The efficacy and safety of cannabidiol (CBD) in pediatric patients with Dravet Syndrome: a narrative review of clinical trials

Eur J Med Res. 2024 Mar 18;29(1):182. doi: 10.1186/s40001-024-01788-6.

Abstract

Background: Dravet Syndrome (DS) is a rare and severe form of childhood epilepsy that is often refractory to conventional antiepileptic drugs. Emerging evidence suggests that Cannabidiol (CBD) offer therapeutic benefits for DS. This review aims to evaluate the efficacy and safety of CBD in pediatric patients with DS based on data from ten clinical trials.

Methods: A review was conducted to identify clinical trials assessing the efficacy and safety of CBD in pediatric patients diagnosed with DS. PubMed, MEDLINE, Scopus, Web of Science, and relevant grey literature were systematically searched for relevant articles up to October 2023, and clinical trials within the last 10 years were included. The search strategy incorporated controlled vocabulary terms and keywords related to "Cannabidiol," "Dravet Syndrome," and "pediatric patients."

Results: The analysis revealed promising efficacy outcomes. Notably, CBD demonstrated substantial reductions in seizure frequency, with some patients achieving seizure freedom. The findings emphasised the consistency of CBD's efficacy across different patient subgroups. The safety profile of CBD was generally acceptable, with adverse events often being manageable.

Conclusion: This review consolidates evidence from multiple clinical trials, affirming the potential of CBD as a promising treatment option for pediatric patients with DS. While further research is needed to address existing knowledge gaps, CBD's efficacy and acceptable safety profile make it a valuable addition to the therapeutic tools for DS.

Keywords: Antiepileptic drugs; Cannabidiol (CBD); Dravet Syndrome; Pediatric patients; Seizure frequency.

Publication types

  • Systematic Review
  • Review

MeSH terms

  • Anticonvulsants
  • Cannabidiol* / therapeutic use
  • Child
  • Epilepsies, Myoclonic* / diagnosis
  • Epilepsies, Myoclonic* / drug therapy
  • Humans
  • Lennox Gastaut Syndrome* / diagnosis
  • Lennox Gastaut Syndrome* / drug therapy
  • Seizures / drug therapy

Substances

  • Anticonvulsants
  • Cannabidiol