Department of Pharmacy, Heart Hospital, Hamad Medical Corporation, Doha, Qatar.
Department of Cardiothoracic Surgery/Cardiac Anesthesia & ICU, Heart Hospital, Hamad Medical Corporation, Doha, Qatar.
J Cardiothorac Vasc Anesth. 2021 Aug;35(8):2483-2495. doi: 10.1053/j.jvca.2021.01.019. Epub 2021 Jan 16.
Veno-arterial extracorporeal membrane oxygenation (VA-ECMO) provides a temporary support system for patients with cardiogenic shock refractory to conventional medical therapies. It has been reported that levosimendan may facilitate VA-ECMO weaning and improve survival. The primary objective of this review was to examine the effect of levosimendan use on VA-ECMO weaning and mortality in critically ill patients on VA-ECMO.
MEDLINE, EMBASE, and CENTRAL were searched. A pair of reviewers identified eligible clinical trials. Two reviewers extracted data and independently assessed the risk of bias. A random-effect model was used to combine data. The primary outcome was the success of weaning from VA-ECMO.
Seven studies of observational design, including a total of 630 patients, were selected in the final analysis. The sample size ranged from ten-to-240 patients, with a mean age between 53 and 65 years, and more than half of them underwent cardiac surgeries. The VA-ECMO durations varied between four and 11.6 days. Overall, levosimendan use was significantly associated with successful weaning compared with control (odds ratio [OR] 2.89, 95% CI, 1.53-5.46; p = 0.001); I = 49%). For survival, six studies (n = 617) were included in the meta-analysis involving 326 patients in the levosimendan group and 291 in the comparator group. Pooled results showed a significantly higher survival rate in the levosimendan group (OR 0.46, 95% CI, 0.30-0.71; p = 0.0004; I = 20%).
Levosimendan therapy was significantly associated with successful weaning and survival benefit in patients with cardiogenic or postcardiotomy shock needing VA-ECMO support for severe cardiocirculatory compromise. To date, there is limited literature and absence of evidence from randomized trials addressing the use of levosimendan in VA-ECMO weaning. This study may be considered a hypothesis-generating research for randomized controlled trials to confirm its findings.
静脉-动脉体外膜肺氧合(VA-ECMO)为对常规药物治疗无反应的心源性休克患者提供了一种临时支持系统。有报道称,左西孟旦有助于 VA-ECMO 脱机,并提高生存率。本综述的主要目的是评估左西孟旦在 VA-ECMO 支持的危重病患者脱机和死亡率方面的作用。
检索 MEDLINE、EMBASE 和 CENTRAL。一对审查员确定了合格的临床试验。两名审查员提取数据并独立评估偏倚风险。使用随机效应模型对数据进行合并。主要结局是 VA-ECMO 脱机的成功。
最终分析中选择了 7 项观察性设计研究,共纳入 630 例患者。样本量从 10 例到 240 例不等,平均年龄在 53 至 65 岁之间,其中一半以上接受了心脏手术。VA-ECMO 持续时间在 4 至 11.6 天之间。总体而言,与对照组相比,左西孟旦的使用与成功脱机显著相关(比值比 [OR] 2.89,95%置信区间,1.53-5.46;p=0.001);I=49%)。关于生存率,纳入了 6 项研究(n=617),涉及左西孟旦组 326 例和对照组 291 例患者。汇总结果显示,左西孟旦组的生存率显著更高(OR 0.46,95%置信区间,0.30-0.71;p=0.0004;I=20%)。
在因严重心肺循环衰竭而需要 VA-ECMO 支持的心源性或心脏手术后休克患者中,左西孟旦治疗与成功脱机和生存获益显著相关。迄今为止,关于左西孟旦在 VA-ECMO 脱机中的应用,文献有限,缺乏随机试验证据。这项研究可以被认为是一个产生假设的研究,为随机对照试验提供了依据。