Syncope in patients with transthyretin amyloid cardiomyopathy: clinical features and outcomes

UDC.coleccionInvestigaciónes_ES
UDC.grupoInvInsuficiencia Cardíaca Avanzada e Transplante Cardíaco (INIBIC)es_ES
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruñaes_ES
UDC.journalTitlePostgraduate Medicinees_ES
dc.contributor.authorBarge-Caballero, Gonzalo
dc.contributor.authorBarge-Caballero, Eduardo
dc.contributor.authorLópez-Pérez, Manuel
dc.contributor.authorBilbao-Quesada, Raquel
dc.contributor.authorGonzález-Babarro, Eva
dc.contributor.authorGómez Otero, Inés
dc.contributor.authorLópez-López, Andrea
dc.contributor.authorGutiérrez-Feijoo, Mario
dc.contributor.authorVarela-Román, Alfonso
dc.contributor.authorGonzález-Juanatey, Carlos
dc.contributor.authorDíaz-Castro, Óscar
dc.contributor.authorCrespo-Leiro, María Generosa
dc.date.accessioned2022-04-19T07:26:47Z
dc.date.embargoEndDate2023-03-23es_ES
dc.date.embargoLift2023-03-23
dc.date.issued2022-03-23
dc.description.abstract[Abstract] Background: We aimed to describe the clinical characteristics, underlying causes and outcomes of syncope in patients with transthyretin amyloid cardiomyopathy (ATTR-CM). Methods: The clinical profile and underlying causes of syncopal episodes were reviewed in a cohort of 128 patients with ATTR-CM enrolled from January 2018 to June 2020 in a prospective multicentre registry in 7 hospitals of Galicia (Spain). After enrollment, patients were followed during a median period of 520 days. The effect of syncope on all-cause mortality was assessed by means of multivariate Cox´s regression. Results: Thirty (23.4%) patients had a history of previous syncope as a clinical antecedent before being enrolled in the prospective phase of the registry, and 4 (3.1%) experienced a first episode of syncope thereafter. The estimated incidence density rate of syncope during the prospective follow-up period after registry enrollment was 71.9 episodes per 1000 patients-year (95% Confidence Interval (CI) 32.8-111.1). The estimated overall prevalence of syncope was 26.6% (95% CI 18.9%-34.2%). Cardiac arrhythmias (n = 11, 32.3%), structural diseases of the heart or great vessels (n = 5, 14.7%), a neurally mediated reflex (n = 6, 17.6%), and orthostatic hypotension (n = 4, 11.8%) were identified as probable underlying causes of syncope; in 8 (23.6%) patients, syncope remained unexplained. Patients with syncope had increased non-adjusted all-cause mortality than patients without it (univariate hazard-ratio 3.37; 95% CI 1.43-7.94). When other independent predictors of survival were added to the survival model, this association was no longer statistically significant (multivariate hazard-ratio 1.81, 95% CI 0.67-4.84). Conclusions: Syncope is frequent in patients with ATTR-CM. This study could not demonstrate an independent association between syncope and mortality in those individuals.Abbreviations: ATTR-CM: Transthyretin amyloid cardiomyopathy; CI: Confidence Interval; HF: Heart Failure; HR: Hazard Ratio; IQR: Interquartile rank; LVEF: Left Ventricular Ejection Fraction; NTproBNP: N-terminal pro-brain natriuretic peptide; SD: Standard Deviation; 99mTc-DPD: technetium-99m-labeled 3,3-diphosphono-1,2-propanodicarboxylic acid.es_ES
dc.identifier.citationBarge-Caballero G, Barge-Caballero E, López-Pérez M, Bilbao-Quesada R, González-Babarro E, Gómez-Otero I, López-López A, Gutiérrez-Feijoo M, Varela-Román A, González-Juanatey C, Díaz-Castro Ó, Crespo-Leiro MG. Syncope in patients with transthyretin amyloid cardiomyopathy: clinical features and outcomes. Postgrad Med. 2022 May;134(4):420-428.es_ES
dc.identifier.issn0032-5481
dc.identifier.urihttp://hdl.handle.net/2183/30482
dc.language.isoenges_ES
dc.publisherTaylor & Francises_ES
dc.relation.urihttps://doi.org/10.1080/00325481.2022.2054174es_ES
dc.rightsThis is an Accepted Manuscript of an article published by Taylor & Francis in "Postgraduate Medicine", available at Taylor and Francis Online web page.es_ES
dc.rights.accessRightsopen accesses_ES
dc.subjectSyncopees_ES
dc.subjectArrhythmiaes_ES
dc.subjectCardiac amyloidosises_ES
dc.subjectSurvivales_ES
dc.subjectTransthyretines_ES
dc.titleSyncope in patients with transthyretin amyloid cardiomyopathy: clinical features and outcomeses_ES
dc.typejournal articlees_ES
dspace.entity.typePublication
relation.isAuthorOfPublication36d178fd-10a0-48a2-925d-71d185a50eda
relation.isAuthorOfPublication.latestForDiscovery36d178fd-10a0-48a2-925d-71d185a50eda

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