Internal Medicine Clinic III, Saarland University Clinic, Saarland University, Homburg, Saar, Germany.
Department of Cardiology, Paris Saint Joseph Hospital, Paris, France.
Eur J Heart Fail. 2018 Feb;20(2):373-381. doi: 10.1002/ejhf.1021. Epub 2017 Oct 12.
In heart failure (HF) with reduced ejection fraction and sinus rhythm, heart rate reduction with ivabradine reduces the composite incidence of cardiovascular death and HF hospitalization.
It is unclear whether the duration of HF prior to therapy independently affects outcomes and whether it modifies the effect of heart rate reduction. In SHIFT, 6505 patients with chronic HF (left ventricular ejection fraction of ≤35%), in sinus rhythm, heart rate of ≥70 b.p.m., treated with guideline-recommended therapies, were randomized to placebo or ivabradine. Outcomes and the treatment effect of ivabradine in patients with different durations of HF were examined. Prior to randomization, 1416 ivabradine and 1459 placebo patients had HF duration of ≥4 weeks and <1.5 years; 836 ivabradine and 806 placebo patients had HF duration of 1.5 years to <4 years, and 989 ivabradine and 999 placebo patients had HF duration of ≥4 years. Patients with longer duration of HF were older (62.5 years vs. 59.0 years; P < 0.0001), had more severe disease (New York Heart Association classes III/IV in 56% vs. 44.9%; P < 0.0001) and greater incidences of co-morbidities [myocardial infarction: 62.9% vs. 49.4% (P < 0.0001); renal dysfunction: 31.5% vs. 21.5% (P < 0.0001); peripheral artery disease: 7.0% vs. 4.8% (P < 0.0001)] compared with patients with a more recent diagnosis. After adjustments, longer HF duration was independently associated with poorer outcome. Effects of ivabradine were independent of HF duration.
Duration of HF predicts outcome independently of risk indicators such as higher age, greater severity and more co-morbidities. Heart rate reduction with ivabradine improved outcomes independently of HF duration. Thus, HF treatments should be initiated early and it is important to characterize HF populations according to the chronicity of HF in future trials.
在射血分数降低的窦性心律心力衰竭患者中,伊伐布雷定降低心率可减少心血管死亡和心力衰竭住院的复合发生率。
在治疗前心力衰竭的持续时间是否独立影响结局,以及它是否改变心率降低的效果尚不清楚。在 SHIFT 中,6505 例慢性心力衰竭(左心室射血分数≤35%)、窦性心律、心率≥70 次/分、接受指南推荐治疗的患者被随机分配至安慰剂或伊伐布雷定组。检查了不同心力衰竭持续时间患者的结局和伊伐布雷定的治疗效果。在随机分组前,1416 例伊伐布雷定和 1459 例安慰剂患者心力衰竭持续时间≥4 周且<1.5 年;836 例伊伐布雷定和 806 例安慰剂患者心力衰竭持续时间为 1.5 年至<4 年,989 例伊伐布雷定和 999 例安慰剂患者心力衰竭持续时间≥4 年。心力衰竭持续时间较长的患者年龄较大(62.5 岁比 59.0 岁;P<0.0001),疾病更严重(纽约心脏协会心功能分级 III/IV 级占 56%比 44.9%;P<0.0001),合并症发生率更高[心肌梗死:62.9%比 49.4%(P<0.0001);肾功能不全:31.5%比 21.5%(P<0.0001);外周动脉疾病:7.0%比 4.8%(P<0.0001)]。校正后,较长的心力衰竭持续时间与较差的结局独立相关。伊伐布雷定的作用与心力衰竭持续时间无关。
心力衰竭的持续时间独立于年龄较大、疾病更严重和合并症更多等风险指标预测结局。伊伐布雷定降低心率可改善结局,与心力衰竭持续时间无关。因此,心力衰竭的治疗应尽早开始,在未来的试验中根据心力衰竭的慢性程度对心力衰竭人群进行特征描述非常重要。