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Non-vitamin K antagonist oral anticoagulants in patients with valvular heart disease
The non-vitamin K antagonist oral anticoagulants (NOACs) dabigatran, rivaroxaban, apixaban, and edoxaban have transformed the management of atrial fibrillation (AF), but are only approved by regulatory authorities for stroke prophylaxis in patients with so-called “non-valvular AF.” This terminology...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850709/ https://www.ncbi.nlm.nih.gov/pubmed/35185406 http://dx.doi.org/10.1093/eurheartj/suab151 |
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author | Fanaroff, Alexander C Vora, Amit N Lopes, Renato D |
author_facet | Fanaroff, Alexander C Vora, Amit N Lopes, Renato D |
author_sort | Fanaroff, Alexander C |
collection | PubMed |
description | The non-vitamin K antagonist oral anticoagulants (NOACs) dabigatran, rivaroxaban, apixaban, and edoxaban have transformed the management of atrial fibrillation (AF), but are only approved by regulatory authorities for stroke prophylaxis in patients with so-called “non-valvular AF.” This terminology has spawned confusion about which patients with valvular heart disease benefit from NOACs and which should be treated with vitamin K antagonists (VKAs) instead. Patients with valvular heart disease other than mechanical prosthetic valves or severe mitral stenosis (including those with bioprosthetic valves) were included in pivotal trials demonstrating the benefit of NOACs over VKAs, and consensus guidelines recommend NOACs over VKAs in these patients. Subsequent devoted randomized controlled trials in patients with AF and bioprosthetic valves, including transcatheter valves, have confirmed the safety of NOACs in this population. In patients with rheumatic mitral stenosis, observational studies indicate that NOACs may be safe and effective, but randomized controlled trials are ongoing. By contrast, a randomized controlled trial showed that dabigatran is harmful in patients with mechanical prosthetic mitral valves; however, these data may not extrapolate to patients with mechanical valve prostheses in other locations or to other NOACs, and randomized controlled trials are ongoing. In this review, we discuss these data in greater depth, and make recommendations for the use of NOACs in patients with valvular heart disease. |
format | Online Article Text |
id | pubmed-8850709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88507092022-02-17 Non-vitamin K antagonist oral anticoagulants in patients with valvular heart disease Fanaroff, Alexander C Vora, Amit N Lopes, Renato D Eur Heart J Suppl Supplement Papers The non-vitamin K antagonist oral anticoagulants (NOACs) dabigatran, rivaroxaban, apixaban, and edoxaban have transformed the management of atrial fibrillation (AF), but are only approved by regulatory authorities for stroke prophylaxis in patients with so-called “non-valvular AF.” This terminology has spawned confusion about which patients with valvular heart disease benefit from NOACs and which should be treated with vitamin K antagonists (VKAs) instead. Patients with valvular heart disease other than mechanical prosthetic valves or severe mitral stenosis (including those with bioprosthetic valves) were included in pivotal trials demonstrating the benefit of NOACs over VKAs, and consensus guidelines recommend NOACs over VKAs in these patients. Subsequent devoted randomized controlled trials in patients with AF and bioprosthetic valves, including transcatheter valves, have confirmed the safety of NOACs in this population. In patients with rheumatic mitral stenosis, observational studies indicate that NOACs may be safe and effective, but randomized controlled trials are ongoing. By contrast, a randomized controlled trial showed that dabigatran is harmful in patients with mechanical prosthetic mitral valves; however, these data may not extrapolate to patients with mechanical valve prostheses in other locations or to other NOACs, and randomized controlled trials are ongoing. In this review, we discuss these data in greater depth, and make recommendations for the use of NOACs in patients with valvular heart disease. Oxford University Press 2022-02-14 /pmc/articles/PMC8850709/ /pubmed/35185406 http://dx.doi.org/10.1093/eurheartj/suab151 Text en Published on behalf of the European Society of Cardiology. © The Author(s) 2022. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Supplement Papers Fanaroff, Alexander C Vora, Amit N Lopes, Renato D Non-vitamin K antagonist oral anticoagulants in patients with valvular heart disease |
title | Non-vitamin K antagonist oral anticoagulants in patients with valvular heart disease |
title_full | Non-vitamin K antagonist oral anticoagulants in patients with valvular heart disease |
title_fullStr | Non-vitamin K antagonist oral anticoagulants in patients with valvular heart disease |
title_full_unstemmed | Non-vitamin K antagonist oral anticoagulants in patients with valvular heart disease |
title_short | Non-vitamin K antagonist oral anticoagulants in patients with valvular heart disease |
title_sort | non-vitamin k antagonist oral anticoagulants in patients with valvular heart disease |
topic | Supplement Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850709/ https://www.ncbi.nlm.nih.gov/pubmed/35185406 http://dx.doi.org/10.1093/eurheartj/suab151 |
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