Phenobarbital Versus Benzodiazepine-Based Pathways for Alcohol Withdrawal Syndrome in Critically Ill Adults: A Systematic Review and Meta-Analysis.

IF 4 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacotherapy Pub Date : 2026-09-01 DOI:10.1002/phar.70197
Zeeshan M Rizwan, Diane Brown, Simone Barry, Kern Guppy, Dana J Gerberi, Ognjen Gajic, Svetlana Herasevich
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引用次数: 0

Abstract

Objective: To compare outcomes of phenobarbital-based versus benzodiazepine-based pathways for alcohol withdrawal syndrome (AWS) in critically ill adults and evaluate whether pathway design and timing of phenobarbital use affect treatment outcomes.

Data sources: A librarian-led search of MEDLINE, Embase, Cochrane Central, CINAHL, Web of Science, Scopus, ClinicalTrials.gov, and the World Health Organization International Clinical Trials Registry Platform was conducted through July 2024, with updates in December 2024, August 2025, and December 2025. Search concepts included phenobarbital, benzodiazepines, and alcohol withdrawal.

Study selection and data extraction: Comparative studies of adults admitted or transferred to an intensive care unit (ICU) with AWS and treated with phenobarbital-based versus benzodiazepine-based pathways were included. Sixteen nonrandomized studies were included in the qualitative synthesis, and 12 treatment-oriented studies were included in the primary meta-analysis. Multiple reviewers independently screened studies, extracted data, and assessed risk of bias using Risk Of Bias In Non-randomized Studies-of Interventions (ROBINS-I).

Data synthesis: Phenobarbital-based pathways were not associated with significantly different intubation (11 studies; odds ratio (OR), 0.62; 95% confidence interval (CI), 0.20-1.87; I2 = 73%) or hospital length of stay (five studies; mean differences [MD], -1.75 days; 95% CI, -5.07 to 1.56; I2 = 63%) compared with benzodiazepine-based pathways. ICU length of stay was shorter with phenobarbital-based pathways (eight studies; MD, -0.60 days; 95% CI, -0.79 to -0.41; I2 = 0%). In exploratory subgroup analyses, front-loaded, protocolized phenobarbital-first pathways were associated with lower intubation and shorter hospital length of stay, but certainty of evidence was very low.

Relevance to patient care and clinical practice: This review distinguishes phenobarbital-first, protocolized ICU pathways from adjunctive or mixed phenobarbital strategies, suggesting that implementation design may influence outcomes.

Conclusions: Although evidence remains very low certainty, these findings suggest that phenobarbital's role in ICU AWS may be pathway dependent. Front-loaded, protocolized phenobarbital-first pathways may be associated with favorable outcomes in exploratory analyses, but these findings should be considered hypothesis-generating and require confirmation in prospective randomized trials.

Trial registration: CRD42024595819.

苯巴比妥与苯二氮卓类药物治疗危重成人酒精戒断综合征的途径:系统回顾和荟萃分析。
目的:比较以苯巴比妥为基础的途径与以苯二氮卓为基础的途径治疗危重成人酒精戒断综合征(AWS)的结果,并评估途径设计和使用苯巴比妥的时机是否影响治疗结果。数据来源:图书馆员主导的MEDLINE、Embase、Cochrane Central、CINAHL、Web of Science、Scopus、ClinicalTrials.gov和世界卫生组织国际临床试验注册平台的搜索持续到2024年7月,更新时间分别为2024年12月、2025年8月和2025年12月。搜索概念包括苯巴比妥、苯二氮卓类药物和酒精戒断。研究选择和数据提取:纳入了以苯巴比妥为基础途径与以苯二氮卓为基础途径治疗的AWS入院或转至重症监护病房(ICU)的成人的比较研究。定性综合纳入16项非随机研究,主要荟萃分析纳入12项以治疗为导向的研究。多名审稿人独立筛选研究,提取数据,并使用非随机干预研究的偏倚风险(ROBINS-I)评估偏倚风险。数据综合:以苯巴比妥为基础的途径与显著不同的插管无关(11项研究,优势比(OR), 0.62;95%置信区间(CI), 0.20-1.87;I2 = 73%)或住院时间(5项研究;平均差异[MD], -1.75天;95% CI, -5.07至1.56;I2 = 63%)与基于苯二氮卓类药物的途径相比。以苯巴比妥为基础的途径的ICU住院时间更短(8项研究;MD, -0.60天;95% CI, -0.79至-0.41;I2 = 0%)。在探索性亚组分析中,预先加载的、协议化的苯巴比妥优先通路与较低的插管率和较短的住院时间相关,但证据的确定性非常低。与患者护理和临床实践的相关性:本综述将苯巴比妥优先、协议化的ICU路径与辅助或混合苯巴比妥策略区分开来,表明实施设计可能会影响结果。结论:尽管证据的确定性仍然很低,但这些发现表明,苯巴比妥在ICU AWS中的作用可能是通路依赖的。在探索性分析中,预先加载的、协议化的苯巴比妥优先途径可能与有利的结果相关,但这些发现应被认为是假设产生的,需要在前瞻性随机试验中得到证实。试验注册:CRD42024595819。
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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来源期刊
Pharmacotherapy
Pharmacotherapy 医学-药学
CiteScore
7.80
自引率
2.40%
发文量
93
审稿时长
4-8 weeks
期刊介绍: Pharmacotherapy is devoted to publication of original research articles on all aspects of human pharmacology and review articles on drugs and drug therapy. The Editors and Editorial Board invite original research reports on pharmacokinetic, bioavailability, and drug interaction studies, clinical trials, investigations of specific pharmacological properties of drugs, and related topics.
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