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在接受体外膜肺氧合支持的患者中,采用治疗药物监测指导的高剂量艾沙康唑治疗侵袭性肺曲霉病。

Therapeutic drug monitoring-guided high-dose isavuconazole therapy for invasive pulmonary aspergillosis in a patient on extracorporeal membrane oxygenation support.

作者信息

Pau-Parra Alba, Sosa Garay Manuel, Doménech Moral Laura, Díez Poch Mónica, Martínez Pla María, Gallart Elisabet, Vima Bofarull Jaume, Nuvials Xavier, García-García Sonia, Doménech Vila Josep María, Planas Viñuales Laura, Cruz López Iván, Lalueza Broto Pilar, Gorgas Torner Maria Queralt, Ferrer Ricard, Riera Jordi

机构信息

Pharmacy Department. Vall d'Hebron University Hospital, Barcelona, Spain.

Basic, Translational and Clinical Pharmacy Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.

出版信息

J Chemother. 2025 Jan 19:1-7. doi: 10.1080/1120009X.2025.2452694.

Abstract

We review the case of a 58-year-old female on extracorporeal membrane oxygenation (ECMO) support diagnosed with invasive pulmonary aspergillosis (IPA). Intravenous isavuconazole was started, requiring dose escalation to achieve isavuconazole trough concentration (ISA-Cmin) within the therapeutic range (2.5-5.0 μg/mL). For more than 4 months, she maintained a dose of 200 mg q12h, with a median ISA-Cmin of 3.4 (interquartile range [IQR]: 3.1-4.9) µg/mL. Throughout this interval, 17 assessments of ISA-Cmin were performed (weekly). Of these, 82% (14/17) were within the therapeutic range, with an intra-individual variability of 36.8%. Although no signs of hepatotoxicity were observed, she experienced short-term gastrointestinal adverse events related to potential isavuconazole over-exposure (ISA-Cmin > 5.0 μg/mL). ECMO circuit changes did not appear to affect ISA-Cmin. She was not obese (IMC ≈ 25 kg/m) and did not require other extracorporeal therapy, but hypoalbuminemia may have contributed to an increase in unbound isavuconazole fraction and consequently its clearance.

摘要

我们回顾了一例接受体外膜肺氧合(ECMO)支持治疗的58岁女性患者,其被诊断为侵袭性肺曲霉病(IPA)。开始静脉注射艾沙康唑,需要增加剂量以将艾沙康唑谷浓度(ISA-Cmin)维持在治疗范围内(2.5 - 5.0μg/mL)。在4个多月的时间里,她维持200mg每12小时一次的剂量,ISA-Cmin中位数为3.4(四分位间距[IQR]:3.1 - 4.9)μg/mL。在此期间,共进行了17次ISA-Cmin评估(每周一次)。其中,82%(14/17)处于治疗范围内,个体内变异性为36.8%。尽管未观察到肝毒性迹象,但她经历了与潜在的艾沙康唑暴露过量(ISA-Cmin > 5.0μg/mL)相关的短期胃肠道不良事件。ECMO回路的改变似乎并未影响ISA-Cmin。她并非肥胖(体重指数[BMI]≈25kg/m²),也不需要其他体外治疗,但低白蛋白血症可能导致游离艾沙康唑分数增加,进而影响其清除率。

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