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   <dc:title>Factors associated with disease progression in patients with atrial fibrillation and heart failure anticoagulated with rivaroxaban</dc:title>
   <dc:creator>Manito Lorite, Nicolás</dc:creator>
   <dc:creator>Cepeda Rodrigo, José María</dc:creator>
   <dc:creator>Farré López, Núria</dc:creator>
   <dc:creator>Castillo Orive, Miguel</dc:creator>
   <dc:creator>Galve, Enrique</dc:creator>
   <dc:creator>Jiménez Candil, Javier</dc:creator>
   <dc:creator>García Pinilla, José M.</dc:creator>
   <dc:creator>López Sánchez, Eduardo Sebastián</dc:creator>
   <dc:creator>Rafols, Carles</dc:creator>
   <dc:creator>Gómez Doblas, Juan José</dc:creator>
   <dc:subject>Anticoagulation</dc:subject>
   <dc:subject>Atrial fibrillation</dc:subject>
   <dc:subject>Direct oral anticoagulant</dc:subject>
   <dc:subject>Heart failure</dc:subject>
   <dc:subject>Rivaroxaban</dc:subject>
   <dc:subject>Worsening heart failure</dc:subject>
   <dcterms:abstract>Background: Patients with atrial fibrillation (AF) and heart failure (HF) have a high risk of thromboembolism and other outcomes and anticoagulation is recommended. Hypothesis: This study was aimed to explore the risk factors associated with HF worsening in patients with AF and HF taking rivaroxaban in Spain. Methods: Multicenter, prospective, observational study that included adults with AF and chronic HF, receiving rivaroxaban ≥4 months before entering. HF worsening was defined as first hospitalization or emergency visit because of HF exacerbation. Results: A total of 672 patients from 71 Spanish centers were recruited, of whom 658 (97.9%) were included in the safety analysis and 552 (82.1%) in the per protocol analysis. At baseline, mean age was 73.7 ± 10.9 years, 64.9% were male, CHA2 DS2 -VASc was 4.1 ± 1.5, HAS-BLED was 1.6 ± 0.9% and 51.3% had HF with preserved ejection fraction. After 24 months of follow-up, 24.9% of patients developed HF worsening, 11.6% died, 2.9% had a thromboembolic event, 3.1% a major bleeding, 0.5% an intracranial bleeding and no patient had a fatal hemorrhage. Older age, the history of chronic obstructive pulmonary disease, the previous use of vitamin K antagonists, and restrictive or infiltrative cardiomyopathies, were independently associated with HF worsening. Only 6.9% of patients permanently discontinued rivaroxaban treatment. Conclusions: Approximately one out of four patients with HF and AF treated with rivaroxaban developed a HF worsening episode after 2 years of follow-up. The identification of those factors that increase the risk of HF worsening could be helpful in the comprehensive management of this population.</dcterms:abstract>
   <dcterms:issued>2024-10-09T06:25:04Z</dcterms:issued>
   <dcterms:issued>2024-10-09T06:25:04Z</dcterms:issued>
   <dcterms:issued>2024</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:relation>Clin Cardiol. 2024 Feb;47(2):e24189</dc:relation>
   <dc:rights>© 2023 The Authors. Clinical Cardiology published by Wiley Periodicals, LLC. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Wiley</dc:publisher>
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