Dosing Recommendations for Vancomycin in Children and Adolescents with Varying Levels of Obesity and Renal Dysfunction: a Population Pharmacokinetic Study in 1892 Children Aged 1-18 Years

被引:12
|
作者
Smit, Cornelis [1 ,2 ]
Goulooze, Sebastiaan C. [1 ]
Bruggemann, Roger J. M. [3 ]
Sherwin, Catherine M. [4 ]
Knibbe, Catherijne A. J. [1 ,5 ]
机构
[1] Leiden Univ, Leiden Acad Ctr Drug Res, Dept Syst Biomed & Pharmacol, Leiden, Netherlands
[2] Univ Childrens Hosp UKBB, Pediat Pharmacol & Pharmacometr, Basel, Switzerland
[3] Radboudumc, Dept Pharm, Radboud Inst Hlth Sci, Nijmegen, Netherlands
[4] Wright State Univ, Dept Pediat, Boonshoft Sch Med, Dayton Childrens Hosp, Dayton, OH USA
[5] St Antonius Hosp, Dept Clin Pharm, Koekoekslaan 1, NL-3435 CM Nieuwegein, Netherlands
来源
AAPS JOURNAL | 2021年 / 23卷 / 03期
关键词
obesity; pediatrics; pharmacokinetics; vancomycin;
D O I
10.1208/s12248-021-00577-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Vancomycin is an effective but potentially nephrotoxic antibiotic commonly used for severe infections. Dosing guidelines for vancomycin in obese children and adolescents with or without renal impairment are currently lacking. This study describes the pharmacokinetics of vancomycin in a large pediatric cohort with varying degrees of obesity and renal function to design practical dosing guidelines for this population. A multi-center retrospective population pharmacokinetic study was conducted using data from patients aged 1-18 years who received >1 dose of vancomycin and had >= 1 vancomycin concentration measured between January 2006 and December 2012. Besides pharmacokinetic data, age, gender, body weight, creatinine clearance (CLcr, bedside Schwartz equation), ward, race, and neutropenic status were collected. Population pharmacokinetic analysis and simulations were performed using NONMEM7.4. A total of 1892 patients (5524 samples) were included, with total body weight (TBW) ranging 6-188 kg (1344 normal weight, 247 overweight, and 301 obese patients) and CLcr down to 8.6 mL/min/1.73 m(2). The two-compartment model, with clearance (CL) significantly increasing with TBW and CLcr, central and peripheral volume of distribution and inter-compartmental clearance increasing with TBW, performed well for all age, weight, and renal function ranges. A dosing guideline is proposed that integrates body weight and CLcr resulting in effective and safe exposures across all ages, body weight, and renal functions in the pediatric population. We have characterized the full pharmacokinetic profile of vancomycin in obese children and adolescents aged 1-18 years and propose a practical dosing guideline that integrates both body weight and renal function.
引用
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页数:10
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