Baysal Ayse, Yanartas Mehmet, Dogukan Mevlut, Gundogus Narin, Kocak Tuncer, Koksal Cengiz
Anesthesiology and Reanimation Clinic, Kartal Kosuyolu High Speciality Training and Research Hospital, Istanbul, Turkey.
Cardiovascular Surgery Clinic, Kartal Kosuyolu High Speciality Training and Research Hospital, Istanbul, Turkey.
J Cardiothorac Vasc Anesth. 2014 Jun;28(3):586-94. doi: 10.1053/j.jvca.2013.09.004. Epub 2014 Jan 18.
The effect of levosimendan on renal function in patients with low ejection fraction undergoing mitral valve surgery was investigated.
A prospective, double-blinded, randomized clinical trial.
Tertiary teaching and research hospital.
Of a total of 147 patients, 128 patients completed the study. In the levosimendan group (n = 64), levosimendan was administered in addition to standard inotropic support; whereas, in the control group (n = 64), only standard inotropic support was given.
In the levosimendan group, a loading dose of levosimendan (6 μg/kg) was administered after removal of the aortic cross-clamp, followed by an infusion (0.1 μg/kg/min) in addition to standard inotropic therapy for 24 hours. In the control group, only standard inotropic therapy was administered. Preoperative characteristics, serum creatinine (sCr) levels, and estimated glomerular filtration rate (eGFR) were determined preoperatively, on postoperative days 1, 3, and 10. Independent risk factors for renal replacement therapy (RRT) requirement were investigated with stepwise multivariate logistic regression analysis.
The primary endpoint was the effect of levosimendan on postoperative renal clearance (sCr and eGFR). The secondary endpoint was the effect of levosimendan on clinical outcomes (length of intensive care unit and hospital stays, need for RRT). Preoperative characteristics and eGFR were similar between the groups (p>0.05). On postoperative days 1 and 3, sCr values were lower and eGFR values were higher in the levosimendan group in comparison with the control group (p = 0.0001, p = 0.009, respectively). Six patients (9.4%) in the levosimendan group and 10 patients (15.6%) in the control group required RRT therapy (p = 0.284). Independent risk factors for need of RRT include preoperative sCr value between 1.2 to 2.09 mg/dL and≥2.1 mg/dL (p< 0.05).
Perioperative treatment with levosimendan in addition to standard inotropic therapy in patients with a low ejection fraction undergoing mitral valve surgery improved immediate postoperative renal function and reduced need for RRT.
研究左西孟旦对接受二尖瓣手术的低射血分数患者肾功能的影响。
一项前瞻性、双盲、随机临床试验。
三级教学研究医院。
总共147例患者,128例完成研究。左西孟旦组(n = 64)除标准的正性肌力支持外还给予左西孟旦;而对照组(n = 6)仅给予标准的正性肌力支持。
左西孟旦组在解除主动脉阻断钳后给予负荷剂量的左西孟旦(6μg/kg),然后除标准的正性肌力治疗外持续输注(0.1μg/kg/min)24小时。对照组仅给予标准的正性肌力治疗。术前测定术前特征、血清肌酐(sCr)水平和估计肾小球滤过率(eGFR),术后第1天、第3天和第10天重复测定。采用逐步多因素逻辑回归分析研究肾脏替代治疗(RRT)需求的独立危险因素。
主要终点是左西孟旦对术后肾脏清除率(sCr和eGFR)的影响。次要终点是左西孟旦对临床结局(重症监护病房住院时间和住院时间、RRT需求)的影响。两组术前特征和eGFR相似(p>0.05)。术后第1天和第3天,左西孟旦组的sCr值较低,eGFR值较高,与对照组相比(分别为p = 0.0001,p = 0.009)。左西孟旦组6例患者(9.4%)和对照组10例患者(15.6%)需要RRT治疗(p = 0.284)。RRT需求的独立危险因素包括术前sCr值在1.2至2.09mg/dL之间和≥2.1mg/dL(p<0.05)。
在接受二尖瓣手术的低射血分数患者中,除标准的正性肌力治疗外,围手术期使用左西孟旦可改善术后即刻肾功能并减少RRT需求。