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纯化大麻二酚作为治疗抵抗性婴儿痉挛综合征患儿的附加疗法。

Purified cannabidiol as add-on therapy in children with treatment-resistant infantile epileptic spasms syndrome.

作者信息

Reyes Valenzuela Gabriela, Gallo Adolfo, Calvo Agustin, Chacón Santiago, Fasulo Lorena, Galicchio Santiago, Adi Javier, Fortini Pablo Sebastian, Caraballo Roberto

机构信息

Department of Neurology, Hospital de Pediatría Juan P Garrahan, Combate de los Pozos, Buenos Aires 1881 Argentina.

Department of Pediatric Neurology, Hospital Regional de Comodoro Rivadavia, Argentina.

出版信息

Seizure. 2024 Feb;115:94-99. doi: 10.1016/j.seizure.2024.01.010. Epub 2024 Jan 15.


DOI:10.1016/j.seizure.2024.01.010
PMID:38237316
Abstract

OBJECTIVE: The aim of this study was to assess efficacy, safety, and tolerability of highly purified cannabidiol oil (CBD) as add-on therapy for the treatment of a series of patients with infantile epileptic spasms syndrome (IESS) who were resistant to antiseizure medications and ketogenic dietary therapy. MATERIAL AND METHODS: We conducted a retrospective analysis of the medical records of 28 infants with treatment-resistant IESS aged 6 to 21 months who received highly purified CBD between July 2021 and June 2023. Data were collected on neurological examinations, EEG, Video-EEG and polygraphic recordings, imaging studies, laboratory testing, and seizure frequency, type, and duration, and adverse effects. As the primary outcome, a reduction of frequency of epileptic spasms (ES) was assessed. ES freedom was considered after a minimal time of 1 month without ES. RESULTS: Sixteen male and 12 female patients, aged 6-21 months, who received CBD for treatment-resistant IESS were included. The etiology was structural in 10, Down syndrome in seven, genetic in nine, and unknown in two. Initial CBD dose was 2 mg/kg/day, which was uptitrated to a median dose of 25 mg/kg/day (range, 2-50). Prior to CBD initiation, patients had a median of 69 ES in clusters per day (range, 41-75) and of 10 focal seizures per week (range, 7-13). After a mean and median follow-up of 15 and 12.5 months (range, 6-26 months), seven patients were ES free and 12 had a >50 % ES reduction. Five of seven patients (71 %) with Down syndrome and 3/5 (60 %) with cerebral palsy responded well. Adverse effects were mild. EEG improvements correlated with ES reductions. CONCLUSION: In this study evaluating the use of CBD in children with IESS, 19/28 (67.8 %) had a more than 50 % ES reduction with good tolerability.

摘要

目的:本研究旨在评估高纯度大麻二酚油(CBD)作为附加疗法治疗一系列对抗癫痫药物和生酮饮食疗法耐药的婴儿痉挛综合征(IESS)患者的疗效、安全性和耐受性。 材料与方法:我们对2021年7月至2023年6月期间接受高纯度CBD治疗的28例6至21个月大的难治性IESS婴儿的病历进行了回顾性分析。收集了神经学检查、脑电图、视频脑电图和多导记录、影像学研究、实验室检查以及癫痫发作频率、类型、持续时间和不良反应的数据。作为主要结局,评估癫痫痉挛(ES)频率的降低情况。在至少1个月无ES后考虑ES缓解。 结果:纳入了16例男性和12例女性患者,年龄6至21个月,接受CBD治疗难治性IESS。病因方面,10例为结构性,7例为唐氏综合征,9例为遗传性,2例病因不明。初始CBD剂量为2mg/kg/天,上调至中位剂量25mg/kg/天(范围2 - 50)。在开始使用CBD之前,患者每天成簇发作的ES中位数为69次(范围41 - 75),每周局灶性发作中位数为10次(范围7 - 13)。在平均和中位随访15个月和12.5个月(范围6 - 26个月)后,7例患者无ES发作,12例患者ES减少>50%。7例唐氏综合征患者中有5例(71%)和5例脑瘫患者中有3例(60%)反应良好。不良反应轻微。脑电图改善与ES减少相关。 结论:在本评估CBD用于IESS儿童的研究中,19/28(67.8%)患者ES减少超过50%,耐受性良好。

相似文献

[1]
Purified cannabidiol as add-on therapy in children with treatment-resistant infantile epileptic spasms syndrome.

Seizure. 2024-2

[2]
Cannabidiol-enriched medical cannabis as add-on therapy in children with treatment-resistant West syndrome: A study of eight patients.

Seizure. 2021-11

[3]
Perceived efficacy of cannabidiol-enriched cannabis extracts for treatment of pediatric epilepsy: A potential role for infantile spasms and Lennox-Gastaut syndrome.

Epilepsy Behav. 2015-6

[4]
Early Response, Long-Term Seizure Outcome, and Very-Low-Dose Adrenocorticotrophic Hormone Therapy for Infantile Epileptic Spasms Syndrome With Down Syndrome.

Pediatr Neurol. 2024-7

[5]
Cannabidiol in treatment of refractory epileptic spasms: An open-label study.

Epilepsy Behav. 2020-5

[6]
Long-term analysis of adrenocorticotropic hormone monotherapy for infantile epileptic spasms syndrome with periventricular leukomalacia.

Seizure. 2023-7

[7]
An Open Retrospective Study of a Standardized Cannabidiol Based-Oil in Treatment-Resistant Epilepsy.

Cannabis Cannabinoid Res. 2022-4

[8]
Long-term efficacy and safety of cannabidiol in patients with tuberous sclerosis complex: 3-year results from the cannabidiol expanded access program.

Epilepsia Open. 2024-10

[9]
Don't Fear the Reefer-Evidence Mounts for Plant-Based Cannabidiol as Treatment for Epilepsy.

Epilepsy Curr. 2019

[10]
[Phenotype of infantile epileptic spasm syndrome in pyridoxin-dependent epilepsy].

Beijing Da Xue Xue Bao Yi Xue Ban. 2024-10-18

引用本文的文献

[1]
Is highly purified cannabidiol a treatment opportunity for drug-resistant epilepsy in subjects with typical Rett syndrome and CDKL5 deficiency disorder?

Epilepsia Open. 2025-8

[2]
Infantile Spasms in Pediatric Down Syndrome: Potential Mechanisms Driving Therapeutic Considerations.

Children (Basel). 2024-12-13

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