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Case Reports
. 2022 Mar 1;68(3):e56-e58.
doi: 10.1097/MAT.0000000000001427.

Voriconazole Sequestration During Extracorporeal Membrane Oxygenation for Invasive Lung Aspergillosis: A Case Report

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Case Reports

Voriconazole Sequestration During Extracorporeal Membrane Oxygenation for Invasive Lung Aspergillosis: A Case Report

Alexandre Mathieu et al. ASAIO J. .

Abstract

The increasing use of extracorporeal membrane oxygenation (ECMO) in critical care introduces new challenges with medication dosing. Voriconazole, a commonly used antifungal and the first-choice agent for the treatment of invasive aspergillosis, is a poorly water-soluble and highly protein-bound drug. Significant sequestration in ECMO circuits can be expected; however, no specific dosing recommendations are available. We report on the therapeutic drug monitoring and clinical evolution of a patient treated with voriconazole for invasive pulmonary aspergillosis while receiving ECMO therapy. Voriconazole trough levels were persistently low (<1 µg/mL) after initiation of ECMO despite additional loading doses and dose increases. Voriconazole dose had to be increased to 6.5 mg/kg three times daily to obtain therapeutic trough levels. The inability to achieve therapeutic levels of voriconazole for a prolonged period (a minimum of 9 days) while undergoing ECMO therapy is believed to have been a significant contributing factor in the patient's fatal outcome. Therapeutic trough levels of voriconazole cannot be guaranteed with standard dosing in patients undergoing ECMO and much higher doses may be necessary. Empirical use of higher doses and/or combination therapy may be reasonable and frequent therapeutic drug monitoring is mandatory.

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Conflict of interest statement

Disclosure: The authors have no conflicts of interest to report.

References

    1. Extracorporeal Life Support Organization. Infection Control and Extracorporeal Life Support. 2017. Available at: https://www.elso.org/Portals/0/Files/Infection-Control-and-Extracorporea... . Accessed September 8, 2020.
    1. Shah AG, Peahota M, Thoma BN, Kraft WK: Medication complications in extracorporeal membrane oxygenation. Crit Care Clin. 33: 897–920, 2017.
    1. Cies JJ, Moore WS 2nd, Giliam N, et al.: Oxygenator impact on voriconazole in extracorporeal membrane oxygenation circuits. Perfusion. 35: 529–533, 2020.
    1. Mehta NM, Halwick DR, Dodson BL, Thompson JE, Arnold JH: Potential drug sequestration during extracorporeal membrane oxygenation: results from an ex vivo experiment. Intensive Care Med. 33: 1018–1024, 2007.
    1. Ruiz S, Papy E, Da Silva D, et al.: Potential voriconazole and caspofungin sequestration during extracorporeal membrane oxygenation. Intensive Care Med. 35: 183–184, 2009.

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