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Population Pharmacokinetics and Dosage Optimization of Teicoplanin in Children With Different Renal Functions

OBJECTIVE: The purposes of our study were to investigate the population pharmacokinetics of teicoplanin in Chinese children with different renal functions and to propose the appropriate dosing regimen for these pediatric patients. METHODS: We performed a prospective pharmacokinetic research on child...

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Autores principales: Gao, Liuliu, Xu, Hua, Ye, Qi, Li, Sichan, Wang, Jun, Mei, Yan, Niu, Changhe, Kang, Ting, Chen, Chen, Wang, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214819/
https://www.ncbi.nlm.nih.gov/pubmed/32431611
http://dx.doi.org/10.3389/fphar.2020.00552
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author Gao, Liuliu
Xu, Hua
Ye, Qi
Li, Sichan
Wang, Jun
Mei, Yan
Niu, Changhe
Kang, Ting
Chen, Chen
Wang, Yang
author_facet Gao, Liuliu
Xu, Hua
Ye, Qi
Li, Sichan
Wang, Jun
Mei, Yan
Niu, Changhe
Kang, Ting
Chen, Chen
Wang, Yang
author_sort Gao, Liuliu
collection PubMed
description OBJECTIVE: The purposes of our study were to investigate the population pharmacokinetics of teicoplanin in Chinese children with different renal functions and to propose the appropriate dosing regimen for these pediatric patients. METHODS: We performed a prospective pharmacokinetic research on children aged 0–10 years, with different renal functions. The population pharmacokinetics model of teicoplanin was developed using NLME program. The individualized optimal dosage regimen was proposed on the basis of the obtained population pharmacokinetics parameters. RESULTS: To achieve the target trough level of 10–30 mg/L, optimal dosing regimen for children with different renal functions are predicted as follows based on the population PK simulations: children with moderate renal insufficiency need three loading doses of 6 mg/kg q12h followed by a maintenance dose of 5 mg/kg qd; children with mild renal insufficiency require three loading doses of 12 mg/kg q12h followed by a maintenance dose of 8 mg/kg qd; children with normal or augmented renal function should be given three loading doses of 12 mg/kg q12h followed by a maintenance doses of 10 mg/kg qd. CONCLUSION: The first study on the population pharmacokinetics of teicoplanin in Chinese children with different renal functions was performed. Individualized dosing regimen was recommended for different renal function groups based on population PK model prediction.
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spelling pubmed-72148192020-05-19 Population Pharmacokinetics and Dosage Optimization of Teicoplanin in Children With Different Renal Functions Gao, Liuliu Xu, Hua Ye, Qi Li, Sichan Wang, Jun Mei, Yan Niu, Changhe Kang, Ting Chen, Chen Wang, Yang Front Pharmacol Pharmacology OBJECTIVE: The purposes of our study were to investigate the population pharmacokinetics of teicoplanin in Chinese children with different renal functions and to propose the appropriate dosing regimen for these pediatric patients. METHODS: We performed a prospective pharmacokinetic research on children aged 0–10 years, with different renal functions. The population pharmacokinetics model of teicoplanin was developed using NLME program. The individualized optimal dosage regimen was proposed on the basis of the obtained population pharmacokinetics parameters. RESULTS: To achieve the target trough level of 10–30 mg/L, optimal dosing regimen for children with different renal functions are predicted as follows based on the population PK simulations: children with moderate renal insufficiency need three loading doses of 6 mg/kg q12h followed by a maintenance dose of 5 mg/kg qd; children with mild renal insufficiency require three loading doses of 12 mg/kg q12h followed by a maintenance dose of 8 mg/kg qd; children with normal or augmented renal function should be given three loading doses of 12 mg/kg q12h followed by a maintenance doses of 10 mg/kg qd. CONCLUSION: The first study on the population pharmacokinetics of teicoplanin in Chinese children with different renal functions was performed. Individualized dosing regimen was recommended for different renal function groups based on population PK model prediction. Frontiers Media S.A. 2020-05-05 /pmc/articles/PMC7214819/ /pubmed/32431611 http://dx.doi.org/10.3389/fphar.2020.00552 Text en Copyright © 2020 Gao, Xu, Ye, Li, Wang, Mei, Niu, Kang, Chen and Wang http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Gao, Liuliu
Xu, Hua
Ye, Qi
Li, Sichan
Wang, Jun
Mei, Yan
Niu, Changhe
Kang, Ting
Chen, Chen
Wang, Yang
Population Pharmacokinetics and Dosage Optimization of Teicoplanin in Children With Different Renal Functions
title Population Pharmacokinetics and Dosage Optimization of Teicoplanin in Children With Different Renal Functions
title_full Population Pharmacokinetics and Dosage Optimization of Teicoplanin in Children With Different Renal Functions
title_fullStr Population Pharmacokinetics and Dosage Optimization of Teicoplanin in Children With Different Renal Functions
title_full_unstemmed Population Pharmacokinetics and Dosage Optimization of Teicoplanin in Children With Different Renal Functions
title_short Population Pharmacokinetics and Dosage Optimization of Teicoplanin in Children With Different Renal Functions
title_sort population pharmacokinetics and dosage optimization of teicoplanin in children with different renal functions
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214819/
https://www.ncbi.nlm.nih.gov/pubmed/32431611
http://dx.doi.org/10.3389/fphar.2020.00552
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