Kim Yong Kyun, Kang Gaeun, Zang Dae Young, Lee Dong Hwan
Division of Infectious Diseases, Department of Internal Medicine, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14066, Republic of Korea.
Division of Clinical Pharmacology, Chonnam National University Hospital, Gfwangju 61469, Republic of Korea.
Antibiotics (Basel). 2024 Sep 5;13(9):849. doi: 10.3390/antibiotics13090849.
This study aimed to develop a population pharmacokinetic (PK) model for meropenem in healthy adults and explore optimal dosing regimens for patients with normal renal function. PK samples were obtained from 12 healthy participants, which were analyzed using noncompartmental analysis and nonlinear mixed-effect modeling. The PK profiles of meropenem were characterized using a two-compartment model, and serum creatinine level was identified as a significant covariate affecting total clearance. Monte Carlo simulations were conducted using this model to inform dosing recommendations. The target index for meropenem efficacy was defined as the cumulative percentage over 24 h during which free () drug concentration exceeded the minimum inhibitory concentration (MIC) under steady state conditions (T). These simulations indicated that the current dosage regimen of 1 g for 30 min infusions every 8 h achieved a 90% probability of target attainment (PTA) for 40%T when the MIC was <2 mg/L. However, to achieve more stringent therapeutic targets, such as a 90%PTA for 100%T or a 90%PTA for 100%T, higher doses administered as 3 h extended infusions or as continuous infusions may be necessary. These results highlight the need for model-informed precision dosing to enhance the efficacy of meropenem therapy across various MIC levels and therapeutic targets.
本研究旨在建立健康成年人美罗培南的群体药代动力学(PK)模型,并探索肾功能正常患者的最佳给药方案。从12名健康受试者获取PK样本,采用非房室分析和非线性混合效应模型进行分析。美罗培南的PK特征用二室模型表征,血清肌酐水平被确定为影响总清除率的显著协变量。使用该模型进行蒙特卡洛模拟以提供给药建议。美罗培南疗效的目标指标定义为稳态条件下(T)游离()药物浓度超过最低抑菌浓度(MIC)的24小时内的累积百分比。这些模拟表明,当MIC<2mg/L时,当前每8小时静脉输注1g共30分钟的给药方案达到40%T目标达成概率(PTA)为90%。然而,为实现更严格的治疗目标,如100%T的90%PTA或100%T的90%PTA,可能需要以3小时延长输注或持续输注的方式给予更高剂量。这些结果凸显了基于模型的精准给药对于提高美罗培南在不同MIC水平和治疗目标下治疗效果的必要性。