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Rivaroxaban and the EINSTEIN clinical trial programme

Rivaroxaban, a direct oral anticoagulant, is widely used for the treatment of venous thromboembolism (VTE) in adult patients. The approval of rivaroxaban for the treatment of deep vein thrombosis and pulmonary embolism and the extended secondary prevention of recurrent VTE is based on the results of...

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Autores principales: Cohen, Alexander T., Bauersachs, Rupert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams And Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504120/
https://www.ncbi.nlm.nih.gov/pubmed/30920394
http://dx.doi.org/10.1097/MBC.0000000000000800
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author Cohen, Alexander T.
Bauersachs, Rupert
author_facet Cohen, Alexander T.
Bauersachs, Rupert
author_sort Cohen, Alexander T.
collection PubMed
description Rivaroxaban, a direct oral anticoagulant, is widely used for the treatment of venous thromboembolism (VTE) in adult patients. The approval of rivaroxaban for the treatment of deep vein thrombosis and pulmonary embolism and the extended secondary prevention of recurrent VTE is based on the results of the EINSTEIN DVT and EINSTEIN PE trials, and the EINSTEIN EXT and EINSTEIN CHOICE trials, respectively. This review provides an updated overview of these completed EINSTEIN studies in adult patients, including results of subanalyses in patients at high risk of recurrent VTE, and discusses the emerging data from the EINSTEIN Junior programme, which is evaluating the use of rivaroxaban for the treatment of paediatric VTE. In the EINSTEIN DVT and EINSTEIN PE trials, rivaroxaban (15 mg twice daily for 21 days, followed by 20 mg once daily thereafter) was shown to be an effective and safe alternative to standard anticoagulation for the treatment of deep vein thrombosis and pulmonary embolism in a broad range of adult patients. These results are supported by increasing amounts of real-world data from patients treated with rivaroxaban in routine clinical practice worldwide. In the EINSTEIN EXT and EINSTEIN CHOICE trials, rivaroxaban was superior to placebo and acetylsalicylic acid, respectively, for the extended treatment of VTE – physicians can now choose between two doses of rivaroxaban (20 mg once daily or 10 mg once daily) for the extended prevention of recurrent VTE, based on a patient's risk of recurrence, bleeding and personal preferences.
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spelling pubmed-65041202019-07-22 Rivaroxaban and the EINSTEIN clinical trial programme Cohen, Alexander T. Bauersachs, Rupert Blood Coagul Fibrinolysis Review Articles Rivaroxaban, a direct oral anticoagulant, is widely used for the treatment of venous thromboembolism (VTE) in adult patients. The approval of rivaroxaban for the treatment of deep vein thrombosis and pulmonary embolism and the extended secondary prevention of recurrent VTE is based on the results of the EINSTEIN DVT and EINSTEIN PE trials, and the EINSTEIN EXT and EINSTEIN CHOICE trials, respectively. This review provides an updated overview of these completed EINSTEIN studies in adult patients, including results of subanalyses in patients at high risk of recurrent VTE, and discusses the emerging data from the EINSTEIN Junior programme, which is evaluating the use of rivaroxaban for the treatment of paediatric VTE. In the EINSTEIN DVT and EINSTEIN PE trials, rivaroxaban (15 mg twice daily for 21 days, followed by 20 mg once daily thereafter) was shown to be an effective and safe alternative to standard anticoagulation for the treatment of deep vein thrombosis and pulmonary embolism in a broad range of adult patients. These results are supported by increasing amounts of real-world data from patients treated with rivaroxaban in routine clinical practice worldwide. In the EINSTEIN EXT and EINSTEIN CHOICE trials, rivaroxaban was superior to placebo and acetylsalicylic acid, respectively, for the extended treatment of VTE – physicians can now choose between two doses of rivaroxaban (20 mg once daily or 10 mg once daily) for the extended prevention of recurrent VTE, based on a patient's risk of recurrence, bleeding and personal preferences. Lippincott Williams And Wilkins 2019-04 2019-03-08 /pmc/articles/PMC6504120/ /pubmed/30920394 http://dx.doi.org/10.1097/MBC.0000000000000800 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Review Articles
Cohen, Alexander T.
Bauersachs, Rupert
Rivaroxaban and the EINSTEIN clinical trial programme
title Rivaroxaban and the EINSTEIN clinical trial programme
title_full Rivaroxaban and the EINSTEIN clinical trial programme
title_fullStr Rivaroxaban and the EINSTEIN clinical trial programme
title_full_unstemmed Rivaroxaban and the EINSTEIN clinical trial programme
title_short Rivaroxaban and the EINSTEIN clinical trial programme
title_sort rivaroxaban and the einstein clinical trial programme
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504120/
https://www.ncbi.nlm.nih.gov/pubmed/30920394
http://dx.doi.org/10.1097/MBC.0000000000000800
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