Hypotension after induction of anesthesia with remimazolam or etomidate: a non-inferiority randomized controlled trial in patients undergoing coronary artery bypass grafting.

IF 4.2 4区 医学 Q1 ANESTHESIOLOGY
Jeong-Jin Min, Eun Jung Oh, Hyun Ji Hwang, Sungwoo Jo, Hyunsung Cho, Chungsu Kim, Jong-Hwan Lee
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Abstract

Background: Remimazolam is a novel ultra-short-acting benzodiazepine known for its hemodynamic stability over propofol. However, its hemodynamic effects compared to those of etomidate are not well established. This study aimed to determine whether the use of remimazolam is non-inferior to etomidate with regard to the occurrence of post-induction hypotension in patients undergoing coronary arterial bypass grafting.

Methods: Patients were randomly assigned to either the remimazolam group (6 m/kg/h) or the etomidate group (0.3 mg/kg) for induction of anesthesia. Anesthetic depth was adjusted based on the bispectral index (BIS). Primary outcome was the incidence of post-induction hypotension, defined as a mean arterial pressure (MAP) less than 65 mmHg within 15 min after endotracheal intubation, with a non-inferiority margin of 12%.

Results: A total of 144 patients were finally analyzed. Incidence of post-induction hypotension was 36 / 71 (50.7%) in the remimazolam group and 25 / 73 (34.2%) in the etomidate group, with a rate difference of 16.5% (95% CI, 3.0-32.6) between the two groups that was beyond the prespecified non-inferiority margin of 12.0%. The number of patients who needed vasopressors was similar in the two groups.

Conclusions: In this non-inferiority trial, remimazolam failed to show non-inferiority to etomidate in terms of post-induction hypotension when used as an induction drug for general anesthesia in patients undergoing coronary arterial bypass grafting. However, different doses or infusion techniques of remimazolam must be compared with etomidate in various patient groups to fully assess its hemodynamic non-inferiority during induction of anesthesia.

雷马唑仑或依托咪酯诱导麻醉后的低血压:冠状动脉旁路移植术患者的非劣效性随机对照试验。
背景介绍雷马唑仑是一种新型超短效苯二氮卓类药物,其血液动力学稳定性优于异丙酚。然而,与依托咪酯相比,它对血液动力学的影响尚未得到充分证实。本研究旨在确定在冠状动脉旁路移植术患者诱导后低血压发生率方面,使用雷马唑仑是否不劣于依托咪酯:将患者随机分配至瑞马唑仑组(6 m/kg/h)或依托咪酯组(0.3 mg/kg)进行麻醉诱导。麻醉深度根据双光谱指数(BIS)进行调整。主要结果是诱导后低血压的发生率,即气管插管后 15 分钟内平均动脉压(MAP)低于 65 mmHg,非劣效差为 12%:最终对 144 名患者进行了分析。雷马唑仑组诱导后低血压发生率为36/71(50.7%),依托咪酯组为25/73(34.2%),两组间的发生率差异为16.5%(95% CI,3.0-32.6),超出了预设的12.0%的非劣效边际。两组需要使用血管加压药的患者人数相似:在这项非劣效性试验中,雷马唑仑作为全身麻醉诱导药物用于冠状动脉旁路移植术患者时,在诱导后低血压方面未能显示出与依托咪酯的非劣效性。不过,必须在不同的患者组别中将不同剂量或输注技术的雷马唑仑与依托咪酯进行比较,以全面评估其在麻醉诱导期间的血流动力学非劣效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
6.90%
发文量
84
审稿时长
16 weeks
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