Extraction of ketamine and dexmedetomidine by extracorporeal life support circuits★.


Journal

The journal of extra-corporeal technology
ISSN: 2969-8960
Titre abrégé: J Extra Corpor Technol
Pays: France
ID NLM: 0267637

Informations de publication

Date de publication:
Sep 2024
Historique:
received: 11 03 2024
accepted: 12 06 2024
medline: 20 9 2024
pubmed: 20 9 2024
entrez: 20 9 2024
Statut: ppublish

Résumé

Patients supported with extracorporeal life support (ECLS) circuits such as ECMO and CRRT often require high doses of sedatives and analgesics, including ketamine and dexmedetomidine. Concentrations of many medications are affected by ECLS circuits through adsorption to the circuit components, dialysis, as well as the large volume of blood used to prime the circuits. However, the impact of ECLS circuits on ketamine and dexmedetomidine pharmacokinetics has not been well described. This study determined ketamine and dexmedetomidine extraction by extracorporeal circuits in an ex-vivo system. Medication was administered at therapeutic concentration to blood-primed, closed-loop ex-vivo ECMO and CRRT circuits. Drug concentrations were measured in plasma, hemofiltrate, and control samples at multiple time points throughout the experiments. At each sample time point, the percentage of drug recovery was calculated. Ketamine plasma concentration in the ECMO and CRRT circuits decreased rapidly, with 43.8% recovery (SD = 0.6%) from ECMO circuits after 8 h and 3.3% (SD = 1.8%) recovery from CRRT circuits after 6 h. Dexmedetomidine was also cleared from CRRT circuits, with 20.3% recovery (SD = 1.8%) after 6 h. Concentrations of both medications were very stable in the control experiments, with approximately 100% drug recovery of both ketamine and dexmedetomidine after 6 h. Ketamine and dexmedetomidine concentrations are significantly affected by ECLS circuits, indicating that dosing adjustments are needed for patients supported with ECMO and CRRT.

Sections du résumé

BACKGROUND BACKGROUND
Patients supported with extracorporeal life support (ECLS) circuits such as ECMO and CRRT often require high doses of sedatives and analgesics, including ketamine and dexmedetomidine. Concentrations of many medications are affected by ECLS circuits through adsorption to the circuit components, dialysis, as well as the large volume of blood used to prime the circuits. However, the impact of ECLS circuits on ketamine and dexmedetomidine pharmacokinetics has not been well described. This study determined ketamine and dexmedetomidine extraction by extracorporeal circuits in an ex-vivo system.
METHODS METHODS
Medication was administered at therapeutic concentration to blood-primed, closed-loop ex-vivo ECMO and CRRT circuits. Drug concentrations were measured in plasma, hemofiltrate, and control samples at multiple time points throughout the experiments. At each sample time point, the percentage of drug recovery was calculated.
RESULTS RESULTS
Ketamine plasma concentration in the ECMO and CRRT circuits decreased rapidly, with 43.8% recovery (SD = 0.6%) from ECMO circuits after 8 h and 3.3% (SD = 1.8%) recovery from CRRT circuits after 6 h. Dexmedetomidine was also cleared from CRRT circuits, with 20.3% recovery (SD = 1.8%) after 6 h. Concentrations of both medications were very stable in the control experiments, with approximately 100% drug recovery of both ketamine and dexmedetomidine after 6 h.
CONCLUSION CONCLUSIONS
Ketamine and dexmedetomidine concentrations are significantly affected by ECLS circuits, indicating that dosing adjustments are needed for patients supported with ECMO and CRRT.

Identifiants

pubmed: 39303131
doi: 10.1051/ject/2024016
pii: ject240012
doi:

Substances chimiques

Ketamine 690G0D6V8H
Dexmedetomidine 67VB76HONO
Hypnotics and Sedatives 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101-107

Informations de copyright

© The Author(s), published by EDP Sciences, 2024.

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Auteurs

Andrew Chevalier (A)

Division of Pediatric Critical Care, Department of Pediatrics, University of Utah, Salt Lake City, UT 84132, USA.

J Porter Hunt (J)

Division of Clinical Pharmacology, Department of Pediatrics, University of Utah, Salt Lake City, UT 84132, USA.

Aviva Whelan (A)

Division of Pediatric Critical Care, Department of Pediatrics, University of Utah, Salt Lake City, UT 84132, USA.

Autumn McKnite (A)

Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT 84132, USA.

Kevin M Watt (KM)

Division of Pediatric Critical Care, Department of Pediatrics, University of Utah, Salt Lake City, UT 84132, USA - Division of Clinical Pharmacology, Department of Pediatrics, University of Utah, Salt Lake City, UT 84132, USA.

Danielle J Green (DJ)

Division of Pediatric Critical Care, Department of Pediatrics, University of Utah, Salt Lake City, UT 84132, USA - Division of Clinical Pharmacology, Department of Pediatrics, University of Utah, Salt Lake City, UT 84132, USA.

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