Effectiveness of Gabapentin as a Benzodiazepine-Sparing Agent in Alcohol Withdrawal Syndrome

Author:

Alzghoul Hamza1,Al-Said Mohammed I.2ORCID,Obeidat Omar3,Al-Ani Hashim3,Tarawneh Mohammad3ORCID,Meadows Robyn4,Youness Houssein5ORCID,Reddy Raju6,Al-Jafari Mohammad7ORCID,Alzghoul Bashar N.8,Khan Akram6ORCID

Affiliation:

1. Graduate Medical Education, University of Central Florida College of Medicine, Orlando, FL 32816, USA

2. Department of Pharmacy, HCA Florida North Florida Hospital, 6500 W Newberry Rd, Gainesville, FL 32605, USA

3. Internal Medicine Residency Program, HCA Florida North Florida Hospital, 6500 W Newberry Rd, Gainesville, FL 32605, USA

4. Graduate Medical Education, HCA Healthcare, Brentwood, TN 37027, USA

5. Section of Pulmonary, Critical Care and Sleep Medicine, The Oklahoma City VA Health Care System and The University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA

6. Department of Internal Medicine, Oregon Health and Science University, Portland, OR 97239, USA

7. Faculty of Medicine, Mutah University, Al-Karak 61710, Jordan

8. Division of Pulmonary, Critical Care and Sleep Medicine, University of Florida, Gainesville, FL 32608, USA

Abstract

Background and Objectives: Gabapentin has shown promise as a potential agent for the treatment of alcohol withdrawal syndrome. We aimed to evaluate the effectiveness of gabapentin as a benzodiazepine-sparing agent in patients undergoing alcohol withdrawal treatment in all the hospitals of a large tertiary healthcare system. Materials and Methods: Medical records of patients admitted to the hospital for alcohol withdrawal management between 1 January 2020 and 31 August 2022 were reviewed. Patients were divided into two cohorts: benzodiazepine-only treatment who received benzodiazepines as the primary pharmacotherapy and gabapentin adjunctive treatment who received gabapentin in addition to benzodiazepines. The outcomes assessed included the total benzodiazepine dosage administered during the treatment and the length of hospital stay. The statistical models were calibrated to account for various factors. Results: A total of 4364 patients were included in the final analysis. Among these, 79 patients (1.8%) received gabapentin in addition to benzodiazepines, and 4285 patients (98.2%) received benzodiazepines only. Patients administered gabapentin required significantly lower average cumulative benzodiazepine dosages, approximately 17.9% less, compared to those not receiving gabapentin (median 2 mg vs. 4 mg of lorazepam equivalent dose (p < 0.01)). However, there were no significant differences in outcomes between the two groups. Conclusions: Our findings demonstrate that using gabapentin with benzodiazepine was associated with a reduction in the cumulative benzodiazepine dosage for alcohol withdrawal. Considering gabapentin as an adjunctive therapy holds promise for patients with comorbidities who could benefit from reducing benzodiazepine dose. This strategy warrants further investigation.

Publisher

MDPI AG

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