Phenobarbital and Alcohol Withdrawal Syndrome: A Systematic Review and Meta-Analysis

Alcohol withdrawal syndrome (AWS) is a complication frequently encountered among patients who are chronic alcohol abusers. It is considered to have a significant impact on the United States healthcare system. It not only has a toll on the healthcare spending but also contributes to significant morbidity and mortality. Benzodiazepines are considered first line in the treatment of AWS. Since patients with alcohol use disorder have downregulated gamma aminobutyric acid (GABA) receptors, this often leads to benzodiazepine resistance. Phenobarbital is also used in the management of alcohol withdrawal syndrome. Here we present a systematic review and meta-analysis of the efficacy and safety of the drug. We conducted an electronic database search for relevant studies published between the inception of the project and November 20, 2022, in three databases, including Medline/PubMed, Embase, and Cochrane Library. Our study included all original studies with prime focus on the baseline characteristics of patients admitted to the intensive care unit (ICU) for alcohol withdrawal syndrome and management/monitoring protocol implemented for its treatment. The primary outcomes that were the focus of our study consisted of changes in the length of hospital stay, length of ICU stay, and changes in scoring systems (for alcohol withdrawal assessment and monitoring) following the implementation of phenobarbital. The secondary outcomes included complications such as intubation and mortality. Based on our analysis, the mean difference in hospital stay was statistically significant at -2.6 (95% CI, -4.48, -0.72, P=0.007) for phenobarbital compared to the benzodiazepine group. We were unable to comment on the heterogeneity in our meta-analysis due to the standard deviation not being reported in one study. There was no statistically significant difference regarding the length of stay in the intensive care unit compared to the control/comparative arm, with a mean difference of -1.17 (95% CI, -1.17, 0.09, P=0.07), with considerable heterogeneity (I2=77%, P=0.002). Our meta-analysis also investigated the risk of intubation between the phenobarbital and the control/comparative group. There was statistically significant difference in the incidence of intubation, relative risk (RR) 0.52 (95% CI, 0.25, 1.08, P=0.08), with considerable heterogeneity (I2=80%, P=0.0001). Our study concludes that phenobarbital is an effective tool in the management of AWS in an ICU setting. However, various studies have reported contradictory results, and vital information appears to be lacking. Moreover, there is a lack of uniformity in terms of phenobarbital dosing. Drug administration should be adapted according to the severity of the symptoms. Further studies need to be conducted discussing the safety profile and adverse effects of the drug when it comes to the management of alcohol withdrawal syndrome.

[1]  P. Shah,et al.  Front-Loaded Versus Low-Intermittent Phenobarbital Dosing for Benzodiazepine-Resistant Severe Alcohol Withdrawal Syndrome , 2022, Journal of Medical Toxicology.

[2]  Julie A. Murphy,et al.  Adjunctive Phenobarbital for Alcohol Withdrawal Syndrome: A Focused Literature Review , 2021, The Annals of pharmacotherapy.

[3]  R. Becher,et al.  Phenobarbital Monotherapy for the Management of Alcohol Withdrawal Syndrome in Surgical-Trauma Patients , 2020, The Annals of pharmacotherapy.

[4]  P. Szumita,et al.  Evaluation of a Phenobarbital-Based Protocol for Severe Alcohol Withdrawal in Critically Ill Patients , 2020, Hospital pharmacy.

[5]  B. Saver,et al.  The ASAM Clinical Practice Guideline on Alcohol Withdrawal Management. , 2020, Journal of addiction medicine.

[6]  S. Lam,et al.  Phenobarbital and symptom-triggered lorazepam versus lorazepam alone for severe alcohol withdrawal in the intensive care unit. , 2020, Alcohol.

[7]  T. Wilens,et al.  Use of Phenobarbital in Alcohol Withdrawal Management - A Retrospective Comparison Study of Phenobarbital and Benzodiazepines for Acute Alcohol Withdrawal Management in General Medical Patients. , 2019, Psychosomatics.

[8]  A. Canonico,et al.  Treatment of Alcohol Withdrawal Syndrome: Phenobarbital vs CIWA‐Ar Protocol , 2018, American journal of critical care : an official publication, American Association of Critical-Care Nurses.

[9]  S. Koenig,et al.  The Safety and Utility of Phenobarbital Use for the Treatment of Severe Alcohol Withdrawal Syndrome in the Medical Intensive Care Unit , 2018, Journal of intensive care medicine.

[10]  S. Kane-Gill,et al.  Patient Outcomes Associated With Phenobarbital Use With or Without Benzodiazepines for Alcohol Withdrawal Syndrome: A Systematic Review , 2017, Hospital pharmacy.

[11]  M. Cohen-Wolkowiez,et al.  Therapeutic Index Estimation of Antiepileptic Drugs: A Systematic Literature Review Approach , 2016, Clinical neuropharmacology.

[12]  Michael C. Thomas,et al.  Barbiturates for the treatment of alcohol withdrawal syndrome: A systematic review of clinical trials. , 2016, Journal of critical care.

[13]  Machelle D. Wilson,et al.  Alcohol withdrawal syndrome in critically ill patients: Protocolized versus nonprotocolized management , 2014, The journal of trauma and acute care surgery.

[14]  B. Bharadwaj,et al.  Clinical management of alcohol withdrawal: A systematic review , 2013, Industrial psychiatry journal.

[15]  D. Moher,et al.  Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement , 2009, BMJ : British Medical Journal.

[16]  M. Enoch The role of GABAA receptors in the development of alcoholism , 2008, Pharmacology Biochemistry and Behavior.

[17]  Lewis S. Nelson,et al.  A strategy of escalating doses of benzodiazepines and phenobarbital administration reduces the need for mechanical ventilation in delirium tremens* , 2007, Critical care medicine.

[18]  Thomas R Kosten,et al.  Management of drug and alcohol withdrawal. , 2003, The New England journal of medicine.

[19]  R. Levy,et al.  Kinetics of phenobarbital in normal subjects and epileptic patients , 2004, European Journal of Clinical Pharmacology.