The Safety of Alcohol Pharmacotherapies in Pregnancy: A Scoping Review of Human and Animal Research.

IF 7.4 2区 医学 Q1 CLINICAL NEUROLOGY CNS drugs Pub Date : 2024-10-10 DOI:10.1007/s40263-024-01126-8
Ebony Quintrell, Danielle J Russell, Sofa Rahmannia, Caitlin S Wyrwoll, Alexander Larcombe, Erin Kelty
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Abstract

Background and objective: Alcohol pharmacotherapies pose unknown teratogenic risks in pregnancy and are therefore recommended to be avoided. This limits treatment options for pregnant individuals with alcohol use disorders (AUD). The information on the safety of these medications during pregnancy is uncertain, prompting a scoping review. The objective of this review was to investigate available information on the safety of alcohol pharmacotherapies in pregnancy.

Methods: Studies published between January 1990 and July 2023 were identified through searches in BIOSIS, Embase, PsycINFO and MEDLINE databases, using terms related to pregnancy and alcohol pharmacotherapies. The alcohol pharmacotherapies investigated were naltrexone, acamprosate, disulfiram, nalmefene, baclofen, gabapentin and topiramate. Studies were screened by two independent reviewers. Covidence software facilitated the management, screening and extraction of studies.

Results: A total of 105 studies were included in the review (naltrexone: 21, acamprosate: 4, disulfiram: 3, baclofen: 3, nalmefene: 0, topiramate: 55, gabapentin: 32) with some studies investigating multiple medications. Studies investigating naltrexone's safety in pregnancy focussed on opioid use disorders, with limited evidence regarding its safety in the context of AUD. Despite concerns about higher rates of some pregnancy complications, studies generally indicate naltrexone as a safer option compared with opioid agonists or alcohol during pregnancy. Acamprosate was not clearly associated with adverse effects of exposure in pregnancy, with two pre-clinical studies suggesting potential neuroprotective properties. Disulfiram has a high risk of congenital anomalies when used in pregnancy, believed to be due to its mechanism of action. Prenatal topiramate has also been associated with an increased risk of congenital anomalies, particularly oral clefts. There were mixed results concerning the safety of prenatal gabapentin and little to no literature investigating the safety of baclofen or nalmefene during pregnancy.

Conclusions: There is insufficient research on the safety of alcohol pharmacotherapies in pregnancy. Despite this, given alcohol's teratogenic effects, naltrexone could be considered to help maintain abstinence in pregnant individuals with AUD, particularly when psychosocial treatments have failed.

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妊娠期酒精药物治疗的安全性:人类和动物研究范围综述》。
背景和目的:酒精药物治疗在妊娠期具有未知的致畸风险,因此建议避免使用。这限制了妊娠期酒精使用障碍(AUD)患者的治疗选择。有关这些药物在孕期安全性的信息尚不确定,因此需要进行一次范围界定综述。本综述旨在调查有关妊娠期酒精药物治疗安全性的现有信息:通过在 BIOSIS、Embase、PsycINFO 和 MEDLINE 数据库中使用与妊娠和酒精药物疗法相关的术语进行检索,确定了 1990 年 1 月至 2023 年 7 月间发表的研究。调查的酒精药物疗法包括纳曲酮、安体舒通、双硫仑、纳美芬、巴氯芬、加巴喷丁和托吡酯。研究报告由两名独立审稿人进行筛选。Covidence 软件为研究的管理、筛选和提取提供了便利:共有 105 项研究被纳入综述(纳曲酮:21 项,阿坎酸:4 项,双硫仑:4 项):4、双硫仑3、巴氯芬:3、纳美芬:0、托吡酯:55、加巴喷丁:32),其中一些研究涉及多种药物。有关纳曲酮在妊娠期安全性的研究主要集中在阿片类药物使用障碍方面,有关其在 AUD 方面安全性的证据有限。尽管人们担心某些妊娠并发症的发生率较高,但研究普遍表明,与阿片类受体激动剂或酒精相比,纳曲酮在妊娠期间是一种更安全的选择。阿坎酸(Acamprosate)与妊娠期接触的不良影响并无明显关联,两项临床前研究表明其具有潜在的神经保护特性。妊娠期使用双硫仑会有很高的先天性畸形风险,这被认为是其作用机制所致。产前服用托吡酯也会增加先天性畸形的风险,尤其是口腔裂缝。有关产前加巴喷丁安全性的研究结果不一,几乎没有文献调查巴氯芬或纳美芬在妊娠期间的安全性:有关妊娠期酒精药物治疗安全性的研究不足。尽管如此,考虑到酒精的致畸作用,可以考虑使用纳曲酮来帮助患有 AUD 的孕妇维持戒酒,尤其是在社会心理治疗无效的情况下。
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来源期刊
CNS drugs
CNS drugs 医学-精神病学
CiteScore
12.00
自引率
3.30%
发文量
82
审稿时长
6-12 weeks
期刊介绍: CNS Drugs promotes rational pharmacotherapy within the disciplines of clinical psychiatry and neurology. The Journal includes: - Overviews of contentious or emerging issues. - Comprehensive narrative reviews that provide an authoritative source of information on pharmacological approaches to managing neurological and psychiatric illnesses. - Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. - Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in neurology and psychiatry. - Original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in CNS Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
期刊最新文献
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