Decreased isavuconazole trough concentrations in the treatment of invasive aspergillosis in an adult patient receiving extracorporeal membrane oxygenation support

Abstract Purpose We present the case of a 56-year-old man with stage IV sarcoidosis on veno-venous extracorporeal membrane oxygenation (VV-ECMO) support for the management of respiratory failure receiving treatment with isavuconazole for invasive aspergillosis. Summary VV-ECMO is an increasingly utilized life support therapy for patients with cardiac and/or respiratory failure, but its impact on medication dosing is poorly understood. In our patient with invasive Aspergillus infection receiving VV-ECMO, because of difficulty achieving therapeutic serum concentrations of voriconazole, we administered isavuconazole 372 mg intravenously (IV) every 8 hours for 6 doses followed by 372 mg IV once daily. Isavuconazole has a favorable pharmacokinetic and safety profile compared to other azole antifungal agents, but its high protein binding and lipophilicity raise concerns about drug sequestration in the VV-ECMO circuit. To optimize the efficacy and safety of this treatment, the isavuconazole trough concentration was measured at days 5 and 17, at which time it was 1.7 and 0.7 μg/mL, respectively. The dose was subsequently increased to 744 mg IV once daily, and serum trough concentrations were measured 5 and 8 days after dose adjustment, corresponding to 3.7 and 2.9 μg/mL, respectively. To our knowledge, this is the third report to describe inadequate isavuconazole trough concentrations during VV-ECMO support when utilizing standard doses. Conclusion In the case described here, standard-dose isavuconazole (372 mg every 8 hours for 6 doses followed by 372 mg daily) did not achieve target trough concentrations in a patient receiving concomitant ECMO support.

[1]  Arun Chopra,et al.  Oxygenator impact on voriconazole in extracorporeal membrane oxygenation circuits , 2020, Perfusion.

[2]  A. Oulhaj,et al.  Isavuconazole Treatment in a Mixed Patient Cohort with Invasive Fungal Infections: Outcome, Tolerability and Clinical Implications of Isavuconazole Plasma Concentrations , 2020, Journal of fungi.

[3]  A. Borman,et al.  Lessons from isavuconazole therapeutic drug monitoring at a United Kingdom Reference Center. , 2020, Medical mycology.

[4]  E. Barreto,et al.  Altered Pharmacokinetics and Dosing of Liposomal Amphotericin B and Isavuconazole during Extracorporeal Membrane Oxygenation , 2019, Pharmacotherapy.

[5]  C. Viscoli,et al.  Serial monitoring of isavuconazole blood levels during prolonged antifungal therapy. , 2019, The Journal of antimicrobial chemotherapy.

[6]  L. Millon,et al.  The pharmacokinetic challenge of treating invasive aspergillosis complicating severe influenzae assisted by extracorporeal membrane oxygenation , 2018, Critical Care.

[7]  T. Walsh,et al.  Isavuconazole Concentration in Real-World Practice: Consistency with Results from Clinical Trials , 2018, Antimicrobial Agents and Chemotherapy.

[8]  J. Roberts,et al.  Optimising drug dosing in patients receiving extracorporeal membrane oxygenation. , 2018, Journal of thoracic disease.

[9]  P. Bonate,et al.  Population Pharmacokinetics of Isavuconazole from Phase 1 and Phase 3 (SECURE) Trials in Adults and Target Attainment in Patients with Invasive Infections Due to Aspergillus and Other Filamentous Fungi , 2016, Antimicrobial Agents and Chemotherapy.

[10]  John F. Fraser,et al.  Can physicochemical properties of antimicrobials be used to predict their pharmacokinetics during extracorporeal membrane oxygenation? Illustrative data from ovine models , 2015, Critical Care.

[11]  J. Fraser,et al.  Pharmacokinetic changes in patients receiving extracorporeal membrane oxygenation. , 2012, Journal of critical care.

[12]  P. Annaert,et al.  Pharmacokinetics of caspofungin and voriconazole in critically ill patients during extracorporeal membrane oxygenation. , 2009, The Journal of antimicrobial chemotherapy.

[13]  J. Arnold,et al.  Potential drug sequestration during extracorporeal membrane oxygenation: results from an ex vivo experiment , 2007, Intensive Care Medicine.