Suppr超能文献

丙戊酸在儿科和成年白种人患者中的群体药代动力学

Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients.

作者信息

Teixeira-da-Silva Paulo, Pérez-Blanco Jonás Samuel, Santos-Buelga Dolores, Otero María José, García María José

机构信息

Pharmaceutical Sciences Department, Universidad de Salamanca, 37007 Salamanca, Spain.

Institute of Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain.

出版信息

Pharmaceutics. 2022 Apr 7;14(4):811. doi: 10.3390/pharmaceutics14040811.

Abstract

(1) Background: The aim of this study was to explore the valproic acid (VPA) pharmacokinetic characteristics in a large population of pediatric and adult Caucasian patients and to establish a robust population pharmacokinetic (PopPK) model. (2) Methods: A total of 2527 serum VPA samples collected from 1204 patients included in a therapeutic drug monitoring program were retrospectively analyzed. Patients were randomly assigned to either a model development group or an external evaluation group. PopPK analysis was performed on 1751 samples from 776 patients with NONMEM using a nonlinear mixed-effect modelling approach. The influence of demographic, anthropometric, treatment and comedication variables on the apparent clearance (CL/F) of VPA was studied. The bootstrap method was used to evaluate the final model internally. External evaluation was carried out using 776 VPA serum samples from 368 patients. (3) Results: A one-compartment model with first-order absorption and elimination successfully described the data. The final model included total body weight, age and comedication with phenytoin, phenobarbital and carbamazepine with a significant impact on VPA elimination. Internal and external evaluations demonstrated the good predictability of the model. (4) Conclusions: A PopPK model of VPA in Caucasian patients was successfully established, which will be helpful for model-informed precision dosing approaches in clinical patient care.

摘要

(1) 背景:本研究旨在探讨丙戊酸(VPA)在大量儿科和成年白种人患者中的药代动力学特征,并建立一个可靠的群体药代动力学(PopPK)模型。(2) 方法:对从1204例纳入治疗药物监测项目的患者中收集的2527份血清VPA样本进行回顾性分析。患者被随机分配到模型开发组或外部评估组。使用非线性混合效应建模方法,对来自776例患者的1751份样本进行PopPK分析。研究了人口统计学、人体测量学、治疗和合并用药变量对VPA表观清除率(CL/F)的影响。采用自举法对最终模型进行内部评估。使用来自368例患者的776份VPA血清样本进行外部评估。(3) 结果:一个具有一级吸收和消除的单室模型成功地描述了数据。最终模型包括总体重、年龄以及与苯妥英、苯巴比妥和卡马西平的合并用药,这些因素对VPA消除有显著影响。内部和外部评估均表明该模型具有良好预测性。(4) 结论:成功建立了白种人患者VPA的PopPK模型,这将有助于在临床患者护理中采用模型指导的精准给药方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f82e/9031051/6915690f7193/pharmaceutics-14-00811-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验