Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22443
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dc.contributor.authorCamaj, Anton-
dc.contributor.authorClaessen, Bimmer E-
dc.contributor.authorMehran, Roxana-
dc.contributor.authorYudi, Matias B-
dc.contributor.authorPower, David-
dc.contributor.authorBaber, Usman-
dc.contributor.authorHengstenberg, Christian-
dc.contributor.authorLefevre, Thierry-
dc.contributor.authorVan Belle, Eric-
dc.contributor.authorGiustino, Gennaro-
dc.contributor.authorGuedeney, Paul-
dc.contributor.authorSorrentino, Sabato-
dc.contributor.authorKupatt, Christian-
dc.contributor.authorWebb, John G-
dc.contributor.authorHildick-Smith, David-
dc.contributor.authorHink, Hans U-
dc.contributor.authorDeliargyris, Efthymios N-
dc.contributor.authorAnthopoulos, Prodromos-
dc.contributor.authorSharma, Samin K-
dc.contributor.authorKini, Annapoorna-
dc.contributor.authorSartori, Samantha-
dc.contributor.authorChandrasekhar, Jaya-
dc.contributor.authorDangas, George D-
dc.date2020-01-13-
dc.date.accessioned2020-01-20T05:24:55Z-
dc.date.available2020-01-20T05:24:55Z-
dc.date.issued2020-12-
dc.identifier.citationCatheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions 2020; 96(7): E688-E694en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22443-
dc.description.abstractClinicians use validated scores to risk-stratify patients undergoing transcatheter aortic valve replacement (TAVR). However, evaluation by the Heart Team often deems patients to be at higher risk than their formal scores suggest. We sought to assess clinical outcomes of TAVR patients defined as high-risk by the Heart Team's assessment versus the patient's logistic EuroSCORE (LES). The BRAVO-3 trial randomized patients at high risk (LES ≥ 18, or deemed inoperable by the Heart Team) to TAVR with periprocedural anticoagulation with unfractionated heparin versus bivalirudin. Endpoints included net adverse cardiac events (NACE: the composite of all-cause mortality, MI, stroke, or bleeding), major adverse cardiovascular events (MACE: death, MI, or stroke), the individual components of MACE, major vascular complications, BARC ≥ 3b bleeding and VARC life-threatening bleeding at 30 days. We compared patients deemed high-risk based on LES ≥ 18 versus high-risk by the Heart Team despite lower LES. A total of 467/800 (58.4%) patients were deemed high-risk by the Heart Team despite LES < 18. After multivariable analysis, there were no differences in the odds of endpoints between groups (NACE, ORLES≥18 : 1.32, 95% CI 0.86-2.02, p = .21; MACE, ORLES≥18 : 1.27, 95% CI 0.72-2.25, p = .41; major vascular complications, ORLES≥18 : 0.97, 95% CI 0.65-1.44, p = .88; BARC ≥3b, ORLES≥18 : 1.38, 95% CI 0.82-2.33, p = .23; and VARC life-threatening bleeding, ORLES≥18 : 0.99, 95% CI 0.69-1.41, p = .95). Patients undergoing TAVR and labeled high-risk by LES ≥ 18 or Heart Team assessment despite LES < 18 have comparable short-term outcomes. Assignment of high-risk status to over 50% of patients is attributable to Heart Team's clinical assessment.en_US
dc.language.isoeng-
dc.subjectHeart Teamen_US
dc.subjectTAVRen_US
dc.subjectlogistic EuroSCOREen_US
dc.titleThe importance of the Heart Team evaluation before transcatheter aortic valve replacement: Results from the BRAVO-3 trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleCatheterization and Cardiovascular Interventions : official journal of the Society for Cardiac Angiography & Interventionsen_US
dc.identifier.affiliationThe Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New Yorken_US
dc.identifier.affiliationInstitut Cardio Vasculaire Paris Sud, Hôpital Privé Jacques Cartier, Massy, Franceen_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationSorbonne Université, ACTION Study Group, INSERM UMRS_1166 Institut de cardiologie (AP-HP), Paris, Franceen_US
dc.identifier.affiliationDepartment of Cardiology and INSERM UMR 1011, University Hospital, and CHRU Lille, Lille, Franceen_US
dc.identifier.affiliationThe Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New Yorken_US
dc.identifier.affiliationDZHK (German Centre for Cardiovascular Research), partner site Munich Heart Alliance, Munich, Germany, and Deutsches Herzzentrum München, Technische Universität München, Munich, Germanyen_US
dc.identifier.affiliationThe Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New Yorken_US
dc.identifier.affiliationDivision of Cardiology, Department of Medical and Surgical Sciences, Magna Graecia University, Catanzaro, Italyen_US
dc.identifier.affiliationLMU Munich, Munich, Germanyen_US
dc.identifier.affiliationSt. Paul's Hospital, Vancouver, British Columbia, Canadaen_US
dc.identifier.affiliationSussex Cardiac Centre-Brighton & Sussex University Hospitals NHS Trust, Brighton, East Sussex, UKen_US
dc.identifier.affiliationUniversitätsmedizin Mainz, Mainz, Germanyen_US
dc.identifier.affiliationScience and Strategy Consulting Group, Basking Ridge, New Jerseyen_US
dc.identifier.affiliationArena Pharmaceuticals, Inc., Zurich, Switzerlanden_US
dc.identifier.affiliationThe Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New Yorken_US
dc.identifier.doi10.1002/ccd.28717en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-2012-4137en_US
dc.identifier.orcid0000-0002-3706-4150en_US
dc.identifier.orcid0000-0002-1888-0793en_US
dc.identifier.orcid0000-0002-7189-3307en_US
dc.identifier.orcid0000-0001-7502-8049en_US
dc.identifier.orcid0000-0002-3706-4150en_US
dc.identifier.pubmedid31943717-
dc.type.austinJournal Article-
local.name.researcherYudi, Matias B
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptCardiology-
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