Rivaroxaban versus Warfarin in Patients with Mechanical Heart Valve: Rationale and Design of the RIWA Study

Abstract Introduction Mechanical heart valves (MHV) are extremely durable, but they require permanent use of anticoagulation to prevent thromboembolic events. The only approved therapeutic options are vitamin K antagonists (VKAs), such as warfarin. As a drug class, clinical management is difficult,...

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Main Authors: André R. Durães, Yasmin de Souza Lima Bitar, José Admirço L. Filho, Igor S. Schonhofen, Edmundo J. N. Camara, Leonardo Roever, Hugo E. D. P. Cardoso, Kevan M. Akrami
Format: Article
Language:English
Published: Adis, Springer Healthcare 2018-10-01
Series:Drugs in R&D
Online Access:http://link.springer.com/article/10.1007/s40268-018-0249-5
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spelling doaj-25ad83f0a0634755a60b092ab7a46fe82020-11-24T21:25:53ZengAdis, Springer HealthcareDrugs in R&D1174-58861179-69012018-10-0118430330810.1007/s40268-018-0249-5Rivaroxaban versus Warfarin in Patients with Mechanical Heart Valve: Rationale and Design of the RIWA StudyAndré R. Durães0Yasmin de Souza Lima Bitar1José Admirço L. Filho2Igor S. Schonhofen3Edmundo J. N. Camara4Leonardo Roever5Hugo E. D. P. Cardoso6Kevan M. Akrami7General Hospital Roberto SantosFederal University of Bahia, Medical School-UFBA/FAMEBGeneral Hospital Roberto SantosGeneral Hospital Roberto SantosFederal University of Bahia, Medical School-UFBA/FAMEBFederal University of UberlândiaGeneral Hospital Roberto SantosDivision of Infectious Disease, Department of Medicine, University of California, San DiegoAbstract Introduction Mechanical heart valves (MHV) are extremely durable, but they require permanent use of anticoagulation to prevent thromboembolic events. The only approved therapeutic options are vitamin K antagonists (VKAs), such as warfarin. As a drug class, clinical management is difficult, therefore new alternatives need to be evaluated. Methods RIWA is a phase II/III, prospective, open-label, randomized, pilot study designed to investigate oral rivaroxaban 15 mg twice daily compared with dose-adjusted warfarin for the prevention of stroke (ischemic or hemorrhagic) and systemic embolism in patients with MHV, from August 2018 to December 2019. Patients will undergo transesophageal echocardiography at the beginning and the end of the study (follow-up time 90 days). On an explanatory basis, all events will be analyzed, including stroke, peripheral systemic embolism, valve thrombosis, significant bleeding and death. Discussion Warfarin and similar VKAs are standard therapy for patients with an MHV. Even with the appropriate use of therapy, the incidence of thromboembolic events is high at 1–4% per year. Furthermore, bleeding risk is significant, ranging from 2 to 9% per year. The new frontier to be overcome in relation to use of the new oral anticoagulants is undoubtedly in patients with MHV. A significant portion of people with MHV worldwide will benefit if noninferiority of these new agents is confirmed. Trial Registration ClinicalTrials.gov identifier: NCT03566303. Recruitment Status: Recruiting. First Posted: 25 June 2018. Last Update Posted: 25 June 2018.http://link.springer.com/article/10.1007/s40268-018-0249-5
collection DOAJ
language English
format Article
sources DOAJ
author André R. Durães
Yasmin de Souza Lima Bitar
José Admirço L. Filho
Igor S. Schonhofen
Edmundo J. N. Camara
Leonardo Roever
Hugo E. D. P. Cardoso
Kevan M. Akrami
spellingShingle André R. Durães
Yasmin de Souza Lima Bitar
José Admirço L. Filho
Igor S. Schonhofen
Edmundo J. N. Camara
Leonardo Roever
Hugo E. D. P. Cardoso
Kevan M. Akrami
Rivaroxaban versus Warfarin in Patients with Mechanical Heart Valve: Rationale and Design of the RIWA Study
Drugs in R&D
author_facet André R. Durães
Yasmin de Souza Lima Bitar
José Admirço L. Filho
Igor S. Schonhofen
Edmundo J. N. Camara
Leonardo Roever
Hugo E. D. P. Cardoso
Kevan M. Akrami
author_sort André R. Durães
title Rivaroxaban versus Warfarin in Patients with Mechanical Heart Valve: Rationale and Design of the RIWA Study
title_short Rivaroxaban versus Warfarin in Patients with Mechanical Heart Valve: Rationale and Design of the RIWA Study
title_full Rivaroxaban versus Warfarin in Patients with Mechanical Heart Valve: Rationale and Design of the RIWA Study
title_fullStr Rivaroxaban versus Warfarin in Patients with Mechanical Heart Valve: Rationale and Design of the RIWA Study
title_full_unstemmed Rivaroxaban versus Warfarin in Patients with Mechanical Heart Valve: Rationale and Design of the RIWA Study
title_sort rivaroxaban versus warfarin in patients with mechanical heart valve: rationale and design of the riwa study
publisher Adis, Springer Healthcare
series Drugs in R&D
issn 1174-5886
1179-6901
publishDate 2018-10-01
description Abstract Introduction Mechanical heart valves (MHV) are extremely durable, but they require permanent use of anticoagulation to prevent thromboembolic events. The only approved therapeutic options are vitamin K antagonists (VKAs), such as warfarin. As a drug class, clinical management is difficult, therefore new alternatives need to be evaluated. Methods RIWA is a phase II/III, prospective, open-label, randomized, pilot study designed to investigate oral rivaroxaban 15 mg twice daily compared with dose-adjusted warfarin for the prevention of stroke (ischemic or hemorrhagic) and systemic embolism in patients with MHV, from August 2018 to December 2019. Patients will undergo transesophageal echocardiography at the beginning and the end of the study (follow-up time 90 days). On an explanatory basis, all events will be analyzed, including stroke, peripheral systemic embolism, valve thrombosis, significant bleeding and death. Discussion Warfarin and similar VKAs are standard therapy for patients with an MHV. Even with the appropriate use of therapy, the incidence of thromboembolic events is high at 1–4% per year. Furthermore, bleeding risk is significant, ranging from 2 to 9% per year. The new frontier to be overcome in relation to use of the new oral anticoagulants is undoubtedly in patients with MHV. A significant portion of people with MHV worldwide will benefit if noninferiority of these new agents is confirmed. Trial Registration ClinicalTrials.gov identifier: NCT03566303. Recruitment Status: Recruiting. First Posted: 25 June 2018. Last Update Posted: 25 June 2018.
url http://link.springer.com/article/10.1007/s40268-018-0249-5
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