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首页> 外文期刊>BMC Anesthesiology >Effect of ramosetron on QTc interval: a randomised controlled trial in patients undergoing off-pump coronary artery bypass surgery
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Effect of ramosetron on QTc interval: a randomised controlled trial in patients undergoing off-pump coronary artery bypass surgery

机译:雷莫司琼对QTc间期的影响:一项针对非体外循环冠状动脉搭桥手术患者的随机对照试验

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Background Ramosetron is a relatively new 5-hydroxytryptamine three receptor antagonist with higher binding affinity and more prolonged duration of action compared to ondansetron. The present study was performed to evaluate the effects of ramosetron on QTc interval and possible cardiovascular adverse effects in patients undergoing cardiac surgery. Method A total of 114 patients who underwent off-pump coronary artery bypass surgery were enrolled in this randomised placebo-controlled trial. Patients were allocated into two groups that received intravenous injection of 0.3?mg ramosetron or normal saline during induction of anaesthesia. QTc intervals were measured before the operation, intraoperatively (0, 1, 2, 3, 5, 10, 15, 30, 45, 60, 90, 120, and 240?min after injection of ramosetron or normal saline), at the end of the operation, and on postoperative day 1. Results There were no differences in mean QTc interval between groups at every time point. However, maximal change in QTc interval during surgery was higher in the ramosetron group than the placebo group (25.1?±?22.0 vs. 17.5?±?14.5?ms, 95?% CI 0.34–14.78, P =?0.040). Also, there were more patients with a QTc interval increase of?>?60?ms in the ramosetron group (5 vs. 0, 95?% CI 1.6–18.0, P =?0.021). There were no significant differences in cardiovascular complications. Conclusions Ramosetron administered during induction of anaesthesia may affect maximal change in QTc interval during off-pump coronary artery bypass surgery. Ramosetron should be used with caution in high risk patients for developing Torsades de Pointes. Trial registration ClinicalTrials.gov NCT02139241. Registered November 12, 2013
机译:背景技术雷莫司琼是相对较新的5-羟色胺三受体拮抗剂,与恩丹西酮相比具有更高的结合亲和力和更长的作用时间。本研究旨在评估雷莫司琼对心脏手术患者QTc间隔的影响以及可能的心血管不良反应。方法该随机安慰剂对照试验共纳入114例接受了非体外循环冠状动脉搭桥手术的患者。将患者分为两组,在麻醉诱导期间接受静脉注射0.3?mg雷莫司琼或生理盐水。术前(注射雷莫司琼或生理盐水后0、1、2、3、5、10、15、30、45、60、90、120和240?min)在手术前测量QTc间隔结果以及术后第1天。结果在每个时间点,两组之间的平均QTc间隔无差异。但是,雷莫司琼组手术期间QTc间隔的最大变化高于安慰剂组(25.1±±22.0 vs. 17.5±±14.5μms,95%CI 0.34–14.78,P = 0.040)。此外,雷莫司琼组中有更多的患者的QTc间隔增加≥60 µms(5 vs. 0,95%CI CI 1.6-18.0,P = 0.012)。心血管并发症没有显着差异。结论麻醉诱导期间使用Ramosetron可能会影响非体外循环冠状动脉搭桥手术期间QTc间隔的最大变化。在高风险患者中发展成Torsades de Pointes时应谨慎使用Ramosetron。试用注册ClinicalTrials.gov NCT02139241。 2013年11月12日注册

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