Intravenous β-blockers for patients undergoing primary percutaneous coronary intervention: A meta-analysis of randomized trials

被引:10
|
作者
Elgendy, Islam Y. [1 ]
Elgendy, Akram Y. [1 ]
Mahmoud, Ahmed N. [1 ]
Mansoor, Hend [2 ]
Mojadidi, Mohammad K. [1 ]
Bavry, Anthony A. [1 ,3 ]
机构
[1] Univ Florida, Dept Med, 1600 SW Archer Rd,POB 100277, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Pharmaceut Outcomes & Policy, Gainesville, FL USA
[3] Georgia Vet Hlth Syst, North Florida South, Gainesville, FL USA
关键词
Adrenergic beta-antagonists; Meta-analysis; Myocardial infarction; Percutaneous coronary intervention; ACUTE MYOCARDIAL-INFARCTION; CLINICAL-OUTCOMES; METOPROLOL; BLOCKADE; THERAPY; SIZE; THROMBOLYSIS; FIBRILLATION; ANGIOPLASTY; IMPACT;
D O I
10.1016/j.ijcard.2016.08.293
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The efficacy and safety of intravenous beta-blockers in patients with ST elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI) are not well known. Methods: Electronic databases were searched for randomized trials that compared intravenous beta-blocker use with routine care or placebo in patients with STEMI undergoing primary PCI. Summary estimates risk ratios (RR) were constructed using DerSimonian and Laird model. Results: Four randomized trials with 1149 Killip class I or II STEMI patients were included. Intravenous beta-blockers were associated with a reduction in the risk of ventricular arrhythmias during hospitalization (RR 0.42, 95% confidence interval [CI] 0.26-0.69, P = 0.001). The risk of cardiogenic shock (RR 0.78, 95% CI 0.31-1.97, P = 0.61), bradycardia (RR 1.54, 95% CI 0.35-6.81, P = 0.57), all-cause mortality (RR 0.71, 95% CI 0.19-3.17, P = 0.72), and cardiovascular mortality (RR 0.93, 95% CI 0.35-2.48, P = 0.88) during hospitalization was similar in both groups. There was a trend towards a lower risk of future heart failure hospitalizations with intravenous beta-blockers (RR 0.32, 95% CI 0.10-1.05, P = 0.06). Conclusion: Intravenous beta-blockers, in STEMI patients (Killip class I or II) undergoing primary PCI, appear to be safe. Intravenous beta-blockers were associated with a reduced risk of ventricular arrhythmias. Due to the small number of patients, the impact on other outcomes could not be determined. Therefore, future trials are recommended to establish the efficacy of intravenous beta-blockers in primary PCI. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:891 / 897
页数:7
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