Impact of an extrafascial versus intrafascial injection for supraclavicular brachial plexus block on respiratory function: a randomized, controlled, double-blind trial.


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:
10 2022
Historique:
received: 13 03 2022
accepted: 20 06 2022
pubmed: 2 7 2022
medline: 26 8 2022
entrez: 1 7 2022
Statut: ppublish

Résumé

Hemidiaphragmatic paresis after ultrasound-guided supraclavicular brachial plexus block is reported to occur in up to 67% of patients. We tested the hypothesis that an injection outside the brachial plexus sheath reduces the incidence of hemidiaphragmatic paresis compared with an intrafascial injection while providing similar analgesia. Fifty American Society of Anesthesiologists I-III patients scheduled for elective upper limb surgery received a supraclavicular brachial plexus block using 30 mL of 1:1 mixture of mepivacaine 1% and ropivacaine 0.5%. The block procedures were randomized to position the needle tip either within the brachial plexus after piercing the sheath (intrafascial injection) or outside the brachial plexus sheath (extrafascial injection). The primary outcome was the incidence of hemidiaphragmatic paresis 30 min after the injection, measured by M-mode ultrasonography. Additional outcomes included time to surgery readiness, and resting and dynamic pain scores at 24 hours postoperatively (Numeric Rating Scale, 0-10). The incidence of hemidiaphragmatic paresis 30 min after the injection was 9% (95% CI 1% to 29%) and 0% (95% CI 0% to 15%) in the intrafascial and extrafascial groups respectively (p=0.14). Extrafascial injection was associated with a longer time to surgery readiness (intrafascial: 18 min (95% CI: 16 to 21 min); extrafascial: 37 min (95% CI: 31 to 42 min); p<0.001). At 24 hours, resting and dynamic pain scores were similar between groups. Ultrasound-guided supraclavicular brachial plexus block with an extrafascial injection does not reduce the incidence of hemidiaphragmatic paresis although it provides similar analgesia, when compared with an intrafascial injection. The longer time to surgery readiness is less compatible with contemporary operating theater efficiency requirements. NCT03957772.

Identifiants

pubmed: 35777931
pii: rapm-2022-103634
doi: 10.1136/rapm-2022-103634
doi:

Substances chimiques

Anesthetics, Local 0

Banques de données

ClinicalTrials.gov
['NCT03957772']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

604-609

Informations de copyright

© American Society of Regional Anesthesia & Pain Medicine 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: EA received grants from the Swiss Academy for Anesthesia Research (SACAR), Lausanne, Switzerland, B. Braun Medical AG, Sempach, Switzerland and the Swiss National Science Foundation, Bern, Switzerland to support his clinical research. EA has also received an honorarium from B. Braun Medical AG Switzerland, Sintetica UK and MSD AG Switzerland. SG received a research grant and an honorarium from MSD AG Switzerland.

Auteurs

Sina Grape (S)

Department of Anaesthesia, Valais Hospital, Sion, Switzerland.
University of Lausanne, Lausanne, Switzerland.

Kyle Kirkham (K)

Department of Anesthesia, Toronto Western Hospital & University of Toronto, Toronto, Ontario, Canada.

Nadjib Zemirline (N)

Department of Anaesthesia, Valais Hospital, Sion, Switzerland.

Alexis Bikfalvi (A)

Department of Anesthesia, University Hospital of Lausanne, Lausanne, Switzerland.

Eric Albrecht (E)

University of Lausanne, Lausanne, Switzerland eric.albrecht@chuv.ch.
Department of Anesthesia, University Hospital of Lausanne, Lausanne, Switzerland.

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