Comparable Benefit of β-Blocker Therapy in Heart Failure Across Regions of the World: Meta-analysis of Randomized Clinical Trials

被引:13
作者
Chatterjee, Saurav [1 ]
Udell, Jacob A. [2 ,3 ]
Sardar, Partha [4 ]
Lichstein, Edgar [5 ,6 ]
Ryan, John J. [7 ]
机构
[1] Mt Sinai Hlth Syst, St Lukes Roosevelt Hosp, Dept Cardiovasc Dis, New York, NY USA
[2] Univ Toronto, Womens Coll Hosp, Dept Med, Womens Coll,Res Inst, Toronto, ON, Canada
[3] Univ Toronto, Womens Coll Hosp, Dept Med, Div Cardiovasc, Toronto, ON, Canada
[4] Texas Tech Univ, Hlth Sci Ctr, Dept Cardiol, El Paso, TX USA
[5] Maimonides Hosp, Dept Med, Brooklyn, NY 11219 USA
[6] SUNY Downstate, Brooklyn, NY USA
[7] Univ Utah, Div Cardiovasc Med, Salt Lake City, UT 84132 USA
关键词
ACUTE MYOCARDIAL-INFARCTION; LEFT-VENTRICULAR FUNCTION; QUALITY-OF-CARE; ELDERLY-PATIENTS; METOPROLOL CR/XL; SURVEY PROGRAM; UNITED-STATES; OUTCOMES; CARVEDILOL; MANAGEMENT;
D O I
10.1016/j.cjca.2014.03.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: There is a concern about geographical region heterogeneity regarding clinical benefit of beta-blocker (BB) therapy in heart failure with reduced ejection fraction (HFrEF). This study sought to compare benefits of BB use within randomized controlled trials (RCTs) that enrolled patients with HFrEF from North America (NA) compared with other regions of the world (ROW). Methods: We conducted a meta-analysis using MEDLINE, EMBASE, Cochrane Library, Web of Science, and Scopus (inceptions-December 2012) of BB RCTs stratified according to NA vs ROW. The primary end point was all-cause mortality and secondary end points were cardiovascular death, sudden death, death due to pump failure, and premature drug discontinuation. Summary odds ratios (ORs) and 95% confidence intervals (CIs) for each outcome were calculated with interaction terms for region. Two-sided P values were calculated with P < 0.05 considered significant. Results: The analysis included 16 RCTs with 14,452 patients; 7 trials were conducted in NA and 9 trials in ROW with follow-up durations of 3-58 months. All-cause mortality was consistently reduced in NA (OR, 0.82; 95% Cl, 0.71-0.96; P = 0.01) and ROW (OR, 0.76; 95% Cl, 0.69-0.84; P < 0.001; P-interaction = 0.40). Overall and according to region, all secondary end points including premature drug discontinuation were also less with BB therapy (P-interactions all >= 0.10). Conclusions: For the regions represented in the included trials, there is no evidence to suggest that geographic region is a significant moderator of clinical outcomes with BB therapy in HFrEF patients.
引用
收藏
页码:898 / 903
页数:6
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