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Infantile epileptic spasms syndrome: a cohort study of 88 children

BACKGROUND: This study aimed to investigate and analyze the risk factors for non-etiology-specific infantile spasms (IS) and unrelieved clinical symptoms after treatment. METHODS: Eighty-eight children with IS who were treated at our hospital from March 2018 to December 2021 were included in the stu...

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Autores principales: Ren, Li-Hong, Zhang, Jing, Li, Si-Xiu, Liu, Ping, Chen, Hui, Hu, Wenguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693141/
https://www.ncbi.nlm.nih.gov/pubmed/38041198
http://dx.doi.org/10.1186/s13052-023-01563-z
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author Ren, Li-Hong
Zhang, Jing
Li, Si-Xiu
Liu, Ping
Chen, Hui
Hu, Wenguang
author_facet Ren, Li-Hong
Zhang, Jing
Li, Si-Xiu
Liu, Ping
Chen, Hui
Hu, Wenguang
author_sort Ren, Li-Hong
collection PubMed
description BACKGROUND: This study aimed to investigate and analyze the risk factors for non-etiology-specific infantile spasms (IS) and unrelieved clinical symptoms after treatment. METHODS: Eighty-eight children with IS who were treated at our hospital from March 2018 to December 2021 were included in the study. The children were divided into etiology-specific (n = 46) and nonetiology-specific (n = 42) groups, based on the diagnostic results, and remission (n = 45) and nonremission (n = 43) groups, based on clinical outcomes after treatment. The clinical data from patients in the etiology-specific and nonetiology-specific groups and the remission and nonremission groups were compared. Risk factors for non-etiology-specific IS were identified using logistic regression analysis. RESULTS: Gender, family history, birth status, and metabolic abnormalities were significantly different between the etiology-specific and non-etiology-specific groups. Gender and metabolic abnormalities were risk factors for nonetiology-specific IS. Family history, birth status, metabolic abnormalities, and brain magnetic resonance imaging were significantly different between the remission and nonremission groups, and different etiologies were risk factors for unrelieved symptoms after treatment. CONCLUSION: The occurrence of nonetiology-specific IS is associated with gender and metabolic abnormalities in children. After medication, unrelieved IS symptoms are associated with etiologies.
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spelling pubmed-106931412023-12-03 Infantile epileptic spasms syndrome: a cohort study of 88 children Ren, Li-Hong Zhang, Jing Li, Si-Xiu Liu, Ping Chen, Hui Hu, Wenguang Ital J Pediatr Research BACKGROUND: This study aimed to investigate and analyze the risk factors for non-etiology-specific infantile spasms (IS) and unrelieved clinical symptoms after treatment. METHODS: Eighty-eight children with IS who were treated at our hospital from March 2018 to December 2021 were included in the study. The children were divided into etiology-specific (n = 46) and nonetiology-specific (n = 42) groups, based on the diagnostic results, and remission (n = 45) and nonremission (n = 43) groups, based on clinical outcomes after treatment. The clinical data from patients in the etiology-specific and nonetiology-specific groups and the remission and nonremission groups were compared. Risk factors for non-etiology-specific IS were identified using logistic regression analysis. RESULTS: Gender, family history, birth status, and metabolic abnormalities were significantly different between the etiology-specific and non-etiology-specific groups. Gender and metabolic abnormalities were risk factors for nonetiology-specific IS. Family history, birth status, metabolic abnormalities, and brain magnetic resonance imaging were significantly different between the remission and nonremission groups, and different etiologies were risk factors for unrelieved symptoms after treatment. CONCLUSION: The occurrence of nonetiology-specific IS is associated with gender and metabolic abnormalities in children. After medication, unrelieved IS symptoms are associated with etiologies. BioMed Central 2023-12-01 /pmc/articles/PMC10693141/ /pubmed/38041198 http://dx.doi.org/10.1186/s13052-023-01563-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ren, Li-Hong
Zhang, Jing
Li, Si-Xiu
Liu, Ping
Chen, Hui
Hu, Wenguang
Infantile epileptic spasms syndrome: a cohort study of 88 children
title Infantile epileptic spasms syndrome: a cohort study of 88 children
title_full Infantile epileptic spasms syndrome: a cohort study of 88 children
title_fullStr Infantile epileptic spasms syndrome: a cohort study of 88 children
title_full_unstemmed Infantile epileptic spasms syndrome: a cohort study of 88 children
title_short Infantile epileptic spasms syndrome: a cohort study of 88 children
title_sort infantile epileptic spasms syndrome: a cohort study of 88 children
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693141/
https://www.ncbi.nlm.nih.gov/pubmed/38041198
http://dx.doi.org/10.1186/s13052-023-01563-z
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