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Clinical risk factors in SUDEP: A nationwide population-based case-control study

OBJECTIVE: We conducted a nationwide case-control study in Sweden to test the hypothesis that specific clinical characteristics are associated with increased risk of sudden unexpected death in epilepsy (SUDEP). METHODS: The study included 255 SUDEP cases (definite and probable) and 1,148 matched con...

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Autores principales: Sveinsson, Olafur, Andersson, Tomas, Mattsson, Peter, Carlsson, Sofia, Tomson, Torbjörn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079690/
https://www.ncbi.nlm.nih.gov/pubmed/31831600
http://dx.doi.org/10.1212/WNL.0000000000008741
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author Sveinsson, Olafur
Andersson, Tomas
Mattsson, Peter
Carlsson, Sofia
Tomson, Torbjörn
author_facet Sveinsson, Olafur
Andersson, Tomas
Mattsson, Peter
Carlsson, Sofia
Tomson, Torbjörn
author_sort Sveinsson, Olafur
collection PubMed
description OBJECTIVE: We conducted a nationwide case-control study in Sweden to test the hypothesis that specific clinical characteristics are associated with increased risk of sudden unexpected death in epilepsy (SUDEP). METHODS: The study included 255 SUDEP cases (definite and probable) and 1,148 matched controls. Clinical information was obtained from medical records and the National Patient Register. The association between SUDEP and potential risk factors was assessed by odds ratios (ORs) and 95% confidence intervals (CIs) and interaction assessed by attributable proportion due to interaction (AP). RESULTS: Experiencing generalized tonic-clonic seizures (GTCS) during the preceding year was associated with a 27-fold increased risk (OR 26.81, 95% CI 14.86–48.38), whereas no excess risk was seen in those with exclusively non-GTCS seizures (OR 1.15, 95% CI 0.54–48.38). The presence of nocturnal GTCS during the last year of observation was associated with a 15-fold risk (OR 15.31, 95% CI 9.57–24.47). Living alone was associated with a 5-fold increased risk of SUDEP (OR 5.01, 95% CI 2.93–8.57) and interaction analysis showed that the combination of not sharing a bedroom and having GTCS conferred an OR of 67.10 (95% CI 29.66–151.88), with AP estimated at 0.69 (CI 0.53–0.85). Among comorbid diseases, a previous diagnosis of substance abuse or alcohol dependence was associated with excess risk of SUDEP. CONCLUSIONS: Individuals with GTCS who sleep alone have a dramatically increased SUDEP risk. Our results indicate that 69% of SUDEP cases in patients who have GTCS and live alone could be prevented if the patients were not unattended at night or were free from GTCS.
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spelling pubmed-70796902020-03-25 Clinical risk factors in SUDEP: A nationwide population-based case-control study Sveinsson, Olafur Andersson, Tomas Mattsson, Peter Carlsson, Sofia Tomson, Torbjörn Neurology Article OBJECTIVE: We conducted a nationwide case-control study in Sweden to test the hypothesis that specific clinical characteristics are associated with increased risk of sudden unexpected death in epilepsy (SUDEP). METHODS: The study included 255 SUDEP cases (definite and probable) and 1,148 matched controls. Clinical information was obtained from medical records and the National Patient Register. The association between SUDEP and potential risk factors was assessed by odds ratios (ORs) and 95% confidence intervals (CIs) and interaction assessed by attributable proportion due to interaction (AP). RESULTS: Experiencing generalized tonic-clonic seizures (GTCS) during the preceding year was associated with a 27-fold increased risk (OR 26.81, 95% CI 14.86–48.38), whereas no excess risk was seen in those with exclusively non-GTCS seizures (OR 1.15, 95% CI 0.54–48.38). The presence of nocturnal GTCS during the last year of observation was associated with a 15-fold risk (OR 15.31, 95% CI 9.57–24.47). Living alone was associated with a 5-fold increased risk of SUDEP (OR 5.01, 95% CI 2.93–8.57) and interaction analysis showed that the combination of not sharing a bedroom and having GTCS conferred an OR of 67.10 (95% CI 29.66–151.88), with AP estimated at 0.69 (CI 0.53–0.85). Among comorbid diseases, a previous diagnosis of substance abuse or alcohol dependence was associated with excess risk of SUDEP. CONCLUSIONS: Individuals with GTCS who sleep alone have a dramatically increased SUDEP risk. Our results indicate that 69% of SUDEP cases in patients who have GTCS and live alone could be prevented if the patients were not unattended at night or were free from GTCS. Lippincott Williams & Wilkins 2020-01-28 /pmc/articles/PMC7079690/ /pubmed/31831600 http://dx.doi.org/10.1212/WNL.0000000000008741 Text en Copyright © 2019 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
Sveinsson, Olafur
Andersson, Tomas
Mattsson, Peter
Carlsson, Sofia
Tomson, Torbjörn
Clinical risk factors in SUDEP: A nationwide population-based case-control study
title Clinical risk factors in SUDEP: A nationwide population-based case-control study
title_full Clinical risk factors in SUDEP: A nationwide population-based case-control study
title_fullStr Clinical risk factors in SUDEP: A nationwide population-based case-control study
title_full_unstemmed Clinical risk factors in SUDEP: A nationwide population-based case-control study
title_short Clinical risk factors in SUDEP: A nationwide population-based case-control study
title_sort clinical risk factors in sudep: a nationwide population-based case-control study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079690/
https://www.ncbi.nlm.nih.gov/pubmed/31831600
http://dx.doi.org/10.1212/WNL.0000000000008741
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