Observational study of medical marijuana as a treatment for treatment-resistant epilepsies.


Journal

Annals of clinical and translational neurology
ISSN: 2328-9503
Titre abrégé: Ann Clin Transl Neurol
Pays: United States
ID NLM: 101623278

Informations de publication

Date de publication:
04 2022
Historique:
revised: 02 02 2022
received: 10 11 2021
accepted: 22 02 2022
pubmed: 11 3 2022
medline: 13 4 2022
entrez: 10 3 2022
Statut: ppublish

Résumé

Medical cannabis formulations with cannabidiol (CBD) and delta-9-tetrahydrocannabinol (THC) are widely used to treat epilepsy. We studied the safety and efficacy of two formulations. We prospectively observed 29 subjects (12 to 46 years old) with treatment-resistant epilepsies (11 Lennox-Gastaut syndrome; 15 with focal or multifocal epilepsy; three generalized epilepsy) were treated with medical cannabis (1THC:20CBD and/or 1THC:50CBD; maximum of 6 mg THC/day) for ≥24 weeks. The primary outcome was change in convulsive seizure frequency from the pre-treatment baseline to the stable optimal dose phase. There were no significant differences during treatment on stable maximal doses for convulsive seizure frequency, seizure duration, postictal duration, or use of rescue medications compared to baseline. No benefits were seen for behavioral disorders or sleep duration; there was a trend for more frequent bowel movements compared to baseline. Ten adverse events occurred in 6/29 patients, all were transient and most unrelated to study medication. No serious adverse events were related to study medication. Our prospective observational study of two high-CBD/low-THC formulations found no evidence of efficacy in reducing seizures, seizure duration, postictal duration, or rescue medication use. Behavioral disorders or sleep duration was unchanged. Study medication was generally well tolerated. The doses of CBD used were lower than prior studies. Randomized trials with larger cohorts are needed, but we found no evidence of efficacy for two CBD:THC products in treating epilepsy, sleep, or behavior in our population.

Identifiants

pubmed: 35267245
doi: 10.1002/acn3.51537
pmc: PMC8994986
doi:

Substances chimiques

Anticonvulsants 0
Medical Marijuana 0
Cannabidiol 19GBJ60SN5
Dronabinol 7J8897W37S

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

497-505

Informations de copyright

© 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

Références

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pubmed: 26352816
Ann Clin Transl Neurol. 2018 Aug 01;5(9):1077-1088
pubmed: 30250864
N Engl J Med. 2017 May 25;376(21):2011-2020
pubmed: 28538134
JAMA Neurol. 2021 Mar 1;78(3):285-292
pubmed: 33346789
Epilepsy Curr. 2012 Jul;12(4):131-2
pubmed: 22936881
Epilepsia. 2021 Sep;62(9):2274-2282
pubmed: 34251027
Epilepsy Behav. 2017 May;70(Pt B):341-348
pubmed: 28188044
Cannabis Cannabinoid Res. 2021 Dec;6(6):528-536
pubmed: 33998885
N Engl J Med. 2018 May 17;378(20):1888-1897
pubmed: 29768152

Auteurs

Orrin Devinsky (O)

NYU Comprehensive Epilepsy Center, New York, New York, USA.

Angelica Marmanillo (A)

The Center for Discovery, Harris, New York, USA.

Theresa Hamlin (T)

The Center for Discovery, Harris, New York, USA.

Philip Wilken (P)

The Center for Discovery, Harris, New York, USA.
Crystal Run Healthcare, Rock Hill, New York, USA.

Daniel Ryan (D)

The Center for Discovery, Harris, New York, USA.

Conor Anderson (C)

The Center for Discovery, Harris, New York, USA.

Daniel Friedman (D)

NYU Comprehensive Epilepsy Center, New York, New York, USA.

George Todd (G)

The Center for Discovery, Harris, New York, USA.
Icahn School of Medicine at Mount Sinai, New York, New York, USA.

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Classifications MeSH