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Anticoagulants for stroke prevention in heart failure with reduced ejection fraction

Impaired left-ventricular ejection-fraction (LV-EF) is a known risk factor for ischemic stroke and systemic embolism in patients with heart failure (HF) even in the absence of atrial fibrillation. While stroke risk is inversely correlated with LV-EF in HF patients with sinus rhythm, strategies using...

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Autores principales: Schäfer, Andreas, Flierl, Ulrike, Bauersachs, Johann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766365/
https://www.ncbi.nlm.nih.gov/pubmed/34448932
http://dx.doi.org/10.1007/s00392-021-01930-y
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author Schäfer, Andreas
Flierl, Ulrike
Bauersachs, Johann
author_facet Schäfer, Andreas
Flierl, Ulrike
Bauersachs, Johann
author_sort Schäfer, Andreas
collection PubMed
description Impaired left-ventricular ejection-fraction (LV-EF) is a known risk factor for ischemic stroke and systemic embolism in patients with heart failure (HF) even in the absence of atrial fibrillation. While stroke risk is inversely correlated with LV-EF in HF patients with sinus rhythm, strategies using anticoagulation with Vitamin-K antagonists (VKA) were futile as the increase in major bleedings outweighed the potential benefit in stroke reduction. Non-Vitamin K oral anticoagulants (NOACs) proved to be an effective and in general safer approach for stroke prevention in patients with atrial fibrillation and may also have a favourable risk–benefit profile in HF patients. In HF patients with sinus rhythm, the COMPASS trial suggested a potential benefit for rivaroxaban, whereas the more dedicated COMMANDER-HF trial remained neutral on overall ischemic benefit owed to a higher mortality which was not influenced by anticoagulation. More recent data from subgroups in the COMMANDER-HF trial, however, suggest that there might be a benefit of rivaroxaban regarding stroke prevention under certain circumstances. In this article, we review the existing evidence for NOACs in HF patients with atrial fibrillation, elaborate the rationale for stroke prevention in HF patients with sinus rhythm, summarise the available data from anticoagulation trials in HF with sinus rhythm, and describe the patient who might eventually profit from an individualised strategy aiming to reduce stroke risk. GRAPHIC ABSTRACT: [Image: see text]
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spelling pubmed-87663652022-01-31 Anticoagulants for stroke prevention in heart failure with reduced ejection fraction Schäfer, Andreas Flierl, Ulrike Bauersachs, Johann Clin Res Cardiol Review Impaired left-ventricular ejection-fraction (LV-EF) is a known risk factor for ischemic stroke and systemic embolism in patients with heart failure (HF) even in the absence of atrial fibrillation. While stroke risk is inversely correlated with LV-EF in HF patients with sinus rhythm, strategies using anticoagulation with Vitamin-K antagonists (VKA) were futile as the increase in major bleedings outweighed the potential benefit in stroke reduction. Non-Vitamin K oral anticoagulants (NOACs) proved to be an effective and in general safer approach for stroke prevention in patients with atrial fibrillation and may also have a favourable risk–benefit profile in HF patients. In HF patients with sinus rhythm, the COMPASS trial suggested a potential benefit for rivaroxaban, whereas the more dedicated COMMANDER-HF trial remained neutral on overall ischemic benefit owed to a higher mortality which was not influenced by anticoagulation. More recent data from subgroups in the COMMANDER-HF trial, however, suggest that there might be a benefit of rivaroxaban regarding stroke prevention under certain circumstances. In this article, we review the existing evidence for NOACs in HF patients with atrial fibrillation, elaborate the rationale for stroke prevention in HF patients with sinus rhythm, summarise the available data from anticoagulation trials in HF with sinus rhythm, and describe the patient who might eventually profit from an individualised strategy aiming to reduce stroke risk. GRAPHIC ABSTRACT: [Image: see text] Springer Berlin Heidelberg 2021-08-27 2022 /pmc/articles/PMC8766365/ /pubmed/34448932 http://dx.doi.org/10.1007/s00392-021-01930-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Schäfer, Andreas
Flierl, Ulrike
Bauersachs, Johann
Anticoagulants for stroke prevention in heart failure with reduced ejection fraction
title Anticoagulants for stroke prevention in heart failure with reduced ejection fraction
title_full Anticoagulants for stroke prevention in heart failure with reduced ejection fraction
title_fullStr Anticoagulants for stroke prevention in heart failure with reduced ejection fraction
title_full_unstemmed Anticoagulants for stroke prevention in heart failure with reduced ejection fraction
title_short Anticoagulants for stroke prevention in heart failure with reduced ejection fraction
title_sort anticoagulants for stroke prevention in heart failure with reduced ejection fraction
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766365/
https://www.ncbi.nlm.nih.gov/pubmed/34448932
http://dx.doi.org/10.1007/s00392-021-01930-y
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