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囊性纤维化儿科患者的抗感染药物:群体药代动力学分析的综合综述

Anti-infectives in Pediatric Patients with Cystic Fibrosis: A Comprehensive Review of Population Pharmacokinetic Analyses.

作者信息

Yaliniz Aysenur, El Hassani Mehdi, Blanchard Ana C, Marsot Amélie

机构信息

Laboratoire de Suivi Thérapeutique Pharmacologique et Pharmacocinétique, Faculty of Pharmacy, Université de Montréal, 2940 chemin de Polytechnique, Montreal, QC, H3T 1J4, Canada.

Faculty of Pharmacy, Université de Montréal, Montreal, Canada.

出版信息

Clin Pharmacokinet. 2025 May;64(5):631-653. doi: 10.1007/s40262-025-01505-4. Epub 2025 Apr 21.

Abstract

Pulmonary complications are the leading cause of morbidity and mortality in pediatric patients with cystic fibrosis. Altered pharmacokinetic parameters in this population, as well as high inter- and intra-individual variability, complicate the optimization of anti-infective treatments. In this review, we aim to summarize and describe all anti-infective population pharmacokinetic (popPK) models applied to pediatric populations with cystic fibrosis. Our objectives were to identify the most-reported structural models and retained covariates and to compare the dosing regimens used in clinical routine with those recommended in literature and guidelines. A literature search was done through the PubMed database from inception to August 2024. Studies were retained only if they complied with the inclusion and exclusion criteria. The review included 21 popPK models covering the pharmacokinetic profiles of eight different molecules. Among these, five are recommended antibiotics for treating pulmonary infections in patients with cystic fibrosis. All models incorporated body composition and/or renal function measures as covariates in their pharmacokinetic parameter equations. Standard dosing regimens in the studies were consistent with guidelines and literature recommendations. This is the first review summarizing and describing all anti-infective popPK models in pediatric patients with cystic fibrosis. Improved estimation of pharmacokinetic parameters and a clearer understanding of variability sources will enhance the optimization of antibiotic treatment in clinical practice. Finally, the impact of new targeted therapies on the management of this population will have to be closely monitored in the years ahead.

摘要

肺部并发症是囊性纤维化儿科患者发病和死亡的主要原因。该人群药代动力学参数的改变以及个体间和个体内的高度变异性,使抗感染治疗的优化变得复杂。在本综述中,我们旨在总结和描述所有应用于囊性纤维化儿科人群的抗感染群体药代动力学(popPK)模型。我们的目标是确定报告最多的结构模型和保留的协变量,并将临床常规使用的给药方案与文献和指南中推荐的方案进行比较。通过PubMed数据库进行了从数据库创建到2024年8月的文献检索。只有符合纳入和排除标准的研究才被保留。该综述包括21个popPK模型,涵盖了八种不同分子的药代动力学概况。其中,五种是治疗囊性纤维化患者肺部感染的推荐抗生素。所有模型在其药代动力学参数方程中都将身体组成和/或肾功能指标作为协变量纳入。研究中的标准给药方案与指南和文献建议一致。这是第一篇总结和描述囊性纤维化儿科患者所有抗感染popPK模型的综述。药代动力学参数估计的改善以及对变异性来源的更清晰理解将加强临床实践中抗生素治疗的优化。最后,在未来几年必须密切监测新的靶向治疗对该人群管理的影响。

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