Total knee arthroplasty under quadruple nerve block with ropivacaine 0.32%: effect of addition of intravenous dexmedetomidine to intravenous dexamethasone on analgesic duration.


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:
02 2021
Historique:
received: 08 06 2020
revised: 10 09 2020
accepted: 25 09 2020
pubmed: 23 10 2020
medline: 29 6 2021
entrez: 22 10 2020
Statut: ppublish

Résumé

Peripheral nerve blocks reduce postoperative pain and enhance recovery after total knee arthroplasty (TKA). This study aims to assess the benefits of addition of intravenous dexmedetomidine (DexM) to intravenous dexamethasone on the analgesic duration of quadruple nerve blocks. This double-blind, randomized, controlled trial prospectively enrolled 90 patients scheduled for TKA under quadruple nerve blocks (sciatic, femoral, obturator, and lateral femoral cutaneous nerves blocks) with 70 mL, 0.32% ropivacaine. All patients received systemic dexamethasone 10 mg. Patients were randomized to receive DexM (2 µg/kg, intravenous) or placebo (1:1 ratio). The primary endpoint was the duration of analgesia defined as the time to first request for rescue analgesia (oxycodone). Kaplan-Meier curves for the first analgesic request were similar between groups (log-rank test; p=0.27). Median (IQR) duration of analgesia was similar between placebo (1575 min (1211-1952)) and DexM (1470 min (1263-1700)) groups (p=0.56). Cumulative consumption of oxycodone at the 48th hour was 20 mg (10-30) and 30 mg (20-40) in placebo and DexM groups, respectively (p=0.14). The day after surgery, 93% and 89% of patients were able to walk in placebo and DexM groups, respectively (p=0.46). Intravenous DexM was associated with bradycardia, hypotension and longer recovery room stay (p<0.05 for all comparisons). In a multimodal analgesic regimen, addition of systemic DexM (2 µg/kg) to systemic dexamethasone does not prolong the analgesic duration of quadruple nerve block with ropivacaine 0.32% after TKA. NCT03834129.

Sections du résumé

BACKGROUND AND OBJECTIVES
Peripheral nerve blocks reduce postoperative pain and enhance recovery after total knee arthroplasty (TKA). This study aims to assess the benefits of addition of intravenous dexmedetomidine (DexM) to intravenous dexamethasone on the analgesic duration of quadruple nerve blocks.
METHODS
This double-blind, randomized, controlled trial prospectively enrolled 90 patients scheduled for TKA under quadruple nerve blocks (sciatic, femoral, obturator, and lateral femoral cutaneous nerves blocks) with 70 mL, 0.32% ropivacaine. All patients received systemic dexamethasone 10 mg. Patients were randomized to receive DexM (2 µg/kg, intravenous) or placebo (1:1 ratio). The primary endpoint was the duration of analgesia defined as the time to first request for rescue analgesia (oxycodone).
RESULTS
Kaplan-Meier curves for the first analgesic request were similar between groups (log-rank test; p=0.27). Median (IQR) duration of analgesia was similar between placebo (1575 min (1211-1952)) and DexM (1470 min (1263-1700)) groups (p=0.56). Cumulative consumption of oxycodone at the 48th hour was 20 mg (10-30) and 30 mg (20-40) in placebo and DexM groups, respectively (p=0.14). The day after surgery, 93% and 89% of patients were able to walk in placebo and DexM groups, respectively (p=0.46). Intravenous DexM was associated with bradycardia, hypotension and longer recovery room stay (p<0.05 for all comparisons).
CONCLUSIONS
In a multimodal analgesic regimen, addition of systemic DexM (2 µg/kg) to systemic dexamethasone does not prolong the analgesic duration of quadruple nerve block with ropivacaine 0.32% after TKA.
TRIAL REGISTRATION NUMBER
NCT03834129.

Identifiants

pubmed: 33087480
pii: rapm-2020-101749
doi: 10.1136/rapm-2020-101749
doi:

Substances chimiques

Analgesics 0
Anesthetics, Local 0
Dexmedetomidine 67VB76HONO
Ropivacaine 7IO5LYA57N
Dexamethasone 7S5I7G3JQL

Banques de données

ClinicalTrials.gov
['NCT03834129']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

104-110

Informations de copyright

© American Society of Regional Anesthesia & Pain Medicine 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Clement Chassery (C)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Philippe Marty (P)

Anesthesia, Clinique Medipole Garonne, Toulouse, France philippemarty@hotmail.com.

Olivier Rontes (O)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Martine Chaubard (M)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Corine Vuillaume (C)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Bertrand Basset (B)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Mehdi Merouani (M)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Constance Marquis (C)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Anne De Lussy (A)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Marie-Claude Delbos (MC)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Julie Casalprim (J)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

Benoit Bataille (B)

Department of Anesthesia and Intensive Care, Narbonne general Hospital, Narbonne, France.

Cecile Naudin (C)

Clinical Research Department, Ambroise Pare Hospital Group, Neuilly-sur-Seine, France.

Fabrice Ferre (F)

Department of Anesthesia, CHU Purpan, Toulouse, France.

Alain Delbos (A)

Anesthesia, Clinique Medipole Garonne, Toulouse, France.

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Classifications MeSH