Pharmacologic Interventions to Prevent Delirium in Trauma Patients: A Systematic Review and Network Meta-Analysis of Randomized Controlled Trials.

Gabriele Zitikyte, Danielle C Roy, Alexandre Tran, Shannon M Fernando, Erin Rosenberg, Salmaan Kanji, Paul T Engels, George A Wells, Christian Vaillancourt
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Abstract

To compare the relative efficacy of pharmacologic interventions in the prevention of delirium in ICU trauma patients.

Data sources: We searched Medical Literature Analysis and Retrieval System Online, Embase, and Cochrane Registry of Clinical Trials from database inception until June 7, 2022. We included randomized controlled trials comparing pharmacologic interventions in critically ill trauma patients.

Study selection: Two reviewers independently screened studies for eligibility, extracted data, and assessed risk of bias.

Data extraction: Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines for network analysis were followed. Random-effects models were fit using a Bayesian approach to network meta-analysis. Between-group comparisons were estimated using hazard ratios (HRs) for dichotomous outcomes and mean differences for continuous outcomes, each with 95% credible intervals. Treatment rankings were estimated for each outcome in the form of surface under the cumulative ranking curve values.

Data synthesis: A total 3,541 citations were screened; six randomized clinical trials (n = 382 patients) were included. Compared with combined propofol-dexmedetomidine, there may be no difference in delirium prevalence with dexmedetomidine (HR 1.44, 95% CI 0.39-6.94), propofol (HR 2.38, 95% CI 0.68-11.36), nor haloperidol (HR 3.38, 95% CI 0.65-21.79); compared with dexmedetomidine alone, there may be no effect with propofol (HR 1.66, 95% CI 0.79-3.69) nor haloperidol (HR 2.30, 95% CI 0.88-6.61).

Conclusions: The results of this network meta-analysis suggest that there is no difference found between pharmacologic interventions on delirium occurrence, length of ICU stay, length of hospital stay, or mortality, in trauma ICU patients.

Abstract Image

Abstract Image

预防创伤患者谵妄的药物干预:随机对照试验的系统回顾和网络荟萃分析。
目的比较不同药物干预预防ICU创伤患者谵妄的相对疗效。数据来源:从数据库建立到2022年6月7日,我们检索了Medical Literature Analysis and Retrieval System Online、Embase和Cochrane Registry of Clinical Trials。我们纳入了比较危重创伤患者的药物干预的随机对照试验。研究选择:两位审稿人独立筛选研究的合格性、提取数据并评估偏倚风险。数据提取:遵循系统评价的首选报告项目和网络分析的元分析指南。随机效应模型使用贝叶斯方法进行网络元分析。组间比较采用二分类结果的风险比(hr)和连续结果的平均差异来估计,每个结果都有95%的可信区间。在累积排名曲线值下以曲面的形式估计每个结果的治疗排名。数据综合:共筛选了3541篇引文;纳入6项随机临床试验(n = 382例)。与异丙酚-右美托咪定联合用药相比,右美托咪定(HR 1.44, 95% CI 0.39-6.94)、异丙酚(HR 2.38, 95% CI 0.68-11.36)和氟哌啶醇(HR 3.38, 95% CI 0.65-21.79)在谵妄患病率方面可能没有差异;与单独使用右美托咪定相比,异丙酚(HR 1.66, 95% CI 0.79-3.69)和氟哌啶醇(HR 2.30, 95% CI 0.88-6.61)可能没有影响。结论:该网络荟萃分析的结果表明,在创伤ICU患者中,药物干预对谵妄发生、ICU住院时间、住院时间或死亡率没有差异。
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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