重症监护病房老年肺炎患者哌拉西林的人群药代动力学及剂量优化。

IF 2.3 4区 医学
Jing Sun, Chuang Yang, Bo-Hao Tang, Guo-Xiang Hao, John van den Anker, Yue-E Wu, De-Qing Sun, Yi Zheng, Wei Zhao
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引用次数: 0

摘要

哌拉西林/他唑巴坦是老年肺炎患者的一线治疗药物。然而,不同中心的给药方案和输注时间存在差异。我们旨在评估哌拉西林在老年肺炎患者中的人群药代动力学,并优化给药方案。这是一项使用机会抽样设计的哌拉西林/他唑巴坦在老年肺炎患者中的前瞻性药代动力学(PK)研究。采用高效液相色谱法测定哌拉西林血药浓度。利用NONMEM软件构建种群PK模型,并在单独的测试队列中进一步验证其预测性能。采用最终种群PK模型进行剂量优化。来自73名患者的151份血液样本被用于建立群体PK模型,来自22名患者的60份治疗药物浓度监测被用于模型验证。建立了一阶消去的单室模型。协变量分析显示,eGFR是唯一的协变量。Monte Carlo模拟结果显示,对于MIC值为8和16 mg/L的病原体,本研究中使用的给药方案(每6/8 h 4000mg,给药30 min)的PTAs为23.5%-64.3%。除eGFR≥50 mL/min/1.73 m2的患者外,不同肾功能水平的患者,4000mg / 6h给药方案的PTAs均超过90%(90.7% ~ 99.8%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Population Pharmacokinetics and Dosing Optimization of Piperacillin in Elderly Patients with Pneumonia in the Intensive Care Unit.

Piperacillin/tazobactam is the first-line treatment for pneumonia in elderly patients. However, there are differences in dosing regimens and infusion times among different centers. We aimed to evaluate the population pharmacokinetics of piperacillin in elderly patients with pneumonia and optimize the dosing regimens. This was a prospective pharmacokinetic (PK) study of piperacillin/tazobactam in elderly patients with pneumonia using an opportunistic sampling design. The blood concentration of piperacillin was determined by high-performance liquid chromatography. A population PK model was constructed using NONMEM software, and its predictive performance was further validated in a separate test cohort. The final population PK model was used for dose optimization. A total of 151 blood samples from 73 patients were used to develop a population PK model, and 60 concentrations of therapeutic drug monitoring from 22 patients were used for model validation. A one-compartment model with first-order elimination was established. Covariate analysis showed that eGFR was the only covariate. Monte Carlo simulation results showed that for pathogens with MIC values of 8 and 16 mg/L, the dosing regimen (4000 mg every 6/8 h administered 30 min) used in this study resulted in PTAs of 23.5%-64.3%. The PTAs of the dosing regimen 4000 mg every 6 h administered by 4-h infusion for patients with different levels of renal function exceeded 90% (90.7%-99.8%), except for patients with eGFR ≥ 50 mL/min/1.73 m2.

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来源期刊
Journal of Clinical Pharmacology
Journal of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
自引率
3.40%
发文量
0
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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