Population Pharmacokinetics Modeling of Vancomycin Among Chinese Infants With Normal and Augmented Renal Function

There have been good amounts of population pharmacokinetics (PPK) models of vancomycin for Chinese pediatric patients, but none of them had a special focus on modeling infant population with different levels of renal function. Since renal function variability is prominent among infant population and...

Full description

Bibliographic Details
Main Authors: De-Yi Li, Ling Li, Gui-Zhou Li, Ya-Hui Hu, Hong-Li Guo, Xia Jing, Feng Chen, Xing Ji, Jing Xu, Hao-Ran Dai
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.713588/full
id doaj-f86f5d18232d495eb676ff16c6b973f5
record_format Article
spelling doaj-f86f5d18232d495eb676ff16c6b973f52021-09-20T14:13:54ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602021-09-01910.3389/fped.2021.713588713588Population Pharmacokinetics Modeling of Vancomycin Among Chinese Infants With Normal and Augmented Renal FunctionDe-Yi Li0Ling Li1Ling Li2Gui-Zhou Li3Gui-Zhou Li4Ya-Hui Hu5Hong-Li Guo6Xia Jing7Feng Chen8Xing Ji9Jing Xu10Hao-Ran Dai11Hao-Ran Dai12Pharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaPharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, ChinaSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, ChinaThere have been good amounts of population pharmacokinetics (PPK) models of vancomycin for Chinese pediatric patients, but none of them had a special focus on modeling infant population with different levels of renal function. Since renal function variability is prominent among infant population and the clearance (CL) of vancomycin is heavily related to renal excretion, it is important to establish precise PPK models based on individual renal function levels. We employed a PPK approach to develop three models of vancomycin in parallel for Chinese pediatric patients with normal renal function [estimated glomerular filtration rate (eGFR) between 30 and 86 ml/min/1.73 m2, Model 1], with augmented renal function (eGFR ≥ 86 ml/min/1.73 m2, Model 2), or with all levels of renal function (Model 3). Three one-compartment models with first-order elimination kinetics were established. The predictive ability of Model 1 and Model 2 among each certain population is comparable with that of Model 3 with no statistical difference. Our study revealed that among the infant population with augmented renal function, only body weight was included as a covariate, which indicated that for an infant whose eGFR ≥ 86 ml/min/1.73 m2, taking blood sample is not compulsory for predicting vancomycin blood concentration, which avoids unnecessary injury to vulnerable infants.https://www.frontiersin.org/articles/10.3389/fped.2021.713588/fullvancomycinpediatricspopulation pharmacokineticsrenal functionexternal validation
collection DOAJ
language English
format Article
sources DOAJ
author De-Yi Li
Ling Li
Ling Li
Gui-Zhou Li
Gui-Zhou Li
Ya-Hui Hu
Hong-Li Guo
Xia Jing
Feng Chen
Xing Ji
Jing Xu
Hao-Ran Dai
Hao-Ran Dai
spellingShingle De-Yi Li
Ling Li
Ling Li
Gui-Zhou Li
Gui-Zhou Li
Ya-Hui Hu
Hong-Li Guo
Xia Jing
Feng Chen
Xing Ji
Jing Xu
Hao-Ran Dai
Hao-Ran Dai
Population Pharmacokinetics Modeling of Vancomycin Among Chinese Infants With Normal and Augmented Renal Function
Frontiers in Pediatrics
vancomycin
pediatrics
population pharmacokinetics
renal function
external validation
author_facet De-Yi Li
Ling Li
Ling Li
Gui-Zhou Li
Gui-Zhou Li
Ya-Hui Hu
Hong-Li Guo
Xia Jing
Feng Chen
Xing Ji
Jing Xu
Hao-Ran Dai
Hao-Ran Dai
author_sort De-Yi Li
title Population Pharmacokinetics Modeling of Vancomycin Among Chinese Infants With Normal and Augmented Renal Function
title_short Population Pharmacokinetics Modeling of Vancomycin Among Chinese Infants With Normal and Augmented Renal Function
title_full Population Pharmacokinetics Modeling of Vancomycin Among Chinese Infants With Normal and Augmented Renal Function
title_fullStr Population Pharmacokinetics Modeling of Vancomycin Among Chinese Infants With Normal and Augmented Renal Function
title_full_unstemmed Population Pharmacokinetics Modeling of Vancomycin Among Chinese Infants With Normal and Augmented Renal Function
title_sort population pharmacokinetics modeling of vancomycin among chinese infants with normal and augmented renal function
publisher Frontiers Media S.A.
series Frontiers in Pediatrics
issn 2296-2360
publishDate 2021-09-01
description There have been good amounts of population pharmacokinetics (PPK) models of vancomycin for Chinese pediatric patients, but none of them had a special focus on modeling infant population with different levels of renal function. Since renal function variability is prominent among infant population and the clearance (CL) of vancomycin is heavily related to renal excretion, it is important to establish precise PPK models based on individual renal function levels. We employed a PPK approach to develop three models of vancomycin in parallel for Chinese pediatric patients with normal renal function [estimated glomerular filtration rate (eGFR) between 30 and 86 ml/min/1.73 m2, Model 1], with augmented renal function (eGFR ≥ 86 ml/min/1.73 m2, Model 2), or with all levels of renal function (Model 3). Three one-compartment models with first-order elimination kinetics were established. The predictive ability of Model 1 and Model 2 among each certain population is comparable with that of Model 3 with no statistical difference. Our study revealed that among the infant population with augmented renal function, only body weight was included as a covariate, which indicated that for an infant whose eGFR ≥ 86 ml/min/1.73 m2, taking blood sample is not compulsory for predicting vancomycin blood concentration, which avoids unnecessary injury to vulnerable infants.
topic vancomycin
pediatrics
population pharmacokinetics
renal function
external validation
url https://www.frontiersin.org/articles/10.3389/fped.2021.713588/full
work_keys_str_mv AT deyili populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT lingli populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT lingli populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT guizhouli populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT guizhouli populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT yahuihu populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT hongliguo populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT xiajing populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT fengchen populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT xingji populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT jingxu populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT haorandai populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
AT haorandai populationpharmacokineticsmodelingofvancomycinamongchineseinfantswithnormalandaugmentedrenalfunction
_version_ 1717374208154009600