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基于性别和性别的药物不良反应分析:药物警戒数据库的范围综述

A Sex- and Gender-Based Analysis of Adverse Drug Reactions: A Scoping Review of Pharmacovigilance Databases.

作者信息

Brabete Andreea C, Greaves Lorraine, Maximos Mira, Huber Ella, Li Alice, Lê Mê-Linh

机构信息

Centre of Excellence for Women's Health, Vancouver, BC V6H 3N1, Canada.

School of Population and Public Health, Faculty of Medicine, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.

出版信息

Pharmaceuticals (Basel). 2022 Feb 28;15(3):298. doi: 10.3390/ph15030298.

Abstract

Drug-related adverse events or adverse drug reactions (ADRs) are currently partially or substantially under-reported. ADR reporting systems need to expand their focus to include sex- and gender-related factors in order to understand, prevent, or reduce the occurrence of ADRs in all people, particularly women. This scoping review describes adverse drug reactions reported to international pharmacovigilance databases. It identifies the drug classes most commonly associated with ADRs and synthesizes the evidence on ADRs utilizing a sex- and gender-based analysis plus (SGBA+) to assess the differential outcomes reported in the individual studies. We developed a systematic search strategy and applied it to six electronic databases, ultimately including 35 papers. Overall, the evidence shows that women are involved in more ADR reports than men across different countries, although in some cases, men experience more serious ADRs. Most studies were conducted in higher-income countries; the terms adverse drug reactions and adverse drug events are used interchangeably, and there is a lack of standardization between systems. Additional research is needed to identify the relationships between sex- and gender-related factors in the occurrence and reporting of ADRs to adequately detect and prevent ADRs, as well as to tailor and prepare effective reporting for the lifecycle management of drugs.

摘要

与药物相关的不良事件或药物不良反应(ADR)目前存在部分或大量漏报的情况。ADR报告系统需要扩大其关注范围,将与性别相关的因素纳入其中,以便了解、预防或减少所有人尤其是女性中ADR的发生。本范围综述描述了向国际药物警戒数据库报告的药物不良反应。它确定了与ADR最常相关的药物类别,并利用基于性别的分析加(SGBA+)对个体研究中报告的不同结果进行评估,从而综合有关ADR的证据。我们制定了系统的检索策略,并将其应用于六个电子数据库,最终纳入35篇论文。总体而言,证据表明,在不同国家,女性参与ADR报告的数量多于男性,尽管在某些情况下,男性经历的ADR更为严重。大多数研究在高收入国家进行;药物不良反应和药物不良事件这两个术语可互换使用,而且各系统之间缺乏标准化。需要开展更多研究,以确定性别相关因素在ADR发生和报告中的关系,从而充分检测和预防ADR,并为药物的生命周期管理定制和准备有效的报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dae5/8950058/b20d76482626/pharmaceuticals-15-00298-g001.jpg

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