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Pregabalin in partial seizures: a pragmatic 21-week, open-label study (PREPS)
P Ryvlin1, R Kälviäinen, F Von Raison
1CTRS-INSERM IDEE, U821, Université Claude Bernard Lyon 1 and Neurological Hospital, Hospices Civils de Lyon, Lyon, France. ryvlin@cermep.fr
This study shows pregabalin effectively reduced seizure frequency in adults with refractory epilepsy. Pregabalin was well-tolerated, with an adverse event profile consistent with prior trials.
Area of Science:
- Neurology
- Clinical Pharmacology
Background:
- Refractory epilepsy poses a significant treatment challenge.
- Controlled trials indicate pregabalin's efficacy as adjunctive therapy.
Purpose of the Study:
- To evaluate the efficacy and tolerability of pregabalin in adults with inadequately controlled partial seizures.
- To assess pregabalin's effectiveness as an add-on treatment in a real-world setting.
Main Methods:
- Open-label, 21-week study involving 476 adult patients.
- Patients received pregabalin (150-600 mg/day) with inadequate seizure control on 1-3 antiepileptic drugs.
- Primary endpoint: mean percentage change in 28-day seizure frequency from baseline.
Main Results:
- A mean seizure frequency reduction of 36% was observed.
- 39% of patients achieved a ≥50% reduction in seizure frequency.
- Common adverse events included dizziness, somnolence, and weight increase.
Conclusions:
- Open-label pregabalin treatment demonstrated efficacy consistent with controlled trials in refractory epilepsy.
- Pregabalin was well-tolerated in this patient population.
- The observed adverse event profile aligns with previous findings.
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