De-mystifying the "Mixifusor".

clinical pharmacology pharmacokinetics propofol remifentanil safety target-controlled infusions

Journal

Paediatric anaesthesia
ISSN: 1460-9592
Titre abrégé: Paediatr Anaesth
Pays: France
ID NLM: 9206575

Informations de publication

Date de publication:
12 2020
Historique:
received: 29 09 2020
accepted: 04 10 2020
pubmed: 15 10 2020
medline: 2 2 2021
entrez: 14 10 2020
Statut: ppublish

Résumé

Total intravenous anesthesia (TIVA) using a mixture of propofol and remifentanil in the same syringe has become an accepted technique in Pediatric Anesthesia. A survey by a group of respected UK anesthetists demonstrated a low incidence of serious complications, related to the pharmacology and dose of the drugs. However, a current guideline for the safe use of TIVA recommends against this practice. Pharmaceutical concerns include the physical stability of the emulsion when remifentanil is mixed with propofol; changes in drug concentration over time; nonuniform mixing of propofol and remifentanil; the risk of bacterial contamination; and the potential for drug administration errors. Propofol and remifentanil have markedly different pharmacokinetic profiles. When remifentanil is mixed with propofol and delivered as a target-controlled infusion (TCI) of propofol, remifentanil delivery is not target-controlled but passively follows the variable infusion rates calculated by the syringe driver to deliver predicted plasma or effect-site concentrations of propofol. The pharmacokinetic consequences can be illustrated using pharmacokinetic modeling similar to that used in TCI pumps. The clinical consequences reflect the dose-dependent pharmacodynamics of remifentanil. Increasing the target propofol concentration produces a rapid increase and peak in remifentanil concentration that risks apnea, bradycardia, and hypotension, especially with higher concentrations of remifentanil. The faster decline in remifentanil concentration with falling propofol concentrations risks inadequate narcosis and unwanted responses to surgical stimuli. Remifentanil delivery is inflexible and dosing cannot be adjusted to the clinical need and responses of individual patients. The medicolegal considerations are stark. In UK and EU Law, mixing propofol and remifentanil creates a new, unlicensed drug and the person mixing takes on the responsibilities of manufacturer. If a patient receiving anesthesia in the form of a mixed propofol-remifentanil infusion suffered a critical incident or actual harm, the clinician's practice may come under scrutiny and criticism, potentially involving a legal challenge and the Medical Regulator.

Identifiants

pubmed: 33051933
doi: 10.1111/pan.14039
pmc: PMC7756545
doi:

Substances chimiques

Piperidines 0
Remifentanil P10582JYYK
Propofol YI7VU623SF

Types de publication

Journal Article Comment

Langues

eng

Sous-ensembles de citation

IM

Pagination

1292-1298

Commentaires et corrections

Type : CommentOn
Type : CommentOn
Type : CommentIn

Informations de copyright

© 2020 The Authors. Pediatric Anesthesia published by John Wiley & Sons Ltd.

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Auteurs

Anthony R Absalom (AR)

University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Ann E Rigby-Jones (AE)

Faculty of Health: Medicine, Dentistry and Human Sciences, University of Plymouth, Plymouth, UK.

Andrew R Rushton (AR)

Department of Anaesthesia, University Hospitals Plymouth, Plymouth, UK.

J Robert Sneyd (J)

Faculty of Health: Medicine, Dentistry and Human Sciences, University of Plymouth, Plymouth, UK.

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