Evidence map›Paper›PMID 38780448›Full record

ArticleJournal of veterinary internal medicine

Clinical efficacy and tolerability of zonisamide monotherapy in dogs with newly diagnosed idiopathic epilepsy: Prospective open-label uncontrolled multicenter trial.

Miyoko Saito, Akinori Nomura, Daisuke Hasegawa, Naoyuki Watanabe, Keiko Uchida, Seiichi Okuno, Masahiro Nakai, Kensuke Orito

Abstract readMulticenter Study
In one paragraph

Article in Journal of veterinary internal medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Miyoko SaitoLaboratory of Small Animal Surgery (Neurology), School of Veterinary Medicine, Azabu University, Sagamihara, Japan.ORCID https://orcid.org/0000-0001-6560-070X
Akinori NomuraDepartment of Product Development, Bussan Animal Health Co, Ltd, Osaka, Japan.
Daisuke HasegawaLaboratory of Veterinary Clinical Neurology, Graduate School of Veterinary Medicine, Nippon Veterinary and Life Science University, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7554-9108
Naoyuki WatanabeWatanabe Animal Hospital, Shizuoka, Japan.
Keiko UchidaAC-plaza Kariya Animal Hospital, Tokyo, Japan.
Seiichi OkunoAnimal Clinic Kobayashi, Saitama, Japan.
Masahiro NakaiDepartment of Product Development, Bussan Animal Health Co, Ltd, Osaka, Japan.
Kensuke OritoLaboratory of Physiology II, School of Veterinary Medicine, Azabu University, Sagamihara, Japan.

Funding

Bussan Animal Health Co., Ltd (former Sumitomo Pharma Animal Health Co., Ltd.)the Center for Diversity, Equity & Inclusion, Azabu University
6 · The paper itself

Abstract

backgroundZonisamide (ZNS) is a newer generation antiseizure medication (ASM) used to treat epilepsy in dogs and cats. However, scientific and clinical information, particularly regarding monotherapy, is limited.

objectivesTo evaluate the antiseizure efficacy and tolerability of ZNS monotherapy in dogs with newly diagnosed idiopathic epilepsy (IE). ANIMALS: Study included 56 client-owned dogs newly diagnosed with IE.

methodsThis was a prospective multicenter, open-label, uncontrolled study. All dogs were ASM-naïve and had ≥2 seizures within 12 weeks. Dogs were administered 2.7-14.4 mg/kg ZNS PO q12h and followed up for ≥12 weeks. Data from the 12-week maintenance treatment period were compared with those from the 4- to 12-week pretreatment period for efficacy evaluation. Data from the entire ZNS administration period were used to assess tolerability.

resultsFifty-six dogs were included in our study. Of the dogs, 53 were assessed for efficacy; 40 (76%) had a ≥ 50% reduction in seizure frequency, and 29 (55%) achieved seizure freedom. For 90% of the dogs with ≥50% reduction in seizure frequency, the mean ZNS dose was 4.8 (range, 2.7-8.6) mg/kg q12h and the mean trough plasma ZNS concentration was 18.9 (range, 8.0-48.0) μg/mL. In 7 of the 56 dogs (13%), reduced activity, decreased appetite, vomiting, hindlimb weakness, soft stools, or constipation was observed, albeit mild and temporary. Laboratory tests revealed no relevant changes. CONCLUSIONS AND CLINICAL IMPORTANCE: Our study suggests that ZNS monotherapy is effective and well-tolerated in dogs with newly diagnosed IE.

Indexed as

AnticonvulsantsDog DiseasesEpilepsyZonisamideAnimalsDogsFemaleMaleProspective StudiesTreatment OutcomeAnticonvulsantsZonisamideantiepileptic drugantiseizure medicationcanineclinical trialseizuretreatment

Identifiers

PMID38780448
PMCPMC11256125

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.