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Peer-reviewed veterinary case report

Pregabalin for nerve pain in dogs with syringomyelia

By Sanchis-Mora, S et al.·Published in Veterinary journal (London, England : 1997)·2019·Royal Veterinary College, United Kingdom·View original on PubMed

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

Species:
dog

Plain-English summary

An 8-year-old dog with Chiari-like malformation and syringomyelia was experiencing severe pain due to nerve issues. The dog was treated with pregabalin, a medication commonly used for neuropathic pain in humans, and the owner reported a significant reduction in pain levels compared to when the dog was given a placebo. The dog showed improved sensitivity to touch and cold, indicating that the medication was effective. Pregabalin was well tolerated, with only mild sedation noted as a side effect.

People also search for: dog syringomyelia pain treatment · pregabalin for dogs · Chiari-like malformation pain relief

Abstract

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&#xb1;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&#xb0;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&#xb0;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&#xb0;C) and allodynia (15&#xb0;C) compared to placebo. Pregabalin was non-cumulative and well tolerated with occasional mild sedation.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/31383420/