Al-Mazraawy Betool O, Girotto Jennifer E
J Pediatr Pharmacol Ther. 2021;26(7):740-745. doi: 10.5863/1551-6776-26.7.740. Epub 2021 Sep 24.
Updated vancomycin guidelines suggest dose adjustment based on area under the curve in a 24-hour period (AUC). This study aims to determine whether a pharmacist managed vancomycin protocol that incorporates maximum dosing paired with trough monitoring can achieve appropriate vancomycin AUC exposures.
A retrospective review was performed evaluating vancomycin usage from October 2018 through September 2019 at a children's hospital. Patients with less than 4 doses or lack a trough concentration were excluded. Vancomycin AUC were estimated using 2 calculations: 1) the Le method, incorporating age and serum creatinine, and 2) the trapezoidal method based upon population data and patient-specific trough. Target AUC ranges were assessed. AUC goals were 400 to 600 mg·hr/L, but due to known variations between calculations, a variance of 20 mg·hr/L was allowed for each end of the goal. Secondary analyses included evaluations of efficacy and toxicity.
Two-hundred twenty-three patients were included. Initial doses were estimated to meet AUC goals in only 63%. After trough-based dose modification, 81% achieved a therapeutic AUC. Using the trapezoidal method, therapeutic concentrations were found in 51% of patients based on the initial dose and 77% after dose modification. Only 6.3% of patients had kidney injury with only 1 of those patients having any calculated AUC > 600 mg·hr/L and none above 620 mg·hr/L. No clinical failures were identified.
Increased initial dosing in infants and children is needed to result in AUC exposures recommended in the guidelines. Maximum dosing paired with trough monitoring may be an alternative to AUC monitoring in areas that are unable to perform AUC calculations. Prospective data are needed to validate these conclusions.
最新的万古霉素指南建议根据24小时曲线下面积(AUC)进行剂量调整。本研究旨在确定由药剂师管理的、结合最大剂量与谷浓度监测的万古霉素方案是否能实现适当的万古霉素AUC暴露。
对一家儿童医院2018年10月至2019年9月期间万古霉素的使用情况进行回顾性评估。排除用药少于4剂或缺乏谷浓度的患者。万古霉素AUC通过两种计算方法估算:1)结合年龄和血清肌酐的Le方法;2)基于群体数据和患者特异性谷浓度的梯形法。评估目标AUC范围。AUC目标为400至600mg·hr/L,但由于计算方法之间存在已知差异,目标两端允许有20mg·hr/L的差异。次要分析包括疗效和毒性评估。
纳入223例患者。初始剂量估计仅63%能达到AUC目标。基于谷浓度调整剂量后,81%达到治疗性AUC。使用梯形法,基于初始剂量,51%的患者达到治疗浓度,剂量调整后为77%。仅6.3%的患者出现肾损伤,其中只有1例患者计算出的AUC>600mg·hr/L,无患者高于620mg·hr/L。未发现临床治疗失败病例。
需要增加婴儿和儿童的初始剂量,以达到指南中推荐的AUC暴露水平。在无法进行AUC计算的地区,最大剂量结合谷浓度监测可能是AUC监测的替代方法。需要前瞻性数据来验证这些结论。