirkland, Quebec, Canada), AstraZeneca (London, United Kingdom), GSK (Brentford, London, United Kingdom), and Sanofi Aventis (Paris, France). Dr. Dzavík reports research, honorarium, and Advisory Board member funds from Cordis, Johnson & Johnson (Bridgewater, New Jersey), and honoraria from Boston Scientific (Natick, Massachusetts). |
Vol 105 - N° 1
P. 10-16 - janvier 2010 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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