COVID-19 Drug Treatments Are Prone to Sequestration in Extracorporeal Membrane Oxygenation Circuits: An Ex Vivo Extracorporeal Membrane Oxygenation Study

Author:

Dhanani Jayesh A.12,Shekar Kiran34,Parmar Dinesh34,Lipman Jeffrey12567,Bristow Debra2,Wallis Steven C.1,Won Hayoung1,Sumi Chandra D.1,Abdul-Aziz Mohd H.1,Roberts Jason A.12567

Affiliation:

1. From the University of Queensland Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Australia

2. Department of Intensive Care Medicine, Royal Brisbane and Women’s Hospital, Herston, Queensland, Australia

3. Adult Intensive Care Services, The Prince Charles Hospital, Chermside, Queensland, Australia

4. School of Medicine, University of Queensland, Brisbane, Queensland, Australia

5. Jamieson Trauma Institute, Royal Brisbane and Womens Hospital

6. Division of Anaesthesiology Critical Care Emergency and Pain Medicine, Nîmes University Hospital, University of Montpellier, Nîmes, France

7. Herston Infectious Diseases Institute (HeIDI), Metro North Health, Brisbane, Australia; and

Abstract

Drug treatments for coronavirus disease 2019 (COVID-19) dramatically improve patient outcomes, and although extracorporeal membrane oxygenation (ECMO) has significant use in these patients, it is unknown whether ECMO affects drug dosing. We used an ex vivo adult ECMO model to measure ECMO circuit effects on concentrations of specific COVID-19 drug treatments. Three identical ECMO circuits used in adult patients were set up. Circuits were primed with fresh human blood (temperature and pH maintained within normal limits). Three polystyrene jars with 75 ml fresh human blood were used as controls. Remdesivir, GS-441524, nafamostat, and tocilizumab were injected in the circuit and control jars at therapeutic concentrations. Samples were taken from circuit and control jars at predefined time points over 6 h and drug concentrations were measured using validated assays. Relative to baseline, mean (± standard deviation [SD]) study drug recoveries in both controls and circuits at 6 h were significantly lower for remdesivir (32.2% [±2.7] and 12.4% [±2.1], p < 0.001), nafamostat (21.4% [±5.0] and 0.0% [±0.0], p = 0.018). Reduced concentrations of COVID-19 drug treatments in ECMO circuits is a clinical concern. Remdesivir and nafamostat may need dose adjustments. Clinical pharmacokinetic studies are suggested to guide optimized COVID-19 drug treatment dosing during ECMO.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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