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Clinical phenotypes within nonconvulsive status epilepticus
The study aimed to identify distinct phenotypes within nonconvulsive status epilepticus (NCSE). Consecutive episodes of NCSE in patients at least 14 years old were included. The level of consciousness was assessed through the Glasgow Coma Scale (GCS). Etiology of NCSE was defined as symptomatic (acu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456934/ https://www.ncbi.nlm.nih.gov/pubmed/34244997 http://dx.doi.org/10.1111/epi.16999 |
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author | Lattanzi, Simona Giovannini, Giada Brigo, Francesco Orlandi, Niccolò Trinka, Eugen Meletti, Stefano |
author_facet | Lattanzi, Simona Giovannini, Giada Brigo, Francesco Orlandi, Niccolò Trinka, Eugen Meletti, Stefano |
author_sort | Lattanzi, Simona |
collection | PubMed |
description | The study aimed to identify distinct phenotypes within nonconvulsive status epilepticus (NCSE). Consecutive episodes of NCSE in patients at least 14 years old were included. The level of consciousness was assessed through the Glasgow Coma Scale (GCS). Etiology of NCSE was defined as symptomatic (acute, remote, progressive) or unknown. Electroencephalographic (EEG) recordings were searched for lateralized periodic discharges (LPDs), generalized sharply and/or triphasic periodic potentials (GPDs), and spontaneous burst suppression (BS). According to treatment response, NCSE was classified as responsive, refractory, or superrefractory. Average linkage hierarchical cluster analysis was performed with Pearson correlation as similarity measure. Two hundred twenty‐nine episodes of NCSE were included. Three clusters were identified. The first cluster linked GCS score 3–8, presence of spontaneous BS on EEG, acute symptomatic etiology, and treatment superrefractoriness. The second cluster gathered GCS score 9–12, presence of LPDs or GPDs on EEG, unknown etiology, and treatment refractoriness. The third cluster associated GCS score 13–15, absence of LPDs, GPDs, and spontaneous BS on EEG, and progressive and remote symptomatic etiology with treatment responsiveness. Phenotyping the heterogeneity of NCSE into electroclinical clusters can contribute to understanding correlations between pathologic and clinical domains, assessing the intrinsic severity of NCSE episodes, and estimating the likelihood of treatment responsiveness. |
format | Online Article Text |
id | pubmed-8456934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84569342021-09-27 Clinical phenotypes within nonconvulsive status epilepticus Lattanzi, Simona Giovannini, Giada Brigo, Francesco Orlandi, Niccolò Trinka, Eugen Meletti, Stefano Epilepsia Brief Communication The study aimed to identify distinct phenotypes within nonconvulsive status epilepticus (NCSE). Consecutive episodes of NCSE in patients at least 14 years old were included. The level of consciousness was assessed through the Glasgow Coma Scale (GCS). Etiology of NCSE was defined as symptomatic (acute, remote, progressive) or unknown. Electroencephalographic (EEG) recordings were searched for lateralized periodic discharges (LPDs), generalized sharply and/or triphasic periodic potentials (GPDs), and spontaneous burst suppression (BS). According to treatment response, NCSE was classified as responsive, refractory, or superrefractory. Average linkage hierarchical cluster analysis was performed with Pearson correlation as similarity measure. Two hundred twenty‐nine episodes of NCSE were included. Three clusters were identified. The first cluster linked GCS score 3–8, presence of spontaneous BS on EEG, acute symptomatic etiology, and treatment superrefractoriness. The second cluster gathered GCS score 9–12, presence of LPDs or GPDs on EEG, unknown etiology, and treatment refractoriness. The third cluster associated GCS score 13–15, absence of LPDs, GPDs, and spontaneous BS on EEG, and progressive and remote symptomatic etiology with treatment responsiveness. Phenotyping the heterogeneity of NCSE into electroclinical clusters can contribute to understanding correlations between pathologic and clinical domains, assessing the intrinsic severity of NCSE episodes, and estimating the likelihood of treatment responsiveness. John Wiley and Sons Inc. 2021-07-09 2021-09 /pmc/articles/PMC8456934/ /pubmed/34244997 http://dx.doi.org/10.1111/epi.16999 Text en © 2021 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Brief Communication Lattanzi, Simona Giovannini, Giada Brigo, Francesco Orlandi, Niccolò Trinka, Eugen Meletti, Stefano Clinical phenotypes within nonconvulsive status epilepticus |
title | Clinical phenotypes within nonconvulsive status epilepticus |
title_full | Clinical phenotypes within nonconvulsive status epilepticus |
title_fullStr | Clinical phenotypes within nonconvulsive status epilepticus |
title_full_unstemmed | Clinical phenotypes within nonconvulsive status epilepticus |
title_short | Clinical phenotypes within nonconvulsive status epilepticus |
title_sort | clinical phenotypes within nonconvulsive status epilepticus |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456934/ https://www.ncbi.nlm.nih.gov/pubmed/34244997 http://dx.doi.org/10.1111/epi.16999 |
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