Seizure Occurring During Baclofen Monotherapy for Phenibut Withdrawal.

IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Clinical Neuropharmacology Pub Date : 2023-03-01 DOI:10.1097/WNF.0000000000000542
Amber Patt, Haley Fox, Lauren Wells, Jillian Theobald, Ryan Feldman
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Abstract

Objective: Phenibut is a widely available gamma-aminobutyric acid B receptor agonist. When taken chronically, phenibut causes dependence and subsequent withdrawal if stopped. Baclofen, a gamma-aminobutyric acid B receptor agonist structurally related to phenibut, has been used to manage phenibut withdrawal (PW), although baclofen doses for PW are not well defined and may exceed Food and Drug Administration-approved doses. Little data described outcomes from baclofen use.

Methods: This case details a patient who experienced a seizure while on baclofen 10 mg thrice daily as monotherapy for PW and highlights a potential risk of underdosing baclofen as monotherapy in the management of PW.

Results: A man in his early 30s with anxiety, depression, and substance use disorder presented to the emergency department by family for lethargy and confusion starting earlier that day. He had been using 25-30 g of phenibut daily for the past 6 months. On arrival, he was hypertensive, tachycardic, tachypneic, and lethargic. The patient received 1 mg of intravenous lorazepam and was admitted to the hospital for presumed PW. His symptoms improved overnight, and he was discharged on 10 mg of baclofen thrice daily. He returned 28 hours later after having a seizure and required intensive care admission in addition to multimodal drug therapy.

Conclusions: Phenibut use is rising, and treatment options for PW, such as baclofen, warrant additional study. Potential risks of underdosing baclofen if used as monotherapy in PW may include seizures as withdrawal progresses. Baclofen's role in therapy may be more appropriate as an adjunct than a cornerstone of therapy. Treatment done in consultation with providers experienced in managing withdrawal such as a toxicologist may help reduce this risk.

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巴氯芬单药治疗戒断非尼特期间发生的癫痫发作。
目的:苯乙酯是一种广泛应用的γ -氨基丁酸B受体激动剂。长期服用时,苯可引起依赖性,如果停止服用则会引起戒断。巴氯芬是一种与非尼布结构相关的γ -氨基丁酸B受体激动剂,已被用于治疗非尼布戒断(PW),尽管巴氯芬治疗PW的剂量尚未明确界定,可能超过美国食品和药物管理局批准的剂量。很少有数据描述使用巴氯芬的结果。方法:本病例详细介绍了一名患者在服用巴氯芬10mg,每日三次单药治疗PW时癫痫发作的情况,并强调了巴氯芬单药治疗PW的潜在风险。结果:一名30岁出头的男性,患有焦虑、抑郁和药物使用障碍,当天早些时候,家人因嗜睡和神志不清而来到急诊室。在过去的6个月里,他每天服用25-30克的菲尼布特。到达时,他有高血压、心动过速、呼吸过速和昏睡。患者接受1毫克劳拉西泮静脉注射,并因推测为PW而入院。他的症状在一夜之间有所改善,出院时给予每日三次10毫克的巴氯芬。他在癫痫发作28小时后返回医院,除多模式药物治疗外,还需要重症监护。结论:非尼布的使用正在增加,治疗PW的选择,如巴氯芬,值得进一步研究。如果单药治疗PW,巴氯芬剂量不足的潜在风险可能包括随着戒断进展而发作。巴氯芬在治疗中的作用可能更适合作为辅助治疗而不是治疗的基石。与毒理学家等有戒断反应管理经验的提供者协商治疗可能有助于降低这种风险。
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来源期刊
Clinical Neuropharmacology
Clinical Neuropharmacology 医学-临床神经学
CiteScore
1.20
自引率
10.00%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Clinical Neuropharmacology is a peer-reviewed journal devoted to the pharmacology of the nervous system in its broadest sense. Coverage ranges from such basic aspects as mechanisms of action, structure-activity relationships, and drug metabolism and pharmacokinetics, to practical clinical problems such as drug interactions, drug toxicity, and therapy for specific syndromes and symptoms. The journal publishes original articles and brief reports, invited and submitted reviews, and letters to the editor. A regular feature is the Patient Management Series: in-depth case presentations with clinical questions and answers.
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