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Young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: A case report
BACKGROUND: Perampanel (PER), a third-generation antiepileptic drug, is a selective and noncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonist, and has been approved for the treatment of adults and adolescents with focal epilepsy. However, there are only a few studie...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048547/ https://www.ncbi.nlm.nih.gov/pubmed/35611206 http://dx.doi.org/10.12998/wjcc.v10.i11.3511 |
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author | Yang, Hua Yu, Dan |
author_facet | Yang, Hua Yu, Dan |
author_sort | Yang, Hua |
collection | PubMed |
description | BACKGROUND: Perampanel (PER), a third-generation antiepileptic drug, is a selective and noncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonist, and has been approved for the treatment of adults and adolescents with focal epilepsy. However, there are only a few studies about the efficacy and tolerability of PER in young children with multidrug-resistant epilepsy. In this case, we aimed to share our clinical experience in this group. CASE SUMMARY: A 4-year-old boy without perinatal asphyxia and familial history of epilepsy began to have ictal seizures from age 14 mo, with jerky movement of four limbs and head nodding. Abnormal multifocal discharge and background activity were recorded through electroencephalography, and no pathogenic mutation was found in the whole exome sequencing for the patient and his parents. He had received valproate, levetiracetam, topiramate, oxcarbazepine, clonazepam and lacosamide sequentially at different times, but he still had frequent seizures even after vagus nerve stimulation (VNS) implantation. He was diagnosed with idiopathic multidrug-resistant epilepsy. However, his seizure frequency was significantly reduced after PER administration in a dose-dependent manner, and better cognitive behavior was observed. In addition, the adverse reactions of anger and aggression also appeared. CONCLUSION: PER is effective as add-on therapy for young children with multidrug-resistant epilepsy who have previously undergone VNS implantation. |
format | Online Article Text |
id | pubmed-9048547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-90485472022-05-23 Young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: A case report Yang, Hua Yu, Dan World J Clin Cases Case Report BACKGROUND: Perampanel (PER), a third-generation antiepileptic drug, is a selective and noncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonist, and has been approved for the treatment of adults and adolescents with focal epilepsy. However, there are only a few studies about the efficacy and tolerability of PER in young children with multidrug-resistant epilepsy. In this case, we aimed to share our clinical experience in this group. CASE SUMMARY: A 4-year-old boy without perinatal asphyxia and familial history of epilepsy began to have ictal seizures from age 14 mo, with jerky movement of four limbs and head nodding. Abnormal multifocal discharge and background activity were recorded through electroencephalography, and no pathogenic mutation was found in the whole exome sequencing for the patient and his parents. He had received valproate, levetiracetam, topiramate, oxcarbazepine, clonazepam and lacosamide sequentially at different times, but he still had frequent seizures even after vagus nerve stimulation (VNS) implantation. He was diagnosed with idiopathic multidrug-resistant epilepsy. However, his seizure frequency was significantly reduced after PER administration in a dose-dependent manner, and better cognitive behavior was observed. In addition, the adverse reactions of anger and aggression also appeared. CONCLUSION: PER is effective as add-on therapy for young children with multidrug-resistant epilepsy who have previously undergone VNS implantation. Baishideng Publishing Group Inc 2022-04-16 2022-04-16 /pmc/articles/PMC9048547/ /pubmed/35611206 http://dx.doi.org/10.12998/wjcc.v10.i11.3511 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Yang, Hua Yu, Dan Young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: A case report |
title | Young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: A case report |
title_full | Young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: A case report |
title_fullStr | Young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: A case report |
title_full_unstemmed | Young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: A case report |
title_short | Young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: A case report |
title_sort | young children with multidrug-resistant epilepsy and vagus nerve stimulation responding to perampanel: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048547/ https://www.ncbi.nlm.nih.gov/pubmed/35611206 http://dx.doi.org/10.12998/wjcc.v10.i11.3511 |
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