Emergency Department, First Affiliated Hospital of Guangxi Medical University, Nanning, China,
Am J Cardiovasc Drugs. 2013 Oct;13(5):365-73. doi: 10.1007/s40256-013-0034-3.
Patients with decompensated heart failure frequently present with volume overload, which is conventionally treated with diuretics. These drugs have been associated with several adverse effects, including increased mortality, leading some clinicians to propose ultrafiltration as a safe alternative to remove sodium and water.
The objective of our study was to compare the safety and efficacy of ultrafiltration and conventional intravenous diuretic therapy for patients with acute heart failure and volume overload.
We searched the following databases through November 2012: Cochrane Library (1993-), PubMed (1988-), OVID (1984-), EBSCO (1984-), CBM (1978-), VIP (1989-), and CNKI (1979-). In addition, we manually searched relevant references and review articles.
Randomized controlled trials comparing the efficacy of ultrafiltration and intravenous diuretics in patients diagnosed with hypervolemic acute heart failure were included. Five trials were found to satisfy all the inclusion criteria.
Two reviewers independently determined study eligibility, assessed methodological quality and extracted the data. We analyzed the data and pooled them, when appropriate, using Revman 5.0. We assessed the risk of bias in the included studies using guidelines in the Cochrane Handbook 5.0 for Systematic Reviews of Interventions, taking into account sequence generation, allocation concealment, blinding, incomplete outcome data, and selective outcome reporting.
Data from the initial phase of five trials involving 477 participants were included. Meta-analysis of the pooled data showed that ultrafiltration was significantly better than diuretic drugs based on 48-h weight loss (Z = 3.72; P < 0.001, weighted mean difference [WMD] = 1.25 kg, 95 % CI 0.59-1.91) and based on 48-h fluid removal (Z = 4.23; P < 0.001, WMD = 1.06 L, 95 % CI 0.57-1.56). Adverse events did not differ significantly between the ultrafiltration and intravenous diuretic treatment groups.
There are several limitations to our review, including publication bias and selection bias. Our review included only a few studies involving relatively few participants.
The available evidence suggests that early ultrafiltration is safe and effective for patients with hypervolemic acute heart failure. It allows greater fluid removal and weight loss by 48 h than do intravenous diuretics, with no significant increase in adverse effects.
失代偿性心力衰竭患者常伴有容量超负荷,传统上使用利尿剂治疗。这些药物与多种不良反应有关,包括死亡率增加,这使得一些临床医生提出超滤作为一种安全的替代方法来去除钠和水。
我们的研究目的是比较超滤和传统静脉内利尿剂治疗急性心力衰竭伴容量超负荷患者的安全性和疗效。
我们通过 2012 年 11 月检索了以下数据库:Cochrane 图书馆(1993 年-)、PubMed(1988 年-)、OVID(1984 年-)、EBSCO(1984 年-)、CBM(1978 年-)、VIP(1989 年-)和中国知网(1979 年-)。此外,我们还手动搜索了相关参考文献和综述文章。
纳入了比较超滤和静脉内利尿剂治疗诊断为高容量性急性心力衰竭患者疗效的随机对照试验。发现有 5 项试验符合所有纳入标准。
两位评审员独立确定研究的合格性、评估方法学质量并提取数据。我们使用 Revman 5.0 分析数据并进行合并,如果合适的话。我们根据 Cochrane 干预系统评价手册 5.0 的指南评估纳入研究的偏倚风险,考虑到序列生成、分配隐藏、盲法、不完整结局数据和选择性结局报告。
纳入了 5 项试验的初始阶段,共涉及 477 名参与者的数据。基于 48 小时体重减轻(Z = 3.72;P < 0.001,加权均数差[WMD] = 1.25kg,95%CI 0.59-1.91)和基于 48 小时液体清除(Z = 4.23;P < 0.001,WMD = 1.06L,95%CI 0.57-1.56),荟萃分析显示超滤明显优于利尿剂。超滤和静脉内利尿剂治疗组的不良事件无显著差异。
我们的综述有几个局限性,包括发表偏倚和选择偏倚。我们的综述只包括了少数几项涉及相对较少参与者的研究。
现有证据表明,早期超滤治疗高容量性急性心力衰竭是安全有效的。与静脉内利尿剂相比,它可在 48 小时内更有效地清除液体和减轻体重,且不良事件发生率无显著增加。