Department of Pediatrics, School of Medicine, University of California, San Diego, San Diego, California.
Department of Pediatrics, Oregon Health and Science University and Doernbecher Children's Hospital, Portland, Oregon.
Hosp Pediatr. 2021 Nov;11(11):e289-e296. doi: 10.1542/hpeds.2020-004465. Epub 2021 Oct 13.
Vancomycin carries risks of treatment failure and emergent resistance with underexposure and renal toxicity with overexposure. Children with overweight or obesity may have altered pharmacokinetics. We aimed to examine how body weight metrics influence vancomycin serum concentrations and to evaluate alternative dosing strategies.
This was a multicenter retrospective cohort study across 3 large, academic hospitals. Patients aged 2 to 18 years old who received ≥3 doses of intravenous vancomycin were included. Weight metrics included total body weight, adjusted body weight, ideal body weight, body surface area, and allometric weight. Outcomes included vancomycin concentration and ratios of area under the curve (AUC) to minimum inhibitory concentration (MIC). Regression analyses were used to examine which body-weight identifier predicted outcomes.
Of the 1099 children, 45% were girls, mean age was 9.0 (SD = 5.4) years, 14% had overweight, and 17% had obesity. Seventy-five percent of children had vancomycin concentrations in the subtherapeutic range by trough <10 µg/mL, and 63% had a ratio of AUC to MIC <400 μg-hr/mL. Three percent had a supratherapeutic initial trough >20 µg/mL or ratio of AUC to MIC >600 μg-hr/mL. Serum vancomycin concentrations were higher in children with overweight or obesity compared with children who were at a normal weight or underweight; the mean ratio of AUC to MIC also trended higher in the groups with overweight or obesity.
Most children received vancomycin regimens that produced suboptimal trough levels. Children with overweight or obesity experienced higher vancomycin trough levels than children of normal weight despite receiving lower total body weight dosing. Using the ratio of AUC to MIC was a better measure of drug exposure.
万古霉素暴露不足会导致治疗失败和耐药性出现,暴露过度则会导致肾毒性。超重或肥胖的儿童可能会改变药代动力学特性。本研究旨在研究体重指标如何影响万古霉素的血清浓度,并评估替代的给药方案。
这是一项在 3 家大型学术医院进行的多中心回顾性队列研究。纳入年龄在 2 至 18 岁之间、接受过至少 3 剂静脉万古霉素治疗的患者。体重指标包括总体重、调整体重、理想体重、体表面积和比例体重。结局指标包括万古霉素浓度和药时曲线下面积(AUC)与最小抑菌浓度(MIC)比值。回归分析用于研究哪种体重指标可以预测结局。
在 1099 名儿童中,45%为女性,平均年龄为 9.0(SD=5.4)岁,14%超重,17%肥胖。75%的儿童谷浓度低于 10μg/ml,属于治疗窗下限;63%的儿童 AUC/MIC 比值小于 400μg·hr/ml。有 3%的儿童初始谷浓度高于 20μg/ml或 AUC/MIC 比值大于 600μg·hr/ml,属于治疗窗上限。与体重正常或体重不足的儿童相比,超重或肥胖的儿童血清万古霉素浓度更高;AUC/MIC 的比值在超重或肥胖组中也呈上升趋势。
大多数儿童接受的万古霉素治疗方案使谷浓度不理想。尽管超重或肥胖儿童的总体重用药剂量较低,但他们的万古霉素谷浓度仍高于体重正常的儿童。AUC/MIC 比值是衡量药物暴露的更好指标。