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Risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs

AIMS: A few studies suggested that epilepsy and antiepileptic drugs with sodium channel‐blocking properties were independently associated with out‐of‐hospital cardiac arrest (OHCA). However, these findings have not yet been replicated. METHODS: Using Danish registries, we conducted a nested case–con...

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Autores principales: Eroglu, Talip E., Folke, Fredrik, Tan, Hanno L., Torp‐Pedersen, Christian, Gislason, Gunnar H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542728/
https://www.ncbi.nlm.nih.gov/pubmed/35293630
http://dx.doi.org/10.1111/bcp.15313
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author Eroglu, Talip E.
Folke, Fredrik
Tan, Hanno L.
Torp‐Pedersen, Christian
Gislason, Gunnar H.
author_facet Eroglu, Talip E.
Folke, Fredrik
Tan, Hanno L.
Torp‐Pedersen, Christian
Gislason, Gunnar H.
author_sort Eroglu, Talip E.
collection PubMed
description AIMS: A few studies suggested that epilepsy and antiepileptic drugs with sodium channel‐blocking properties were independently associated with out‐of‐hospital cardiac arrest (OHCA). However, these findings have not yet been replicated. METHODS: Using Danish registries, we conducted a nested case–control study in a cohort of individuals between 1 June 2001 and 31 December 2015. Cases were defined as OHCA from presumed cardiac causes, and were matched with non‐OHCA‐controls based on sex, and age on the date of OHCA. Exposure of interest was epilepsy or antiepileptic drug use. To study the association between individual antiepileptic drug use and the rate of OHCA, we compared each antiepileptic drug with valproic acid. Cox regression with time‐dependent covariates was conducted to calculate hazard ratio (HR) and 95% confidence interval (CI). RESULTS: We identified 35 195 OHCA‐cases and 351 950 matched non‐OHCA controls. Epilepsy (cases: 3.58%, controls: 1.60%) was associated with increased rate of OHCA compared with the general population (HR: 1.76, 95%CI: 1.64–1.88) when common OHCA risk factors were taken into account. When we studied antiepileptic drug use, we found that 2 antiepileptic drugs without sodium channel blockage, clonazepam (HR: 1.88, 95%CI: 1.45–2.44) and pregabalin (HR: 1.33, 95%CI: 1.05–1.69), were associated with OHCA, whereas none of the antiepileptic drugs with sodium channel blockage were associated with OHCA. CONCLUSION: Epilepsy is associated with increased rate of OHCA. Our findings do not support a possible association between antiepileptic drugs with sodium channel‐blocking properties and OHCA.
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spelling pubmed-95427282022-10-14 Risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs Eroglu, Talip E. Folke, Fredrik Tan, Hanno L. Torp‐Pedersen, Christian Gislason, Gunnar H. Br J Clin Pharmacol Original Articles AIMS: A few studies suggested that epilepsy and antiepileptic drugs with sodium channel‐blocking properties were independently associated with out‐of‐hospital cardiac arrest (OHCA). However, these findings have not yet been replicated. METHODS: Using Danish registries, we conducted a nested case–control study in a cohort of individuals between 1 June 2001 and 31 December 2015. Cases were defined as OHCA from presumed cardiac causes, and were matched with non‐OHCA‐controls based on sex, and age on the date of OHCA. Exposure of interest was epilepsy or antiepileptic drug use. To study the association between individual antiepileptic drug use and the rate of OHCA, we compared each antiepileptic drug with valproic acid. Cox regression with time‐dependent covariates was conducted to calculate hazard ratio (HR) and 95% confidence interval (CI). RESULTS: We identified 35 195 OHCA‐cases and 351 950 matched non‐OHCA controls. Epilepsy (cases: 3.58%, controls: 1.60%) was associated with increased rate of OHCA compared with the general population (HR: 1.76, 95%CI: 1.64–1.88) when common OHCA risk factors were taken into account. When we studied antiepileptic drug use, we found that 2 antiepileptic drugs without sodium channel blockage, clonazepam (HR: 1.88, 95%CI: 1.45–2.44) and pregabalin (HR: 1.33, 95%CI: 1.05–1.69), were associated with OHCA, whereas none of the antiepileptic drugs with sodium channel blockage were associated with OHCA. CONCLUSION: Epilepsy is associated with increased rate of OHCA. Our findings do not support a possible association between antiepileptic drugs with sodium channel‐blocking properties and OHCA. John Wiley and Sons Inc. 2022-03-26 2022-08 /pmc/articles/PMC9542728/ /pubmed/35293630 http://dx.doi.org/10.1111/bcp.15313 Text en © 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Eroglu, Talip E.
Folke, Fredrik
Tan, Hanno L.
Torp‐Pedersen, Christian
Gislason, Gunnar H.
Risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs
title Risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs
title_full Risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs
title_fullStr Risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs
title_full_unstemmed Risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs
title_short Risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs
title_sort risk of out‐of‐hospital cardiac arrest in patients with epilepsy and users of antiepileptic drugs
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542728/
https://www.ncbi.nlm.nih.gov/pubmed/35293630
http://dx.doi.org/10.1111/bcp.15313
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