Building functional and sustainable pharmacovigilance systems: an analysis of pharmacovigilance development across high-, middle- and low-income countries.

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Therapeutic Advances in Drug Safety Pub Date : 2025-06-10 eCollection Date: 2025-01-01 DOI:10.1177/20420986251342941
Olga Menang, Peter van Eeuwijk, Karen Maigetter, Andrea de Soyres-Kuemmerle, Edinam Agbenu, Christian Burri
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引用次数: 0

Abstract

Background: There has been notable progress in pharmacovigilance (PV) in low- and middle-income countries (LMIC) in the last decade. However, only a few of these PV systems are fully functional, unlike in high-income countries where stringent legislation, regulations and operational guidelines have enabled the establishment of effective PV systems. The key challenges faced in LMIC include organisational inefficiencies; weak infrastructure; inconsistent and poorly enforced regulations; and inadequate financing and shortage of trained personnel. Furthermore, low adverse event volume and poor data quality hinder the capacity for safety data generation and utilisation. With the increasing availability of essential and innovative medicines in LMIC, establishing robust PV systems is crucial for effective safety surveillance.

Objectives: This research aims to analyse the development of PV systems across high-, middle- and low-income countries and to carve out essential elements for functionality and sustainability of PV systems in LMIC.

Design: A convergent parallel mixed-methods design, combining qualitative and quantitative methods.

Methods: Qualitative and quantitative research consisted of semi-structured interviews and an online survey, respectively.

Results: Twelve key informants from 10 countries were interviewed and 52 respondents from 36 countries completed the online survey. From the qualitative and quantitative data, we identified nine essential elements for sustainable PV development in LMIC: understanding the drivers of PV development; adequately resolving core system challenges; implementing an efficient organisational structure and good governance; establishing procedures for PV activities; ensuring availability of qualified and trained staff; identifying alternate sources of financing; having a strategic development plan; adequately leveraging the health system; and effectively integrating the pharmaceutical sector in the national PV system.

Conclusion: Findings from this research indicate that significant efforts are still needed to upgrade PV systems in LMIC to meet global standards despite the progress achieved in recent years. Developing the different areas emerging from this research, within the framework of a holistic, fit-for-purpose PV system strengthening, would enable a comprehensive progression from basic to functional and thus sustainable PV systems in LMIC.

建立功能性和可持续的药物警戒系统:高、中、低收入国家药物警戒发展分析。
背景:在过去十年中,低收入和中等收入国家(LMIC)在药物警戒(PV)方面取得了显著进展。然而,这些光伏系统中只有少数能够充分发挥作用,这与高收入国家的情况不同,在高收入国家,严格的立法、条例和操作准则能够建立有效的光伏系统。中低收入国家面临的主要挑战包括组织效率低下;基础设施薄弱;规章不一致且执行不力;资金不足和训练有素的人员短缺。此外,不良事件数量少和数据质量差阻碍了安全数据生成和利用的能力。随着低收入和中等收入国家基本药物和创新药物供应的增加,建立健全的光伏系统对于有效的安全监测至关重要。目的:本研究旨在分析高、中、低收入国家光伏系统的发展情况,并找出中低收入国家光伏系统功能和可持续性的基本要素。设计:收敛并行混合方法设计,定性与定量相结合。方法:定性研究和定量研究分别采用半结构化访谈和在线调查。结果:来自10个国家的12名关键信息提供者接受了采访,来自36个国家的52名受访者完成了在线调查。从定性和定量数据中,我们确定了中低收入国家光伏可持续发展的九个基本要素:了解光伏发展的驱动因素;充分解决核心系统挑战;建立高效的组织架构和良好的管治;制定PV活动的程序;确保有合格和训练有素的工作人员;确定其他资金来源;有战略发展规划的;充分利用卫生系统;有效将医药行业纳入国家光伏产业体系。结论:这项研究的结果表明,尽管近年来取得了进展,但仍需要做出重大努力来升级LMIC的光伏系统以达到全球标准。在整体的、适合用途的光伏系统加强框架内发展这项研究产生的不同领域,将使低收入和中等收入国家的光伏系统从基本发展到功能,从而实现可持续发展。
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
Therapeutic Advances in Drug Safety
Therapeutic Advances in Drug Safety Medicine-Pharmacology (medical)
CiteScore
6.70
自引率
4.50%
发文量
31
审稿时长
9 weeks
期刊介绍: Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in drug safety, providing a forum in print and online for publishing the highest quality articles in this area. The editors welcome articles of current interest on research across all areas of drug safety, including therapeutic drug monitoring, pharmacoepidemiology, adverse drug reactions, drug interactions, pharmacokinetics, pharmacovigilance, medication/prescribing errors, risk management, ethics and regulation.
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