Pregabalin for the treatment of syringomyelia-associated neuropathic pain in dogs: A randomised, placebo-controlled, double-masked clinical trial.


Journal

Veterinary journal (London, England : 1997)
ISSN: 1532-2971
Titre abrégé: Vet J
Pays: England
ID NLM: 9706281

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 11 10 2018
revised: 27 06 2019
accepted: 30 06 2019
entrez: 7 8 2019
pubmed: 7 8 2019
medline: 24 12 2019
Statut: ppublish

Résumé

Pregabalin is the first-line treatment for neuropathic pain (NeP) in humans. Dogs with Chiari-like malformation and syringomyelia (CM/SM) associated with NeP could benefit from pregabalin. The aim of this study was to evaluate the efficacy of pregabalin for NeP in dogs with CM/SM. Eight dogs with symptomatic CM/SM were included in a double-masked, randomised, crossover placebo-controlled clinical trial. All dogs received anti-inflammatory drugs as base-line treatment during placebo or pregabalin phase of 14±4 days each. Analgesic efficacy was assessed with a daily numerical rating scale (NRS) recorded by dog owners (0-10, 10=worst pain) and quantitative sensory testing at baseline, placebo and pregabalin phases. Blood samples were collected to report pregabalin exposure and to assess renal function. Daily NRS scores recorded by dog owners in the pregabalin group were lower than in the placebo group (P=0.006). Mechanical thresholds were higher with pregabalin compared to baseline or placebo (P=0.037, P<0.001). Cold latency at 15°C was prolonged on the neck and humeri with pregabalin compared to baseline (P<0.001 for both) or placebo (P=0.02, P=0.0001). Cold latency at 0°C was longer on pregabalin compared to baseline and placebo (P=0.001, P=0.004). There was no pregabalin accumulation between first and last dose. This study demonstrates the efficacy of pregabalin for the treatment of NeP due to CM/SM on daily pain scores recorded by dog owners. Pregabalin significantly reduced mechanical hyperalgesia, cold hyperalgesia (0°C) and allodynia (15°C) compared to placebo. Pregabalin was non-cumulative and well tolerated with occasional mild sedation.

Identifiants

pubmed: 31383420
pii: S1090-0233(18)30619-1
doi: 10.1016/j.tvjl.2019.06.006
pii:
doi:

Substances chimiques

Analgesics 0
Pregabalin 55JG375S6M

Types de publication

Journal Article Randomized Controlled Trial, Veterinary

Langues

eng

Sous-ensembles de citation

IM

Pagination

55-62

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

S Sanchis-Mora (S)

Comparative Biomedical Sciences, Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL97TA, UK. Electronic address: ssanchismora@rvc.ac.uk.

Y M Chang (YM)

Research Office, Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL97TA, UK.

S M Abeyesinghe (SM)

Production and Population Health, Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL97TA, UK.

A Fisher (A)

Transpharmation Ltd, 2 Royal College Street, London, NW10NH, UK.

N Upton (N)

Transpharmation Ltd, 2 Royal College Street, London, NW10NH, UK.

H A Volk (HA)

Clinical Sciences and Services Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL97TA, UK; Department of Small Animal Medicine and Surgery, University of Veterinary Medicine, Bünteweg 9, 30559, Hannover, Germany.

L Pelligand (L)

Comparative Biomedical Sciences, Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL97TA, UK; Clinical Sciences and Services Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL97TA, UK.

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Classifications MeSH