Kennedy KaShena L, Ristagno Elizabeth H, Marshall Linda K, Mara Kristin C, Lee Grace, Dinnes Laura M
Department of Pharmacy (KLK), Children's Health Dallas, Dallas, TX.
Department of Pharmacy (LKM, GL, LMD), Mayo Clinic, Division of Pediatric Infectious Diseases, Department of Pediatric and Adolescent Medicine (EHR), Mayo Clinic, Department of Quantitative Health Sciences (KCM), Mayo Clinic, Rochester, MN.
J Pediatr Pharmacol Ther. 2025 Feb;30(1):112-122. doi: 10.5863/1551-6776-30.1.112. Epub 2025 Feb 10.
The optimal dose for triazoles in pediatric patients may substantially vary given the dynamic changes in pharmacokinetics and pharmacodynamics, based on disease severity. Therapeutic drug monitoring has been a valuable tool to help guide management and avoid potential toxicities associated with treatment of invasive fungal infections (IFIs). Goal azole serum concentrations are based on specific drug, indication, and minimum inhibitory concentration when known. This study aimed to determine the optimal pediatric azole doses needed to achieve targeted serum concentrations of isavuconazole, itraconazole, posaconazole, and voriconazole.
This is a single center, retrospective chart review of pediatric patients who received isavuconazole, itraconazole, posaconazole, or voriconazole between January 1, 2011, and August 31, 2021.
A total of 273 pediatric patients received isavuconazole, itraconazole, posaconazole, or voriconazole in the inpatient or outpatient setting during the study period. Of the 273 patients, only 122 met criteria for inclusion in the analysis. Eighty-three percent of patients reached a goal serum concentration. Patients younger than 12 years required a higher dose (mg/kg/day) to achieve goal serum concentrations. Patients who received an azole in the form of an oral tablet or intravenously were more likely to reach a goal concentration than those not receiving these formulations. Median time to goal concentration occurred at 20 days for isavuconazole, 34 days for itraconazole, 11 days for posaconazole, and 10 days for voriconazole.
Higher starting azole doses are needed to obtain goal concentrations quickly, especially for children younger than 12 years.
鉴于药代动力学和药效学随疾病严重程度的动态变化,三唑类药物在儿科患者中的最佳剂量可能有很大差异。治疗药物监测一直是帮助指导治疗管理并避免与侵袭性真菌感染(IFI)治疗相关潜在毒性的重要工具。目标唑类血清浓度基于特定药物、适应证以及已知时的最低抑菌浓度。本研究旨在确定达到艾沙康唑、伊曲康唑、泊沙康唑和伏立康唑目标血清浓度所需的最佳儿科唑类剂量。
这是一项对2011年1月1日至2021年8月31日期间接受艾沙康唑、伊曲康唑、泊沙康唑或伏立康唑治疗的儿科患者进行的单中心回顾性病历审查。
在研究期间,共有273名儿科患者在住院或门诊环境中接受了艾沙康唑、伊曲康唑、泊沙康唑或伏立康唑治疗。在这273名患者中,只有122名符合纳入分析的标准。83%的患者达到了目标血清浓度。12岁以下的患者需要更高的剂量(毫克/千克/天)才能达到目标血清浓度。接受口服片剂或静脉注射形式唑类药物的患者比未接受这些剂型的患者更有可能达到目标浓度。达到目标浓度的中位时间,艾沙康唑为20天,伊曲康唑为34天,泊沙康唑为11天,伏立康唑为10天。
需要更高的起始唑类剂量才能快速达到目标浓度,尤其是对于12岁以下的儿童。