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首页> 外文期刊>Journal of the American College of Cardiology >A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study of the Effects of Qili Qiangxin Capsules in Patients With Chronic Heart Failure
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A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study of the Effects of Qili Qiangxin Capsules in Patients With Chronic Heart Failure

机译:多中心,随机,双盲,并行组,安慰剂对照研究祁利羌新胶囊在慢性心力衰竭患者中的影响研究

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摘要

The purpose of this study was to assess the effects of qili qiangxin capsules in patients with chronic heart failure (CHF).Qili qiangxin capsules are a traditional Chinese medicine that has been approved in China for the treatment of CHF, but the evidence supporting its efficacy remains unclear.A total of 512 patients with CHF were enrolled and randomly assigned to receive the placebo or qili qiangxin capsules in addition to their standard medications for the treatment of CHF. The primary endpoint was the reduction or percent change in the plasma N-terminal pro-B-type natriuretic peptide (NT-proBNP) level during 12 weeks of treatment.At the 12-week follow-up, a significant reduction in the NT-proBNP level from baseline was observed in both groups, but the qili qiangxin capsule group demonstrated a significantly greater reduction than the placebo group (p = 0.002); 47.95% of patients in the qiii qiangxin capsule group demonstrated reductions in NT-proBNP levels of at least 30% compared with 31.98% of patients in the placebo group (p < 0.001). Treatment with qili qiangxin capsules also demonstrated superior performance in comparison to the placebo with respect to New York Heart Association functional classification, left ventricular ejection fraction, 6-min walking distance, and quality of life.On a background of standard treatment, qili qiangxin capsules further reduced the levels of NT-proBNP. Together, our data suggest that qiii qiangxin capsules could be used in combination therapy for CHF.
机译:本研究的目的是评估祁利羌新胶囊在慢性心力衰竭(CHF)患者中的影响。季齐羌新胶囊是中国批准的中医,用于治疗CHF,但证据支持其疗效仍然不清楚。除了用于治疗CHF的标准药物外,还注册了512例CHF患者,以接受安慰剂或祁利羌昔胶囊。初级终点是在治疗12周内血浆N-末端Pro-B型利钠尿肽(NT-proPNP)水平的减少或百分比。该12周随访,NT-显着减少 - 两组中观察到基线的ProBNP水平,但齐丽羌新胶囊组均比安慰剂组明显更大(P = 0.002); 47.95%的秋肝素胶囊组患者患者患有至少30%的NT-ProPNP水平减少,与31.98%的安慰剂组(P <0.001)。与齐丽羌新胶囊的治疗还展现出卓越的性能与安慰剂相对于纽约心脏关联功能分类,左心室喷射分数,6分钟的步行距离和生活质量。标准治疗背景,齐丽羌新胶囊。进一步降低了NT-probnp的水平。我们的数据表明,秋齐羌新胶囊可用于CHF的联合治疗。

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