Kong D, Koomen J V, Vanommeslaeghe F, Delanghe S, Van Biesen W, Colin P J, Eloot S
Department of Anesthesiology, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713GZ, Groningen, The Netherlands.
Department of Pharmacology, Toxicology and Kinetics, Dutch Medicines Evaluation Board, Utrecht, The Netherlands.
Clin Pharmacokinet. 2025 Aug;64(8):1165-1178. doi: 10.1007/s40262-025-01527-y. Epub 2025 Jun 3.
End-stage kidney disease (ESKD) patients undergoing haemodialysis (HD) require a dosing regimen that balances the low endogenous clearance with the additional dialyser clearance. This study aimed to expand a previously proposed general-purpose pharmacokinetic model for piperacillin/tazobactam with a new population of ESKD patients undergoing intermittent high-flux haemodialysis.
Inter- and intradialytic blood samples were collected in ESKD patients undergoing intermittent high-flux haemodialysis, in HD or haemodiafiltration (HDF) mode, who received piperacillin/tazobactam during routine care. The previous general-purpose model was expanded to reflect changes in the pharmacokinetics in the new patient population. A covariate search was performed focussing on factors that explained variability between patients in endogenous and dialysis clearance. Simulations were performed to determine the probability of target attainment with current dosing recommendations in this specific population.
In 20 ESKD patients, 195 piperacillin/tazobactam concentrations were determined. The general-purpose model was successfully expanded, wherein endogenous piperacillin/tazobactam clearance in patients with/without residual diuresis was 63% (95% confidence interval [CI] 49.5-73.0%) and 78.6% (95% CI 66.3-86.4%) lower compared with the general population, respectively. Extraction ratios of piperacillin and tazobactam ranged from 64 to 80%. Differences in probability of target attainment (PTA) for piperacillin were observed between patients with normal kidney function and ESKD patients undergoing haemodialysis with current dosing recommendations.
We successfully expanded a general-purpose model to reflect the piperacillin/tazobactam pharmacokinetics in ESKD patients undergoing intermittent haemodialysis using high-flux dialysers. The current dosing recommendations provide inconsistent probability of target attainment in ESKD patients compared with the general population.
接受血液透析(HD)的终末期肾病(ESKD)患者需要一种给药方案,以平衡内源性清除率低与透析器额外清除率之间的关系。本研究旨在将先前提出的哌拉西林/他唑巴坦通用药代动力学模型扩展至接受间歇性高通量血液透析的新的ESKD患者群体。
在接受间歇性高通量血液透析(HD或血液透析滤过[HDF]模式)的ESKD患者进行常规治疗期间接受哌拉西林/他唑巴坦治疗时,采集透析期间和透析后的血样。扩展先前的通用模型以反映新患者群体药代动力学的变化。进行协变量搜索,重点关注解释患者内源性和透析清除率差异的因素。进行模拟以确定在该特定人群中按照当前给药建议达到目标的概率。
在20例ESKD患者中,测定了195个哌拉西林/他唑巴坦浓度。通用模型成功扩展,其中有/无残余利尿的患者内源性哌拉西林/他唑巴坦清除率分别比普通人群低63%(95%置信区间[CI]49.5 - 73.0%)和78.6%(95%CI 66.3 - 86.4%)。哌拉西林和他唑巴坦的提取率范围为64%至80%。按照当前给药建议,肾功能正常的患者与接受血液透析的ESKD患者之间,哌拉西林达到目标的概率(PTA)存在差异。
我们成功扩展了一个通用模型,以反映使用高通量透析器进行间歇性血液透析的ESKD患者的哌拉西林/他唑巴坦药代动力学。与普通人群相比,当前给药建议在ESKD患者中达到目标的概率不一致。