Anantha Narayanan Mahesh, Reddy Yogesh N V, Baskaran Janani, Deshmukh Abhishek, Benditt David G, Raveendran Ganesh
Mahesh Anantha Narayanan, Janani Baskaran, David G Benditt, Ganesh Raveendran, Division of Cardiovascular Diseases, University of Minnesota Medical Center, Minneapolis, MN 55455, United States.
World J Cardiol. 2017 Feb 26;9(2):182-190. doi: 10.4330/wjc.v9.i2.182.
To perform a systematic-review and meta-analysis to compare outcomes of ivabradine combined with beta-blocker to beta-blocker alone in heart failure with reduced ejection fraction (HFrEF).
We searched PubMed, Cochrane, EMBASE, CINAHL and Web of Science for trials comparing ivabradine + beta-blocker to beta-blocker alone in HFrEF. We performed a systematic-review and meta-analysis of published literature. Primary end-point was combined end point of cardiac death and hospitalization for heart failure.
Six studies with 17671 patients were included. Mean follow-up was 8.7 ± 7.9 mo. Combined end-point of heart failure readmission and cardiovascular death was better in ivabradine + beta-blocker group compared to beta-blocker alone (RR: 0.93, 95%CI: 0.79-1.09, = 0.354). Mean difference (MD) in heart rate was higher in the ivabradine + beta-blocker group (MD: 6.14, 95%CI: 3.80-8.48, < 0.001). There was no difference in all cause mortality (RR: 0.98, 95%CI: 0.89-1.07, = 0.609), cardiovascular mortality (RR: 0.99, 95%CI: 0.86-1.15, = 0.908) or heart failure hospitalization (RR: 0.87, 95%CI: 0.68-1.11, = 0.271).
From the available clinical trials, ivabradine + beta-blocker resulted in a significantly greater reduction in HR coupled with improvement in combined end-point of heart failure readmission and cardiovascular death but with no improvement in all cause or cardiovascular mortality. Given the limited evidence, further randomized controlled trials are essential before widespread clinical application of ivabradine + beta-blocker is advocated for HFrEF.
进行一项系统评价和荟萃分析,比较伊伐布雷定联合β受体阻滞剂与单用β受体阻滞剂治疗射血分数降低的心力衰竭(HFrEF)的疗效。
我们检索了PubMed、Cochrane、EMBASE、CINAHL和Web of Science数据库,查找比较伊伐布雷定+β受体阻滞剂与单用β受体阻滞剂治疗HFrEF的试验。我们对已发表的文献进行了系统评价和荟萃分析。主要终点是心源性死亡和因心力衰竭住院的联合终点。
纳入6项研究,共17671例患者。平均随访时间为8.7±7.9个月。与单用β受体阻滞剂相比,伊伐布雷定+β受体阻滞剂组心力衰竭再入院和心血管死亡的联合终点更好(RR:0.93,95%CI:0.79-1.09,P=0.354)。伊伐布雷定+β受体阻滞剂组心率的平均差值(MD)更高(MD:6.14,95%CI:3.80-8.48,P<0.001)。全因死亡率(RR:0.98,95%CI:0.89-1.07,P=0.609)、心血管死亡率(RR:0.99,95%CI:0.86-1.15,P=0.908)或心力衰竭住院率(RR:0.87,95%CI:0.68-1.11,P=0.271)无差异。
从现有临床试验来看,伊伐布雷定+β受体阻滞剂能显著降低心率,同时改善心力衰竭再入院和心血管死亡的联合终点,但对全因死亡率或心血管死亡率无改善。鉴于证据有限,在提倡将伊伐布雷定+β受体阻滞剂广泛应用于HFrEF的临床治疗之前,有必要进一步开展随机对照试验。