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Status Epilepticus Manifested as Continuous Epileptic Spasms

Objective: The etiology and outcome of status epilepticus with continuous epileptic spasms have not been fully understood; and only rare cases have been reported in the literature. Here, we described 11 children, who manifested continuous epileptic spasms with various etiologies and different outcom...

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Autores principales: Liao, Jianxiang, Huang, Tieshuan, Srour, Myriam, Xiao, Yuhan, Chen, Yan, Lin, Sufang, Chen, Li, Hu, Yan, Men, Lina, Wen, Jialun, Li, Bing, Wen, Feiqiu, Xiong, Lan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034528/
https://www.ncbi.nlm.nih.gov/pubmed/32117026
http://dx.doi.org/10.3389/fneur.2020.00065
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author Liao, Jianxiang
Huang, Tieshuan
Srour, Myriam
Xiao, Yuhan
Chen, Yan
Lin, Sufang
Chen, Li
Hu, Yan
Men, Lina
Wen, Jialun
Li, Bing
Wen, Feiqiu
Xiong, Lan
author_facet Liao, Jianxiang
Huang, Tieshuan
Srour, Myriam
Xiao, Yuhan
Chen, Yan
Lin, Sufang
Chen, Li
Hu, Yan
Men, Lina
Wen, Jialun
Li, Bing
Wen, Feiqiu
Xiong, Lan
author_sort Liao, Jianxiang
collection PubMed
description Objective: The etiology and outcome of status epilepticus with continuous epileptic spasms have not been fully understood; and only rare cases have been reported in the literature. Here, we described 11 children, who manifested continuous epileptic spasms with various etiologies and different outcomes. Methods: This is a case series study designed to systematically review the charts, video-electroencephalography (video-EEG), magnetic resonance images, and longitudinal follow-up of patients who presented continuous epileptic spasms lasting more than 30 min. Results: Median age at onset was 2 years old, ranging from 2 months to 5.6 years. The etiology of continuous epileptic spasms for these 11 cases consisted of not only some known electro-clinical epilepsy syndromes like West Syndrome and Ohtahara Syndrome, but also secondary symptomatic continuous epileptic spasms, caused by acute encephalitis or encephalopathy, which extends the etiological spectrum of continuous epileptic spasms. The most characteristic feature of these 11 cases was prolonged epileptic spasms, lasting for a median of 13.00 days (95% CI: 7.26–128.22 days). The interictal EEG findings typically manifested as hypsarrhythmia or its variants, including burst suppression. Hospital stays were much longer in acute symptomatic cases than in primary epileptic syndromic cases (59.67 ± 50.82 vs. 15.00 ± 1.41 days). However, the long-term outcomes were extremely poor in the patients with defined electro-clinical epilepsy syndromes, including severe motor and intellectual developmental deficits (follow-up of 4.94 ± 1.56 years), despite early diagnosis and treatment. Continuous epileptic spasms were refractory to corticosteroids, immuno-modulation or immunosuppressive therapies, and ketogenic diet. Conclusion: Continuous epileptic spasms were associated with severe brain impairments in patients with electro-clinical syndromes; and required long hospital stays in patients with acute symptomatic causes. We suggest to include continuous epileptic spasms in the international classification of status epilepticus, as a special form. Further investigations are required to better recognize this condition, better understand the etiology, as well as to explore more effective treatments to improve outcomes.
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spelling pubmed-70345282020-02-28 Status Epilepticus Manifested as Continuous Epileptic Spasms Liao, Jianxiang Huang, Tieshuan Srour, Myriam Xiao, Yuhan Chen, Yan Lin, Sufang Chen, Li Hu, Yan Men, Lina Wen, Jialun Li, Bing Wen, Feiqiu Xiong, Lan Front Neurol Neurology Objective: The etiology and outcome of status epilepticus with continuous epileptic spasms have not been fully understood; and only rare cases have been reported in the literature. Here, we described 11 children, who manifested continuous epileptic spasms with various etiologies and different outcomes. Methods: This is a case series study designed to systematically review the charts, video-electroencephalography (video-EEG), magnetic resonance images, and longitudinal follow-up of patients who presented continuous epileptic spasms lasting more than 30 min. Results: Median age at onset was 2 years old, ranging from 2 months to 5.6 years. The etiology of continuous epileptic spasms for these 11 cases consisted of not only some known electro-clinical epilepsy syndromes like West Syndrome and Ohtahara Syndrome, but also secondary symptomatic continuous epileptic spasms, caused by acute encephalitis or encephalopathy, which extends the etiological spectrum of continuous epileptic spasms. The most characteristic feature of these 11 cases was prolonged epileptic spasms, lasting for a median of 13.00 days (95% CI: 7.26–128.22 days). The interictal EEG findings typically manifested as hypsarrhythmia or its variants, including burst suppression. Hospital stays were much longer in acute symptomatic cases than in primary epileptic syndromic cases (59.67 ± 50.82 vs. 15.00 ± 1.41 days). However, the long-term outcomes were extremely poor in the patients with defined electro-clinical epilepsy syndromes, including severe motor and intellectual developmental deficits (follow-up of 4.94 ± 1.56 years), despite early diagnosis and treatment. Continuous epileptic spasms were refractory to corticosteroids, immuno-modulation or immunosuppressive therapies, and ketogenic diet. Conclusion: Continuous epileptic spasms were associated with severe brain impairments in patients with electro-clinical syndromes; and required long hospital stays in patients with acute symptomatic causes. We suggest to include continuous epileptic spasms in the international classification of status epilepticus, as a special form. Further investigations are required to better recognize this condition, better understand the etiology, as well as to explore more effective treatments to improve outcomes. Frontiers Media S.A. 2020-02-14 /pmc/articles/PMC7034528/ /pubmed/32117026 http://dx.doi.org/10.3389/fneur.2020.00065 Text en Copyright © 2020 Liao, Huang, Srour, Xiao, Chen, Lin, Chen, Hu, Men, Wen, Li, Wen and Xiong. 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 Neurology
Liao, Jianxiang
Huang, Tieshuan
Srour, Myriam
Xiao, Yuhan
Chen, Yan
Lin, Sufang
Chen, Li
Hu, Yan
Men, Lina
Wen, Jialun
Li, Bing
Wen, Feiqiu
Xiong, Lan
Status Epilepticus Manifested as Continuous Epileptic Spasms
title Status Epilepticus Manifested as Continuous Epileptic Spasms
title_full Status Epilepticus Manifested as Continuous Epileptic Spasms
title_fullStr Status Epilepticus Manifested as Continuous Epileptic Spasms
title_full_unstemmed Status Epilepticus Manifested as Continuous Epileptic Spasms
title_short Status Epilepticus Manifested as Continuous Epileptic Spasms
title_sort status epilepticus manifested as continuous epileptic spasms
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034528/
https://www.ncbi.nlm.nih.gov/pubmed/32117026
http://dx.doi.org/10.3389/fneur.2020.00065
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