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老年患者程序性镇静中使用瑞米唑仑:一项采用试验序贯分析的系统评价和荟萃分析

Remimazolam for Procedural Sedation in Older Patients: A Systematic Review and Meta-Analysis with Trial Sequential Analysis.

作者信息

Lee Myeongjong, Lee Cheol, Choi Guen Joo, Kang Hyun

机构信息

Department of Anesthesiology and Pain Medicine, Research Institute of Medical Science, Konkuk University Medical School, 82 Guwondae-ro, Chungju 27376, Republic of Korea.

Department of Anesthesiology and Pain Medicine, Wonkwang University School of Medicine, 895 Muwang-ro, Iksan 54538, Republic of Korea.

出版信息

J Pers Med. 2024 Feb 29;14(3):276. doi: 10.3390/jpm14030276.

Abstract

This systematic review and meta-analysis with trial sequential analysis (TSA) aimed to evaluate the efficacy and safety of remimazolam compared to other sedatives for procedural sedation in older patients. We registered the protocol of this systematic review and meta-analysis with TSA in the PROSPERO network (CRD42023441209). Two investigators performed a systematic, comprehensive, and independent search of the PubMed, EMBASE, and Cochrane Central Register of Controlled Trials databases to identify randomized controlled trials (RCTs) comparing remimazolam with other sedatives in older patients undergoing procedural sedation. Conventional meta-analysis and TSA were also performed. Seven RCTs (1502 patients) were included. Pooled results demonstrated that remimazolam was associated with a low incidence of hypoxemia, hypotension, bradycardia, respiratory depression, and injection pain. Remimazolam also required a long time to cause loss of consciousness. There were no differences in rates of sedation success, dizziness/headache, postoperative nausea and vomiting, or recovery time. Older patients receiving procedural sedation with remimazolam had a lower risk of hypoxemia, hypotension, bradycardia, respiratory depression, and injection pain than those receiving other sedatives, suggesting that remimazolam may be more suitable for procedural sedation in older patients.

摘要

本项采用试验序贯分析(TSA)的系统评价和荟萃分析旨在评估与其他镇静剂相比,瑞马唑仑用于老年患者程序性镇静的疗效和安全性。我们在PROSPERO网络(CRD42023441209)中注册了本系统评价和采用TSA的荟萃分析方案。两名研究者对PubMed、EMBASE和Cochrane对照试验中央注册库数据库进行了系统、全面且独立的检索,以识别比较瑞马唑仑与其他镇静剂用于接受程序性镇静的老年患者的随机对照试验(RCT)。同时还进行了传统的荟萃分析和TSA。纳入了7项RCT(1502例患者)。汇总结果表明,瑞马唑仑与低氧血症、低血压、心动过缓、呼吸抑制和注射痛的发生率较低相关。瑞马唑仑导致意识丧失也需要较长时间。镇静成功率、头晕/头痛、术后恶心和呕吐或恢复时间方面没有差异。接受瑞马唑仑程序性镇静的老年患者发生低氧血症、低血压、心动过缓、呼吸抑制和注射痛的风险低于接受其他镇静剂的患者,这表明瑞马唑仑可能更适合老年患者的程序性镇静。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3f4/10971009/b9fe11e39e08/jpm-14-00276-g001.jpg

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