Evidence map›Paper›PMID 42180250›Full record

ArticleFrontiers in cellular and infection microbiology2026

Physiologically based pharmacokinetic modeling and dose adjustment of imipenem in pediatric patients with renal impairment.

Chen Feng, Peng Xiao, Yuchen Qu, Kai Fan, Yueyuan Wang, Xinyun Zhang, Xiaolan Wang, Jie Pan, Yang Deng, Yunli Yu

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Chen FengDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Peng XiaoDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Yuchen QuDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Kai FanDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Yueyuan WangDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Xinyun ZhangDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Xiaolan WangDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Jie PanDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Yang DengHunan Provincial Key Laboratory of Anti-Resistance Microbial Drugs, The Third Hospital of Changsha, Changsha, Hunan, China.
Yunli YuDepartment of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To establish a physiologically based pharmacokinetic (PBPK) model of imipenem, predict its exposure in pediatric patients with different renal function, and optimize the dosing regimen. Methods: GastroPlus™ was used to construct PBPK models for healthy adults, adults with renal impairment (RI), and children with normal renal function, validated by fold error (<2) between predicted and observed pharmacokinetic parameters. Based on the established PBPK models, the exposure of imipenem in pediatric patients with different renal function was predicted. Monte carlo simulations were used to evaluate the probability of target attainment (PTA) for optimized doses and to determine appropriate dosing regimens for pediatric patients with RI. Results: The PBPK model could adequately predict the exposure of imipenem in different populations after single and multiple administrations (fold error <2). For 15 mg/kg doses, the AUC of imipenem in children with mild RI, moderate RI and severe RI was 1.05-fold, 1.26-fold, and 2.14-fold that of healthy children, respectively. Prolonging infusion from 30 min to 3 h significantly increased PTA. In addition, for susceptible bacteria with the minimum inhibitory concentration (MIC) < 4 mg/L, the recommended doses for pediatric patients aged ≥ 3 years with normal renal function, mild RI, moderate RI, and severe RI were 15, 15, 12, and 7 mg/kg every 6 hours, respectively, with a 3-hour infusion. Conclusion: This PBPK model can accurately predict the exposure of imipenem in pediatric patients with renal impairment, and the optimized dosing regimen can meet the pharmacodynamic targets, providing support for the precise use of imipenem.

Indexed as

Anti-Bacterial AgentsImipenemRenal InsufficiencyAdolescentAdultChildChild, PreschoolFemaleHumansInfantMaleMicrobial Sensitivity TestsModels, BiologicalMonte Carlo MethodAnti-Bacterial AgentsImipenemimipenempediatric patientsphysiologically based pharmacokinetic modelprobability of target attainmentrenal impairment

Identifiers

PMID42180250
PMCPMC13194417

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