Comparison of Intravenous Microdialysis and Standard Plasma Sampling for Monitoring of Vancomycin and Meropenem Plasma Concentrations-An Experimental Porcine Study.

meropenem microdialysis pharmacokinetics plasma sampling vancomycin

Journal

Antibiotics (Basel, Switzerland)
ISSN: 2079-6382
Titre abrégé: Antibiotics (Basel)
Pays: Switzerland
ID NLM: 101637404

Informations de publication

Date de publication:
21 Apr 2023
Historique:
received: 23 02 2023
revised: 13 04 2023
accepted: 19 04 2023
medline: 28 4 2023
pubmed: 28 4 2023
entrez: 28 4 2023
Statut: epublish

Résumé

Microdialysis is a catheter-based method suitable for dynamic sampling of unbound antibiotic concentrations. Intravenous antibiotic concentration sampling by microdialysis has several advantages and may be a superior alternative to standard plasma sampling. We aimed to compare concentrations obtained by continuous intravenous microdialysis sampling and by standard plasma sampling of both vancomycin and meropenem in a porcine model. Eight female pigs received 1 g of both vancomycin and meropenem, simultaneously over 100 and 10 min, respectively. Prior to drug infusion, an intravenous microdialysis catheter was placed in the subclavian vein. Microdialysates were collected for 8 h. From a central venous catheter, plasma samples were collected in the middle of every dialysate sampling interval. A higher area under the concentration/time curve and peak drug concentration were found in standard plasma samples compared to intravenous microdialysis samples, for both vancomycin and meropenem. Both vancomycin and meropenem concentrations obtained with intravenous microdialysis were generally lower than from standard plasma sampling. The differences in key pharmacokinetic parameters between the two sampling techniques underline the importance of further investigations to find the most suitable and reliable method for continuous intravenous antibiotic concentration sampling.

Identifiants

pubmed: 37107154
pii: antibiotics12040791
doi: 10.3390/antibiotics12040791
pmc: PMC10135263
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Johanne Gade Lilleøre (JG)

Department of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Aarhus Denmark Microdialysis Research Group (ADMIRE), Aarhus University Hospital, 8200 Aarhus, Denmark.

Sofus Vittrup (S)

Department of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Aarhus Denmark Microdialysis Research Group (ADMIRE), Aarhus University Hospital, 8200 Aarhus, Denmark.

Sara Kousgaard Tøstesen (SK)

Department of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Aarhus Denmark Microdialysis Research Group (ADMIRE), Aarhus University Hospital, 8200 Aarhus, Denmark.

Pelle Hanberg (P)

Department of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Aarhus Denmark Microdialysis Research Group (ADMIRE), Aarhus University Hospital, 8200 Aarhus, Denmark.

Maiken Stilling (M)

Department of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Aarhus Denmark Microdialysis Research Group (ADMIRE), Aarhus University Hospital, 8200 Aarhus, Denmark.
Department of Orthopedic Surgery, Aarhus University Hospital, 8200 Aarhus, Denmark.

Mats Bue (M)

Department of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Aarhus Denmark Microdialysis Research Group (ADMIRE), Aarhus University Hospital, 8200 Aarhus, Denmark.
Department of Orthopedic Surgery, Aarhus University Hospital, 8200 Aarhus, Denmark.

Classifications MeSH