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Clinical profile of patients with nascent alcohol related seizures

AIM: The aim of this study is to characterize the clinical profile of patients with alcohol related seizures (ARS) and to identify the prevalence of idiopathic generalized epilepsy (IGE) in the same. MATERIALS AND METHODS: 100 consecutive male patients presenting to a tertiary care center in South I...

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Autores principales: Sandeep, P., Cherian, Ajith, Iype, Thomas, Chitra, P., Suresh, M. K., Ajitha, K. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841594/
https://www.ncbi.nlm.nih.gov/pubmed/24339573
http://dx.doi.org/10.4103/0972-2327.120454
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author Sandeep, P.
Cherian, Ajith
Iype, Thomas
Chitra, P.
Suresh, M. K.
Ajitha, K. C.
author_facet Sandeep, P.
Cherian, Ajith
Iype, Thomas
Chitra, P.
Suresh, M. K.
Ajitha, K. C.
author_sort Sandeep, P.
collection PubMed
description AIM: The aim of this study is to characterize the clinical profile of patients with alcohol related seizures (ARS) and to identify the prevalence of idiopathic generalized epilepsy (IGE) in the same. MATERIALS AND METHODS: 100 consecutive male patients presenting to a tertiary care center in South India with new onset ARS were analyzed with alcohol use disorders identification test (AUDIT) score. All underwent 19 channel digital scalp electroencephalography (EEG) and at least computed tomography (CT) scan. RESULTS: A total of 27 patients (27%) who had cortical atrophy on CT had a mean duration of alcohol intake of 23.62 years compared with 14.55 years in patients with no cortical atrophy (P < 0.001). Twenty-two patients (22%) had clustering in the current episode of whom 18 had cortical atrophy. Nearly, 88% patients had generalized tonic clonic seizures while 12% who had partial seizures underwent magnetic resonance imaging (MRI), which identified frontal focal cortical dysplasia in one. Mean lifetime duration of alcohol intake in patients presenting with seizures within 6 hours (6H-gp) of intake of alcohol was significantly lower (P = 0.029). One patient in the 6H-gp with no withdrawal symptoms had EEG evidence for IGE and had a lower AUDIT score compared with the rest. CONCLUSION: CT evidence of cortical atrophy is related to the duration of alcohol intake and portends an increased risk for clustering. Partial seizures can be a presenting feature of ARS and those patients may benefit from MRI to identify underlying symptomatic localization related epilepsy (8.3% of partial seizures). IGE is more likely in patients presenting with ARS within first 6 hours especially if they do not have alcohol withdrawal symptoms and scalp EEG is helpful to identify this small subgroup (~1%) who may require long-term anti-epileptic medication.
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spelling pubmed-38415942013-12-11 Clinical profile of patients with nascent alcohol related seizures Sandeep, P. Cherian, Ajith Iype, Thomas Chitra, P. Suresh, M. K. Ajitha, K. C. Ann Indian Acad Neurol Original Article AIM: The aim of this study is to characterize the clinical profile of patients with alcohol related seizures (ARS) and to identify the prevalence of idiopathic generalized epilepsy (IGE) in the same. MATERIALS AND METHODS: 100 consecutive male patients presenting to a tertiary care center in South India with new onset ARS were analyzed with alcohol use disorders identification test (AUDIT) score. All underwent 19 channel digital scalp electroencephalography (EEG) and at least computed tomography (CT) scan. RESULTS: A total of 27 patients (27%) who had cortical atrophy on CT had a mean duration of alcohol intake of 23.62 years compared with 14.55 years in patients with no cortical atrophy (P < 0.001). Twenty-two patients (22%) had clustering in the current episode of whom 18 had cortical atrophy. Nearly, 88% patients had generalized tonic clonic seizures while 12% who had partial seizures underwent magnetic resonance imaging (MRI), which identified frontal focal cortical dysplasia in one. Mean lifetime duration of alcohol intake in patients presenting with seizures within 6 hours (6H-gp) of intake of alcohol was significantly lower (P = 0.029). One patient in the 6H-gp with no withdrawal symptoms had EEG evidence for IGE and had a lower AUDIT score compared with the rest. CONCLUSION: CT evidence of cortical atrophy is related to the duration of alcohol intake and portends an increased risk for clustering. Partial seizures can be a presenting feature of ARS and those patients may benefit from MRI to identify underlying symptomatic localization related epilepsy (8.3% of partial seizures). IGE is more likely in patients presenting with ARS within first 6 hours especially if they do not have alcohol withdrawal symptoms and scalp EEG is helpful to identify this small subgroup (~1%) who may require long-term anti-epileptic medication. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3841594/ /pubmed/24339573 http://dx.doi.org/10.4103/0972-2327.120454 Text en Copyright: © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sandeep, P.
Cherian, Ajith
Iype, Thomas
Chitra, P.
Suresh, M. K.
Ajitha, K. C.
Clinical profile of patients with nascent alcohol related seizures
title Clinical profile of patients with nascent alcohol related seizures
title_full Clinical profile of patients with nascent alcohol related seizures
title_fullStr Clinical profile of patients with nascent alcohol related seizures
title_full_unstemmed Clinical profile of patients with nascent alcohol related seizures
title_short Clinical profile of patients with nascent alcohol related seizures
title_sort clinical profile of patients with nascent alcohol related seizures
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841594/
https://www.ncbi.nlm.nih.gov/pubmed/24339573
http://dx.doi.org/10.4103/0972-2327.120454
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