Comparative efficacy of remifentanil and fentanyl in mechanically ventilated ICU patients: a systematic review and meta-analysis on ventilation duration and delirium incidence.

IF 3.1
Hiromu Okano, Eriya Imai, Hiroshi Okamoto, Masaaki Sakuraya, Yoshitaka Aoki, Shun Muramatsu, Misa Kitamura, Tsutomu Yamazaki, Yuki Kataoka
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引用次数: 0

Abstract

Background: The ultrashort-acting properties and organ-independent metabolism of remifentanil may be advantageous in mechanical ventilation management. Unlike fentanyl, which accumulates over time and may prolong sedation, remifentanil enables more predictable titration and rapid weaning. This study aimed to determine the effect of remifentanil on shortening the duration of mechanical ventilation in comparison with fentanyl in adult intensive care unit (ICU) patients.

Methods: A systematic review and meta-analysis was conducted, including randomised controlled trials (RCTs) and observational studies from MEDLINE, Cochrane, EMBASE, ICTRP, and ClinicalTrials.gov, from inception to July 2024. Studies comparing remifentanil with fentanyl in mechanically ventilated ICU patients were included, whereas those that used only remifentanil or fentanyl intraoperatively were excluded. The primary outcome was ventilation duration, with a minimal important difference (MID) of 90 min. A random-effects meta-analysis was performed and the certainty of evidence was assessed using the GRADE approach. The risk of bias was evaluated using RoB 2.0 and ROBINS-I tools.

Results: We included 18 studies (14 RCTs and 4 observational studies). Ten studies (8 RCTs and 2 observational studies; 901 patients) were analysed. Remifentanil may reduce ventilation duration compared to fentanyl (8 RCTs: MD -6.70 h, 95% CI -14.36 to 0.97; low certainty; 2 observational studies: MD -21.26 h, 95% CI -37.29 to -5.24; low certainty).

Conclusions: Remifentanil may reduce the duration of mechanical ventilation, potentially improving patient outcomes. However, owing to the low certainty of the evidence and study heterogeneity, further high-quality RCTs are required to validate these findings.

Trial registration: PROSPERO 2024 and CRD42024557414.

瑞芬太尼与芬太尼在ICU机械通气患者中的比较疗效:通气时间与谵妄发生率的系统回顾与meta分析。
背景:瑞芬太尼的超短效特性和不依赖于器官的代谢可能有利于机械通气管理。与芬太尼不同,芬太尼会随着时间的推移而积累,并可能延长镇静时间,瑞芬太尼可以实现更可预测的滴定和快速脱机。本研究旨在确定瑞芬太尼与芬太尼在缩短成人重症监护病房(ICU)患者机械通气时间方面的效果。方法:系统回顾和荟萃分析,包括随机对照试验(rct)和观察性研究,来自MEDLINE、Cochrane、EMBASE、ICTRP和ClinicalTrials.gov,从成立到2024年7月。比较瑞芬太尼和芬太尼在机械通气ICU患者中的应用的研究被纳入,而那些术中仅使用瑞芬太尼或芬太尼的研究被排除。主要结局为通气时间,最小重要差异(MID)为90分钟。进行随机效应荟萃分析,并使用GRADE方法评估证据的确定性。使用rob2.0和ROBINS-I工具评估偏倚风险。结果:纳入18项研究(14项随机对照试验和4项观察性研究)。10项研究(8项随机对照试验和2项观察性研究;901例患者)进行分析。与芬太尼相比,瑞芬太尼可能缩短通气时间(8项随机对照试验:MD -6.70 h, 95% CI -14.36至0.97;低确定性;2项观察性研究:MD -21.26 h, 95% CI -37.29 ~ -5.24;低确定性)。结论:瑞芬太尼可能减少机械通气的持续时间,潜在地改善患者的预后。然而,由于证据的低确定性和研究的异质性,需要进一步的高质量随机对照试验来验证这些发现。试验注册:PROSPERO 2024和CRD42024557414。
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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