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Recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants

The direct oral anticoagulants (DOACs) have now supplanted vitamin K antagonists (VKAs) for the treatment of venous thromboembolism (VTE). The DOACs include dabigatran, which inhibits thrombin, and rivaroxaban, apixaban, and edoxaban, which inhibit factor Xa. The DOACs are as effective for the preve...

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Detalles Bibliográficos
Autores principales: Weitz, Jeffrey I., Jaffer, Iqbal H., Fredenburgh, James C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490483/
https://www.ncbi.nlm.nih.gov/pubmed/28713563
http://dx.doi.org/10.12688/f1000research.11174.1
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author Weitz, Jeffrey I.
Jaffer, Iqbal H.
Fredenburgh, James C.
author_facet Weitz, Jeffrey I.
Jaffer, Iqbal H.
Fredenburgh, James C.
author_sort Weitz, Jeffrey I.
collection PubMed
description The direct oral anticoagulants (DOACs) have now supplanted vitamin K antagonists (VKAs) for the treatment of venous thromboembolism (VTE). The DOACs include dabigatran, which inhibits thrombin, and rivaroxaban, apixaban, and edoxaban, which inhibit factor Xa. The DOACs are as effective for the prevention of recurrence as conventional VTE treatment, consisting of a parenteral anticoagulant followed by a VKA, and are associated with less bleeding. Because of these properties and the convenience of fixed dosing without the need for routine coagulation monitoring, guidelines now recommend DOACs over VKAs for VTE treatment in patients without active cancer. This paper examines the increasing role of the DOACs for VTE treatment.
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spelling pubmed-54904832017-07-13 Recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants Weitz, Jeffrey I. Jaffer, Iqbal H. Fredenburgh, James C. F1000Res Review The direct oral anticoagulants (DOACs) have now supplanted vitamin K antagonists (VKAs) for the treatment of venous thromboembolism (VTE). The DOACs include dabigatran, which inhibits thrombin, and rivaroxaban, apixaban, and edoxaban, which inhibit factor Xa. The DOACs are as effective for the prevention of recurrence as conventional VTE treatment, consisting of a parenteral anticoagulant followed by a VKA, and are associated with less bleeding. Because of these properties and the convenience of fixed dosing without the need for routine coagulation monitoring, guidelines now recommend DOACs over VKAs for VTE treatment in patients without active cancer. This paper examines the increasing role of the DOACs for VTE treatment. F1000Research 2017-06-23 /pmc/articles/PMC5490483/ /pubmed/28713563 http://dx.doi.org/10.12688/f1000research.11174.1 Text en Copyright: © 2017 Weitz JI et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Weitz, Jeffrey I.
Jaffer, Iqbal H.
Fredenburgh, James C.
Recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants
title Recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants
title_full Recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants
title_fullStr Recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants
title_full_unstemmed Recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants
title_short Recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants
title_sort recent advances in the treatment of venous thromboembolism in the era of the direct oral anticoagulants
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490483/
https://www.ncbi.nlm.nih.gov/pubmed/28713563
http://dx.doi.org/10.12688/f1000research.11174.1
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