危险系数
射血分数
心力衰竭
医学
安慰剂
随机对照试验
置信区间
不利影响
心脏病学
内科学
替代医学
病理
作者
Iokfai Cheang,Wenming Yao,Yanli Zhou,Xu Zhu,Gehui Ni,Xinyi Lu,Shengen Liao,Rongrong Gao,Fang Zhou,Jiangang Shen,Alice Yeuk Lan Leung,Meng Jiang,Hong Kong,Ling Bai,Ailiman Mahemuti,Haitao Yuan,Yugang Dong,Chun‐Ka Wong,Qinghua Xu,Gaoxing Zhang
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2024-08-01
卷期号:30 (8): 2295-2302
被引量:56
标识
DOI:10.1038/s41591-024-03169-2
摘要
Abstract Previous findings have indicated the potential benefits of the Chinese traditional medicine Qiliqiangxin (QLQX) in heart failure. Here we performed a double-blind, randomized controlled trial to evaluate the efficacy and safety of QLQX in patients with heart failure and reduced ejection fraction (HFrEF). This multicenter trial, conducted in 133 hospitals in China, enrolled 3,110 patients with HFrEF with NT-proBNP levels of ≥450 pg ml −1 and left ventricular ejection fraction of ≤40%. Participants were randomized to receive either QLQX capsules or placebo (four capsules three times daily) alongside standard heart failure therapy. The trial met its primary outcome, which was a composite of hospitalization for heart failure and cardiovascular death: over a median follow-up of 18.3 months, the primary outcome occurred in 389 patients (25.02%) in the QLQX group and 467 patients (30.03%) in the placebo group (hazard ratio (HR), 0.78; 95% confidence interval (CI), 0.68−0.90; P < 0.001). In an analysis of secondary outcomes, the QLQX group showed reductions in both hospitalization for heart failure (15.63% versus 19.16%; HR, 0.76; 95% CI, 0.64−0.90; P = 0.002) and cardiovascular death (13.31% versus 15.95%; HR, 0.83; 95% CI, 0.68−0.996; P = 0.045) compared to the placebo group. All-cause mortality did not differ significantly between the two groups (HR, 0.84; 95% CI, 0.70−1.01; P = 0.058) and adverse events were also comparable between the groups. The results of this trial indicate that QLQX may improve clinical outcomes in patients with HFrEF when added to conventional therapy. ChiCTR registration: ChiCTR1900021929 .
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