Isavuconazole plasma concentrations in critically ill patients during extracorporeal membrane oxygenation

Author:

Kriegl Lisa1,Hatzl Stefan2,Zurl Christoph34ORCID,Reisinger Alexander Christian2,Schilcher Gernot2,Eller Philipp2,Gringschl Yvonne5,Muhr Tina6,Meinitzer Andreas7,Prattes Juergen1,Hoenigl Martin14ORCID,Krause Robert14

Affiliation:

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

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

3. Division of General Paediatrics, Department of Paediatrics and Adolescent Medicine, Medical University of Graz , Graz , Austria

4. BioTechMed-Graz , Graz , Austria

5. Department of Anesthesiology and Intensive Care Medicine, Medical University of Graz , Graz , Austria

6. Department of Internal Medicine, Landeskrankenhaus Graz 2 , Graz , Austria

7. Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz , Graz , Austria

Abstract

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.

Funder

Pfizer

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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