Antiretroviral Use for HIV Prevention During Pregnancy: The Need to Strengthen Regulatory and Surveillance Systems in Africa.

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Safety Pub Date : 2025-01-26 DOI:10.1007/s40264-024-01494-6
Robin Schaefer, L Donaldson, A Chigome, M Escudeiro Dos Santos, S Lamprianou, N Ndembi, J I Nwokike, P Nyambayo, V Palmi, F Renaud, M Gonzalez Tome, V Miller
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Abstract

HIV-prevention efforts focusing on women of child-bearing potential are needed to end the HIV epidemic in the African region. The use of antiretroviral drugs as pre-exposure prophylaxis (PrEP) is a critical HIV prevention tool. However, safety data on new antiretrovirals during pregnancy are often limited because pregnant people are excluded from drug development studies. Calls from communities, healthcare professionals, and regulators to improve the information supporting decision-making around the use of medical products during pregnancy have been increasing. Post-marketing safety surveillance is an essential tool for detecting adverse outcomes and evaluating real-world, longer-term effects of drugs. Detecting and evaluating uncommon pregnancy outcomes requires large sample sizes, highlighting the benefits of and need for safety surveillance. Surveillance systems vary widely across Africa, and the need for enhanced surveillance of PrEP use during pregnancy highlights the limitations of current regulatory and surveillance systems. Challenges include weak regulation and insufficient resources. Pooling of resources and regulatory harmonization could address resource challenges. The African Medicines Agency, as a specialized agency of the African Union, has the potential to improve African medical product regulation, including post-marketing safety surveillance. This can strengthen regulation and ensure that market authorization holders meet their responsibility to invest in post-marketing surveillance systems, such as pregnancy registries. At the same time, independent post-marketing studies are needed to ensure generation of essential safety data. The Forum for Collaborative Research has initiated a project to facilitate interactions between regulators in Africa, the USA, and Europe, as well as other stakeholders, and to work toward consensus on safety data generation from PrEP during pregnancy before and after marketing authorization.

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要想在非洲地区结束艾滋病毒的流行,就必须以有生育能力的妇女为重点开展艾滋病毒预防工作。使用抗逆转录病毒药物作为接触前预防(PrEP)是一种重要的艾滋病毒预防工具。然而,由于孕妇被排除在药物开发研究之外,因此孕期使用新型抗逆转录病毒药物的安全性数据往往十分有限。社区、医疗保健专业人士和监管机构要求改进支持孕期使用医疗产品决策的信息的呼声越来越高。上市后安全监测是检测不良后果和评估药物在现实世界中的长期影响的重要工具。检测和评估不常见的妊娠结局需要大量样本,这就凸显了安全监测的益处和必要性。非洲各地的监测系统差异很大,需要加强对孕期使用 PrEP 的监测,这凸显了当前监管和监测系统的局限性。面临的挑战包括监管不力和资源不足。集中资源和统一监管可以应对资源挑战。非洲药品管理局作为非洲联盟的一个专门机构,有可能改善非洲医疗产品的监管,包括上市后的安全监测。这可以加强监管,确保市场授权持有人履行投资于上市后监测系统(如妊娠登记)的责任。与此同时,还需要开展独立的上市后研究,以确保生成基本的安全数据。合作研究论坛发起了一个项目,以促进非洲、美国和欧洲的监管机构以及其他利益相关者之间的互动,并努力就妊娠期 PrEP 在上市授权前后安全性数据的生成达成共识。
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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. 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 Drug Safety 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.
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