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Pharmacologic treatment and SUDEP risk: A nationwide, population-based, case-control study
OBJECTIVE: We conducted a nationwide case–control study in Sweden to test the hypothesis that antiepileptic drugs (AEDs) mono- or polytherapy, adherence, antidepressants, neuroleptics, β-blockers, and statins are associated with sudden unexpected death in epilepsy (SUDEP) risk. METHODS: Included wer...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682832/ https://www.ncbi.nlm.nih.gov/pubmed/32967928 http://dx.doi.org/10.1212/WNL.0000000000010874 |
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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 antiepileptic drugs (AEDs) mono- or polytherapy, adherence, antidepressants, neuroleptics, β-blockers, and statins are associated with sudden unexpected death in epilepsy (SUDEP) risk. METHODS: Included were 255 SUDEP cases and 1,148 matched controls. Information on clinical factors and medications came from medical records and the National Patient and Prescription Registers. The association between SUDEP and medications was assessed by odds ratios (ORs) with 95% confidence intervals (CIs) adjusted for potential risk factors including type of epilepsy, living conditions, comorbidity, and frequency of generalized tonic-clonic seizures (GTCS). RESULTS: Polytherapy, especially taking 3 or more AEDs, was associated with a substantially reduced risk of SUDEP (OR 0.31, 95% CI 0.14–0.67). Combinations including lamotrigine (OR 0.55, 95% CI 0.31–0.97), valproic acid (OR 0.53, 95% CI 0.29–0.98), and levetiracetam (OR 0.49, 95% CI 0.27–0.90) were associated with reduced risk. No specific AED was associated with increased risk. Regarding monotherapy, although numbers were limited, the lowest SUDEP risk was seen in users of levetiracetam (0.10, 95% CI 0.02–0.61). Having nonadherence mentioned in the medical record was associated with an OR of 2.75 (95% CI 1.58–4.78). Statin use was associated with a reduced SUDEP risk (OR 0.34, 95% CI 0.11–0.99) but selective serotonin reuptake inhibitor use was not. CONCLUSION: These results provide support for the importance of medication adherence and intensified AED treatment for patients with poorly controlled GTCS in the effort to reduce SUDEP risk and suggest that comedication with statins may reduce risk. |
format | Online Article Text |
id | pubmed-7682832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-76828322020-11-24 Pharmacologic treatment and SUDEP risk: 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 antiepileptic drugs (AEDs) mono- or polytherapy, adherence, antidepressants, neuroleptics, β-blockers, and statins are associated with sudden unexpected death in epilepsy (SUDEP) risk. METHODS: Included were 255 SUDEP cases and 1,148 matched controls. Information on clinical factors and medications came from medical records and the National Patient and Prescription Registers. The association between SUDEP and medications was assessed by odds ratios (ORs) with 95% confidence intervals (CIs) adjusted for potential risk factors including type of epilepsy, living conditions, comorbidity, and frequency of generalized tonic-clonic seizures (GTCS). RESULTS: Polytherapy, especially taking 3 or more AEDs, was associated with a substantially reduced risk of SUDEP (OR 0.31, 95% CI 0.14–0.67). Combinations including lamotrigine (OR 0.55, 95% CI 0.31–0.97), valproic acid (OR 0.53, 95% CI 0.29–0.98), and levetiracetam (OR 0.49, 95% CI 0.27–0.90) were associated with reduced risk. No specific AED was associated with increased risk. Regarding monotherapy, although numbers were limited, the lowest SUDEP risk was seen in users of levetiracetam (0.10, 95% CI 0.02–0.61). Having nonadherence mentioned in the medical record was associated with an OR of 2.75 (95% CI 1.58–4.78). Statin use was associated with a reduced SUDEP risk (OR 0.34, 95% CI 0.11–0.99) but selective serotonin reuptake inhibitor use was not. CONCLUSION: These results provide support for the importance of medication adherence and intensified AED treatment for patients with poorly controlled GTCS in the effort to reduce SUDEP risk and suggest that comedication with statins may reduce risk. Lippincott Williams & Wilkins 2020-11-03 /pmc/articles/PMC7682832/ /pubmed/32967928 http://dx.doi.org/10.1212/WNL.0000000000010874 Text en Copyright © 2020 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 Pharmacologic treatment and SUDEP risk: A nationwide, population-based, case-control study |
title | Pharmacologic treatment and SUDEP risk: A nationwide, population-based, case-control study |
title_full | Pharmacologic treatment and SUDEP risk: A nationwide, population-based, case-control study |
title_fullStr | Pharmacologic treatment and SUDEP risk: A nationwide, population-based, case-control study |
title_full_unstemmed | Pharmacologic treatment and SUDEP risk: A nationwide, population-based, case-control study |
title_short | Pharmacologic treatment and SUDEP risk: A nationwide, population-based, case-control study |
title_sort | pharmacologic treatment and sudep risk: a nationwide, population-based, case-control study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682832/ https://www.ncbi.nlm.nih.gov/pubmed/32967928 http://dx.doi.org/10.1212/WNL.0000000000010874 |
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