Oxygenator impact on meropenem/vaborbactam in extracorporeal membrane oxygenation circuits.

drug sequestration extracorporeal membrane oxygenation meropenem pharmacodynamic pharmacokinetics quadrox vaborbactam oxygenator

Journal

Perfusion
ISSN: 1477-111X
Titre abrégé: Perfusion
Pays: England
ID NLM: 8700166

Informations de publication

Date de publication:
10 2022
Historique:
pubmed: 27 5 2021
medline: 24 9 2022
entrez: 26 5 2021
Statut: ppublish

Résumé

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 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. 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. 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.

Identifiants

pubmed: 34034594
doi: 10.1177/02676591211018985
doi:

Substances chimiques

Boronic Acids 0
vaborbactam 1C75676F8V
Meropenem FV9J3JU8B1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

729-737

Auteurs

Jeffrey J Cies (JJ)

The Center for Pediatric Pharmacotherapy LLC, Pottstown, PA, USA.
St. Christopher's Hospital for Children, Philadelphia, PA, USA.
Drexel University College of Medicine, Philadelphia, PA, USA.

Peter Nikolos (P)

Arnold and Marie Schwartz College of Pharmacy and Health Sciences, Brooklyn, NY, USA.
New York Presbyterian Weill Cornell Medical Center, New York, NY, USA.

Wayne S Moore (WS)

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

Nadji Giliam (N)

St. Christopher's Hospital for Children, Philadelphia, PA, USA.

Tracy Low (T)

St. Christopher's Hospital for Children, Philadelphia, PA, USA.

Daniel Marino (D)

St. Christopher's Hospital for Children, Philadelphia, PA, USA.

Jillian Deacon (J)

St. Christopher's Hospital for Children, Philadelphia, PA, USA.

Adela Enache (A)

Atlantic Diagnostic Laboratories, Bensalem, PA, USA.

Arun Chopra (A)

The Center for Pediatric Pharmacotherapy LLC, Pottstown, PA, USA.
NYU Langone Medical Center, New York, NY, USA.
NYU School of Medicine, New York, NY, USA.

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Classifications MeSH