Comparing the safety and efficacy of remimazolam-based total intravenous anesthesia versus volatile agent-based anesthesia: a meta-analysis of randomized controlled trials.

IF 4.2 4区 医学 Q1 ANESTHESIOLOGY Korean Journal of Anesthesiology Pub Date : 2025-02-01 Epub Date: 2024-12-12 DOI:10.4097/kja.24444
Ji-In Park, Hyo-Seok Na, Keum-O Lee, Jung-Hee Ryu, Hyun-Jung Shin
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Abstract

Background: Remimazolam is a novel short-acting benzodiazepine that has recently been used for general anesthesia. This study compared the safety and efficacy of remimazolam-based total intravenous anesthesia (TIVA) and volatile agent-based anesthesia in adults undergoing general anesthesia.

Methods: We searched electronic databases including PubMed, Embase, CENTRAL, and Scopus for relevant studies. The primary outcome was the proportion of patients who experienced hypotension during surgery. Secondary outcomes included incidence of bradycardia, extubation time, duration in the post-anesthesia care unit hospital stay, and incidence of postoperative nausea and/or vomiting (PONV). We estimated the relative risk (RR) and mean difference with 95% CIs using a random-effects model.

Results: A total of 969 patients from 12 randomized controlled trials were included. The incidence of hypotension was 14% and 34% in the remimazolam and volatile agent groups, respectively. Remimazolam significantly lowered the incidence of hypotension (RR: 0.43, 95% CI [0.29-0.63], P = 0.0000, I2 = 26%). The remimazolam group had a PONV incidence of 13%, compared to 28% in the volatile agent group, indicating a significant difference (RR: 0.51, 95% CI [0.37-0.72], P = 0.0001, I2 = 15%). No significant differences were observed in the other outcomes.

Conclusions: Remimazolam-based TIVA demonstrated favorable hemodynamic effects, with a lower incidence of hypotension and similar bradycardia rates, compared to volatile agent-based anesthesia. Furthermore, the reduction in PONV supports the use of remimazolam-based TIVA as a valuable method for general anesthesia.

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比较雷马唑仑全静脉麻醉与挥发性药物麻醉的安全性和有效性:一项随机对照试验的荟萃分析。
背景:雷马唑仑是一种新型短效苯二氮卓类药物,最近被用于全身麻醉。本研究比较了雷马唑仑为基础的全静脉麻醉(TIVA)和挥发性药物为基础的麻醉在成人全身麻醉中的安全性和有效性。方法:检索PubMed、EMBASE、CENTRAL、Scopus等电子数据库进行相关研究。主要结局是手术期间出现低血压的患者比例。次要结局包括心动过缓发生率、拔管时间、麻醉后护理病房(PACU)住院时间、术后恶心和/或呕吐(PONV)发生率。我们使用随机效应模型估计了95% ci的相对风险(RR)和平均差异(MD)。结果:12项随机对照试验共纳入969例患者。雷马唑仑组和挥发剂组低血压发生率分别为14%和34%。雷马唑仑显著降低低血压发生率(RR: 0.43, 95 CI [0.29, 0.63], P = 0.0000, I2 = 26%)。雷马唑仑组PONV发生率为13%,而挥发剂组为28%,差异有统计学意义(RR: 0.51, 95% CI [0.37, 0.72], P = 0.0001, I2 = 15%)。其他结果无显著差异。结论:与挥发性药物麻醉相比,以雷马唑仑为基础的TIVA具有良好的血流动力学效果,低血压发生率较低,心动过缓率相似。此外,PONV的减少支持了以雷马唑仑为基础的TIVA作为一种有价值的全身麻醉方法的使用。
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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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