Valproic Acid-Induced Congenital Disorders, an Analysis in EudraVigilance and a Literature Review of Valproic Acid Utilization During Pregnancy.

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Mădălina Hurubă, Andreea Farcaș, Daniel Leucuța, Cristina Mogoșan
{"title":"Valproic Acid-Induced Congenital Disorders, an Analysis in EudraVigilance and a Literature Review of Valproic Acid Utilization During Pregnancy.","authors":"Mădălina Hurubă, Andreea Farcaș, Daniel Leucuța, Cristina Mogoșan","doi":"10.1002/pds.70134","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Valproic acid (VPA) is known to increase the risk of congenital malformations during pregnancy. We evaluated VPA-induced congenital disorder reports in EudraVigilance (EV), before and after the most recent EU risk minimization recommendations in 2018, and conducted a literature review of studies capturing pregnancy exposure data to VPA.</p><p><strong>Methods: </strong>EV public database of reports was searched for congenital ADRs for VPA, between Jan 2013 and Jun 2023. Descriptive analysis was performed to evaluate demographic data, year trends, outcomes, indications, and concomitant folic acid. A structured review of the literature based on explicit key words and eligibility criteria was conducted in PubMed and EU PAS Register (now HMA-EMA Catalogue for RWD sources) to capture pregnancy exposure to VPA. Data on study design, objectives, and results, particularly pregnancy exposure, were extracted.</p><p><strong>Results: </strong>A total of 2021 reports containing 3210 VPA-induced congenital disorders were identified (2068 congenital malformations, 634 neural tube defects, 614 cardiac malformations). Most ages reported were between 0 and 1 months (n, 387) and for the male sex (n, 833). Generally, the outcome was \"not recovered/not resolved,\" with 2.8% fatal ADRs reported. The number of reports slightly decreased through the years (lowest in 2015 [n, 154]; highest in 2013 [n, 669]). The literature review included 24 eligible studies, depicting varying levels of pregnancy exposure depending on the study aims and population, with an overall vast heterogeneity in presenting the study results.</p><p><strong>Conclusions: </strong>The number of VPA-induced congenital disorder reports slightly decreased. Despite absolute contraindications, pregnancy exposure to VPA continues to occur. The present analysis signals that VPA use during pregnancy is still an actual issue despite constant risk mitigation measures.</p>","PeriodicalId":19782,"journal":{"name":"Pharmacoepidemiology and Drug Safety","volume":"34 6","pages":"e70134"},"PeriodicalIF":2.4000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacoepidemiology and Drug Safety","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/pds.70134","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: Valproic acid (VPA) is known to increase the risk of congenital malformations during pregnancy. We evaluated VPA-induced congenital disorder reports in EudraVigilance (EV), before and after the most recent EU risk minimization recommendations in 2018, and conducted a literature review of studies capturing pregnancy exposure data to VPA.

Methods: EV public database of reports was searched for congenital ADRs for VPA, between Jan 2013 and Jun 2023. Descriptive analysis was performed to evaluate demographic data, year trends, outcomes, indications, and concomitant folic acid. A structured review of the literature based on explicit key words and eligibility criteria was conducted in PubMed and EU PAS Register (now HMA-EMA Catalogue for RWD sources) to capture pregnancy exposure to VPA. Data on study design, objectives, and results, particularly pregnancy exposure, were extracted.

Results: A total of 2021 reports containing 3210 VPA-induced congenital disorders were identified (2068 congenital malformations, 634 neural tube defects, 614 cardiac malformations). Most ages reported were between 0 and 1 months (n, 387) and for the male sex (n, 833). Generally, the outcome was "not recovered/not resolved," with 2.8% fatal ADRs reported. The number of reports slightly decreased through the years (lowest in 2015 [n, 154]; highest in 2013 [n, 669]). The literature review included 24 eligible studies, depicting varying levels of pregnancy exposure depending on the study aims and population, with an overall vast heterogeneity in presenting the study results.

Conclusions: The number of VPA-induced congenital disorder reports slightly decreased. Despite absolute contraindications, pregnancy exposure to VPA continues to occur. The present analysis signals that VPA use during pregnancy is still an actual issue despite constant risk mitigation measures.

丙戊酸诱发的先天性疾病、妊娠期丙戊酸使用的预警分析及文献综述。
目的:丙戊酸(VPA)已知会增加怀孕期间先天性畸形的风险。我们在2018年欧盟最新的风险最小化建议之前和之后评估了EudraVigilance (EV)中VPA诱导的先天性疾病报告,并对获取VPA妊娠暴露数据的研究进行了文献综述。方法:检索EV公共报告数据库2013年1月- 2023年6月先天性VPA不良反应报告。进行描述性分析以评估人口统计数据、年度趋势、结果、适应症和伴随的叶酸。在PubMed和EU PAS Register(现为RWD来源的HMA-EMA目录)中,基于明确的关键词和资格标准对文献进行结构化审查,以捕获妊娠暴露于VPA。提取有关研究设计、目标和结果的数据,特别是妊娠暴露。结果:共发现vpa诱发的先天性疾病报告2021例,共3210例(其中先天性畸形2068例,神经管缺陷634例,心脏畸形614例)。大多数报告的年龄在0到1个月之间(387例),男性(833例)。一般来说,结果是“未恢复/未解决”,有2.8%的致命不良反应报告。报告数量逐年略有下降(2015年最低[n, 154];2013年最高[n, 669])。文献综述包括24项符合条件的研究,根据研究目标和人群的不同,描述了不同程度的妊娠暴露,研究结果总体上存在巨大的异质性。结论:vpa诱发的先天性疾病报告数量略有下降。尽管有绝对禁忌症,妊娠暴露于VPA仍在继续发生。目前的分析表明,尽管采取了持续的风险缓解措施,但妊娠期间使用VPA仍然是一个实际问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
4.80
自引率
7.70%
发文量
173
审稿时长
3 months
期刊介绍: The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信