4.3 Editorial Material

Perampanel as add-on treatment in refractory focal epilepsy. The Dianalund experience

Journal

ACTA NEUROLOGICA SCANDINAVICA
Volume 134, Issue 5, Pages 374-377

Publisher

WILEY-BLACKWELL
DOI: 10.1111/ane.12558

Keywords

perampanel; drug-refractory focal epilepsy; efficacy; safety; tolerability; psychiatric adverse events

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Background - Perampanel (PER) is an antagonist of AMPA receptors that has been approved for adjunctive treatment of partial-onset seizures. Aims -To evaluate effectiveness and safety of PER as add-on treatment in patients with severely refractory focal epilepsy. Methods - PER was introduced as add-on treatment in 22 consecutive patients with drug-resistant focal epilepsy. PER was started with 2 mg/day at bedtime and was up-titrated by 2 mg/day every 24 weeks. Results - All patients suffered from severely refractory focal epilepsy (86% took 2 or more AEDs prior PER initiation; 40% had been submitted to surgery or were surgery candidates; 7 had VNS). After 12 months since PER initiation, the retention rate was 54.5% and the responder rate was 27.2%, including 9.1% seizure-free patients. Mean PER dose in the responders was 8 mg/day (range 4-10). Most common side effects were tiredness, behavioral changes (primarily aggressivity), dizziness and were reported in 59.1% of patients, leading to PER discontinuation in 31.8% of subjects. Conclusions - PER as add-on treatment can achieve clinically meaningful improvement in patients suffering from severely refractory focal epilepses. Further studies are warranted to explore the tolerability profile, with particular focus on psychiatric adverse events.

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