Remimazolam for procedural sedation

医学 镇静 咪唑安定 麻醉 安慰剂 相对风险 子群分析 置信区间 随机对照试验 异丙酚 不利影响 外科 内科学 替代医学 病理
作者
Lasse Stehr‐Pingel,Mathias Maagaard,Casper D. Tvarnø,S Sörenson,Shaheer Bukhari,Lars Peter Kloster Andersen,Jakob Hessel Andersen,Ole Mathiesen
出处
期刊:European Journal of Anaesthesiology [Lippincott Williams & Wilkins]
卷期号:42 (4): 298-312
标识
DOI:10.1097/eja.0000000000002126
摘要

BACKGROUND Midazolam and propofol are frequently used for procedural sedation. Remimazolam may provide a more controllable sedation with fewer adverse effects. OBJECTIVE To assess the sedation success rate and respiratory and cardiovascular complications of remimazolam versus placebo and other sedatives in adults undergoing procedural sedation. DESIGN A systematic review of randomised controlled trials (RCTs) with meta-analyses, trial sequential analyses (TSA), and GRADE evaluations of the certainty of evidence. DATA SOURCES We searched Medline, Embase, CENTRAL, BIOSIS, CINAHL, and Web of Science Core Collection from their inception to 22 June 2024. ELIGIBILITY CRITERIA RCTs allocating participants undergoing procedural sedation to remimazolam versus placebo or any active comparator. RESULTS We included 63 trials randomising 13 953 participants. All included trial results were judged to be at high risk of bias. The sedation success rate was similar with remimazolam versus active comparators, relative risk (RR) 1.04, [97.5% confidence interval (CI), 0.96 to 1.14; TSA-adjusted CI, 0.95 to 1.18], P = 0.26, GRADE: very low. Subgroup analyses indicated that remimazolam versus midazolam increased sedation success rate, while the risks were similar with remimazolam versus comparators. Remimazolam versus active comparators decreased the risk of respiratory complications, RR 0.47, (97.5% CI, 0.36 to 0.61; TSA-adjusted CI, 0.35 to 0.61), P < 0.01; and cardiovascular complications, RR 0.46, (97.5% CI, 0.37 to 0.56; TSA-adjusted CI, 0.38 to 0.57), P < 0.01. Subgroup analyses indicated that remimazolam versus propofol reduced respiratory and cardiovascular complications, while the risks were similar versus midazolam. CONCLUSION Remimazolam seems to provide a similar sedation success rate as other active comparators (propofol, ciprofol, midazolam, dexmedetomidine, etomidate), although subgroup analyses indicated that remimazolam increased sedation success rate compared to midazolam. Remimazolam compared to propofol may decrease the risk of respiratory and cardiovascular complications. The certainty of the evidence was very low to low, and firm conclusions could not be drawn.
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