Crystallization of mixtures of local anesthetics with and without select adjuvants: a semiquantitative light microscopy analysis.

Anesthesia, Local Obstetrics Pharmacology REGIONAL ANESTHESIA

Journal

Regional anesthesia and pain medicine
ISSN: 1532-8651
Titre abrégé: Reg Anesth Pain Med
Pays: England
ID NLM: 9804508

Informations de publication

Date de publication:
05 Mar 2024
Historique:
received: 13 12 2023
accepted: 28 02 2024
medline: 6 3 2024
pubmed: 6 3 2024
entrez: 5 3 2024
Statut: aheadofprint

Résumé

Injecting mixtures of local anesthetics with or without adjuvants is a common practise in regional and particularly obstetric anesthesia to decrease block onset time and/or augment epidural analgesia for cesarean section. While evidence on the efficacy of this practise is equivocal, little is known about its safety in terms of the pharmacologic compatibility of local anesthetics. We assessed the grade of crystallization in individual mixtures of seven local anesthetics (bupivacaine, ropivacaine, lidocaine, procaine, chloroprocaine, mepivacaine, prilocaine) with or without four adjuvants (sodium bicarbonate, dexamethasone, clonidine, fentanyl) using a semiquantitative light microscopy scale (ranging from 0 to 5), repeatedly for up to 60 min and performed correlation analysis between grade of crystallization and initial solution pH. Of the 50 mixtures tested, 26 showed grades of crystallization ≥4 at admixture and 41 showed grades of crystallization ≥4 after 60 min. The addition of adjuvants to local anesthetic mixtures did not substantially change the grades of crystallization. Bupivacaine has a slightly lower precipitation tendency, compared with ropivacaine. A moderate relationship was found between initial pH and grade of crystallization after 15 min for the adjuvant mixtures (R=0.33, p=0.04), but not at other time points. The preparation of local anesthetic (±adjuvant) mixtures leads to high grades of crystallization, which increase over 60 min and appear independent of solution pH. The risk of mixing medications with unknown physical or chemical compatibility profiles in regional anesthesia should be critically appraised and its clinical significance elucidated in future translational research.

Identifiants

pubmed: 38443138
pii: rapm-2023-105229
doi: 10.1136/rapm-2023-105229
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© American Society of Regional Anesthesia & Pain Medicine 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Elisabeth Hoerner (E)

Department of Anesthesiology and Intensive Care, Medical University of Innsbruck, Innsbruck, Austria.

Ottokar Stundner (O)

Department of Anesthesiology and Intensive Care, Medical University of Innsbruck, Innsbruck, Austria otto.stundner@gmail.com.
Department of Anesthesiology, Perioperative Medicine and Intensive Care, Paracelsus Medical University, Salzburg, Austria.

Anna Seisl (A)

Department of Anesthesiology and Intensive Care, Medical University of Innsbruck, Innsbruck, Austria.

Heidi Fiegl (H)

Department of Obstetrics and Gynecology, Medical University of Innsbruck, Innsbruck, Austria.

Lukas Gasteiger (L)

Department of Anesthesiology and Intensive Care, Medical University of Innsbruck, Innsbruck, Austria.

Classifications MeSH