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Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation

Atrial fibrillation (AF) is associated with significant risk of stroke and other thromboembolic events, which can be effectively prevented using oral anticoagulation (OAC) with either vitamin K antagonists (VKAs) or non-VKA oral anticoagulants (NOACs) dabigatran, rivaroxaban, apixaban, or edoxaban....

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Autores principales: Ueberham, Laura, Dagres, Nikolaos, Potpara, Tatjana S., Bollmann, Andreas, Hindricks, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656712/
https://www.ncbi.nlm.nih.gov/pubmed/28956288
http://dx.doi.org/10.1007/s12325-017-0616-6
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author Ueberham, Laura
Dagres, Nikolaos
Potpara, Tatjana S.
Bollmann, Andreas
Hindricks, Gerhard
author_facet Ueberham, Laura
Dagres, Nikolaos
Potpara, Tatjana S.
Bollmann, Andreas
Hindricks, Gerhard
author_sort Ueberham, Laura
collection PubMed
description Atrial fibrillation (AF) is associated with significant risk of stroke and other thromboembolic events, which can be effectively prevented using oral anticoagulation (OAC) with either vitamin K antagonists (VKAs) or non-VKA oral anticoagulants (NOACs) dabigatran, rivaroxaban, apixaban, or edoxaban. Until recently, VKAs were the only available means for OAC treatment. NOACs had similar efficacy and were safer than or as safe as warfarin with respect to reduced rates of hemorrhagic stroke or other intracranial bleeding in the respective pivotal randomized clinical trials (RCTs) of stroke prevention in non-valvular AF patients. Increasing “real-world” evidence on NOACs broadly confirms the results of the RCTs. However, individual patient characteristics including renal function, age, or prior bleeding should be taken into account when choosing the OAC with best risk–benefit profile. In patients ineligible for OACs, surgical or interventional stroke prevention strategies should be considered. In patients undergoing cardiac surgery for other reasons, the left atrial appendage excision, ligation, or amputation may be the best option. Importantly, residual stumps or insufficient ligation may result in even higher stroke risk than without intervention. Percutaneous left atrial appendage occlusion, although requiring minimally invasive access, failed to demonstrate reduced ischemic stroke events compared to warfarin. In this review article, we summarize current treatment options and discuss the strengths and major limitations of the therapies for stroke risk reduction in patients with AF.
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spelling pubmed-56567122017-11-01 Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation Ueberham, Laura Dagres, Nikolaos Potpara, Tatjana S. Bollmann, Andreas Hindricks, Gerhard Adv Ther Review Atrial fibrillation (AF) is associated with significant risk of stroke and other thromboembolic events, which can be effectively prevented using oral anticoagulation (OAC) with either vitamin K antagonists (VKAs) or non-VKA oral anticoagulants (NOACs) dabigatran, rivaroxaban, apixaban, or edoxaban. Until recently, VKAs were the only available means for OAC treatment. NOACs had similar efficacy and were safer than or as safe as warfarin with respect to reduced rates of hemorrhagic stroke or other intracranial bleeding in the respective pivotal randomized clinical trials (RCTs) of stroke prevention in non-valvular AF patients. Increasing “real-world” evidence on NOACs broadly confirms the results of the RCTs. However, individual patient characteristics including renal function, age, or prior bleeding should be taken into account when choosing the OAC with best risk–benefit profile. In patients ineligible for OACs, surgical or interventional stroke prevention strategies should be considered. In patients undergoing cardiac surgery for other reasons, the left atrial appendage excision, ligation, or amputation may be the best option. Importantly, residual stumps or insufficient ligation may result in even higher stroke risk than without intervention. Percutaneous left atrial appendage occlusion, although requiring minimally invasive access, failed to demonstrate reduced ischemic stroke events compared to warfarin. In this review article, we summarize current treatment options and discuss the strengths and major limitations of the therapies for stroke risk reduction in patients with AF. Springer Healthcare 2017-09-27 2017 /pmc/articles/PMC5656712/ /pubmed/28956288 http://dx.doi.org/10.1007/s12325-017-0616-6 Text en © The Author(s) 2017 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Ueberham, Laura
Dagres, Nikolaos
Potpara, Tatjana S.
Bollmann, Andreas
Hindricks, Gerhard
Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation
title Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation
title_full Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation
title_fullStr Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation
title_full_unstemmed Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation
title_short Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation
title_sort pharmacological and non-pharmacological treatments for stroke prevention in patients with atrial fibrillation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656712/
https://www.ncbi.nlm.nih.gov/pubmed/28956288
http://dx.doi.org/10.1007/s12325-017-0616-6
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