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CHARM 中射血分数中间值的心衰:特征、结局和坎地沙坦在整个射血分数谱中的作用。

Heart failure with mid-range ejection fraction in CHARM: characteristics, outcomes and effect of candesartan across the entire ejection fraction spectrum.

机构信息

Unit of Cardiology, Department of Medicine, Karolinska Institutet, and Heart and Vascular Theme, Karolinska University Hospital, Stockholm, Sweden.

Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.

出版信息

Eur J Heart Fail. 2018 Aug;20(8):1230-1239. doi: 10.1002/ejhf.1149. Epub 2018 Feb 12.

Abstract

AIMS

We tested the hypothesis that candesartan improves outcomes in heart failure (HF) with mid-range ejection fraction [HFmrEF; ejection fraction (EF) 40-49%].

METHODS AND RESULTS

In 7598 patients enrolled in the CHARM Programme (HF across the spectrum of EF), we assessed characteristics, outcomes and treatment effect of candesartan according to EF. Patients with HFmrEF (n = 1322, 17%) were similar to those with HF with reduced EF (HFrEF; n = 4323, 57%) with respect to some characteristics, and intermediate between HFrEF and HF with preserved EF (HFpEF; n = 1953, 26%) with respect to others. Over a mean follow-up of 2.9 years, the incidence rates for the primary outcome of cardiovascular death or HF hospitalization were 15.9, 8.5 and 8.9 per 100 patient-years in HFrEF, HFmrEF and HFpEF. In adjusted analyses, the rates of the primary outcome declined with increasing EF up to 50%. For treatment effect, the incidence rates for the primary outcome for candesartan vs. placebo were 14.4 vs. 17.5 per 100 patient-years in HFrEF [hazard ratio (HR) 0.82, 95% confidence interval (CI) 0.75-0.91; P < 0.001], 7.4 vs. 9.7 per 100 patient-years in HFmrEF (HR 0.76, 95% CI 0.61-0.96; P = 0.02), and 8.6 vs. 9.1 per 100 patient-years in HFpEF (HR 0.95, 95% CI 0.79-1.14; P = 0.57). For recurrent HF hospitalization, the incidence rate ratios were 0.68 in HFrEF (95% CI 0.58-0.80; P < 0.001), 0.48 in HFmrEF (95% CI 0.33-0.70; P < 0.001), and 0.78 in HFpEF (95% CI 0.59-1.03; P = 0.08). With EF as a continuous spline variable, candesartan significantly reduced the primary outcome until EF well over 50% and recurrent HF hospitalizations until EF well over 60%.

CONCLUSION

Candesartan improved outcomes in HFmrEF to a similar degree as in HFrEF. ClinicalTrials.gov: CHARM Alternative NCT00634400, CHARM Added NCT00634309, CHARM Preserved NCT00634712.

摘要

目的

我们检验了坎地沙坦是否能改善射血分数处于中间范围的心衰(HFmrEF;射血分数 40%-49%)患者的预后的假说。

方法和结果

在 CHARM 计划(EF 谱中的心衰)的 7598 名患者中,我们根据 EF 评估了坎地沙坦的特征、结局和治疗效果。HFmrEF(n=1322,17%)患者与射血分数降低的心衰(HFrEF;n=4323,57%)患者在某些特征上相似,而与射血分数保留的心衰(HFpEF;n=1953,26%)在其他特征上则处于中间位置。平均随访 2.9 年后,HFrEF、HFmrEF 和 HFpEF 患者主要终点(心血管死亡或心衰住院)的发生率分别为 15.9、8.5 和 8.9/100 患者年。在调整后的分析中,主要终点发生率随着 EF 的增加而降低,直至 EF 超过 50%。坎地沙坦治疗组与安慰剂组的主要终点发生率分别为 HFrEF 中 14.4 和 17.5/100 患者年(HR 0.82,95%CI 0.75-0.91;P<0.001)、HFmrEF 中 7.4 和 9.7/100 患者年(HR 0.76,95%CI 0.61-0.96;P=0.02)和 HFpEF 中 8.6 和 9.1/100 患者年(HR 0.95,95%CI 0.79-1.14;P=0.57)。心衰再住院的发生率比值分别为 HFrEF 中 0.68(95%CI 0.58-0.80;P<0.001)、HFmrEF 中 0.48(95%CI 0.33-0.70;P<0.001)和 HFpEF 中 0.78(95%CI 0.59-1.03;P=0.08)。EF 作为连续样条变量,坎地沙坦显著降低了主要终点的发生率,直至 EF 超过 50%,并降低了心衰再住院的发生率,直至 EF 超过 60%。

结论

坎地沙坦改善 HFmrEF 患者的预后的效果与 HFrEF 相似。临床试验.gov:CHARM 替代试验 NCT00634400、CHARM 附加试验 NCT00634309、CHARM 保留试验 NCT00634712。

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