Vonoprazan-associated Clostridioides difficile infection: an analysis of the Japanese Adverse Drug Event Report and the FDA Adverse Event Reporting System

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Drug Safety Pub Date : 2024-07-31 DOI:10.1177/20420986241260211
Mengling Ouyang, Shupeng Zou, Qian Cheng, Xuan Shi, Yazheng Zhao, Minghui Sun
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Abstract

Background:Prolonged or excessive use of acid suppressants may increase the risk of Clostridioides difficile infection (CDI) by altering the intestinal microecosystem. Vonoprazan, a novel potassium-competitive acid blocker, exhibits a faster and more sustained acid-suppressive effect than proton pump inhibitors (PPIs). Therefore, vonoprazan may have a greater impact on the gut microbiota, potentially resulting in CDI.Objectives:This study aimed to explore the potential relationship between acid suppressants and CDI by the Japan Adverse Drug Event Report (JADER) and the FDA Adverse Event Reporting System (FAERS) databases.Design:A retrospective analysis of the JADER and FAERS databases was examined by disproportionality analysis.Methods:We performed signal detection analyses of CDI induced by vonoprazan and PPIs using the JADER and FAERS databases. The association between acid suppressants and CDI was calculated using the reporting odds ratio (ROR) and corresponding 95% confidence interval (95% CI). When the lower limit of the 95% CI is exceeded by 1, the association is considered statistically significant.Results:In the JADER database, the ROR (95% CI) for vonoprazan and PPIs based on suspect drug reports was 15.84 (12.23–20.50) and 2.51 (1.92–3.28), respectively. In the FAERS database, the ROR (95% CI) for vonoprazan and PPIs based on primary and secondary suspect drug reports was 11.50 (6.36–20.82) and 1.42 (1.34–1.51), respectively. Subgroup analysis showed that elderly patients aged 60 years and older were more strongly associated with CDI. The ROR (95% CI) for vonoprazan and PPIs in patients aged 60 years and older in the JADER database was 15.35 (11.59–20.33) and 1.65 (1.14–2.39), respectively. Similarly, the ROR (95% CI) for vonoprazan and PPIs in the FAERS database was 12.56 (6.26–25.20) and 1.43 (1.31–1.57), respectively. Excluding the effect of Helicobacter pylori ( H. pylori) infection, the use of acid suppressants was still associated with CDI.Conclusion:While signal detection analysis based on the JADER and FAERS databases could not establish causality, our study demonstrated that both vonoprazan and PPIs were significantly associated with CDI. Vonoprazan showed a stronger association with CDI in both databases.
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沃诺普拉赞相关艰难梭菌感染:对日本药物不良事件报告和美国食品药品管理局不良事件报告系统的分析
背景:长期或过量使用抑酸剂可能会改变肠道微生态系统,从而增加艰难梭菌感染(CDI)的风险。Vonoprazan是一种新型钾竞争性酸阻滞剂,与质子泵抑制剂(PPI)相比,它具有更快、更持久的抑酸效果。目的:本研究旨在通过日本药物不良事件报告(JADER)和美国食品药品管理局不良事件报告系统(FAERS)数据库,探讨抑酸剂与 CDI 之间的潜在关系。方法:我们利用 JADER 和 FAERS 数据库,对 Vonoprazan 和 PPIs 引起的 CDI 进行了信号检测分析。抑酸剂与 CDI 之间的关联采用报告几率比(ROR)和相应的 95% 置信区间(95% CI)进行计算。结果:在JADER数据库中,根据可疑药物报告,vonoprazan和PPIs的ROR(95% CI)分别为15.84(12.23-20.50)和2.51(1.92-3.28)。在 FAERS 数据库中,根据主要和次要可疑药物报告,vonoprazan 和 PPIs 的 ROR(95% CI)分别为 11.50(6.36-20.82)和 1.42(1.34-1.51)。亚组分析显示,60 岁及以上的老年患者与 CDI 的关联性更强。在 JADER 数据库中,60 岁及以上患者服用 vonoprazan 和 PPIs 的 ROR(95% CI)分别为 15.35(11.59-20.33)和 1.65(1.14-2.39)。同样,FAERS 数据库中 vonoprazan 和 PPIs 的 ROR(95% CI)分别为 12.56(6.26-25.20)和 1.43(1.31-1.57)。结论:虽然基于JADER和FAERS数据库的信号检测分析不能确定因果关系,但我们的研究表明,伏诺普拉赞和PPIs与CDI有显著相关性。在这两个数据库中,沃诺普拉赞与 CDI 的相关性更强。
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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