Laboratory of Regulatory Science, Faculty of Pharmacy, Musashino University, 1-1-20 Shinmachi, Nishitokyo-shi, Tokyo, 202-8585, Japan.
Research Institute of Pharmaceutical Sciences, Musashino University, 1-1-20 Shinmachi, Nishitokyo-shi, Tokyo, 202-8585, Japan.
BMC Pharmacol Toxicol. 2024 Sep 3;25(1):60. doi: 10.1186/s40360-024-00777-z.
Triazolam is a typical drug commonly used in the elderly; however, there have been concerns about its adverse events resulting from age-related changes in physiological function and drug interactions with concomitant drugs. Thus, updated information contributing to the appropriate use based on the latest pharmacokinetic and post-marketing surveillance methods is needed. In this study, we evaluated the appropriate use of triazolam in the elderly by integrating real-world data with a modeling and simulation approach.
The occurrence risk of adverse events in the elderly was evaluated using the spontaneous adverse event reporting regulatory databases from Japan and the United States. Information on drug concentrations and reactions was extracted from previous publications to estimate the threshold for plasma triazolam concentrations that cause adverse events. The pharmacokinetic/pharmacodynamic (PK/PD) model was then constructed, and the dose and administration were evaluated in various situations anticipated in medical practice.
Among all prescriptions, 25.4% were prescribed to individuals aged 80 years or above, and 51.8% were for those aged 70 years or above. A majority of cases involved CYP3A-metabolized drug combinations, accounting for 85.6%. Elderly individuals were at a higher risk of developing delirium and fall-fracture. Based on the constructed PK/PD model, the risk of adverse events increased when the plasma concentration of triazolam exceeded the calculated threshold of 0.44 ng/mL at approximately 6 h after administration. Administering 0.125 mg of triazolam, is half the approved dose for the elderly in Japan was deemed appropriate. Moreover, there was a substantial risk of adverse events even at a dosage of 0.0625 mg in combination with a moderate or strong inhibitor of cytochrome P450 3 A.
Analyzing large-scale databases and existing research publications on PK/PD can practically contribute to optimizing triazolam drug therapy for the elderly in the daily clinical setting.
三唑仑是一种常用于老年人的典型药物;然而,由于与年龄相关的生理功能变化和与伴随药物的药物相互作用,人们对其不良反应感到担忧。因此,需要基于最新的药代动力学和上市后监测方法提供有助于适当使用的最新信息。在这项研究中,我们通过整合真实世界数据和建模与模拟方法来评估三唑仑在老年人中的适当使用。
使用来自日本和美国的自发不良事件报告监管数据库评估老年人发生不良事件的风险。从以前的出版物中提取有关药物浓度和反应的信息,以估计引起不良事件的血浆三唑仑浓度阈值。然后构建药代动力学/药效学(PK/PD)模型,并在预期在医学实践中出现的各种情况下评估剂量和给药。
所有处方中,有 25.4%开给 80 岁或以上的人,51.8%开给 70 岁或以上的人。大多数病例涉及 CYP3A 代谢药物组合,占 85.6%。老年人发生谵妄和跌倒骨折的风险较高。根据构建的 PK/PD 模型,当三唑仑的血浆浓度在给药后约 6 小时超过计算出的 0.44 ng/mL 阈值时,不良事件的风险增加。给予 0.125 毫克三唑仑被认为是合适的,这是日本批准的老年剂量的一半。此外,即使与中度或强 CYP3A 抑制剂联合使用 0.0625 毫克剂量,也存在很大的不良事件风险。
分析大规模数据库和现有的 PK/PD 研究出版物可以实际有助于优化老年人在日常临床环境中的三唑仑药物治疗。