Back to Search
Start Over
Recovery of echocardiographic function in children with idiopathic dilated cardiomyopathy: results from the pediatric cardiomyopathy registry.
- Source :
-
Journal of the American College of Cardiology [J Am Coll Cardiol] 2014 Apr 15; Vol. 63 (14), pp. 1405-13. Date of Electronic Publication: 2014 Feb 19. - Publication Year :
- 2014
-
Abstract
- Objectives: This study sought to determine the incidence and predictors of recovery of normal echocardiographic function among children with idiopathic dilated cardiomyopathy (DCM).<br />Background: Most children with idiopathic DCM have poor outcomes; however, some improve.<br />Methods: We studied children <18 years of age from the Pediatric Cardiomyopathy Registry who had both depressed left ventricular (LV) function (fractional shortening or ejection fraction z-score <-2) and LV dilation (end-diastolic dimension [LVEDD] z-score >2) at diagnosis and who had at least 1 follow-up echocardiogram 30 days to 2 years from the initial echocardiogram. We estimated the cumulative incidence and predictors of normalization.<br />Results: Among 868 children who met the inclusion criteria, 741 (85%) had both echocardiograms. At 2 years, 22% had recovered normal LV function and size; 51% had died or undergone heart transplantation (median, 3.2 months), and 27% had persistently abnormal echocardiograms. Younger age (hazard ratio [HR]: 0.92; 95% confidence interval [CI]: 0.88 to 0.97) and lower LVEDD z-score (HR: 0.78; 95% CI: 0.70 to 0.87) independently predicted normalization. Nine children (9%) with normal LV function and size within 2 years of diagnosis later underwent heart transplantation or died.<br />Conclusions: Despite marked LV dilation and depressed function initially, children with idiopathic DCM can recover normal LV size and function, particularly those younger and with less LV dilation at diagnosis. Investigations related to predictors of recovery, such as genetic associations, serum markers, and the impact of medical therapy or ventricular unloading with assist devices are important next steps. Longer follow-up after normalization is warranted as cardiac failure can recur. (Pediatric Cardiomyopathy Registry; NCT00005391).<br /> (Copyright © 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Adolescent
Age Distribution
Cardiomyopathy, Dilated congenital
Cardiomyopathy, Dilated therapy
Child
Child, Preschool
Female
Follow-Up Studies
Humans
Incidence
Infant
Male
Recovery of Function
Retrospective Studies
Risk Assessment
Severity of Illness Index
Sex Distribution
Stroke Volume
Survival Rate
Time Factors
Treatment Outcome
Ventricular Dysfunction, Left mortality
Ventricular Dysfunction, Left physiopathology
Cardiomyopathy, Dilated diagnostic imaging
Cardiomyopathy, Dilated epidemiology
Echocardiography, Doppler
Registries
Ventricular Dysfunction, Left diagnostic imaging
Ventricular Remodeling physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1558-3597
- Volume :
- 63
- Issue :
- 14
- Database :
- MEDLINE
- Journal :
- Journal of the American College of Cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 24561146
- Full Text :
- https://doi.org/10.1016/j.jacc.2013.11.059