Phenobarbital Versus Benzodiazepine-Based Pathways for Alcohol Withdrawal Syndrome in Critically Ill Adults: A Systematic Review and Meta-Analysis
- Journal
- Pharmacotherapy (Q1)
- Published
- 1 September 2026
- Study design
- Systematic review / meta-analysis of RCTs
- Evidence level
- Level 1, High (CEBM 1a)
- Authors
- Zeeshan M Rizwan, Diane Brown, Simone Barry, Kern Guppy, Dana J Gerberi, Ognjen Gajic, et al.
- PMID
- 42634386
- DOI
- 10.1002/phar.70197
Why clinicians should know about it
- Picked for Critical Care and Intensive Care Medicine (top studies of the week, 30 August 2026): Phenobarbital vs benzodiazepine pathways for AWS in ICU
- Picked for Pharmacology (medical) (top studies of the week, 30 August 2026): Phenobarbital vs benzodiazepine pathways for alcohol withdrawal
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.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.