Peer-reviewed veterinary case report
Phenobarbital or potassium bromide as an add-on antiepileptic drug for the management of canine idiopathic epilepsy refractory to imepitoin.
- Journal:
- Veterinary journal (London, England : 1997)
- Year:
- 2017
- Authors:
- Royaux, E et al.
- Affiliation:
- Department of Small Animal Medicine and Clinical Biology
- Species:
- dog
Plain-English summary
This study looked at how well two medications, phenobarbital and potassium bromide (KBr), work when added to imepitoin for dogs with idiopathic epilepsy (a type of epilepsy with no known cause) that isn't well controlled. Twenty-seven dogs participated, with some receiving phenobarbital and others getting KBr. Both groups showed a significant drop in the number of seizures and the frequency of seizure days, and most dogs had fewer cluster seizures, which are groups of seizures occurring close together. About 79% of the dogs on phenobarbital and 69% on KBr responded positively to the treatment. Overall, adding either medication helped reduce seizures in these dogs and was generally well tolerated.
Abstract
Imepitoin has recently been approved in Europe for the management of dogs with idiopathic epilepsy. Currently, there is no evidence-based information available on the efficacy of antiepileptic drugs used as additions to the therapeutic regimen in dogs with idiopathic epilepsy that are not well controlled with imepitoin. The goal of this study was to evaluate the efficacy of phenobarbital or potassium bromide (KBr) as add-on antiepileptic drugs for controlling dogs refractory to a maximum dose of imepitoin (30 mg/kg twice daily). The study was performed as a prospective, randomised, controlled clinical trial. The efficacy of phenobarbital and KBr was evaluated by comparing monthly seizure frequency (MSF), monthly seizure day frequency (MSDF), the presence of cluster seizures during a retrospective 2-month period with a prospective follow-up of 6 months, and the overall responder rate. Twenty-seven dogs were included in the study, 14 dogs in the phenobarbital group and 13 dogs in the KBr group. Both median MSF and MSDF decreased in the phenobarbital group (both P = 0.001) and in the KBr group (P = 0.004 and P = 0.003, respectively). Overall, the number of dogs with cluster seizures decreased (P = 0.0005). The responder rate was 79% vs. 69% in the phenobarbital and KBr groups, respectively. We conclude that phenobarbital or KBr add-on treatment decreases median MSF and MSDF in epileptic dogs refractory to a maximum dose of imepitoin. Combination therapy was generally well tolerated and resulted in an improvement in seizure management in the majority of the dogs.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/28190495/