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Recurrence risk of ictal asystole in epilepsy

OBJECTIVE: To determine the recurrence risk of ictal asystole (IA) and its determining factors in people with epilepsy. METHODS: We performed a systematic review of published cases with IA in 3 databases and additionally searched our local database for patients with multiple seizures simultaneously...

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Autores principales: Hampel, Kevin G., Thijs, Roland D., Elger, Christian E., Surges, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580865/
https://www.ncbi.nlm.nih.gov/pubmed/28747444
http://dx.doi.org/10.1212/WNL.0000000000004266
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author Hampel, Kevin G.
Thijs, Roland D.
Elger, Christian E.
Surges, Rainer
author_facet Hampel, Kevin G.
Thijs, Roland D.
Elger, Christian E.
Surges, Rainer
author_sort Hampel, Kevin G.
collection PubMed
description OBJECTIVE: To determine the recurrence risk of ictal asystole (IA) and its determining factors in people with epilepsy. METHODS: We performed a systematic review of published cases with IA in 3 databases and additionally searched our local database for patients with multiple seizures simultaneously recorded with ECG and EEG and at least one IA. IA recurrence risk was estimated by including all seizures without knowledge of the chronological order. Various clinical features were assessed by an individual patient data meta-analysis. A random mixed effect logistic regression model was applied to estimate the average recurrence risk of IA. Plausibility of the calculated IA recurrence risk was checked by analyzing the local dataset with available information in chronological order. RESULTS: Eighty patients with 182 IA in 537 seizures were included. Recurrence risk of IA amounted to 40% (95% confidence interval [CI] 32%–50%). None of the clinical factors (age, sex, type and duration of epilepsy, hemispheric lateralization, duration of IA per patient) appeared to have a significant effect on the short-term recurrence risk of IA. When considering the local dataset only, IA recurrence risk was estimated to 30% (95% CI 14%–53%). Information whether IA coincided with symptoms (i.e., syncope) or not was given in 60 patients: 100 out of 142 IAs were symptomatic. CONCLUSION: Our data suggest that in case of clinically suspected IA, the recording of 1 or 2 seizures is not sufficient to rule out IA. Furthermore, the high short-term recurrence risk favors aggressive treatment, including pacemaker implantation if seizure freedom cannot be achieved.
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spelling pubmed-55808652017-09-08 Recurrence risk of ictal asystole in epilepsy Hampel, Kevin G. Thijs, Roland D. Elger, Christian E. Surges, Rainer Neurology Article OBJECTIVE: To determine the recurrence risk of ictal asystole (IA) and its determining factors in people with epilepsy. METHODS: We performed a systematic review of published cases with IA in 3 databases and additionally searched our local database for patients with multiple seizures simultaneously recorded with ECG and EEG and at least one IA. IA recurrence risk was estimated by including all seizures without knowledge of the chronological order. Various clinical features were assessed by an individual patient data meta-analysis. A random mixed effect logistic regression model was applied to estimate the average recurrence risk of IA. Plausibility of the calculated IA recurrence risk was checked by analyzing the local dataset with available information in chronological order. RESULTS: Eighty patients with 182 IA in 537 seizures were included. Recurrence risk of IA amounted to 40% (95% confidence interval [CI] 32%–50%). None of the clinical factors (age, sex, type and duration of epilepsy, hemispheric lateralization, duration of IA per patient) appeared to have a significant effect on the short-term recurrence risk of IA. When considering the local dataset only, IA recurrence risk was estimated to 30% (95% CI 14%–53%). Information whether IA coincided with symptoms (i.e., syncope) or not was given in 60 patients: 100 out of 142 IAs were symptomatic. CONCLUSION: Our data suggest that in case of clinically suspected IA, the recording of 1 or 2 seizures is not sufficient to rule out IA. Furthermore, the high short-term recurrence risk favors aggressive treatment, including pacemaker implantation if seizure freedom cannot be achieved. Lippincott Williams & Wilkins 2017-08-22 /pmc/articles/PMC5580865/ /pubmed/28747444 http://dx.doi.org/10.1212/WNL.0000000000004266 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Hampel, Kevin G.
Thijs, Roland D.
Elger, Christian E.
Surges, Rainer
Recurrence risk of ictal asystole in epilepsy
title Recurrence risk of ictal asystole in epilepsy
title_full Recurrence risk of ictal asystole in epilepsy
title_fullStr Recurrence risk of ictal asystole in epilepsy
title_full_unstemmed Recurrence risk of ictal asystole in epilepsy
title_short Recurrence risk of ictal asystole in epilepsy
title_sort recurrence risk of ictal asystole in epilepsy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580865/
https://www.ncbi.nlm.nih.gov/pubmed/28747444
http://dx.doi.org/10.1212/WNL.0000000000004266
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