Oxygenator impact on meropenem/vaborbactam in extracorporeal membrane oxygenation circuits

Author:

Cies Jeffrey J123ORCID,Nikolos Peter45,Moore Wayne S1,Giliam Nadji2,Low Tracy2,Marino Daniel2,Deacon Jillian2,Enache Adela6,Chopra Arun178

Affiliation:

1. The Center for Pediatric Pharmacotherapy LLC, Pottstown, PA, USA

2. St. Christopher’s Hospital for Children, Philadelphia, PA, USA

3. Drexel University College of Medicine, Philadelphia, PA, USA

4. Arnold and Marie Schwartz College of Pharmacy and Health Sciences, Brooklyn, NY, USA

5. New York Presbyterian Weill Cornell Medical Center, New York, NY, USA

6. Atlantic Diagnostic Laboratories, Bensalem, PA, USA

7. NYU Langone Medical Center, New York, NY, USA

8. NYU School of Medicine, New York, NY, USA

Abstract

Introduction: To determine the oxygenator impact on alterations of meropenem (MEM)/vaborbactam (VBR) in a contemporary neonatal/pediatric (1/4-inch) and adolescent/adult (3/8-inch) extra corporeal membrane oxygenation (ECMO) circuit including the Quadrox-i® oxygenator. Methods: 1/4-inch and 3/8-inch, simulated closed-loop ECMO circuits were prepared with a Quadrox-i pediatric and Quadrox-i adult oxygenator and blood primed. Additionally, 1/4-inch and 3/8-inch circuits were also prepared without an oxygenator in series. A one-time dose of MEM/VBR was administered into the circuits and serial pre- and post-oxygenator concentrations were obtained at 5 minutes, 1, 2, 3, 4, 5, 6, 8, 12, and 24-hour time points. MEM/VBR was also maintained in a glass vial and samples were taken from the vial at the same time periods for control purposes to assess for spontaneous drug degradation. Results: For the 1/4-inch circuit, there was an approximate mean 55% MEM loss with the oxygenator in series and a mean 33%–40% MEM loss without an oxygenator in series at 24 hours. For the 3/8-inch circuit, there was an approximate mean 70% MEM loss with the oxygenator in series and a mean 30%–38% MEM loss without an oxygenator in series at 24 hours. For both the 1/4-inch circuit and 3/8-inch circuits with and without an oxygenator, there was <10% VBR loss for the duration of the experiment. Conclusions: This ex-vivo investigation demonstrated substantial MEM loss within an ECMO circuit with an oxygenator in series with both sizes of the Quadrox-i oxygenator at 24 hours and no significant VBR loss. Further evaluations with multiple dose in-vitro and in-vivo investigations are needed before specific MEM/VBR dosing recommendations can be made for clinical application with ECMO.

Funder

melinta therapeutics

Publisher

SAGE Publications

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Safety Research,Radiology, Nuclear Medicine and imaging,General Medicine

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