Department of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, USA.
Clin Pharmacol Ther. 2021 Apr;109(4):952-957. doi: 10.1002/cpt.2179. Epub 2021 Mar 3.
Kidney function is a common parameter used to define antimicrobial drug dosage and frequency of administration. Several methods exist to measure kidney function but for pragmatic reasons rely on estimated kidney function equations based on the endogenous biomarker serum creatinine and common clinical variables. Current regulatory guidance on the design of studies in patients with abnormal kidney function in the United States also recommend consideration of estimated kidney function for this reason. Over the past few decades, alternate endogenous biomarkers, administration of exogenous biomarkers for noninvasive measurement, use of probe substrates to characterize individual kidney drug clearance pathways, modifications to conventional equations to account for time-varying clearance, and improved clinical trial modeling and simulation to factor in these uncertainties have occurred. Furthermore, major changes to kidney replacement therapy delivery in the outpatient, inpatient, and at-home setting are occurring. Antimicrobial drug dose adjustment in this diverse population is complex and in a state of flux due to technical innovations. Over-reliance on kidney function estimates to guide drug dosing in patients with infectious diseases can bias underdosing especially among the acutely ill. A holistic approach to drug dose adjustment in patients with abnormal kidney function is necessary to optimize clinical outcomes.
肾功能是定义抗菌药物剂量和给药频率的常用参数。有几种方法可以测量肾功能,但出于实际原因,这些方法依赖于基于内源性生物标志物血清肌酐和常见临床变量的估算肾功能方程。美国关于异常肾功能患者研究设计的现行监管指南也出于这个原因建议考虑估算的肾功能。在过去几十年中,出现了替代内源性生物标志物、用于非侵入性测量的外源性生物标志物的给药、使用探针底物来描述个体肾脏药物清除途径、修改常规方程以考虑随时间变化的清除率,以及改进临床试验建模和模拟以考虑这些不确定性。此外,门诊、住院和家庭环境中肾脏替代治疗的主要变化正在发生。由于技术创新,在这个多样化的人群中调整抗菌药物剂量非常复杂,并且处于不断变化的状态。过度依赖肾功能估计值来指导传染病患者的药物剂量可能会导致剂量不足,尤其是在急性疾病患者中。需要采取整体方法来调整肾功能异常患者的药物剂量,以优化临床结果。