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Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities

Objective: Children with autism spectrum disorder (ASD) commonly exhibit comorbid symptoms such as aggression, hyperactivity and anxiety. Several studies are being conducted worldwide on cannabidiol use in ASD; however, these studies are still ongoing, and data on the effects of its use is very limi...

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Autores principales: Barchel, Dana, Stolar, Orit, De-Haan, Tal, Ziv-Baran, Tomer, Saban, Naama, Fuchs, Danny Or, Koren, Gideon, Berkovitch, Matitiahu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333745/
https://www.ncbi.nlm.nih.gov/pubmed/30687090
http://dx.doi.org/10.3389/fphar.2018.01521
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author Barchel, Dana
Stolar, Orit
De-Haan, Tal
Ziv-Baran, Tomer
Saban, Naama
Fuchs, Danny Or
Koren, Gideon
Berkovitch, Matitiahu
author_facet Barchel, Dana
Stolar, Orit
De-Haan, Tal
Ziv-Baran, Tomer
Saban, Naama
Fuchs, Danny Or
Koren, Gideon
Berkovitch, Matitiahu
author_sort Barchel, Dana
collection PubMed
description Objective: Children with autism spectrum disorder (ASD) commonly exhibit comorbid symptoms such as aggression, hyperactivity and anxiety. Several studies are being conducted worldwide on cannabidiol use in ASD; however, these studies are still ongoing, and data on the effects of its use is very limited. In this study we aimed to report the experience of parents who administer, under supervision, oral cannabinoids to their children with ASD. Methods: After obtaining a license from the Israeli Ministry of Health, parents of children with ASD were instructed by a nurse practitioner how to administer oral drops of cannabidiol oil. Information on comorbid symptoms and safety was prospectively recorded biweekly during follow-up interviews. An independent group of specialists analyzed these data for changes in ASD symptoms and drug safety. Results: 53 children at a median age of 11 (4–22) year received cannabidiol for a median duration of 66 days (30–588). Self-injury and rage attacks (n = 34) improved in 67.6% and worsened in 8.8%. Hyperactivity symptoms (n = 38) improved in 68.4%, did not change in 28.9% and worsened in 2.6%. Sleep problems (n = 21) improved in 71.4% and worsened in 4.7%. Anxiety (n = 17) improved in 47.1% and worsened in 23.5%. Adverse effects, mostly somnolence and change in appetite were mild. Conclusion: Parents’ reports suggest that cannabidiol may improve ASD comorbidity symptoms; however, the long-term effects should be evaluated in large scale studies.
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spelling pubmed-63337452019-01-25 Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities Barchel, Dana Stolar, Orit De-Haan, Tal Ziv-Baran, Tomer Saban, Naama Fuchs, Danny Or Koren, Gideon Berkovitch, Matitiahu Front Pharmacol Pharmacology Objective: Children with autism spectrum disorder (ASD) commonly exhibit comorbid symptoms such as aggression, hyperactivity and anxiety. Several studies are being conducted worldwide on cannabidiol use in ASD; however, these studies are still ongoing, and data on the effects of its use is very limited. In this study we aimed to report the experience of parents who administer, under supervision, oral cannabinoids to their children with ASD. Methods: After obtaining a license from the Israeli Ministry of Health, parents of children with ASD were instructed by a nurse practitioner how to administer oral drops of cannabidiol oil. Information on comorbid symptoms and safety was prospectively recorded biweekly during follow-up interviews. An independent group of specialists analyzed these data for changes in ASD symptoms and drug safety. Results: 53 children at a median age of 11 (4–22) year received cannabidiol for a median duration of 66 days (30–588). Self-injury and rage attacks (n = 34) improved in 67.6% and worsened in 8.8%. Hyperactivity symptoms (n = 38) improved in 68.4%, did not change in 28.9% and worsened in 2.6%. Sleep problems (n = 21) improved in 71.4% and worsened in 4.7%. Anxiety (n = 17) improved in 47.1% and worsened in 23.5%. Adverse effects, mostly somnolence and change in appetite were mild. Conclusion: Parents’ reports suggest that cannabidiol may improve ASD comorbidity symptoms; however, the long-term effects should be evaluated in large scale studies. Frontiers Media S.A. 2019-01-09 /pmc/articles/PMC6333745/ /pubmed/30687090 http://dx.doi.org/10.3389/fphar.2018.01521 Text en Copyright © 2019 Barchel, Stolar, De-Haan, Ziv-Baran, Saban, Fuchs, Koren and Berkovitch. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Barchel, Dana
Stolar, Orit
De-Haan, Tal
Ziv-Baran, Tomer
Saban, Naama
Fuchs, Danny Or
Koren, Gideon
Berkovitch, Matitiahu
Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities
title Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities
title_full Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities
title_fullStr Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities
title_full_unstemmed Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities
title_short Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities
title_sort oral cannabidiol use in children with autism spectrum disorder to treat related symptoms and co-morbidities
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333745/
https://www.ncbi.nlm.nih.gov/pubmed/30687090
http://dx.doi.org/10.3389/fphar.2018.01521
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