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dc.contributor.authorNitsche, C
dc.contributor.authorScully, PR
dc.contributor.authorPatel, KP
dc.contributor.authorKammerlander, AA
dc.contributor.authorKoschutnik, M
dc.contributor.authorDona, C
dc.contributor.authorWollenweber, T
dc.contributor.authorAhmed, N
dc.contributor.authorThornton, GD
dc.contributor.authorKelion, AD
dc.contributor.authorSabharwal, N
dc.contributor.authorNewton, JD
dc.contributor.authorOzkor, M
dc.contributor.authorKennon, S
dc.contributor.authorMullen, M
dc.contributor.authorLloyd, G
dc.contributor.authorFontana, M
dc.contributor.authorHawkins, PN
dc.contributor.authorPugliese, F
dc.contributor.authorMenezes, LJ
dc.contributor.authorMoon, JC
dc.contributor.authorMascherbauer, J
dc.contributor.authorTreibel, TA
dc.date.accessioned2021-04-06T14:38:06Z
dc.date.available2020-11-04
dc.date.available2021-04-06T14:38:06Z
dc.date.issued2021-01-19
dc.identifier.citationristian Nitsche, Paul R. Scully, Kush P. Patel, Andreas A. Kammerlander, Matthias Koschutnik, Carolina Dona, Tim Wollenweber, Nida Ahmed, George D. Thornton, Andrew D. Kelion, Nikant Sabharwal, James D. Newton, Muhiddin Ozkor, Simon Kennon, Michael Mullen, Guy Lloyd, Marianna Fontana, Philip N. Hawkins, Francesca Pugliese, Leon J. Menezes, James C. Moon, Julia Mascherbauer, Thomas A. Treibel, Prevalence and Outcomes of Concomitant Aortic Stenosis and Cardiac Amyloidosis, Journal of the American College of Cardiology, Volume 77, Issue 2, 2021, Pages 128-139, https://doi.org/10.1016/j.jacc.2020.11.006.en_US
dc.identifier.issn0735-1097
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/71083
dc.description.abstractBACKGROUND: Older patients with severe aortic stenosis (AS) are increasingly identified as having cardiac amyloidosis (CA). It is unknown whether concomitant AS-CA has worse outcomes or results in futility of transcatheter aortic valve replacement (TAVR). OBJECTIVES: This study identified clinical characteristics and outcomes of AS-CA compared with lone AS. METHODS: Patients who were referred for TAVR at 3 international sites underwent blinded research core laboratory 99mtechnetium-3,3-diphosphono-1,2-propanodicarboxylic acid (DPD) bone scintigraphy (Perugini grade 0: negative; grades 1 to 3: increasingly positive) before intervention. Transthyretin-CA (ATTR) was diagnosed by DPD and absence of a clonal immunoglobulin, and light-chain CA (AL) was diagnosed via tissue biopsy. National registries captured all-cause mortality. RESULTS: A total of 407 patients (age 83.4 6.5 years; 49.8% men) were recruited. DPD was positive in 48 patients (11.8%; grade 1: 3.9% [n ¼ 16]; grade 2/3: 7.9% [n ¼ 32]). AL was diagnosed in 1 patient with grade 1. Patients with grade 2/3 had worse functional capacity, biomarkers (N-terminal pro-brain natriuretic peptide and/or high-sensitivity troponin T), and biventricular remodeling. A clinical score (RAISE) that used left ventricular remodeling (hypertrophy/diastolic dysfunction), age, injury (high-sensitivity troponin T), systemic involvement, and electrical abnormalities (right bundle branch block/low voltages) was developed to predict the presence of AS-CA (area under the curve: 0.86; 95% confidence interval: 0.78 to 0.94; p < 0.001). Decisions by the heart team (DPD-blinded) resulted in TAVR (333 [81.6%]), surgical AVR (10 [2.5%]), or medical management (65 [15.9%]). After a median of 1.7 years, 23% of patients died. One-year mortality was worse in all patients with AS-CA (grade: 1 to 3) than those with lone AS (24.5% vs. 13.9%; p ¼ 0.05). TAVR improved survival versus medical management; AS-CA survival post-TAVR did not differ from lone AS (p ¼ 0.36). CONCLUSIONS: Concomitant pathology of AS-CA is common in older patients with AS and can be predicted clinically. AS-CA has worse clinical presentation and a trend toward worse prognosis, unless treated. Therefore, TAVR should not be withheld in AS-CA. (J Am Coll Cardiol 2021;77:128–39) © 2021 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.format.extent128 - 139
dc.relation.ispartofJOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
dc.rightsCC BY-NC-ND LICENSE
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectaortic stenosisen_US
dc.subjectcardiac amyloidosisen_US
dc.subjectTAVRen_US
dc.titlePrevalence and Outcomes of Concomitant Aortic Stenosis and Cardiac Amyloidosisen_US
dc.typeArticleen_US
dc.rights.holder© 2021 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.
dc.identifier.doi10.1016/j.jacc.2020.11.006
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000608973900003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue2en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume77en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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