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Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic

AIMS: We aimed to study the frequency, age, and gender distribution of paroxysmal nonepileptic events (PNEs) in children referred to epilepsy clinic with the diagnosis of epilepsy. We also evaluated the therapeutic implications of correct diagnosis and co-existence of true epilepsy in this populatio...

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Autores principales: Mandli, Ashfak H., Desai, Neelu A., Badheka, Rahul S., Udani, Vrajesh P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8276968/
https://www.ncbi.nlm.nih.gov/pubmed/34316303
http://dx.doi.org/10.4103/jpn.JPN_33_20
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author Mandli, Ashfak H.
Desai, Neelu A.
Badheka, Rahul S.
Udani, Vrajesh P.
author_facet Mandli, Ashfak H.
Desai, Neelu A.
Badheka, Rahul S.
Udani, Vrajesh P.
author_sort Mandli, Ashfak H.
collection PubMed
description AIMS: We aimed to study the frequency, age, and gender distribution of paroxysmal nonepileptic events (PNEs) in children referred to epilepsy clinic with the diagnosis of epilepsy. We also evaluated the therapeutic implications of correct diagnosis and co-existence of true epilepsy in this population. SETTINGS AND DESIGN: All new patients below 18 years attending the Pediatric epilepsy out-patient clinic of PD Hinduja hospital over 6 months were evaluated. MATERIALS AND METHODS: Patients with history of paroxysmal events characterized by abrupt changes in consciousness or behavior or movement were included. They were assessed on description of events aided by recorded videos. If the diagnosis was not confirmed by this preliminary evaluation, further investigations were advised. STATISTICAL ANALYSIS USED: Chi-square/Fisher’s exact test was used to analyze differences between categorical variables and Kruskal–Wallis test between continuous variables. The data were analyzed by SAS University Edition. All significance tests were two-tailed with α <0.05. RESULTS: Two hundred new patients presenting with paroxysmal events were enrolled over 6 months. After diagnoses, 19% of these children had PNEs, 80% had epileptic events, and 1% remained undiagnosed. Common nonepileptic events seen were physiological in patients below 5 years and psychogenic in older children. Thirty-four percent of patients with PNEs were on anti-epileptic drugs (AEDs). After confirming nonepileptic attacks, only 2.6% patients needed AEDs for coexisting epilepsy which was statistically significant (P < 0.001) change in treatment. CONCLUSIONS: Epilepsy mimics are common in children and are often misdiagnosed causing undue stress. Correct diagnosis leads to a drastic change in management like withdrawal of drugs, commencing new treatment if needed, and appropriate referrals.
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spelling pubmed-82769682021-07-26 Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic Mandli, Ashfak H. Desai, Neelu A. Badheka, Rahul S. Udani, Vrajesh P. J Pediatr Neurosci Original Article AIMS: We aimed to study the frequency, age, and gender distribution of paroxysmal nonepileptic events (PNEs) in children referred to epilepsy clinic with the diagnosis of epilepsy. We also evaluated the therapeutic implications of correct diagnosis and co-existence of true epilepsy in this population. SETTINGS AND DESIGN: All new patients below 18 years attending the Pediatric epilepsy out-patient clinic of PD Hinduja hospital over 6 months were evaluated. MATERIALS AND METHODS: Patients with history of paroxysmal events characterized by abrupt changes in consciousness or behavior or movement were included. They were assessed on description of events aided by recorded videos. If the diagnosis was not confirmed by this preliminary evaluation, further investigations were advised. STATISTICAL ANALYSIS USED: Chi-square/Fisher’s exact test was used to analyze differences between categorical variables and Kruskal–Wallis test between continuous variables. The data were analyzed by SAS University Edition. All significance tests were two-tailed with α <0.05. RESULTS: Two hundred new patients presenting with paroxysmal events were enrolled over 6 months. After diagnoses, 19% of these children had PNEs, 80% had epileptic events, and 1% remained undiagnosed. Common nonepileptic events seen were physiological in patients below 5 years and psychogenic in older children. Thirty-four percent of patients with PNEs were on anti-epileptic drugs (AEDs). After confirming nonepileptic attacks, only 2.6% patients needed AEDs for coexisting epilepsy which was statistically significant (P < 0.001) change in treatment. CONCLUSIONS: Epilepsy mimics are common in children and are often misdiagnosed causing undue stress. Correct diagnosis leads to a drastic change in management like withdrawal of drugs, commencing new treatment if needed, and appropriate referrals. Wolters Kluwer - Medknow 2021 2021-06-25 /pmc/articles/PMC8276968/ /pubmed/34316303 http://dx.doi.org/10.4103/jpn.JPN_33_20 Text en Copyright: © 2021 Journal of Pediatric Neurosciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Mandli, Ashfak H.
Desai, Neelu A.
Badheka, Rahul S.
Udani, Vrajesh P.
Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic
title Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic
title_full Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic
title_fullStr Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic
title_full_unstemmed Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic
title_short Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic
title_sort paroxysmal nonepileptic events in a pediatric epilepsy clinic
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8276968/
https://www.ncbi.nlm.nih.gov/pubmed/34316303
http://dx.doi.org/10.4103/jpn.JPN_33_20
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