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Developmental population pharmacokinetics-pharmacodynamics and dosing optimization of cefoperazone in children.

Authors :
Shi, Hai-Yan
Wang, Kai
Wang, Rong-Hua
Wu, Yue-E
Tang, Bo-Hao
Li, Xue
Du, Bin
Kan, Min
Zheng, Yi
Xu, Bao-Ping
Shen, A-Dong
Su, Le-Qun
Jacqz-Aigrain, Evelyne
Huang, Xin
Zhao, Wei
Source :
Journal of Antimicrobial Chemotherapy (JAC). Jul2020, Vol. 75 Issue 7, p1917-1924. 8p.
Publication Year :
2020

Abstract

<bold>Objectives: </bold>To evaluate the population pharmacokinetics of cefoperazone in children and establish an evidence-based dosing regimen using a developmental pharmacokinetic-pharmacodynamic approach in order to optimize cefoperazone treatment.<bold>Methods: </bold>A model-based, open-label, opportunistic-sampling pharmacokinetic study was conducted in China. Blood samples from 99 cefoperazone-treated children were collected and quantified by HPLC/MS. NONMEM software was used for population pharmacokinetic-pharmacodynamic analysis. This study was registered at ClinicalTrials.gov (NCT03113344).<bold>Results: </bold>A two-compartment model with first-order elimination agreed well with the experimental data. Covariate analysis showed that current body weight had a significant effect on the pharmacokinetics of cefoperazone. Monte Carlo simulation showed that for bacteria for which cefoperazone has an MIC of 0.5 mg/L, 78.1% of hypothetical children treated with '40 mg/kg/day, q8h, IV drip 3 h' would reach the pharmacodynamic target. For bacteria for which cefoperazone has an MIC of 8 mg/L, 88.4% of hypothetical children treated with 80 mg/kg/day (continuous infusion) would reach the treatment goal. A 160 mg/kg/day (continuous infusion) regimen can cover bacteria for which cefoperazone has an MIC of 16 mg/L. Nevertheless, even if using the maximum reported dose of 160 mg/kg/day (continuous infusion), the ratio of hypothetical children reaching the treatment target was only 9.9% for bacteria for which cefoperazone has an MIC of 32 mg/L.<bold>Conclusions: </bold>For cefoperazone, population pharmacokinetics were evaluated in children and an appropriate dosing regimen was developed based on developmental pharmacokinetics-pharmacodynamics. The dose indicated in the instructions (20-160 mg/kg/day) can basically cover the clinically common bacteria for which cefoperazone has an MIC of ≤16 mg/L. However, for bacteria for which the MIC is >16 mg/L, cefoperazone is not a preferred choice. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03057453
Volume :
75
Issue :
7
Database :
Academic Search Index
Journal :
Journal of Antimicrobial Chemotherapy (JAC)
Publication Type :
Academic Journal
Accession number :
144244976
Full Text :
https://doi.org/10.1093/jac/dkaa071