Skip navigation
  •  Home
  • UDC 
    • Getting started
    • RUC Policies
    • FAQ
    • FAQ on Copyright
    • More information at INFOguias UDC
  • Browse 
    • Communities
    • Browse by:
    • Issue Date
    • Author
    • Title
    • Subject
  • Help
    • español
    • Gallegan
    • English
  • Login
  •  English 
    • Español
    • Galego
    • English
  
View Item 
  •   DSpace Home
  • Facultade de Ciencias da Saúde
  • Investigación (FCS)
  • View Item
  •   DSpace Home
  • Facultade de Ciencias da Saúde
  • Investigación (FCS)
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

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

Thumbnail
View/Open
BargeCaballero_Syncope.pdf (271.1Kb)
Use this link to cite
http://hdl.handle.net/2183/30482
Collections
  • Investigación (FCS) [1293]
Metadata
Show full item record
Title
Syncope in patients with transthyretin amyloid cardiomyopathy: clinical features and outcomes
Author(s)
Barge-Caballero, Gonzalo
Barge-Caballero, Eduardo
López-Pérez, Manuel
Bilbao-Quesada, Raquel
González-Babarro, Eva
Gómez Otero, Inés
López-López, Andrea
Gutiérrez-Feijoo, Mario
Varela-Román, Alfonso
González-Juanatey, Carlos
Díaz-Castro, Óscar
Crespo-Leiro, María Generosa
Date
2022-03-23
Citation
Barge-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.
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.
Keywords
Syncope
Arrhythmia
Cardiac amyloidosis
Survival
Transthyretin
 
Editor version
https://doi.org/10.1080/00325481.2022.2054174
Rights
This is an Accepted Manuscript of an article published by Taylor & Francis in "Postgraduate Medicine", available at Taylor and Francis Online web page.
ISSN
0032-5481

Browse

All of DSpaceCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsResearch GroupAcademic DegreeThis CollectionBy Issue DateAuthorsTitlesSubjectsResearch GroupAcademic Degree

My Account

LoginRegister

Statistics

View Usage Statistics
Sherpa
OpenArchives
OAIster
Scholar Google
UNIVERSIDADE DA CORUÑA. Servizo de Biblioteca.    DSpace Software Copyright © 2002-2013 Duraspace - Send Feedback