Lee Hyoeun, Yoon Seonghae, Chung Jae Yong
Department of Clinical Pharmacology and Therapeutics, Seoul National University Bundang Hospital, Seongnam 13620, Korea.
Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine, Seoul 03080, Korea.
Transl Clin Pharmacol. 2024 Sep;32(3):150-158. doi: 10.12793/tcp.2024.32.e14. Epub 2024 Sep 25.
This study aimed to estimate individual pharmacokinetic (PK) parameters in an obese hemodialysis (HD) patient receiving gentamicin and to assess the impact of obesity on gentamicin clearance (CL). A 53-year-old obese Korean woman underwent HD and received gentamicin. To estimate individual PK parameters, we employed the POSTHOC option using NONMEM 7.4.4. A priori model contained HD as a covariate for CL during HD, and creatinine CL (CrCL), normalized by the group mean value from the a priori model, as a covariate for non-HD CL (CLNHD). Individual CLNHD exhibited a substantial reduction from the population CLNHD, with the value corresponding to 36% of the a priori model's population PK (popPK) parameter. The patient's CrCL exceeded the group maximum of the a priori information, suggesting inaccurate renal function representation. After adjusting CrCL to the group mean from the a priori model, the patient's CLNHD was 138% of the population's typical value. The objective function value for each run was 0.53 and -4.49, respectively. The patient's CLNHD was greater than the popPK parameter value but less than the popPK parameter value when estimated using the patient's original CrCL. Meanwhile, another software (Monolix; version 2024R1) gave similar results. This study shows the importance of individualized PK parameter estimation, particularly in obese HD patients, and highlights the potential impact of factors including obesity on gentamicin CL.
本研究旨在估算接受庆大霉素治疗的肥胖血液透析(HD)患者的个体药代动力学(PK)参数,并评估肥胖对庆大霉素清除率(CL)的影响。一名53岁的肥胖韩国女性接受了血液透析并使用了庆大霉素。为了估算个体PK参数,我们使用NONMEM 7.4.4软件的事后分析选项。先验模型将血液透析期间的CL中的血液透析作为协变量,将根据先验模型的组均值标准化的肌酐CL(CrCL)作为非血液透析CL(CLNHD)的协变量。个体CLNHD较群体CLNHD大幅降低,其值相当于先验模型群体药代动力学(popPK)参数的36%。患者的CrCL超过了先验信息的组最大值,提示肾功能表示不准确。将CrCL调整为先验模型的组均值后,患者的CLNHD为群体典型值的138%。每次运行的目标函数值分别为0.53和 -4.49。患者的CLNHD大于popPK参数值,但小于使用患者原始CrCL估算时的popPK参数值。同时,另一个软件(Monolix;2024R1版)给出了类似结果。本研究表明了个体PK参数估算的重要性,尤其是在肥胖血液透析患者中,并强调了包括肥胖在内的因素对庆大霉素CL的潜在影响。