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Updated: Feb 3, 2026

Brain Source Imaging in Preclinical Rat Models of Focal Epilepsy using High-Resolution EEG Recordings
Published on: June 6, 2015
Zonisamide add-on therapy for focal epilepsy
Francesco Brigo1, Simona Lattanzi, Stanley C Igwe
1Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, P.le L.A. Scuro, 10, Verona, Verona, Italy, 37134.
Zonisamide effectively reduces seizure frequency by at least 50% in individuals with refractory focal epilepsy when used as an add-on therapy. Moderate-quality evidence supports its efficacy, though adverse effects like ataxia and somnolence were noted.
Area of Science:
- Neurology
- Pharmacology
- Clinical Trials
Background:
- Refractory epilepsy affects up to 30% of epilepsy patients, particularly those with focal seizures.
- Zonisamide is an antiepileptic drug used in treatment regimens.
- This review is an update of a previous Cochrane review from 2013.
Purpose of the Study:
- To evaluate the efficacy and tolerability of zonisamide as an add-on treatment for focal epilepsy.
- To assess zonisamide's effectiveness in patients whose seizures are not controlled by existing antiepileptic drugs.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials (RCTs).
- Searched multiple databases including Cochrane Epilepsy Group Register, MEDLINE, and ClinicalTrials.gov.
- Assessed risk of bias using the Cochrane 'Risk of bias' tool and evidence quality using the GRADE approach.
Main Results:
- Zonisamide (300-500 mg/day) significantly reduced seizure frequency by at least 50% compared to placebo (RR 1.90, moderate-quality evidence).
- The number needed to treat for an additional beneficial outcome was six.
- Adverse effects associated with zonisamide included ataxia, somnolence, agitation, and anorexia.
Conclusions:
- Zonisamide demonstrates moderate-quality evidence of efficacy in reducing seizure frequency for refractory focal epilepsy.
- Longer-term efficacy and optimal dosing require further investigation.
- Results are not generalizable to monotherapy or other epilepsy types.
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