PCSK9 Inhibitors and Infection-Related Adverse Events: A Pharmacovigilance Study Using the World Health Organization VigiBase.

IF 1.9 Q3 PHARMACOLOGY & PHARMACY Drugs - Real World Outcomes Pub Date : 2024-09-01 Epub Date: 2024-07-02 DOI:10.1007/s40801-024-00430-5
Dahyun Park, Sungho Bea, Ji-Hwan Bae, Hyesung Lee, Young June Choe, Ju-Young Shin, Hoon Kim
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Abstract

Aims: Protein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) are novel lipid-lowering agents used in patients with cardiovascular disease. Despite reassuring safety data from pivotal trials, increasing evidence from real-world studies suggests that PCSK9i increase the risk of bacterial and viral infections. Therefore, this study aimed to identify signals of infection-related adverse events (AEs) associated with PCSK9i.

Methods: We performed an observational pharmacovigilance study using the World Health Organization's VigiBase, recorded up to December 2022. We included individual case safety reports (ICSRs) of PCSK9 inhibitors, alirocumab and evolocumab, and compared them with those of other drugs. Infection-related ICSRs were retrieved from the Medical Dictionary for Regulatory Activities System Organ Class 'infections and infestations.'

Results: Among 114,293 reports (258,099 drug-AE pairs) related to PCSK9 inhibitors, 54% included female patients, 41% included patients aged ≥65 years, and 82% included patients who received evolocumab. Additionally, beyond AEs recognized by regulatory authorities, organ infections such as influenza (reporting odds ratio [ROR] 2.89, 95% confidence interval [CI] 2.74-3.05), gastric infections (ROR 2.47, 95% CI 1.63-3.75), and kidney infections (ROR 1.36, 95% CI 1.06-1.73) were observed. Sensitivity analysis indicated a heightened risk of infection-related AEs associated with PCSK9i regardless of the specific drug type.

Conclusions: In addition to the labelled respiratory infections, six infection-related symptoms in the gastrointestinal, urinary, and renal organs were identified. Our findings support the need for systematic surveillance of infections among PCSK9i users.

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PCSK9 抑制剂与感染相关不良事件:使用世界卫生组织 VigiBase 的药物警戒研究。
目的:蛋白转化酶枯草酶/kexin 9 型抑制剂(PCSK9i)是用于心血管疾病患者的新型降脂药物。尽管关键试验的安全性数据令人放心,但越来越多的实际研究证据表明,PCSK9i 会增加细菌和病毒感染的风险。因此,本研究旨在确定与 PCSK9i 相关的感染相关不良事件(AEs)的信号:我们使用世界卫生组织的 VigiBase 进行了一项观察性药物警戒研究,记录截至 2022 年 12 月。我们纳入了 PCSK9 抑制剂、阿利珠单抗和依维莫司的个体病例安全报告(ICSR),并将其与其他药物的个体病例安全报告进行了比较。感染相关的 ICSR 从《监管活动系统医学字典》器官类 "感染和侵袭 "中检索:在与 PCSK9 抑制剂相关的 114,293 份报告(258,099 对药物-AE)中,54% 包括女性患者,41% 包括年龄≥65 岁的患者,82% 包括接受 evolocumab 治疗的患者。此外,除了监管机构认可的 AE 外,还观察到器官感染,如流感(报告几率比 [ROR] 2.89,95% 置信区间 [CI] 2.74-3.05)、胃部感染(ROR 2.47,95% CI 1.63-3.75)和肾脏感染(ROR 1.36,95% CI 1.06-1.73)。敏感性分析表明,无论具体药物类型如何,与PCSK9i相关的感染相关AEs风险都会增加:结论:除了标记的呼吸道感染外,还发现了胃肠道、泌尿系统和肾脏器官的六种感染相关症状。我们的研究结果表明,有必要对 PCSK9i 使用者的感染情况进行系统监测。
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来源期刊
Drugs - Real World Outcomes
Drugs - Real World Outcomes PHARMACOLOGY & PHARMACY-
CiteScore
3.60
自引率
5.00%
发文量
49
审稿时长
8 weeks
期刊介绍: Drugs - Real World Outcomes targets original research and definitive reviews regarding the use of real-world data to evaluate health outcomes and inform healthcare decision-making on drugs, devices and other interventions in clinical practice. The journal includes, but is not limited to, the following research areas: Using registries/databases/health records and other non-selected observational datasets to investigate: drug use and treatment outcomes prescription patterns drug safety signals adherence to treatment guidelines benefit : risk profiles comparative effectiveness economic analyses including cost-of-illness Data-driven research methodologies, including the capture, curation, search, sharing, analysis and interpretation of ‘big data’ Techniques and approaches to optimise real-world modelling.
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