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准备:环利尿剂在慢性收缩性心力衰竭患者中的相对疗效:一项随机试验的系统评价和网络荟萃分析。

READY: relative efficacy of loop diuretics in patients with chronic systolic heart failure-a systematic review and network meta-analysis of randomised trials.

机构信息

Department of Cardiology, Angiology, and Pulmonology, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.

出版信息

Heart Fail Rev. 2019 Jul;24(4):461-472. doi: 10.1007/s10741-019-09771-8.

Abstract

The majority of patients with chronic heart failure (HF) receive long-term treatment with loop diuretics. The comparative effectiveness of different loop diuretics is unknown. We searched PubMed, clinicaltrials.gov , the Cochrane Central Register of Controlled Trials and the European Union Clinical Trials Register for randomised clinical trials exploring the efficacy of the loop diuretics azosemide, bumetanide, furosemide or torasemide in patients with HF. Comparators included placebo, standard medical care or any other active treatment. The primary endpoint was all-cause mortality. Secondary endpoints included cardiovascular mortality, HF-related hospitalisation and any combined endpoint thereof. Hypokalaemia and acute renal failure were defined as additional safety endpoints. Evidence was synthesised using network meta-analysis (NMA). Thirty-four trials reporting on 2647 patients were included. The overall quality of evidence was rated as moderate. NMA demonstrated no significant differences between loop diuretics with respect to all-cause mortality, cardiovascular mortality or hypokalaemia. In contrast, torasemide ranked best in terms of HF hospitalisation, and there was a trend towards benefits with torasemide with regard to occurrence of acute renal failure. Sensitivity analyses excluding trials with a follow-up < 6 months, trials with a cross-over design and those including < 25 patients confirmed the main results. We found no significant superiority of either loop diuretic with respect to mortality and safety endpoints. However, clinicians may prefer torasemide, as it was associated with fewer HF-related hospitalisations.

摘要

大多数慢性心力衰竭(HF)患者接受长期的袢利尿剂治疗。不同袢利尿剂的疗效比较尚不清楚。我们检索了 PubMed、clinicaltrials.gov、Cochrane 对照试验中心注册库和欧盟临床试验注册库,以寻找探索噻嗪类利尿剂阿佐塞米、布美他尼、呋塞米或托拉塞米在 HF 患者中的疗效的随机临床试验。对照剂包括安慰剂、标准医疗护理或任何其他活性治疗。主要终点是全因死亡率。次要终点包括心血管死亡率、HF 相关住院和任何联合终点。低钾血症和急性肾衰竭被定义为额外的安全终点。使用网络荟萃分析(NMA)综合证据。纳入了 34 项试验,共 2647 名患者。证据的整体质量评分为中等。NMA 表明,在全因死亡率、心血管死亡率或低钾血症方面,各种袢利尿剂之间没有显著差异。相比之下,托拉塞米在 HF 住院方面排名最佳,并且托拉塞米在急性肾衰竭方面有获益的趋势。排除随访时间<6 个月的试验、交叉设计的试验和纳入<25 名患者的试验进行敏感性分析,确认了主要结果。我们没有发现任何一种袢利尿剂在死亡率和安全性终点方面具有显著优势。然而,由于托拉塞米与较少的 HF 相关住院相关,临床医生可能更倾向于使用托拉塞米。

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