Literature DB >> 29154821

Heterotaxy syndrome and associated arrhythmias in pediatric patients.

Mary C Niu1, Heather A Dickerson2, Judson A Moore3, Caridad de la Uz2, Santiago O Valdés2, Jeffrey J Kim2, David E Bard4, Shaine A Morris2, Christina Y Miyake2.   

Abstract

BACKGROUND: Heterotaxy syndrome (HS) is a rare disorder with complex anatomy involving misarrangements of the cardiac conduction system. Arrhythmias may be related to anatomic variations and contribute to morbidity.
OBJECTIVE: The purpose of this study was to investigate the associations between arrhythmias, anatomy, and outcomes in a large HS cohort.
METHODS: A single-center retrospective review of patients ≤21 years of age diagnosed with HS was performed.
RESULTS: A total of 337 patients were included in the study. During median follow-up of 7 years (interquartile range 2-16 years), 129 patients (38%) had ≥1 clinically significant rhythm disturbance: tachyarrhythmias in 75 (22%), bradyarrhythmias in 29 (9%), and both in 25 (7%). Factors associated with tachyarrhythmia by multivariate analysis were at least moderate atrioventricular valve regurgitation (hazard ratio [HR] 1.66; 95% confidence interval [CI] 1.11-2.50), single ventricle anatomy (HR 2.30; 95% CI 1.09-4.85), and pulmonary venous obstruction (HR 2.33; 95% CI 1.45-3.76). Isomerism subtype was not associated with tachyarrhythmias. In adjusted and unadjusted analyses, bradyarrhythmias (symptomatic sinus/atrial bradycardia and high-grade or complete heart block) were associated with left atrial isomerism (LAI) compared to right atrial isomerism (HR 7.12; 95% CI 3.01-16.9). The overall transplant-free survival of the cohort was 66%. Tachyarrhythmias, but not bradyarrhythmias, were associated with mortality or need for transplant (HR 2.24; 95% CI 1.45-3.46).
CONCLUSION: Clinically significant arrhythmias are common in HS. Although bradyarrhythmias are associated with LAI, tachyarrhythmia occurrence may depend more on hemodynamic and anatomic factors than isomerism subtype. Tachyarrhythmias, but not bradyarrhythmias, are associated with death or need for transplant.
Copyright © 2017 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Arrhythmia; Congenital heart defects; Heart block; Heterotaxy; Outcome

Mesh:

Year:  2017        PMID: 29154821     DOI: 10.1016/j.hrthm.2017.11.013

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  3 in total

1.  Bradyarrhythmias in Repaired Atrioventricular Septal Defects: Single-Center Experience Based on 34 Years of Follow-Up of 522 Patients.

Authors:  Corrado Di Mambro; Camilla Calvieri; Massimo Stefano Silvetti; Ilaria Tamburri; Salvatore Giannico; Anwar Baban; Sonia Albanese; Gianluca Brancaccio; Adriano Carotti; Fiore Salvatore Iorio; Fabrizio Drago
Journal:  Pediatr Cardiol       Date:  2018-06-13       Impact factor: 1.655

2.  Incidental Finding of Heterotaxy Syndrome in a Patient With Pulmonary Embolism: A Case Report and Concise Review.

Authors:  Mohamed Mahmoud; Khadija El Kortbi; Hayoung Wang; Joseph Wang
Journal:  Cureus       Date:  2022-04-20

3.  Predictors and outcomes of heart block during surgical stage I palliation of patients with a single ventricle: A report from the NPC-QIC.

Authors:  Richard J Czosek; Jeffrey B Anderson; Shankar Baskar; Philip R Khoury; Natalie Jayaram; David S Spar
Journal:  Heart Rhythm       Date:  2021-05-21       Impact factor: 6.343

  3 in total

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