Doménech-Moral Laura, García-García Sonia, Pau-Parra Alba, Sosa Manuel, Puertas Sanjuan Adrian, Bonilla Camilo, Gallart Elisabeth, Castellote Laura, Faixó Patricia, Guevara Jessica, Vilanova Albert, Martínez-Pla María, Conto Aldair, Nuvials Xavier, Lalueza Pilar, Ferrer Ricard, Gorgas Maria Queralt, Riera Jordi
Pharmacy Department, Vall d'Hebron University Hospital, Basic, Translational and Clinical Pharmacy Research Group, Vall d'Hebron Research Institute, 08035 Barcelona, Spain.
Critical Care Department, Vall d'Hebron University Hospital, SODIR, Vall d'Hebron Research Institute, 08035 Barcelona, Spain.
Antibiotics (Basel). 2025 Jun 12;14(6):600. doi: 10.3390/antibiotics14060600.
BACKGROUND/OBJECTIVES: Extracorporeal membrane oxygenation (ECMO) is increasingly used in critically ill patients, but may significantly alter the pharmacokinetics (PK) of antifungals. Data on plasma concentrations of Isavuconazole (IsaPlasm) in ECMO patients are limited. Our objective is to evaluate Isavuconazole exposure and variability in critically ill COVID-19 patients receiving ECMO.
We conducted a pharmacokinetic analysis of Isavuconazole in critically ill patients receiving Veno-Venous ECMO for respiratory support. Plasma concentrations were measured using therapeutic drug monitoring (TDM) at multiple time points, including sampling before and after the membrane oxygenator. PK parameters-Area Under Curve (AUC), Minimum Plasma Concentration (Cmin), Elimination Half-Life (T), volume of distribution (Vd), and clearance (CL)-were estimated and compared with published data in non-ECMO populations.
Five patients were included. The median AUC was 227.3 µg·h/mL (IQR 182.4-311.35), higher than reported in non-ECMO patients. The median Vd was 761 L (727-832), suggesting extensive peripheral distribution and potential drug sequestration in the ECMO circuit. CL was increased (1.6 L/h, IQR 1.5-3.4). Two patients with recently replaced ECMO circuits exhibited significant drug loss across the membrane. Obesity and hypoalbuminemia were identified as factors associated with altered drug exposure.
Isavuconazole pharmacokinetics show marked variability in critically ill ECMO patients. Increased AUC and Vd, along with reduced clearance, highlight the need for individualized dosing.
背景/目的:体外膜肺氧合(ECMO)在重症患者中的应用日益广泛,但可能会显著改变抗真菌药物的药代动力学(PK)。关于接受ECMO治疗患者的艾沙康唑血浆浓度(IsaPlasm)的数据有限。我们的目的是评估接受ECMO治疗的重症COVID-19患者的艾沙康唑暴露量及变异性。
我们对接受静脉-静脉ECMO进行呼吸支持的重症患者的艾沙康唑进行了药代动力学分析。在多个时间点使用治疗药物监测(TDM)测量血浆浓度,包括在膜式氧合器前后取样。估算药代动力学参数——曲线下面积(AUC)、最低血浆浓度(Cmin)、消除半衰期(T)、分布容积(Vd)和清除率(CL),并与非ECMO人群的已发表数据进行比较。
纳入了5名患者。AUC中位数为227.3µg·h/mL(IQR 182.4 - 311.35),高于非ECMO患者的报告值。Vd中位数为761L(727 - 832),表明外周分布广泛且药物可能在ECMO回路中滞留。CL增加(1.6L/h,IQR 1.5 - 3.4)。两名最近更换ECMO回路的患者在膜上出现了显著的药物损失。肥胖和低白蛋白血症被确定为与药物暴露改变相关的因素。
在重症ECMO患者中,艾沙康唑的药代动力学表现出明显的变异性。AUC和Vd增加,以及清除率降低,凸显了个体化给药的必要性。