Search Results

You are looking at 1 - 3 of 3 items for

  • Author or Editor: Julie M. Ducoté x
  • Refine by Access: All Content x
Clear All Modify Search
History

A 5-year-old sexually intact male Welsh Corgi was evaluated for progressive ambulatory paraparesis of the pelvic limbs of approximately 9 months' duration. Bilateral pelvic limb ataxia and paresis had been noticed by the owner during the 9 months prior to referral. There was no history of trauma, and the dog did not have signs of pain. On physical examination, conscious proprioception in the pelvic limbs was absent, the patellar reflexes were exaggerated, severe wear was evident on the toenails of each pelvic limb, and the dog's body condition was thin. The neurologic lesion was localized to the area from

Restricted access
in Journal of the American Veterinary Medical Association
in Journal of the American Veterinary Medical Association

Abstract

Objective—To assess tolerability and short-term efficacy of oral administration of pregabalin as an adjunct to phenobarbital, potassium bromide, or a combination of phenobarbital and potassium bromide for treatment of dogs with poorly controlled suspected idiopathic epilepsy.

Design—Open-label, noncomparative clinical trial.

Animals—11 client-owned dogs suspected of having idiopathic epilepsy that was inadequately controlled with phenobarbital, potassium bromide, or a combination of these 2 drugs.

Procedures—Dogs were treated with pregabalin (3 to 4 mg/kg [1.4 to 1.8 mg/lb], PO, q 8 h) for 3 months. Number of generalized seizures in the 3 months before and after initiation of pregabalin treatment was recorded. Number of responders (≥ 50% reduction in seizure frequency) was recorded, and seizure frequency before and after initiation of pregabalin treatment was compared by use of a nonparametric Wilcoxon signed rank test.

Results—Seizures were significantly reduced (mean, 57%; median, 50%) after pregabalin administration in the 9 dogs that completed the study; 7 were considered responders with mean and median seizure reductions of 64% and 58%, respectively. Adverse effects for pregabalin were reported in 10 dogs. Mean and median plasma pregabalin concentrations for all dogs were 6.4 and 7.3 μg/mL, respectively.

Conclusions and Clinical Relevance—Pregabalin may hold promise as a safe and effective adjunct anticonvulsant drug for epileptic dogs poorly controlled with the standard drugs phenobarbital or potassium bromide. Adverse effects of pregabalin appeared to be mild. Additional studies with larger numbers of dogs and longer follow-up intervals are warranted.

Restricted access
in Journal of the American Veterinary Medical Association