TY - JOUR
T1 - Real-Life Experience With Purified Cannabidiol Treatment for Refractory Epilepsy
T2 - A Multicenter Retrospective Study
AU - Tzadok, Michal
AU - Gur-Pollack, Rotem
AU - Florh, Hadar
AU - Michaeli, Yael
AU - Gilboa, Tal
AU - Lezinger, Mirit
AU - Heyman, Eli
AU - Chernuha, Veronika
AU - Gudis, Irina
AU - Nissenkorn, Andreea
AU - Lerman-Sagie, Tally
AU - Ben Zeev, Bruria
AU - Uliel-Sibony, Shimrit
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2024/1
Y1 - 2024/1
N2 - Background: Drug-resistant epilepsy (DRE) affects the development and quality of life of children and young adults. We analyzed the effectiveness and safety of purified CBD in this population. Methods: A retrospective analysis of medical records of 139 children and young adults (54.7% female, median age 12.0 years) with DRE treated with purified CBD from 2018 to 2022 at five medical centers in Israel. Results: The most common diagnosis was Lennox-Gastaut syndrome (37.4%) followed by Dravet syndrome (16.5%) and tuberous sclerosis complex (16.5%). Median purified CBD dose was 12.5 mg/kg (range 2.5 to 20.0), and median treatment duration was 9.0 months (range 0.5 to 48.0). Most patients (92.2%) had a reduced seizure frequency following treatment initiation; 41.1% had >50% reduction. Fifty-three patients (38.1%) had positive effects: improved alertness (31.7%), improved speech (10.1%), and achievement of new developmental milestones (2.2%). A multivariate linear model assessing predictive factors for seizure reduction demonstrated that patients previously treated with CBD oils, especially those with >50% seizure reduction on prior treatment, were also more likely to have a reduced seizure frequency while they were treated with purified CBD (P = 0.01, P < 0.0001). Development, diagnosis, age, purified CBD dose (0 to 10 mg/kg/day vs 10 to 20 mg/kg/day), and concomitant treatment with clobazam, valproic acid, or everolimus did not affect seizure reduction by purified CBD. The most common adverse events were irritability (20.9%) and drowsiness (12.9%). Conclusion: Purified CBD is well-tolerated and effective in reducing seizure frequency in children and young adults with DRE.
AB - Background: Drug-resistant epilepsy (DRE) affects the development and quality of life of children and young adults. We analyzed the effectiveness and safety of purified CBD in this population. Methods: A retrospective analysis of medical records of 139 children and young adults (54.7% female, median age 12.0 years) with DRE treated with purified CBD from 2018 to 2022 at five medical centers in Israel. Results: The most common diagnosis was Lennox-Gastaut syndrome (37.4%) followed by Dravet syndrome (16.5%) and tuberous sclerosis complex (16.5%). Median purified CBD dose was 12.5 mg/kg (range 2.5 to 20.0), and median treatment duration was 9.0 months (range 0.5 to 48.0). Most patients (92.2%) had a reduced seizure frequency following treatment initiation; 41.1% had >50% reduction. Fifty-three patients (38.1%) had positive effects: improved alertness (31.7%), improved speech (10.1%), and achievement of new developmental milestones (2.2%). A multivariate linear model assessing predictive factors for seizure reduction demonstrated that patients previously treated with CBD oils, especially those with >50% seizure reduction on prior treatment, were also more likely to have a reduced seizure frequency while they were treated with purified CBD (P = 0.01, P < 0.0001). Development, diagnosis, age, purified CBD dose (0 to 10 mg/kg/day vs 10 to 20 mg/kg/day), and concomitant treatment with clobazam, valproic acid, or everolimus did not affect seizure reduction by purified CBD. The most common adverse events were irritability (20.9%) and drowsiness (12.9%). Conclusion: Purified CBD is well-tolerated and effective in reducing seizure frequency in children and young adults with DRE.
KW - Children
KW - Drug-resistant epilepsy
KW - Purified cannabidiol
KW - Seizure reduction
KW - Young adults
UR - http://www.scopus.com/inward/record.url?scp=85177865763&partnerID=8YFLogxK
U2 - 10.1016/j.pediatrneurol.2023.10.012
DO - 10.1016/j.pediatrneurol.2023.10.012
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C2 - 37995414
AN - SCOPUS:85177865763
SN - 0887-8994
VL - 150
SP - 91
EP - 96
JO - Pediatric Neurology
JF - Pediatric Neurology
ER -