Suppr超能文献

药物性帕金森样事件:一项基于美国食品药品监督管理局不良事件报告系统(FAERS)的2004年至2024年第一季度的真实世界研究

Drug-induced Parkinson-like events: a real-world study from 2004 to the first quarter of 2024 based on FAERS.

作者信息

Wang Ke, Chen Junyan, Huang Mingquan, Zeng Xinhao, Ren Xiaoqun, Liu Xiuqiong, Tao Chao, Yang Liuxuan, Shang Jinlu, Zhou Meiling

机构信息

Department of Pharmacy, The Affiliated Hospital, Southwest Medical University, Luzhou, China.

Department of Clinical Pharmacy, School of Pharmacy, Southwest Medical University, Luzhou, China.

出版信息

Front Pharmacol. 2025 Jan 3;15:1529260. doi: 10.3389/fphar.2024.1529260. eCollection 2024.

Abstract

BACKGROUND

Timely identification of drug-induced Parkinson-like events is essential to improve clinical management and enhance patients' quality of life. However, there is a significant lack of studies addressing these events in real-world settings.

METHODS

To bridge this gap, we analyzed adverse event (AE) reports related to Parkinson-like events from the FDA Adverse Event Reporting System (FAERS) database from the first quarter of 2004 to the first quarter of 2024. Our objective was to summarize a list of potential drugs at high risk for Parkinson-like events and their corresponding proportions of AE reports.

RESULTS

As a result, a total of 54,639 AE reports linked to Parkinson-like events involving 1,224 drugs were identified. Among these, carbidopa/levodopa exhibited the highest number of reports, followed by baclofen and pimavanserin. The most frequently reported drug class was antiparkinsonian drugs and psycholeptics, followed by psychoanaleptics. Using two disproportionate analysis methods, the reporting odds ratio and proportional reporting ratio, we found that 136 drugs exhibited positive results in both methods, while 1,063 drugs did not show any positive signals.

CONCLUSION

This study provides a comprehensive pharmacovigilance analysis of drugs associated with Parkinson-like events, aiming to promote rational drug use and inform clinical practice.

摘要

背景

及时识别药物诱发的帕金森样事件对于改善临床管理和提高患者生活质量至关重要。然而,在现实环境中,针对这些事件的研究严重不足。

方法

为弥补这一差距,我们分析了美国食品药品监督管理局不良事件报告系统(FAERS)数据库中2004年第一季度至2024年第一季度与帕金森样事件相关的不良事件(AE)报告。我们的目标是总结出一份帕金森样事件高风险潜在药物清单及其相应的AE报告比例。

结果

结果共确定了54639份与帕金森样事件相关的AE报告,涉及1224种药物。其中,卡比多巴/左旋多巴的报告数量最多,其次是巴氯芬和匹莫范色林。报告频率最高的药物类别是抗帕金森病药物和抗精神病药物,其次是精神兴奋药。使用两种不成比例分析方法,即报告比值比和比例报告比,我们发现有136种药物在两种方法中均呈现阳性结果,而1063种药物未显示任何阳性信号。

结论

本研究对与帕金森样事件相关的药物进行了全面的药物警戒分析,旨在促进合理用药并为临床实践提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/219e/11739097/ecc78ef7ce3f/fphar-15-1529260-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验