Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/39435
Title: Electrical Dyssynchrony in Cardiac Amyloidosis: Prevalence, Predictors, Clinical Correlates, and Outcomes
Authors: MARTENS, Pieter 
Hanna, Mazen
Valent, Jason
MULLENS, Wilfried 
Ives, Lauren
Kwon, Debbie H.
Rickard, John
Tang, W. H. Wilson
Issue Date: 2022
Publisher: CHURCHILL LIVINGSTONE INC MEDICAL PUBLISHERS
Source: Journal of Cardiac Failure, 28 (12) , p. 1664 -1672
Abstract: Background: 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)
Notes: Martens, 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.
pieter_martens@icloud.com
Keywords: Cardiac amyloidosis;Cardiac amyloidosis;electrical dyssynchrony;electrical dyssynchrony;disease severity;disease severity;natural history;natural history
Document URI: http://hdl.handle.net/1942/39435
ISSN: 1071-9164
e-ISSN: 1532-8414
DOI: 10.1016/j.cardfail.2022.07.046
ISI #: 000905073900004
Rights: 2022 Elsevier Inc. All rights reserved
Category: A1
Type: Journal Contribution
Validations: ecoom 2024
Appears in Collections:Research publications

Files in This Item:
File Description SizeFormat 
Electrical Dyssynchrony in Cardiac Amyloidosis_ Prevalence, Predictors, Clinical Correlates, and Outcomes.pdf
  Restricted Access
Published version789.47 kBAdobe PDFView/Open    Request a copy
Show full item record

SCOPUSTM   
Citations

10
checked on Jul 2, 2026

WEB OF SCIENCETM
Citations

10
checked on Jul 8, 2026

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.