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Movement Disorders Secondary to Novel Antiseizure Medications in Pediatric Populations: A Systematic Review and Meta-analysis of Risk

Novel antiseizure medications are thought to be safer than their conventional counterparts, though no dedicated analysis of movement disorder risk among pediatric populations using novel antiseizure medications has been completed. We report a systematic review with meta-analysis describing the relat...

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Autores principales: Peacock, Dakota J. S. J., Yoneda, Joshua R. K., Siever, Jodi E., Vis-Dunbar, Mathew, Boelman, Cyrus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160953/
https://www.ncbi.nlm.nih.gov/pubmed/35392704
http://dx.doi.org/10.1177/08830738221089742
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author Peacock, Dakota J. S. J.
Yoneda, Joshua R. K.
Siever, Jodi E.
Vis-Dunbar, Mathew
Boelman, Cyrus
author_facet Peacock, Dakota J. S. J.
Yoneda, Joshua R. K.
Siever, Jodi E.
Vis-Dunbar, Mathew
Boelman, Cyrus
author_sort Peacock, Dakota J. S. J.
collection PubMed
description Novel antiseizure medications are thought to be safer than their conventional counterparts, though no dedicated analysis of movement disorder risk among pediatric populations using novel antiseizure medications has been completed. We report a systematic review with meta-analysis describing the relationship between novel antiseizure medications and movement disorders in pediatrics. MEDLINE, EMBASE, and the World Health Organization’s International Clinical Trials Registry Platform were searched up to October 2020 for randomized controlled trials investigating novel antiseizure medications in pediatric populations. Antiseizure medications included lacosamide, perampanel, eslicarbazepine, rufinamide, fenfluramine, cannabidiol, and brivaracetam. Outcomes were pooled using random effects models; risk difference (RD) and 95% confidence intervals (CIs) were calculated. Twenty-three studies were selected from 1690 nonredundant manuscripts (n = 1912 total). There was a significantly increased risk of movement disorders associated with perampanel (RD 0.07, 95% CI 0.01-0.13; n = 133), though only 1 relevant trial was found. No increased risk of movement disorders was found with other antiseizure medications. Our findings indicate most novel antiseizure medications are safe to use in pediatric populations with respect to movement disorders. However, findings were limited by quality of adverse event reporting.
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spelling pubmed-91609532022-06-03 Movement Disorders Secondary to Novel Antiseizure Medications in Pediatric Populations: A Systematic Review and Meta-analysis of Risk Peacock, Dakota J. S. J. Yoneda, Joshua R. K. Siever, Jodi E. Vis-Dunbar, Mathew Boelman, Cyrus J Child Neurol Original Articles Novel antiseizure medications are thought to be safer than their conventional counterparts, though no dedicated analysis of movement disorder risk among pediatric populations using novel antiseizure medications has been completed. We report a systematic review with meta-analysis describing the relationship between novel antiseizure medications and movement disorders in pediatrics. MEDLINE, EMBASE, and the World Health Organization’s International Clinical Trials Registry Platform were searched up to October 2020 for randomized controlled trials investigating novel antiseizure medications in pediatric populations. Antiseizure medications included lacosamide, perampanel, eslicarbazepine, rufinamide, fenfluramine, cannabidiol, and brivaracetam. Outcomes were pooled using random effects models; risk difference (RD) and 95% confidence intervals (CIs) were calculated. Twenty-three studies were selected from 1690 nonredundant manuscripts (n = 1912 total). There was a significantly increased risk of movement disorders associated with perampanel (RD 0.07, 95% CI 0.01-0.13; n = 133), though only 1 relevant trial was found. No increased risk of movement disorders was found with other antiseizure medications. Our findings indicate most novel antiseizure medications are safe to use in pediatric populations with respect to movement disorders. However, findings were limited by quality of adverse event reporting. SAGE Publications 2022-04-07 2022-05 /pmc/articles/PMC9160953/ /pubmed/35392704 http://dx.doi.org/10.1177/08830738221089742 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Peacock, Dakota J. S. J.
Yoneda, Joshua R. K.
Siever, Jodi E.
Vis-Dunbar, Mathew
Boelman, Cyrus
Movement Disorders Secondary to Novel Antiseizure Medications in Pediatric Populations: A Systematic Review and Meta-analysis of Risk
title Movement Disorders Secondary to Novel Antiseizure Medications in Pediatric Populations: A Systematic Review and Meta-analysis of Risk
title_full Movement Disorders Secondary to Novel Antiseizure Medications in Pediatric Populations: A Systematic Review and Meta-analysis of Risk
title_fullStr Movement Disorders Secondary to Novel Antiseizure Medications in Pediatric Populations: A Systematic Review and Meta-analysis of Risk
title_full_unstemmed Movement Disorders Secondary to Novel Antiseizure Medications in Pediatric Populations: A Systematic Review and Meta-analysis of Risk
title_short Movement Disorders Secondary to Novel Antiseizure Medications in Pediatric Populations: A Systematic Review and Meta-analysis of Risk
title_sort movement disorders secondary to novel antiseizure medications in pediatric populations: a systematic review and meta-analysis of risk
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160953/
https://www.ncbi.nlm.nih.gov/pubmed/35392704
http://dx.doi.org/10.1177/08830738221089742
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