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Expanding use of new oral anticoagulants

New, non-vitamin K antagonist oral anticoagulants (NOACs) have been developed to overcome the limitations of warfarin. These include dabigatran, which inhibits thrombin, and rivaroxaban, apixaban, and edoxaban, which inhibit factor Xa. In the US, rivaroxaban and apixaban are licensed for thromboprop...

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Autor principal: Weitz, Jeffrey I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculty of 1000 Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191267/
https://www.ncbi.nlm.nih.gov/pubmed/25374671
http://dx.doi.org/10.12703/P6-93
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author Weitz, Jeffrey I.
author_facet Weitz, Jeffrey I.
author_sort Weitz, Jeffrey I.
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description New, non-vitamin K antagonist oral anticoagulants (NOACs) have been developed to overcome the limitations of warfarin. These include dabigatran, which inhibits thrombin, and rivaroxaban, apixaban, and edoxaban, which inhibit factor Xa. In the US, rivaroxaban and apixaban are licensed for thromboprophylaxis after elective hip or knee arthroplasty, and rivaroxaban and dabigatran are approved for treatment of venous thromboembolism. Dabigatran, rivaroxaban, and apixaban also are licensed for stroke prevention in eligible patients with atrial fibrillation. Designed to be given in fixed doses without routine coagulation monitoring, the NOACs are more convenient to administer than warfarin. Phase III clinical trials have shown that the NOACs are at least as effective as warfarin and are associated with less intracranial bleeding. This article compares the pharmacological properties of the NOACs with those of warfarin, describes the clinical trial data with the NOACs in the approved indications, outlines the unmet medical needs that the NOACs address, highlights the potential limitations of the NOACs, and provides guidance on the optimal use of the NOACs.
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spelling pubmed-41912672014-11-05 Expanding use of new oral anticoagulants Weitz, Jeffrey I. F1000Prime Rep Review Article New, non-vitamin K antagonist oral anticoagulants (NOACs) have been developed to overcome the limitations of warfarin. These include dabigatran, which inhibits thrombin, and rivaroxaban, apixaban, and edoxaban, which inhibit factor Xa. In the US, rivaroxaban and apixaban are licensed for thromboprophylaxis after elective hip or knee arthroplasty, and rivaroxaban and dabigatran are approved for treatment of venous thromboembolism. Dabigatran, rivaroxaban, and apixaban also are licensed for stroke prevention in eligible patients with atrial fibrillation. Designed to be given in fixed doses without routine coagulation monitoring, the NOACs are more convenient to administer than warfarin. Phase III clinical trials have shown that the NOACs are at least as effective as warfarin and are associated with less intracranial bleeding. This article compares the pharmacological properties of the NOACs with those of warfarin, describes the clinical trial data with the NOACs in the approved indications, outlines the unmet medical needs that the NOACs address, highlights the potential limitations of the NOACs, and provides guidance on the optimal use of the NOACs. Faculty of 1000 Ltd 2014-10-01 /pmc/articles/PMC4191267/ /pubmed/25374671 http://dx.doi.org/10.12703/P6-93 Text en © 2014 Faculty of 1000 Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode All F1000Prime Reports articles are distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Weitz, Jeffrey I.
Expanding use of new oral anticoagulants
title Expanding use of new oral anticoagulants
title_full Expanding use of new oral anticoagulants
title_fullStr Expanding use of new oral anticoagulants
title_full_unstemmed Expanding use of new oral anticoagulants
title_short Expanding use of new oral anticoagulants
title_sort expanding use of new oral anticoagulants
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191267/
https://www.ncbi.nlm.nih.gov/pubmed/25374671
http://dx.doi.org/10.12703/P6-93
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