Misumida Naoki, Harjai Kishore, Kernis Steven, Kanei Yumiko
Department of Internal Medicine, Mount Sinai Beth Israel, New York, NY, USA
Department of Cardiology, Geisinger Clinic, Wilkes-Barre, PA, USA.
J Cardiovasc Pharmacol Ther. 2016 May;21(3):280-5. doi: 10.1177/1074248415608011. Epub 2015 Sep 29.
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.
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.
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).
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.
对于接受直接经皮冠状动脉介入治疗(PCI)且左心室射血分数(LVEF)保留的ST段抬高型心肌梗死(STEMI)患者,口服β受体阻滞剂治疗对长期死亡率的影响尚不清楚。
我们检索了MEDLINE、EMBASE和Cochrane对照试验中心注册库,以查找评估口服β受体阻滞剂治疗对接受直接PCI且LVEF保留的STEMI患者疗效的研究。主要结局为全因死亡率。纳入随访时间等于或超过6个月的随机对照试验和报告了校正风险比(或倾向评分匹配患者的风险比)的观察性研究。使用随机效应模型计算合并风险比及95%置信区间(CI)。
无随机对照试验符合纳入标准。7项观察性研究共10857例患者符合纳入标准。随访时间为6个月至5.2年。4项研究将LVEF保留定义为40%,3项研究定义为50%。根据汇总估计,口服β受体阻滞剂治疗与全因死亡率降低相关(合并风险比0.79,95%CI 0.65 - 0.97)。
这项荟萃分析表明,口服β受体阻滞剂治疗与接受直接PCI且LVEF保留的STEMI患者全因死亡率降低相关。这支持了美国心脏病学会基金会/美国心脏协会2013年STEMI管理指南。