Assessment of the Effective Dose of Isavuconazole, Itraconazole, Posaconazole, and Voriconazole to Achieve Goal Serum Concentrations in Pediatric Patients at a Single Center.

Q2 Medicine
KaShena L Kennedy, Elizabeth H Ristagno, Linda K Marshall, Kristin C Mara, Grace Lee, Laura M Dinnes
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引用次数: 0

Abstract

Objective: 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.

Methods: 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.

Results: 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.

Conclusions: Higher starting azole doses are needed to obtain goal concentrations quickly, especially for children younger than 12 years.

单中心儿科患者依沙乌康唑、伊曲康唑、泊沙康唑和伏立康唑达到目标血清浓度的有效剂量评估
目的:考虑到基于疾病严重程度的药代动力学和药效学的动态变化,儿科患者三唑类药物的最佳剂量可能会有很大差异。治疗性药物监测一直是帮助指导管理和避免与侵袭性真菌感染(IFIs)治疗相关的潜在毒性的有价值的工具。目标唑的血清浓度是基于特定的药物、适应症和已知的最低抑制浓度。本研究旨在确定达到伊萨乌康唑、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童唑剂量。方法:这是一项单中心、回顾性的图表研究,对2011年1月1日至2021年8月31日期间接受依舒康唑、伊曲康唑、泊沙康唑或伏立康唑治疗的儿科患者进行回顾性分析。结果:在研究期间,共有273名儿科患者在住院或门诊接受了依舒康唑、伊曲康唑、泊沙康唑或伏立康唑治疗。在273例患者中,只有122例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(mg/kg/天)才能达到目标血清浓度。接受口服片剂或静脉注射形式的唑类药物的患者比不接受这些制剂的患者更有可能达到目标浓度。异戊康唑达到目标浓度的中位时间为20天,伊曲康唑为34天,泊沙康唑为11天,伏立康唑为10天。结论:需要更高的起始剂量来快速获得目标浓度,特别是对于12岁以下的儿童。
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来源期刊
Journal of Pediatric Pharmacology and Therapeutics
Journal of Pediatric Pharmacology and Therapeutics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.40
自引率
0.00%
发文量
90
期刊介绍: The Journal of Pediatric Pharmacology and Therapeutics is the official journal of the Pediatric Pharmacy Advocacy Group. JPPT is a peer-reviewed multi disciplinary journal that is devoted to promoting the safe and effective use of medications in infants and children. To this end, the journal publishes practical information for all practitioners who provide care to pediatric patients. Each issue includes review articles, original clinical investigations, case reports, editorials, and other information relevant to pediatric medication therapy. The Journal focuses all work on issues related to the practice of pediatric pharmacology and therapeutics. The scope of content includes pharmacotherapy, extemporaneous compounding, dosing, methods of medication administration, medication error prevention, and legislative issues. The Journal will contain original research, review articles, short subjects, case reports, clinical investigations, editorials, and news from such organizations as the Pediatric Pharmacy Advocacy Group, the FDA, the American Academy of Pediatrics, the American Society of Health-System Pharmacists, and so on.
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