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Authordc.contributor.authorRodes Cabau, Josep 
Authordc.contributor.authorMasson, Jean Bernard 
Authordc.contributor.authorWelsh, Robert C. 
Authordc.contributor.authorGarcía del Blanco, Bruno 
Authordc.contributor.authorPelletier, Marc 
Authordc.contributor.authorWebb, John G. 
Authordc.contributor.authorAl Qoofi, Faisal 
Authordc.contributor.authorGenereux, Philippe 
Authordc.contributor.authorMaluenda Razeto, Gabriel 
Authordc.contributor.authorThoenes, Martin 
Admission datedc.date.accessioned2018-05-23T13:30:33Z
Available datedc.date.available2018-05-23T13:30:33Z
Publication datedc.date.issued2017
Cita de ítemdc.identifier.citationJacc-Cardiovascular Interventions Vol.10 (13): 1357-1365es_ES
Identifierdc.identifier.other10.1016/j.jcin.2017.04.014
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/148050
Abstractdc.description.abstractOBJECTIVES The aim of this study was to compare aspirin plus clopidogrel with aspirin alone as antithrombotic treatment following transcatheter aortic valve replacement (TAVR) for the prevention of ischemic events, bleeding events, and death. BACKGROUND Few data exist on the optimal antithrombotic therapy following TAVR. METHODS This was a randomized controlled trial comparing aspirin (80 to 100 mg/day) plus clopidogrel (75 mg/day) (dual antiplatelet therapy [DAPT]) versus aspirin alone (single-antiplatelet therapy [SAPT]) in patients undergoing TAVR with a balloon-expandable valve. The primary endpoint was the occurrence of death, myocardial infarction (MI), stroke or transient ischemic attack, or major or life-threatening bleeding (according to Valve Academic Research Consortium 2 definitions) within the 3 months following the procedure. The trial was prematurely stopped after the inclusion of 74% of the planned study population. RESULTS A total of 222 patients were included, 111 allocated to DAPT and 111 to SAPT. The composite of death, MI, stroke or transient ischemic attack, or major or life-threatening bleeding tended to occur more frequently in the DAPT group (15.3% vs. 7.2%, p = 0.065). There were no differences between groups in the occurrence of death (DAPT, 6.3%; SAPT, 3.6%; p = 0.37), MI (DAPT, 3.6%; SAT, 0.9%; p = 0.18), or stroke or transient ischemic attack (DAPT, 2.7%; SAPT, 0.9%; p = 0.31) at 3 months. DAPT was associated with a higher rate of major or life-threatening bleeding events (10.8% vs. 3.6% in the SAPT group, p = 0.038). There were no differences between groups in valve hemodynamic status post-TAVR. CONCLUSIONS This small trial showed that SAPT (vs. DAPT) tended to reduce the occurrence of major adverse events following TAVR. SAPT reduced the risk for major or life-threatening events while not increasing the risk for MI or stroke. Larger studies are needed to confirm these results. (Aspirin Versus Aspirin + Clopidogrel Following Transcatheter Aortic Valve Implantation: The ARTE Trial [ARTE], NCT01559298; Aspirin Versus Aspirin + Clopidogrel as Antithrombotic Treatment Following TAVI [ARTE], NCT02640794) (C) 2017 by the American College of Cardiology Foundation.es_ES
Patrocinadordc.description.sponsorshipEdwards Lifesciences / Foundation of the Research Center of the Quebec Heart Lung Institute / AstraZeneca / Amgen Bayer / Janssen Bristol-Myers Squibb-Pfizer / Boehringer Ingelheimes_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherElsevieres_ES
Sourcedc.sourceJacc-Cardiovascular Interventionses_ES
Keywordsdc.subjectAortic stenosises_ES
Keywordsdc.subjectAspirines_ES
Keywordsdc.subjectBleedinges_ES
Keywordsdc.subjectClopidogreles_ES
Keywordsdc.subjectStrokees_ES
Keywordsdc.subjectTranscatheter aortic valve replacementes_ES
Títulodc.titleAspirin versus aspirin plus clopidogrel as antithrombotic treatment following transcatheter aortic valve replacement with a balloon-expandable valve the ARTE (aspirin versus aspirin plus clopidogrel following transcatheter aortic valve implantation) randomized clinical triales_ES
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso a solo metadatoses_ES
Catalogueruchile.catalogadortjnes_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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