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

被引:0
|
作者
Valenzuela, Gabriela Reyes [1 ]
Gallo, Adolfo [1 ]
Calvo, Agustin [2 ]
Chacon, Santiago [3 ]
Fasulo, Lorena [4 ]
Galicchio, Santiago [4 ]
Adi, Javier [5 ]
Fortini, Pablo Sebastian [1 ]
Caraballo, Roberto [1 ]
机构
[1] Hosp Pediat Juan P Garrahan, Dept Neurol, RA-1881 Buenos Aires, Argentina
[2] Hosp Reg Comodoro Rivadavia, Dept Pediat Neurol, Comodoro Rivadavia, Argentina
[3] Pediat Neurol Ctr CENI, Gualeguaychu, Argentina
[4] Clin San Lucas, Dept Neurol, Neuquen, Argentina
[5] Hosp Notti, Dept Pediat Neurol, Mendoza, Argentina
来源
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2024年 / 115卷
关键词
Purified cannabidiol; Infantile epileptic spasms; Treatment; -resistant; Cerebral palsy; ILAE COMMISSION; POSITION PAPER; SEIZURES; CLASSIFICATION;
D O I
10.1016/j.seizure.2024.01.010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 treatmentresistant 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.
引用
收藏
页码:94 / 99
页数:6
相关论文
共 28 条
  • [1] Cannabidiol-enriched medical cannabis as add-on therapy in children with treatment-resistant West syndrome: A study of eight patients
    Caraballo, Roberto
    Valenzuela, Gabriela Reyes
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2021, 92 : 238 - 243
  • [2] Brivaracetam as add-on therapy in children with developmental epileptic encephalopathies: A study of 42 patients
    Caraballo, Roberto H.
    Reyes, Gabriela
    Chacon, Santiago
    Fortini, Pablo Sebastian
    EPILEPSY & BEHAVIOR, 2024, 150
  • [3] Safety and efficacy of melatonin supplementation as an add-on treatment for infantile epileptic spasms syndrome: A randomized, placebo-controlled, double-blind trial
    Sun, Yulin
    Chen, Jian
    Shi, Xiuyu
    Li, Zhichao
    Wan, Lin
    Yan, Huimin
    Chen, Yuehao
    Wang, Jiaxin
    Wang, Jing
    Zou, Liping
    Reiter, Russel
    Zhang, Bo
    Yang, Guang
    JOURNAL OF PINEAL RESEARCH, 2024, 76 (01)
  • [4] Sulthiame add-on therapy in children with Lennox-Gastaut syndrome: A study of 44 patients
    Caraballo, Roberto H.
    Flesler, Santiago
    Reyes Valenzuela, Gabriela
    Fortini, Sebastian
    Chacon, Santiago
    Ross, Lucas
    Noli, Daniel
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2018, 62 : 55 - 58
  • [5] Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India
    Nagarajan, Balamurugan
    Gowda, Vykuntaraju K.
    Yoganathan, Sangeetha
    Sharawat, Indar Kumar
    Srivastava, Kavita
    Vora, Nitish
    Badheka, Rahul
    Danda, Sumita
    Kalane, Umesh
    Kaur, Anupriya
    Madaan, Priyanka
    Mehta, Sanjiv
    Negi, Sandeep
    Panda, Prateek Kumar
    Rajadhyaksha, Surekha
    Saini, Arushi Gahlot
    Saini, Lokesh
    Shah, Siddharth
    Srinivasan, Varunvenkat M.
    Suthar, Renu
    Thomas, Maya
    Vyas, Sameer
    Sankhyan, Naveen
    Sahu, Jitendra Kumar
    EPILEPSIA OPEN, 2023, 8 (04) : 1383 - 1404
  • [6] Cost-Utility Analysis of Add-on Cannabidiol vs Usual Care Alone for the Treatment of Seizures in Patients With Treatment-Resistant Lennox-Gastaut Syndrome or Dravet Syndrome in the Netherlands
    Siddiqui, Jamshaed
    Bowditch, Sally
    JOURNAL OF HEALTH ECONOMICS AND OUTCOMES RESEARCH, 2024, 11 (02): : 168 - 179
  • [7] Infantile epileptic spasms syndrome in children with cardiofaciocutanous syndrome: Clinical presentation and associations with genotype
    Kenney-Jung, Daniel. L. L.
    Rogers, Dante. J. J.
    Kroening, Samuel. J. J.
    Zatkalik, Abigail. L. L.
    Whitmarsh, Ashley. E. E.
    Roberts, Amy. E. E.
    Zenker, Martin
    Gambardella, Maria Luigia
    Contaldo, Ilaria
    Leoni, Chiara
    Onesimo, Roberta
    Zampino, Giuseppe
    Tartaglia, Marco
    Battaglia, Domenica. I. I.
    Pierpont, Elizabeth. I. I.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2022, 190 (04) : 501 - 509
  • [8] Purified cannabidiol leads to improvement of severe treatment-resistant behavioral symptoms in children with autism spectrum disorder
    Fortini, Pablo Sebastian
    Toibaro, Javier J.
    Caraballo, Roberto H.
    PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2025, 249
  • [9] Cohort study of infantile epileptic spasms syndrome: etiological analysis and treatment of corticosteroids
    Jiang, Yu
    Zou, Nan
    Luo, Yuanyuan
    Cheng, Min
    Liao, Shuang
    Hong, Siqi
    Liang, Xiaohua
    Zhong, Min
    Li, Tingsong
    Jiang, Li
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2022, 101 : 120 - 126
  • [10] Treatment outcomes for infantile spasms in Japanese children with Down syndrome
    Nishimoto, Satomi
    Shimakawa, Shuichi
    Fukui, Miho
    Ogino, Motoko
    Tsuda-Kitahara, Hikaru
    Toshikawa, Hiromitsu
    Nomura, Shohei
    Kunisada, Kayo
    Kashiwagi, Mitsuru
    Miyamoto, Ryohei
    Tamai, Hiroshi
    Ashida, Akira
    PEDIATRICS INTERNATIONAL, 2021, 63 (12) : 1495 - 1503