Levosimendan in patients with reduced left ventricular function undergoing isolated coronary or valve surgery

医学 左旋西孟旦 心脏病学 内科学 危险系数 体外循环 心肌梗塞 心脏外科 冠状动脉搭桥手术 置信区间 动脉 心力衰竭
作者
Sean van Diepen,Rajendra H. Mehta,Jeffrey D. Leimberger,Shaun G. Goodman,Stephen E. Fremes,Rachael Jankowich,Matthias Heringlake,Kevin J. Anstrom,Jerrold H. Levy,John M. Luber,A. Dave Nagpal,Andra E. Duncan,Michael Argenziano,Wolfgang Toller,Kevin Teoh,J. David Knight,Renato D. Lópes,Patricia A. Cowper,Daniel B. Mark,John H. Alexander
出处
期刊:The Journal of Thoracic and Cardiovascular Surgery [American Association for Thoracic Surgery]
卷期号:159 (6): 2302-2309.e6 被引量:52
标识
DOI:10.1016/j.jtcvs.2019.06.020
摘要

Abstract Objective In the Levosimendan in Patients with Left Ventricular Systolic Dysfunction Undergoing Cardiac Surgery Requiring Cardiopulmonary Bypass (LEVO-CTS) trial, no differences in clinical outcomes were observed between levosimendan and placebo in a broad population of patients undergoing cardiac surgery. In previous studies, the benefits of levosimendan were most clearly evident in patients undergoing isolated coronary artery bypass grafting (CABG) surgery. In a prespecified analysis of LEVO-CTS, we compared treatment-related outcomes and costs across types of cardiac surgical procedures. Methods Overall, 563 (66.4%) patients underwent isolated CABG, 97 (11.4%) isolated valve, and 188 (22.2%) combined CABG/valve surgery. Outcomes included the co-primary 4-component composite (30-day mortality, 30-day renal replacement, 5-day myocardial infarction, or 5-day mechanical circulatory support), the 2-component composite (30-day mortality or 5-day mechanical circulatory support), 90-day mortality, low cardiac output syndrome (LCOS), and 30-day medical costs. Results The 4- and 2-component outcomes were not significantly different with levosimendan and placebo in patients undergoing CABG (15.2% vs 19.3% and 7.8% vs 10.4%), valve (49.0% vs 33.3% and 22.4% vs 2.1%), or combined procedures (39.6% vs 35.9% and 24.0% vs 19.6%). Ninety-day mortality was lower with levosimendan in isolated CABG (2.1% vs 7.9%; hazard ratio [HR], 0.26; 95% confidence interval [CI], 0.11-0.64), but not significantly different in valve (8.3% vs 2.0%; HR, 4.10; 95% CI, 0.46-36.72) or combined procedures (10.4% vs 7.6%; HR, 1.39; 95% CI, 0.53-3.64; interaction P = .011). LCOS (12.0% vs 22.1%; odds ratio, 0.48; 95% CI, 0.30-0.76; interaction P = .118) was significantly lower in levosimendan-treated patients undergoing isolated CABG. Excluding study drug costs, median and mean 30-day costs were $53,707 and $65,852 for levosimendan and $54,636 and $67,122 for placebo, with a 30-day mean difference (levosimendan – placebo) of −$1270 (bootstrap 95% CI, −$8722 to $6165). Conclusions Levosimendan was associated with lower 90-day mortality and LCOS in patients undergoing isolated CABG, but not in those undergoing isolated valve or combined CABG/valve procedures.
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