利用国际非专利名称(INN)系统加强药物警戒信号检测。

IF 3.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Raffaella Balocco, Jeffrey K Aronson, Sarel F Malan, Albert Figueras
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引用次数: 0

摘要

“茎”标志着物质之间的药理学关系,构成了世界卫生组织在20世纪50年代开发的国际非专利名称(INN)系统的主干。在本文中,我们建议使用INN系统来增强药物警戒信号的检测。在分析了历史病例和当前的药物警戒实践之后,我们讨论了基于干细胞的分类如何促进对每个干细胞的不良反应特征的理解,并将其用作早期识别偏离预期类别效应的药物不良反应的基准,换句话说,与新上市药物或知名药物的不同用途相关的信号。我们提出了一个潜在的框架,将基于干细胞的分析整合到现有的药物警戒数据库中,辅以人工智能方法,如机器学习。虽然承认局限性,如干细胞变异性和报告偏差,但我们认为这种方法为监管当局和医疗保健专业人员在上市后监督中提供了潜在的优势。实施基于干细胞的上市后监测可以提高信号检测效率,并通过早期识别意外的不良反应和不良反应,有助于提高患者的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strengthening Signal Detection in Pharmacovigilance by Using International Nonproprietary Name (INN) Stems.

'Stems', which mark pharmacological relationships between substances, form the backbone of the International Nonproprietary Name (INN) system, developed by the WHO in the 1950s. In this paper, we propose using the INN stems to enhance pharmacovigilance signal detection. After analysis of historical cases and current pharmacovigilance practices, we discuss how stem-based classification could facilitate understanding of the adverse-effects profile of each stem, to be used as a benchmark for early identification of adverse drug reactions that deviate from expected class effects, in other words signals associated with newly marketed medicines or different uses of well-known medicines. We propose a potential framework for integrating stem-based analysis into existing pharmacovigilance databases, supplemented by artificial intelligence approaches, such as machine learning. While acknowledging limitations, such as stem variability and reporting bias, we suggest that this approach offers potential advantages for regulatory authorities and healthcare professionals in post-marketing surveillance. Implementation of stem-based post-marketing surveillance could enhance signal-detection efficiency and contribute to improved patient safety through earlier identification of unexpected adverse effects and adverse reactions.

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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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