Impact of Gabapentin as a Benzodiazepine-Sparing Medication During Acute Alcohol Withdrawal.

IF 4 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacotherapy Pub Date : 2025-11-01 Epub Date: 2025-11-11 DOI:10.1002/phar.70074
William G Cordell, Leah A Surbaugh, Kelsey Inman, Dennis Grauer, Megan Stewart, Jace Knutson
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引用次数: 0

Abstract

Background: Abrupt cessation of alcohol consumption after prolonged periods of use leaves patients at risk for experiencing withdrawal symptoms. Alcohol is a central nervous system depressant that increases the activity of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) and suppresses the activity of the excitatory neurotransmitter glutamate. Stopping consumption of alcohol reduces this inhibitory response and leads to a net excitatory state and symptoms of withdrawal, including anxiety, tremors, and even seizures. Benzodiazepines have traditionally been the treatment of choice for patients with alcohol withdrawal. Gabapentin has recently been studied as an adjunctive agent for the treatment and prevention of alcohol withdrawal, given its structural similarity to GABA and lower risk for dependence compared with benzodiazepines.

Objective: The primary objective of this study was to determine if a gabapentin-based regimen is benzodiazepine-sparing in patients experiencing alcohol withdrawal.

Methods: This was a retrospective, single center, pre- and post-implementation analysis of a gabapentin taper-based alcohol withdrawal protocol in place of a traditional benzodiazepine-based protocol used in patients admitted to a large, urban academic medical center in the Midwest for alcohol withdrawal between January 1, 2017, and January 1, 2023. The primary outcome was a comparison of cumulative benzodiazepine dose (in lorazepam equivalents) received throughout admission between groups.

Results: This study included 200 patients with 100 patients in each of the pre- and post-implementation groups. Baseline characteristics were similar between groups except for baseline serum alcohol level, which was higher in the pre-implementation group. Patients in the post-implementation group on average were exposed to 9.7-mg lorazepam equivalents during admission compared with 22.8-mg lorazepam equivalents in the pre-implementation group (p = 0.001). Patients between groups had similar symptom progression as characterized by average daily alcohol withdrawal assessment scale (AWAS) scores and length of stay.

Conclusion: Utilization of a gabapentin taper resulted in significantly lower cumulative exposure to benzodiazepines and similar clinical outcomes in patients admitted for acute alcohol withdrawal.

加巴喷丁作为苯二氮卓类药物在急性酒精戒断中的影响。
背景:长时间饮酒后突然停止饮酒使患者有出现戒断症状的危险。酒精是一种中枢神经系统抑制剂,可增加抑制性神经递质γ -氨基丁酸(GABA)的活性,抑制兴奋性神经递质谷氨酸的活性。停止饮酒会减少这种抑制反应,导致净兴奋状态和戒断症状,包括焦虑、颤抖,甚至癫痫发作。传统上,苯二氮卓类药物是酒精戒断患者的治疗选择。由于加巴喷丁的结构与GABA相似,且与苯二氮卓类药物相比,其依赖风险较低,因此最近研究了加巴喷丁作为治疗和预防酒精戒断的辅助药物。目的:本研究的主要目的是确定以加巴喷丁为基础的方案是否对酒精戒断患者节省苯二氮卓类药物。方法:对2017年1月1日至2023年1月1日在中西部一家大型城市学术医疗中心接受酒精戒断治疗的患者进行回顾性、单中心、实施前和实施后分析,以加巴喷丁逐渐减少的酒精戒断方案取代传统的苯二氮卓类药物戒断方案。主要结局是比较两组在入院期间接受的累积苯二氮卓剂量(劳拉西泮当量)。结果:本研究纳入200例患者,实施前后组各100例。除了实施前组的基线血清酒精水平较高外,各组之间的基线特征相似。实施后组患者入院时平均暴露于9.7 mg劳拉西泮当量,而实施前组为22.8 mg劳拉西泮当量(p = 0.001)。两组患者的症状进展相似,以平均每日酒精戒断评估量表(AWAS)评分和住院时间为特征。结论:在急性酒精戒断患者中,使用加巴喷丁可显著降低苯二氮卓类药物的累积暴露,并具有相似的临床结果。
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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