Efficacy and tolerance of cannabidiol in the treatment of epilepsy in patients with Rett syndrome

Author:

Desnous Béatrice1ORCID,Beretti Thibault1,Muller Nathan1,Neveu Julien2,Villeneuve Nathalie1,Lépine Anne1,Daquin Géraldine3,Milh Mathieu1ORCID

Affiliation:

1. Pediatric Neurology Department Timone Enfant, APHM Marseille France

2. Pediatric Neurology Department Lenval Nice France

3. Epileptology and Cerebral Rhythmology Department Timone Adulte, APHM Marseille France

Abstract

AbstractWe aim to assess the efficacy and tolerance of cannabidiol as adjunctive therapy for Rett syndrome (RTT) patients with epilepsy. We conducted a longitudinal observational study through a monocentric cohort of 46 patients with RTT. Patients were recruited from March 2020 to October 2022 and were treated with Epidyolex® (cannabidiol, CBD, 100 mg/mL oral solution). In our cohort, 26 patients had associated epilepsy (26/46 [56%]), and 10/26 (38%) were treated with CBD, in combination with clobazam in 50% of cases. The median dose at their last follow‐up was 15 mg/kg/day. The median treatment duration was 13 months (range: 1–32 months). CBD reduced the incidence of seizures in seven out of 10 patients (70%) with one seizure‐free patient, two patients with a reduction of seizures of more than 75%, and four patients with a decrease of more than 50%. No aggravation of symptoms or adverse effects were observed. Only one patient experienced a transitory drooling and somnolence episode at the CBD initiation. Half of the patients showed a reduction in agitation and/or anxiety attacks, and an improvement in spasticity was reported in 4/10 (40%) of patients. CBD appears to have potential therapeutic value for the treatment of drug‐resistant epilepsy in Rett syndrome. CBD is well tolerated and, when used in combination with clobazam, may increase the effectiveness of clobazam alone.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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