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.
Eur J Heart Fail. 2018 Aug;20(8):1230-1239. doi: 10.1002/ejhf.1149. Epub 2018 Feb 12.
We tested the hypothesis that candesartan improves outcomes in heart failure (HF) with mid-range ejection fraction [HFmrEF; ejection fraction (EF) 40-49%].
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%.
Candesartan improved outcomes in HFmrEF to a similar degree as in HFrEF. ClinicalTrials.gov: CHARM Alternative NCT00634400, CHARM Added NCT00634309, CHARM Preserved NCT00634712.
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。
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%。
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。