A Controlled Trial of Rivaroxaban after Transcatheter Aortic-Valve Replacement

Patients who had undergone successful TAVR were randomly assigned to receive either a rivaroxaban-based antithrombotic regimen or an antiplatelet-based antithrombotic regimen. At 17 months, the primary outcome of death or thromboembolic complications occurred more frequently with rivaroxaban.

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Published inThe New England journal of medicine Vol. 382; no. 2; pp. 120 - 129
Main Authors Dangas, George D, Tijssen, Jan G.P, Wöhrle, Jochen, Søndergaard, Lars, Gilard, Martine, Möllmann, Helge, Makkar, Raj R, Herrmann, Howard C, Giustino, Gennaro, Baldus, Stephan, De Backer, Ole, Guimarães, Ana H.C, Gullestad, Lars, Kini, Annapoorna, von Lewinski, Dirk, Mack, Michael, Moreno, Raúl, Schäfer, Ulrich, Seeger, Julia, Tchétché, Didier, Thomitzek, Karen, Valgimigli, Marco, Vranckx, Pascal, Welsh, Robert C, Wildgoose, Peter, Volkl, Albert A, Zazula, Ana, van Amsterdam, Ronald G.M, Mehran, Roxana, Windecker, Stephan
Format Journal Article Web Resource
LanguageEnglish
Published United States Massachusetts Medical Society 09.01.2020
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ISSN0028-4793
1533-4406
1533-4406
DOI10.1056/NEJMoa1911425

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Summary:Patients who had undergone successful TAVR were randomly assigned to receive either a rivaroxaban-based antithrombotic regimen or an antiplatelet-based antithrombotic regimen. At 17 months, the primary outcome of death or thromboembolic complications occurred more frequently with rivaroxaban.
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scopus-id:2-s2.0-85075993796
ISSN:0028-4793
1533-4406
1533-4406
DOI:10.1056/NEJMoa1911425