Effect of level of sedation on outcomes in critically ill adult patients: a systematic review of clinical trials with meta-analysis and trial sequential analysis.

IF 9.6 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL EClinicalMedicine Pub Date : 2024-03-28 eCollection Date: 2024-05-01 DOI:10.1016/j.eclinm.2024.102569
Ameldina Ceric, Johan Holgersson, Teresa L May, Markus B Skrifvars, Johanna Hästbacka, Manoj Saxena, Anders Aneman, Anthony Delaney, Michael C Reade, Candice Delcourt, Janus Christian Jakobsen, Niklas Nielsen
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Abstract

Background: Sedation is routinely administered to critically ill patients to alleviate anxiety, discomfort, and patient-ventilator asynchrony. However, it must be balanced against risks such as delirium and prolonged intensive care stays. This study aimed to investigate the effects of different levels of sedation in critically ill adults.

Methods: Systematic review with meta-analysis and trial sequential analysis (TSA) of randomised clinical trials including critically ill adults admitted to the intensive care unit. CENTRAL, MEDLINE, Embase, LILACS, and Web of Science were searched from their inception to 13 June 2023. Risks of bias were assessed using the Cochrane risk of bias tool. Primary outcome was all-cause mortality. Aggregate data were synthesised with meta-analyses and TSA, and the certainty of the evidence was assessed using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) approach. This study is registered with PROSPERO: CRD42023386960.

Findings: Fifteen trials randomising 4352 patients were included, of which 13 were assessed high risk of bias. Meta-analyses comparing lighter to deeper sedation showed no evidence of a difference in all-cause mortality (risk ratio (RR) 0.94, 95% confidence interval (CI) 0.83-1.06; p = 0.28; 15 trials; moderate certainty evidence), serious adverse events (RR 0.99, CI 0.92-1.06; p = 0.80; 15 trials; moderate certainty evidence), or delirium (RR 1.01, 95% CI 0.94-1.09; p = 0.78; 11 trials; moderate certainty evidence). TSA showed that when assessing mortality, a relative risk reduction of 16% or more between the compared interventions could be rejected.

Interpretation: The level of sedation has not been shown to affect the risks of death, delirium, and other serious adverse events in critically ill adult patients. While TSA suggests that additional trials are unlikely to significantly change the conclusion of the meta-analyses, the certainty of evidence was moderate. This suggests a need for future high-quality studies with higher methodological rigor.

Funding: None.

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镇静水平对重症成人患者预后的影响:临床试验系统回顾及荟萃分析和试验序列分析。
背景:重症患者通常会使用镇静剂来缓解焦虑、不适和患者与呼吸机的不同步。然而,镇静必须与谵妄和延长重症监护时间等风险相平衡。本研究旨在调查不同程度的镇静剂对成人重症患者的影响:方法:对包括重症监护室收治的成人重症患者在内的随机临床试验进行系统回顾、荟萃分析和试验序列分析(TSA)。对 CENTRAL、MEDLINE、Embase、LILACS 和 Web of Science 进行了检索,检索时间从开始至 2023 年 6 月 13 日。使用 Cochrane 偏倚风险工具评估偏倚风险。主要结果为全因死亡率。通过荟萃分析和TSA对总体数据进行综合,并采用建议、评估、发展和评价分级(GRADE)方法对证据的确定性进行评估。本研究已在 PROSPERO 注册:CRD42023386960.研究结果:研究结果:共纳入了 15 项试验,随机抽取了 4352 名患者,其中 13 项被评估为高偏倚风险。比较轻度镇静与深度镇静的 Meta 分析表明,没有证据表明两者在全因死亡率(风险比 (RR)0.94,95% 置信区间 (CI)0.83-1.06;P = 0.28;15 项试验;中等确定性证据)、严重不良事件(RR 0.99,CI 0.92-1.06;P = 0.80;15 项试验;中等确定性证据)或谵妄(RR 1.01,95% CI 0.94-1.09;P = 0.78;11 项试验;中等确定性证据)方面存在差异。TSA显示,在评估死亡率时,可以拒绝比较干预措施之间16%或更高的相对风险降低:解释:镇静程度尚未被证明会影响重症成年患者的死亡、谵妄和其他严重不良事件的风险。虽然TSA表明额外的试验不太可能显著改变荟萃分析的结论,但证据的确定性为中等。这表明今后需要进行方法更严谨的高质量研究:无。
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来源期刊
EClinicalMedicine
EClinicalMedicine Medicine-Medicine (all)
CiteScore
18.90
自引率
1.30%
发文量
506
审稿时长
22 days
期刊介绍: eClinicalMedicine is a gold open-access clinical journal designed to support frontline health professionals in addressing the complex and rapid health transitions affecting societies globally. The journal aims to assist practitioners in overcoming healthcare challenges across diverse communities, spanning diagnosis, treatment, prevention, and health promotion. Integrating disciplines from various specialties and life stages, it seeks to enhance health systems as fundamental institutions within societies. With a forward-thinking approach, eClinicalMedicine aims to redefine the future of healthcare.
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