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体外膜肺氧合患者中重症患者的伊曲康唑血浆浓度。

Isavuconazole plasma concentrations in critically ill patients during extracorporeal membrane oxygenation.

机构信息

Division of Infectious Diseases, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Intensive Care Unit, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

出版信息

J Antimicrob Chemother. 2022 Aug 25;77(9):2500-2505. doi: 10.1093/jac/dkac196.

Abstract

BACKGROUND

Isavuconazole is an antifungal drug used for treatment of invasive fungal infections. Critically ill COVID-19 and influenza patients require extracorporeal membrane oxygenation (ECMO) in cases with severe acute respiratory distress syndrome and have risk factors for invasive pulmonary aspergillosis. Little is known about isavuconazole plasma concentrations during ECMO.

OBJECTIVES

To determine isavuconazole plasma concentrations in seven patients treated with intravenous isavuconazole under ECMO and the influence of the ECMO circuit immediately after the first isavuconazole dose.

METHODS

Critically ill patients treated with isavuconazole (standard doses) and ECMO were included in this study. Sixty-four blood samples used for measurement of isavuconazole concentrations were collected at several timepoints starting 2 h after the first isavuconazole dose up to 168 h. An additional 27 blood samples were drawn from the inflow and outflow line of the membrane oxygenator to assess any potential isavuconazole clearance effect of the ECMO oxygenation device and the lines.

RESULTS

Median isavuconazole trough levels above 1 μg/mL (min. 0.83, max. 1.73) or 2 μg/mL (min. 0.84, max. 2.97) were achieved 24 h or 96 h after the first dose of isavuconazole. The isavuconazole plasma concentrations pre (inflow line) and post (outflow line) the membrane oxygenator were directly correlated (ρ = 0.987, R2 = 0.994, P < 0.001). Post membrane oxygenator isavuconazole concentrations were directly correlated to contemporaneous samples obtained from the arterial lines of patients (ρ = 0.942, R2 = 0.945, P < 0.001).

CONCLUSIONS

Isavuconazole concentrations might be influenced by the higher volume of distribution due to ECMO therapy, but were not altered by the ECMO oxygenator and achieved median plasma concentrations >1 μg/mL 24 h after the first loading dose.

摘要

背景

伊曲康唑是一种抗真菌药物,用于治疗侵袭性真菌感染。患有严重急性呼吸窘迫综合征的 COVID-19 和流感重症患者需要体外膜肺氧合(ECMO)治疗,并且存在侵袭性肺曲霉病的危险因素。关于 ECMO 期间伊曲康唑的血药浓度知之甚少。

目的

测定 7 例 ECMO 下接受静脉伊曲康唑治疗的患者的伊曲康唑血药浓度,并测定首次伊曲康唑剂量后 ECMO 回路对其的影响。

方法

本研究纳入了接受伊曲康唑(标准剂量)和 ECMO 治疗的重症患者。在首次伊曲康唑剂量后 2 小时至 168 小时,采集 64 个时间点的 64 个血样用于测量伊曲康唑浓度。另外从膜氧合器的流入和流出管路中抽取 27 个血样,以评估 ECMO 氧合装置和管路对伊曲康唑的潜在清除作用。

结果

首次伊曲康唑剂量后 24 小时或 96 小时,伊曲康唑谷浓度中位数>1μg/ml(最低 0.83,最高 1.73)或>2μg/ml(最低 0.84,最高 2.97)。膜氧合器前后的伊曲康唑血药浓度直接相关(ρ=0.987,R2=0.994,P<0.001)。膜氧合器后伊曲康唑浓度与同时取自患者动脉管路的样本直接相关(ρ=0.942,R2=0.945,P<0.001)。

结论

伊曲康唑浓度可能受到 ECMO 治疗导致的分布容积增加的影响,但不受 ECMO 氧合器的影响,首次负荷剂量后 24 小时达到中位数>1μg/ml 的血药浓度。

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