Downes Kevin J, Zane Nicole R, Zuppa Athena F
The Center for Clinical Pharmacology, Children's Hospital of Philadelphia.
The Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia.
Ther Drug Monit. 2020 Dec;42(6):848-855. doi: 10.1097/FTD.0000000000000796.
Vancomycin is eliminated by glomerular filtration, but current approaches to estimate kidney function in children are unreliable. The authors sought to compare the suitability of cystatin C (CysC)-based glomerular filtration rate equations with the most commonly used creatinine-based equation, bedside Schwartz, to estimate vancomycin clearance (CL).
This prospective observational study enrolled critically ill patients (2-18 years) receiving intravenous vancomycin at the Children's Hospital of Philadelphia during December 2015-November 2017. Vancomycin levels were collected during clinical care and at 3 times during a single dosing interval. Plasma CysC was measured within 24 hours before intravenous vancomycin (baseline) initiation or immediately after enrollment and along with the third pharmacokinetic sample. Nonlinear mixed effects modeling was performed using NONMEM software. Covariate selection was used to test model fit with inclusion of the estimated glomerular filtration rate (eGFR) on CL using bedside Schwartz versus various published CysC-based equations.
In total, 83 vancomycin levels were obtained from 20 children. The median age was 12.7 years; 6 patients were women. A 1-compartment model best described the data; CL was allometrically scaled to 0.75. During covariate selection, inclusion of the eGFR calculated using a CysC-based equation significantly improved model fit [reduction in objective function value (OFV) range: -17.191 to -18.704] than bedside Schwartz ([INCREMENT]OFV -12.820). Including the full age spectrum equation, an eGFR equation based on both creatinine and CysC, led to the largest OFV reduction (-22.913); female sex was also a significant covariate of CL in the model. Final model pharmacokinetic indices were CL = 0.29 L/h/kg and volume of distribution = 0.48 L/kg.
CysC-based equations help better estimate vancomycin CL than bedside Schwartz in critically ill children.
万古霉素通过肾小球滤过清除,但目前评估儿童肾功能的方法并不可靠。作者旨在比较基于胱抑素C(CysC)的肾小球滤过率方程与最常用的基于肌酐的方程(床边施瓦茨方程)在估计万古霉素清除率(CL)方面的适用性。
这项前瞻性观察性研究纳入了2015年12月至2017年11月期间在费城儿童医院接受静脉注射万古霉素的重症患者(2至18岁)。在临床护理期间以及单次给药间隔内的3个时间点采集万古霉素血药浓度。在静脉注射万古霉素(基线)开始前24小时内或入组后立即测定血浆CysC,并与第三个药代动力学样本同时测定。使用NONMEM软件进行非线性混合效应建模。使用协变量选择来测试模型拟合情况,将基于床边施瓦茨方程与各种已发表的基于CysC的方程估算的肾小球滤过率(eGFR)纳入对CL的影响。
共从20名儿童中获得了83个万古霉素血药浓度数据。中位年龄为12.7岁;6例为女性。一个一室模型能最好地描述数据情况;CL经异速生长标度调整为0.75。在协变量选择过程中,与床边施瓦茨方程相比,纳入基于CysC的方程计算得到的eGFR能显著改善模型拟合情况(目标函数值(OFV)降低范围:-17.191至-18.704),而床边施瓦茨方程使OFV增加了-12.820。纳入全年龄谱方程(一种基于肌酐和CysC的eGFR方程)导致OFV降低幅度最大(-22.913);女性性别在该模型中也是CL的一个显著协变量。最终模型的药代动力学指标为CL = 0.29 L/h/kg,分布容积 = 0.48 L/kg。
在重症儿童中,基于CysC的方程比床边施瓦茨方程能更好地估计万古霉素CL。