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Zonisamide add-on for drug-resistant partial epilepsy.
1Department of Neurological Science, Room 2.26 - Clinical Science Centre for Research & Education, Lower Lane, Liverpool, Merseyside, UK L9 7LJ. r.jowett@liv.ac.uk
The Cochrane Database of Systematic Reviews
|October 20, 2005
Summary
Zonisamide effectively reduces seizure frequency in individuals with drug-resistant partial epilepsy when used as an add-on therapy. However, optimal dosing and long-term effectiveness require further investigation.
Area of Science:
- Neurology
- Pharmacology
- Clinical Trials
Background:
- Up to 30% of epilepsy patients develop drug-resistant epilepsy, particularly those with partial seizures.
- Zonisamide is an antiepileptic agent evaluated for add-on treatment in refractory epilepsy.
Purpose of the Study:
- To evaluate the efficacy and safety of zonisamide as an add-on treatment for drug-resistant partial epilepsy.
- To assess seizure frequency reduction, treatment withdrawal, and adverse events associated with zonisamide therapy.
Main Methods:
- Systematic review of randomized placebo-controlled add-on trials of zonisamide.
- Searched Cochrane Epilepsy Group Specialized Register and contacted drug manufacturers and experts.
- Data extracted on seizure reduction, withdrawal rates, and adverse events; intention-to-treat analyses performed.
Main Results:
- Zonisamide (100-500 mg/day) significantly increased the likelihood of a 50% or greater seizure frequency reduction (RR 2.35, 95% CI 1.74 to 3.17).
- Higher zonisamide doses (300-500 mg/day) were associated with increased treatment withdrawal (RR 1.64, 95% CI 1.20 to 2.26).
- Significantly associated adverse effects included ataxia, dizziness, somnolence, agitation, and anorexia.
Conclusions:
- Zonisamide demonstrates efficacy as an add-on treatment for drug-resistant partial epilepsy.
- Minimum effective and maximum tolerated doses were not identified.
- Study duration was limited to 12 weeks, precluding conclusions on long-term effectiveness or use in monotherapy or other epilepsy types.