Population pharmacokinetics and thrombocytopenia risk assessment of linezolid in liver transplant recipients.

IF 3.9 2区 医学 Q1 INFECTIOUS DISEASES
Xiaoping Shi, Wenyu Yang, Fanyu Zhao, Donghui Lao, Qing Xu, Xiaoyu Li, Qianzhou Lv, Qingfeng He, Xiaoqiang Xiang, Ting Wang, Xiao Zhu
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引用次数: 0

Abstract

Background: Linezolid is a commonly prescribed antibiotic for multidrug-resistant enterococcal infections in liver transplant recipients (LTRs). However, changes in pharmacokinetics due to fluctuations in liver and renal functions, combined with the increased risk of thrombocytopenia, complicate its clinical use. This study aimed to characterize the exposure-thrombocytopenia risk relationship of linezolid in LTRs, and to identify safe dosing thresholds to promote rational drug use.

Methods: A retrospective analysis was conducted on adult LTRs treated with linezolid at Zhongshan Hospital between January 2019 and May 2022. A population exposure-safety model was developed and used to establish a thrombocytopenia risk threshold and optimize initial dosing strategies through Monte Carlo simulations. An area under the concentration-time curve (AUC) calculator was developed to facilitate individualized dose adjustments.

Results: Exposure-safety analysis revealed that an AUCss,24h threshold of 291.7 mg/L·h was associated with an increased risk of thrombocytopenia. Monte Carlo simulations showed that current covariate-based initial dosing recommendations were suboptimal, highlighting the necessity of therapeutic drug monitoring (TDM) to improve outcomes in LTRs. The online AUC calculator developed in this study offers a practical tool for clinicians to implement timely dose adjustments (https://optimaldose.shinyapps.io/LinezolidAUC/).

Conclusions: This study provides the first comprehensive analysis of linezolid exposure and its relationship to thrombocytopenia risk in LTRs. The findings underscore the importance of AUC-guided dosing and TDM in optimizing treatment outcomes.

肝移植受者利奈唑胺的人群药代动力学和血小板减少风险评估。
背景:利奈唑胺是肝移植受者(LTRs)多药耐药肠球菌感染的常用抗生素。然而,由于肝肾功能波动引起的药代动力学变化,加上血小板减少的风险增加,使其临床应用复杂化。本研究旨在表征利奈唑胺在ltr中暴露与血小板减少的风险关系,并确定安全剂量阈值,以促进合理用药。方法:回顾性分析2019年1月至2022年5月中山医院利奈唑胺治疗的成人ltr。建立了人群暴露-安全模型,并通过蒙特卡罗模拟建立了血小板减少风险阈值和优化初始剂量策略。开发了浓度-时间曲线下面积(AUC)计算器,便于个体化剂量调整。结果:暴露-安全分析显示,auss 24h阈值为291.7 mg/L·h与血小板减少的风险增加有关。蒙特卡罗模拟显示,目前基于协变量的初始剂量建议是次优的,强调了治疗药物监测(TDM)改善ltr预后的必要性。本研究开发的在线AUC计算器为临床医生及时调整剂量提供了实用工具(https://optimaldose.shinyapps.io/LinezolidAUC/)。结论:本研究首次全面分析了利奈唑胺暴露及其与ltr患者血小板减少风险的关系。研究结果强调了auc引导剂量和TDM在优化治疗结果中的重要性。
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
CiteScore
9.20
自引率
5.80%
发文量
423
审稿时长
2-4 weeks
期刊介绍: The Journal publishes articles that further knowledge and advance the science and application of antimicrobial chemotherapy with antibiotics and antifungal, antiviral and antiprotozoal agents. The Journal publishes primarily in human medicine, and articles in veterinary medicine likely to have an impact on global health.
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