Does Oral Beta-Blocker Therapy Improve Long-Term Survival in ST-Segment Elevation Myocardial Infarction With Preserved Systolic Function? A Meta-Analysis

被引:25
|
作者
Misumida, Naoki [1 ]
Harjai, Kishore [2 ]
Kernis, Steven [3 ]
Kanei, Yumiko [4 ]
机构
[1] Mt Sinai Beth Israel, Dept Internal Med, 1st Ave,16th St, New York, NY 10003 USA
[2] Geisinger Med Clin, Dept Cardiol, Wilkes Barre, PA USA
[3] Lourdes Med Ctr, Dept Cardiol, Cherry Hill, NJ USA
[4] Mt Sinai Beth Israel, Dept Cardiol, New York, NY 10003 USA
关键词
beta-blocker; ST-segment elevation myocardial infarction; percutaneous coronary intervention; left ventricular ejection fraction; meta-analysis; PERCUTANEOUS CORONARY INTERVENTION; CLINICAL-OUTCOMES; PRIMARY ANGIOPLASTY; DISCHARGE; IMPACT; ASSOCIATION; MANAGEMENT; MORTALITY;
D O I
10.1177/1074248415608011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The effect of oral beta-blocker therapy on long-term mortality in patients with ST-segment elevation myocardial infarction (STEMI) who are treated with primary percutaneous coronary intervention (PCI) and who have preserved left ventricular ejection fraction (LVEF) remains unclear. Methods: We searched MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials for studies evaluating the effect of oral beta-blocker therapy in patients with STEMI who underwent primary PCI and who had preserved LVEF. The primary outcome was all-cause mortality. Randomized controlled trials and the observational studies that reported an adjusted hazard ratio (or hazard ratio in the propensity score-matched patients) with follow-up duration equal to or more than 6 months were included. Pooled hazard ratio with 95% confidence interval (CI) was calculated using a random effect model. Results: No randomized controlled trials met the inclusion criteria. Seven observational studies totaling 10 857 patients met the inclusion criteria. Follow-up duration ranged from 6 months to 5.2 years. Preserved LVEF was defined as 40% in 4 studies and 50% in 3 studies. Based on the pooled estimate, oral beta-blocker therapy was associated with a reduction in all-cause mortality (combined hazard ratio 0.79, 95% CI 0.65-0.97). Conclusion: This meta-analysis demonstrates that oral beta-blocker therapy is associated with decreased all-cause mortality in patients with STEMI who are treated with primary PCI and who have preserved LVEF. This supports the current American College of Cardiology Foundation/American Heart Association 2013 Guideline for the Management of STEMI.
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页码:280 / 285
页数:6
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