Department of Systems Biomedicine and Pharmacology, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
Pediatric Pharmacology and Pharmacometrics, University Children's Hospital (UKBB), Basel, Switzerland.
AAPS J. 2021 Apr 11;23(3):53. doi: 10.1208/s12248-021-00577-x.
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 (CL, 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 CL down to 8.6 mL/min/1.73 m. The two-compartment model, with clearance (CL) significantly increasing with TBW and CL, 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 CL 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.
万古霉素是一种有效的但潜在肾毒性抗生素,常用于严重感染。目前缺乏肥胖儿童和青少年(无论是否有肾功能损害)使用万古霉素的剂量指南。本研究描述了在具有不同程度肥胖和肾功能的大量儿科队列中万古霉素的药代动力学,旨在为该人群设计实用的剂量指南。使用 2006 年 1 月至 2012 年 12 月期间接受>1 次万古霉素治疗且至少有 1 次万古霉素浓度测量的年龄在 1-18 岁的患者的数据,进行了一项多中心回顾性群体药代动力学研究。除了药代动力学数据外,还收集了年龄、性别、体重、肌酐清除率(CL,床边 Schwartz 方程)、病房、种族和中性粒细胞减少状态。使用 NONMEM7.4 进行群体药代动力学分析和模拟。共纳入 1892 例患者(5524 个样本),总体重(TBW)范围为 6-188kg(1344 例正常体重、247 例超重和 301 例肥胖患者),CL 低至 8.6mL/min/1.73m。两室模型,CL 随 TBW 和 CL 显著增加,中央和外周分布容积和隔室间清除率随 TBW 增加,在所有年龄、体重和肾功能范围内表现良好。提出了一种剂量指南,该指南将体重和 CL 整合在一起,在儿科人群中所有年龄、体重和肾功能范围内实现了有效和安全的暴露。我们已经描述了肥胖儿童和青少年(1-18 岁)万古霉素的完整药代动力学特征,并提出了一种实用的剂量指南,该指南将体重和肾功能整合在一起。