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老年患者阿米卡星初始给药方案的群体药代动力学分析

Population Pharmacokinetics Analysis of Amikacin Initial Dosing Regimen in Elderly Patients.

作者信息

Kato Hideo, Parker Suzanne L, Roberts Jason A, Hagihara Mao, Asai Nobuhiro, Yamagishi Yuka, Paterson David L, Mikamo Hiroshige

机构信息

Department of Clinical Infectious Diseases, Aichi Medical University, Aichi 480-1195, Japan.

University of Queensland Centre for Clinical Research, The University of Queensland, Royal Brisbane & Women's Hospital, Brisbane, QLD 4029, Australia.

出版信息

Antibiotics (Basel). 2021 Jan 20;10(2):100. doi: 10.3390/antibiotics10020100.

Abstract

There are limited data of amikacin pharmacokinetics (PK) in the elderly population. Hence, we aimed to describe the population PK of amikacin in elderly patients (>70 years old) and to establish optimized initial dosing regimens. We simulated individual maximum concentrations in plasma (Cmax) and minimal concentrations (Cmin) for several dosing regimens (200-2000 mg every 24, 48, and 72 h) for patients with creatinine clearance (CCr) of 10-90 mL/min and analyzed efficacy (Cmax/minimal inhibitory concentration (MIC) ≥ 8) for MICs of 4, 8, and 16 mg/L and safety (Cmin < 4 mg/L). A one-compartment model best described the data. CCr was the only covariate associated with amikacin clearance. The population PK parameter estimates were 2.25 L/h for clearance and 18.0 L for volume of distribution. Dosing simulations recommended the dosing regimens (1800 mg) with dosing intervals ranging 48-72 h for patients with CCr of 40-90 mL/min based on achievement of both efficacy for the MIC of 8 mg/L and safety. None of the dosing regimens achieved the targets for an MIC of 16 mg/L. We recommend the initial dosing regimen using a nomogram based on CCr for an MIC of ≤8 mg/L in elderly patients with CCr of 40-90 mL/min.

摘要

关于老年人群中阿米卡星药代动力学(PK)的数据有限。因此,我们旨在描述老年患者(>70岁)中阿米卡星的群体PK,并建立优化的初始给药方案。我们模拟了肌酐清除率(CCr)为10 - 90 mL/min的患者在几种给药方案(每24、48和72小时200 - 2000 mg)下的个体血浆最大浓度(Cmax)和最小浓度(Cmin),并分析了对于4、8和16 mg/L的最低抑菌浓度(MIC)的疗效(Cmax/最低抑菌浓度(MIC)≥8)和安全性(Cmin < 4 mg/L)。单室模型最能描述这些数据。CCr是与阿米卡星清除率相关的唯一协变量。群体PK参数估计值为清除率2.25 L/h,分布容积18.0 L。给药模拟建议,基于对8 mg/L的MIC达到疗效和安全性,对于CCr为40 - 90 mL/min的患者,给药方案为(1800 mg),给药间隔为48 - 72小时。没有一种给药方案能达到16 mg/L的MIC目标。我们建议在CCr为40 - 90 mL/min的老年患者中,针对≤8 mg/L的MIC使用基于CCr的列线图制定初始给药方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0580/7909551/95881300e1fe/antibiotics-10-00100-g001a.jpg

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