Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/39435
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dc.contributor.authorMARTENS, Pieter-
dc.contributor.authorHanna, Mazen-
dc.contributor.authorValent, Jason-
dc.contributor.authorMULLENS, Wilfried-
dc.contributor.authorIves, Lauren-
dc.contributor.authorKwon, Debbie H.-
dc.contributor.authorRickard, John-
dc.contributor.authorTang, W. H. Wilson-
dc.date.accessioned2023-02-15T09:49:04Z-
dc.date.available2023-02-15T09:49:04Z-
dc.date.issued2022-
dc.date.submitted2023-02-13T13:36:35Z-
dc.identifier.citationJournal of Cardiac Failure, 28 (12) , p. 1664 -1672-
dc.identifier.urihttp://hdl.handle.net/1942/39435-
dc.description.abstractBackground: Conduction-system involvement in cardiac amyloidosis (CA) is common. The prevalence, clinical correlates and impact on outcome related to ventricular electrical dyssynchrony in CA remain insufficiently elucidated. Methods: Data from a prospectively maintained registry of patients with CA diagnosed in the Cleveland Clinic's amyloidosis clinic was used to determine the frequency of electrical dyssynchrony (defined as a QRS > 130 msec). The relation with the clinical profile and clinical outcome was assessed. To determine the impact of hypertrophy on QRS prolongation, a QRSmatched cohort without CA was used for comparison of cardiac magnetic resonance imaging. Results: A total of 1140 patients with CA (39% AL, 61% TTR) were evaluated, of whom 230 (20%) had electrical dyssynchrony. The type of conduction block was predominantly a right bundle branch block (BBB, 48%) followed by left BBB (35%) and intraventricular conduction delay (17%). Presence of transthyretin amyloidosis (ATTR-CA), older age, male gender, white race, and coronary artery disease were independently (P< 0.05 for all) associated with electrical dyssynchrony, and patients were more commonly prescribed a mineralocorticoid receptor antagonist. In ATTR-CA, specifically, every increase in ATTR-CA disease stage was associated with a 1.55-fold (1.23-1.95; P< 0.001) increased odds for electrical dyssynchrony. In a subset of patients with CA who underwent cardiac magnetic resonance imaging (n = 41), left ventricular mass index was unrelated to the QRS duration (r = 0.187; P = 0.283) in CA, in contrast to a nonCA QRS-matched cohort (r = 0.397; P< 0.001). Patients with electrical dyssynchrony were more symptomatic at initial presentation, as illustrated by a higher New York Heart Association class (P= 0.041). During a median follow-up of 462 days (IQR:138-996 days), a higher proportion of patients with electrical dyssynchrony died from all-cause death (P= 0.037) or developed a permanent pacing indication (3% vs 10.4%; P< 0.001) during follow-up. Conclusion: Electrical dyssynchrony is common in CA, especially in ATTR-CA, and is associated with worse functional status and clinical outcome. Given the high rate of permanent pacing indications at follow-up, additional studies are necessary to determine the best monitoring and pacing strategies in CA. (J Cardiac Fail 2022;28:1664-1672)-
dc.description.sponsorshipThe Cleveland Clinic Amyloidosis Registry is supported by Dr. Hanna’s Term Chair for Amyloid Heart Disease. Dr. Pieter Martens is supported by a grant from the Belgian American Educational Foundation and by the Frans Van de Werf Fund.-
dc.language.isoen-
dc.publisherCHURCHILL LIVINGSTONE INC MEDICAL PUBLISHERS-
dc.rights2022 Elsevier Inc. All rights reserved-
dc.subject.otherCardiac amyloidosis-
dc.subject.otherCardiac amyloidosis-
dc.subject.otherelectrical dyssynchrony-
dc.subject.otherelectrical dyssynchrony-
dc.subject.otherdisease severity-
dc.subject.otherdisease severity-
dc.subject.othernatural history-
dc.subject.othernatural history-
dc.titleElectrical Dyssynchrony in Cardiac Amyloidosis: Prevalence, Predictors, Clinical Correlates, and Outcomes-
dc.typeJournal Contribution-
dc.identifier.epage1672-
dc.identifier.issue12-
dc.identifier.spage1664-
dc.identifier.volume28-
local.format.pages9-
local.bibliographicCitation.jcatA1-
dc.description.notesMartens, P (corresponding author), Cleveland Clin, Heart Vasc & Thorac Inst, Dept Cardiovasc Med, Cleveland, OH 44195 USA.; Martens, P (corresponding author), Ziekenhuis Oost Limburg, Dept Cardiol, Genk, Belgium.; Martens, P (corresponding author), Univ Hasselt, Hasselt, Belgium.-
dc.description.notespieter_martens@icloud.com-
local.publisher.placeCURTIS CENTER, INDEPENDENCE SQUARE WEST, PHILADELPHIA, PA 19106-3399 USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1016/j.cardfail.2022.07.046-
dc.identifier.pmid35882259-
dc.identifier.isi000905073900004-
dc.contributor.orcidMartens, Pieter/0000-0002-6036-2113-
local.provider.typewosris-
local.description.affiliation[Martens, Pieter; Hanna, Mazen; Ives, Lauren; Kwon, Debbie H.; Rickard, John; Tang, W. H. Wilson] Cleveland Clin, Heart Vasc & Thorac Inst, Dept Cardiovasc Med, Cleveland, OH 44195 USA.-
local.description.affiliation[Martens, Pieter; Mullens, Wilfried] Ziekenhuis Oost Limburg, Dept Cardiol, Genk, Belgium.-
local.description.affiliation[Martens, Pieter; Mullens, Wilfried] Univ Hasselt, Hasselt, Belgium.-
local.description.affiliation[Valent, Jason] Cleveland Clin, Taussig Canc Inst, Dept Hematol & Med Oncol, Cleveland, OH USA.-
local.uhasselt.internationalyes-
item.fulltextWith Fulltext-
item.accessRightsRestricted Access-
item.validationecoom 2024-
item.fullcitationMARTENS, Pieter; Hanna, Mazen; Valent, Jason; MULLENS, Wilfried; Ives, Lauren; Kwon, Debbie H.; Rickard, John & Tang, W. H. Wilson (2022) Electrical Dyssynchrony in Cardiac Amyloidosis: Prevalence, Predictors, Clinical Correlates, and Outcomes. In: Journal of Cardiac Failure, 28 (12) , p. 1664 -1672.-
item.contributorMARTENS, Pieter-
item.contributorHanna, Mazen-
item.contributorValent, Jason-
item.contributorMULLENS, Wilfried-
item.contributorIves, Lauren-
item.contributorKwon, Debbie H.-
item.contributorRickard, John-
item.contributorTang, W. H. Wilson-
crisitem.journal.issn1071-9164-
crisitem.journal.eissn1532-8414-
Appears in Collections:Research publications
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