Center for Experiential Pharmacy Practice, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan;
Center for Experiential Pharmacy Practice, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
In Vivo. 2024 May-Jun;38(3):1285-1291. doi: 10.21873/invivo.13567.
BACKGROUND/AIM: Recent research has increasingly demonstrated an association between proton pump inhibitors (PPIs) and serious adverse events. This study aimed to evaluate the association between PPI and rhabdomyolysis (RM), examining its time-to-onset profiles using the Japanese Adverse Drug Event Report (JADER) database.
Data spanning from April 2004 to March 2022 were used. The association between PPIs and RM was evaluated using the reporting odds ratio (ROR), adjusted for sex and age. Subsequent analyses were conducted after excluding cases involving concomitant use of statins or fibrates. Furthermore, the onset time of RM and Weibull distribution parameters were calculated to evaluate the expression profile of RM, and the outcomes were examined.
RM was associated with the use of esomeprazole, omeprazole, and rabeprazole, even in the absence of concomitant statin or fibrate use. The median time to RM onset varied among PPIs, ranging from 6.5 to 127 d. The Weibull distribution parameters indicated that the hazard types of nearly all orally administered PPIs were classified as early failure or close to random failure. Regarding outcomes, cases of death were reported for all PPIs except vonoprazan.
The findings suggest the need for vigilant monitoring of RM during PPI administration, particularly in the early stages, considering the varying onset times.
背景/目的:最近的研究越来越多地表明质子泵抑制剂 (PPI) 与严重不良事件之间存在关联。本研究旨在使用日本药物不良反应报告 (JADER) 数据库评估 PPI 与横纹肌溶解症 (RM) 之间的关联,并检查其发病时间谱。
使用了 2004 年 4 月至 2022 年 3 月的数据。使用报告比值比 (ROR) 评估了 PPI 与 RM 之间的关联,同时调整了性别和年龄因素。在排除了同时使用他汀类药物或贝特类药物的病例后,进行了后续分析。此外,计算了 RM 的发病时间和威布尔分布参数,以评估 RM 的表达谱,并检查了结果。
即使没有同时使用他汀类药物或贝特类药物,RM 也与埃索美拉唑、奥美拉唑和雷贝拉唑的使用相关。RM 发病的中位时间因 PPI 而异,范围为 6.5 至 127 天。威布尔分布参数表明,几乎所有口服 PPI 的危险类型均归类为早期失效或接近随机失效。关于结局,除了沃诺拉赞外,所有 PPI 都报告了死亡病例。
这些发现表明,在使用 PPI 期间需要密切监测 RM,特别是在早期阶段,需要考虑到不同的发病时间。