In a retrospective study of 29 pediatric patients with intractable epilepsy, adjunctive CBD therapy showed retention rates above 86% at both 12 and 24 months, with 79.3% achieving at least 50% seizure reduction at one year.
Families of children with treatment-resistant epilepsy, pediatric neurologists, and researchers studying CBD across epilepsy subtypes.
79.3% achieved 50%+ seizure reduction at 12 months
What the researchers found
At 12 months, 79.3% of patients achieved 50% or greater seizure reduction and 34.5% achieved 75% or greater reduction without generalized motor seizures. The retention rate exceeded 86% at both 12 and 24 months. One patient with a GABRB3 variant achieved seizure freedom.
Why it matters
Children with intractable epilepsy have often exhausted conventional treatment options. This study shows CBD maintained effectiveness across a range of genetic and non-genetic epilepsy causes, including some rarely studied variants.
The numbers in context
29 patients. Median maintenance dose 14.2 mg/kg/day. Retention above 86% at 12 and 24 months. 79.3% achieved 50%+ seizure reduction at 12 months. 34.5% achieved 75%+ reduction. Adverse events in 37.9%, mostly somnolence and lethargy. 3 discontinuations.
How the study worked
Retrospective cohort study of 29 patients aged 6-24 years with pediatric-onset intractable epilepsy treated at Korea University Hospitals between April 2019 and May 2024. Median follow-up was 14.3 months. Patients were on a median of 5 antiseizure medications at CBD initiation.
What this study cannot tell us
Retrospective design with a small sample of 29 patients. Single center in South Korea. No control group. Patients were on multiple concurrent medications, making it difficult to isolate CBD effects.
How to read the evidence
Moderate: retrospective cohort with reasonable follow-up duration but small sample, no control group, and single-center design.
When this study was published
Published 2026. Data from April 2019 to May 2024.
The bigger picture
Most CBD epilepsy research focuses on Dravet and Lennox-Gastaut syndromes. This study extends the evidence across diverse etiologies including GABRB3, SCN2A, KCNT1, and KIF1A variants, Angelman syndrome, and acquired causes like hypoxic brain injury.
Questions still open
- Which genetic epilepsy subtypes respond best to CBD? Could earlier introduction of CBD (before trying 5+ medications) improve outcomes? What explains the high retention rate compared to other antiseizure medications?
Common questions
How effective is CBD for treatment-resistant epilepsy in children?
Does CBD work for different types of epilepsy?
Read the original research
Adjunctive cannabidiol in intractable pediatric epilepsy: A retrospective study on tolerability, efficacy, and safety across genetic and nongenetic etiologies.
Medicine, 105(5), e47425
Citation
Shim, Youngkyu; Yang, Dong Hwa; Byeon, Jung Hye; Eun, Baik-Lin. (2026). Adjunctive cannabidiol in intractable pediatric epilepsy: A retrospective study on tolerability, efficacy, and safety across genetic and nongenetic etiologies.. Medicine, 105(5), e47425. https://doi.org/10.1097/MD.0000000000047425
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