体外膜氧合过程中两性霉素B和异戊康唑脂质体药代动力学和剂量的改变

Yanjun Zhao, T. Seelhammer, E. Barreto, John W. Wilson
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引用次数: 35

摘要

接受体外膜氧合(ECMO)的患者可能会显著改变药物的药代动力学。确保体外膜肺组织中抗菌药物的最佳有效剂量仍然是一个挑战。迄今为止,关于ECMO期间两性霉素和三唑的最佳使用的数据有限。我们报告了一例药代动力学改变,脂质体两性霉素B和异唑康唑水平不足,以及在肺芽孢菌病患者继发严重急性呼吸窘迫综合征的ECMO期间需要增加剂量的病例。两种药物的标准每日总剂量增加2倍是必要的,以克服被认为是继发于ECMO回路隔离的药物损失的低血清浓度。这些发现对于优化ECMO患者的抗菌治疗以最大化治疗效果具有重要意义。对接受抗菌药物治疗并同时进行体外膜肺mo的患者进行治疗药物监测,可以促进适当的药物剂量,以达到足够的血清浓度,并优化有利的患者预后。需要进一步研究ECMO期间的抗菌药代动力学,为危重患者的剂量建议提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Altered Pharmacokinetics and Dosing of Liposomal Amphotericin B and Isavuconazole during Extracorporeal Membrane Oxygenation
Drug pharmacokinetics may be significantly altered in patients receiving extracorporeal membrane oxygenation (ECMO). Ensuring the optimized effective dosing of antimicrobials on ECMO remains a challenge. To date, limited data are available regarding the optimal use of amphotericin and triazoles during ECMO. We report a case of altered pharmacokinetics, insufficient liposomal amphotericin B and isavuconazole levels, and the need for escalated doses during ECMO in a patient with severe acute respiratory distress syndrome secondary to pulmonary blastomycosis. A 2‐fold increase in the standard total daily dose of both drugs was necessary to overcome low serum concentrations thought to be secondary to drug loss from ECMO circuit sequestration. These findings have important implications for optimizing antimicrobial therapy in patients receiving ECMO to maximize therapeutic efficacy. The use of therapeutic drug monitoring for patients receiving antimicrobial therapy with concurrent ECMO may facilitate appropriate drug dosing to achieve adequate serum concentrations and optimize favorable patient outcomes. Further studies exploring antimicrobial pharmacokinetics during ECMO are needed to inform dosing recommendations in critically ill patients.
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