Department of Anesthesia and Intensive Care, Istituto Mediterraneo per i Trapianti e Terapie ad alta specializzazione (IRCCS-ISMETT), Via Tricomi 5, 90127, Palermo, Italy.
Department of Anesthesiology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Crit Care. 2017 Oct 19;21(1):252. doi: 10.1186/s13054-017-1849-0.
Previous studies have shown beneficial effects of levosimendan in high-risk patients undergoing cardiac surgery. Two large randomized controlled trials (RCTs), however, showed no advantages of levosimendan.
We performed a systematic review and meta-analysis (MEDLINE and Embase from inception until March 30, 2017), investigating whether levosimendan offers advantages compared with placebo in high-risk cardiac surgery patients, as defined by preoperative left ventricular ejection fraction (LVEF) ≤ 35% and/or low cardiac output syndrome (LCOS). The primary outcomes were mortality at longest follow-up and need for postoperative renal replacement therapy (RRT). Secondary postoperative outcomes investigated included myocardial injury, supraventricular arrhythmias, development of LCOS, acute kidney injury (AKI), duration of mechanical ventilation, intensive care unit and hospital lengths of stay, and incidence of hypotension during drug infusion.
Six RCTs were included in the meta-analysis, five of which investigated only patients with LVEF ≤ 35% and one of which included predominantly patients with LCOS. Mortality was similar overall (OR 0.64 [0.37, 1.11], p = 0.11) but lower in the subgroup with LVEF < 35% (OR 0.51 [0.32, 0.82], p = 0.005). Need for RRT was reduced by levosimendan both overall (OR 0.63 [0.42, 0.94], p = 0.02) and in patients with LVEF < 35% (OR 0.55 [0.31, 0.97], p = 0.04). Among secondary outcomes, we found lower postoperative LCOS in patients with LVEF < 35% receiving levosimendan (OR 0.49 [0.27, 0.89], p = 0.02), lower overall AKI (OR 0.62 [0.42, 0.92], p = 0.02), and a trend toward lower mechanical support, both overall (p = 0.07) and in patients with LVEF < 35% (p = 0.05).
Levosimendan reduces mortality in patients with preoperative severely reduced LVEF but does not affect overall mortality. Levosimendan reduces the need for RRT after high-risk cardiac surgery.
先前的研究表明左西孟旦对接受心脏手术的高危患者有益。然而,两项大型随机对照试验(RCT)并未显示左西孟旦的优势。
我们进行了系统评价和荟萃分析(从 MEDLINE 和 Embase 检索到 2017 年 3 月 30 日),以调查左西孟旦与安慰剂相比在术前左心室射血分数(LVEF)≤35%和/或低心输出量综合征(LCOS)的高危心脏手术患者中是否具有优势。主要结局为最长随访时的死亡率和术后需要肾脏替代治疗(RRT)。次要术后结局包括心肌损伤、室上性心律失常、LCOS 的发展、急性肾损伤(AKI)、机械通气时间、重症监护病房和住院时间以及药物输注期间低血压的发生率。
荟萃分析纳入了 6 项 RCT,其中 5 项仅调查了 LVEF≤35%的患者,1 项主要纳入了 LCOS 患者。总体死亡率相似(OR 0.64 [0.37, 1.11],p=0.11),但 LVEF<35%的亚组较低(OR 0.51 [0.32, 0.82],p=0.005)。左西孟旦降低了 RRT 的需求,总体上(OR 0.63 [0.42, 0.94],p=0.02)和 LVEF<35%的患者中(OR 0.55 [0.31, 0.97],p=0.04)。在次要结局中,我们发现 LVEF<35%接受左西孟旦治疗的患者术后 LCOS 发生率较低(OR 0.49 [0.27, 0.89],p=0.02),总体 AKI 发生率较低(OR 0.62 [0.42, 0.92],p=0.02),机械支持的总体趋势较低(p=0.07)和 LVEF<35%的患者(p=0.05)。
左西孟旦降低了术前 LVEF 严重降低的患者的死亡率,但不影响总体死亡率。左西孟旦降低高危心脏手术后 RRT 的需求。