Department of Pharmacy, Xiangya Hospital of Central South University, Changsha, Hunan, China.
School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, China.
Antimicrob Agents Chemother. 2018 Nov 26;62(12). doi: 10.1128/AAC.00955-18. Print 2018 Dec.
Voriconazole is a broad-spectrum triazole antifungal and the first-line treatment for invasive aspergillosis (IA). The aim of this research was to study the dose adjustments of voriconazole as well as the affecting factors influencing voriconazole trough concentrations in Asian children to optimize its daily administration. Clinical data were analyzed of inpatients 2 to 14 years old who were subjected to voriconazole trough concentration monitoring from 1 June 2015 to 1 December 2017. A total of 138 voriconazole trough concentrations from 42 pediatric patients were included. Voriconazole trough concentrations at steady state ranged from 0.02 to 9.35 mg/liter, with high inter- and intraindividual variability. Only 50.0% of children achieved the target range (1.0 to 5.5 mg/liter) at initial dosing, while 35.7% of children were subtherapeutic, and 14.3% of children were supratherapeutic at initial dosing. There was no correlation between initial trough concentrations and initial dosing. A total of 28.6% of children (12/42) received an adjusted dose according to trough concentrations. Children <6, 6 to 12, and >12 years old required a median oral maintenance dose to achieve the target range of 11.1, 7.2, and 5.3 mg/kg twice daily, respectively ( = 0.043). The average doses required to achieved the target range were 7.7 mg/kg and 5.6 mg/kg, respectively, and were lower than the recommended dosage ( = 0.033 and 0.003, respectively). Affecting factors such as administration routes and coadministration with proton pump inhibitors (PPIs) explained 55.3% of the variability in voriconazole exposure. Therapeutic drug monitoring (TDM) of voriconazole could help to individualize antifungal therapy for children and provide guidelines for TDM and dosing optimization in Asian children.
伏立康唑是一种广谱三唑类抗真菌药物,也是侵袭性曲霉菌病(IA)的一线治疗药物。本研究旨在研究伏立康唑的剂量调整以及影响伏立康唑谷浓度的影响因素,以优化其日常给药。分析了 2015 年 6 月 1 日至 2017 年 12 月 1 日期间接受伏立康唑谷浓度监测的 2 至 14 岁住院患者的临床数据。共纳入 42 例儿科患者的 138 个伏立康唑谷浓度。稳态时伏立康唑谷浓度范围为 0.02 至 9.35 毫克/升,个体内和个体间差异很大。只有 50.0%的儿童在初始剂量时达到目标范围(1.0 至 5.5 毫克/升),35.7%的儿童治疗不足,14.3%的儿童治疗过度。初始谷浓度与初始剂量之间无相关性。共有 28.6%(12/42)的儿童根据谷浓度调整剂量。<6 岁、6 至 12 岁和>12 岁的儿童需要中位数口服维持剂量,以实现目标范围 11.1、7.2 和 5.3 毫克/公斤,每日两次(=0.043)。达到目标范围所需的平均剂量分别为 7.7 毫克/公斤和 5.6 毫克/公斤,均低于推荐剂量(=0.033 和 0.003)。给药途径和与质子泵抑制剂(PPIs)联合用药等影响因素解释了伏立康唑暴露变异性的 55.3%。伏立康唑治疗药物监测(TDM)有助于个体化儿童抗真菌治疗,并为亚洲儿童提供 TDM 和剂量优化指南。