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Updated: Mar 2, 2026

Magnetic Resonance Derived Myocardial Strain Assessment Using Feature Tracking
Published on: February 12, 2011
Distribution of strain patterns in children with dilated cardiomyopathy
Susanna L den Boer1, Gideon J du Marchie Sarvaas2, Liselotte M Klitsie3
1Departments of Pediatrics, Division of Pediatric Cardiology, Sophia Children's Hospital, Erasmus University Medical Center, Rotterdam, The Netherlands.
Insights
Quantitative and qualitative dyssynchrony parameters assessed by two-dimensional speckle tracking echocardiography (STE) are not reproducible in children with dilated cardiomyopathy (DCM). Reduced strain, not dyssynchrony, was the main finding, suggesting dyssynchrony is a minor issue in pediatric DCM.
Area of Science:
- Pediatric cardiology
- Cardiovascular imaging
- Echocardiography
Background:
- Dyssynchrony parameters predict outcomes in adult heart failure.
- Limited data exists on dyssynchrony in pediatric dilated cardiomyopathy (DCM).
Purpose of the Study:
- Evaluate predictive value of quantitative and qualitative dyssynchrony parameters using STE in pediatric DCM.
- Assess reproducibility of these STE-derived parameters in children.
Main Methods:
- Prospective, multicenter study of 75 children with DCM and 75 controls.
- Two-dimensional speckle tracking echocardiography (STE) assessed quantitative and qualitative dyssynchrony.
- Cox regression identified risk factors for death or heart transplantation.
Main Results:
- 13% of patients reached endpoint during 21-month follow-up.
- Quantitative dyssynchrony measures were higher in DCM patients but had high variability.
- Qualitative analysis revealed reduced strain, not dyssynchronous patterns.
Conclusions:
- Quantitative dyssynchrony parameters lack reproducibility in children, limiting clinical use.
- Qualitative analysis suggests reduced strain, not dyssynchrony, is characteristic of pediatric DCM.
- Dyssynchrony appears to be a minor problem in children with DCM.
Objectives:
This study aimed to evaluate the predicting value of quantitative and qualitative dyssynchrony parameters as assessed by two-dimensional speckle tracking echocardiography (STE) on outcome in children with dilated cardiomyopathy (DCM). Furthermore, the reproducibility of these parameters was investigated.
Background:
In previous studies in adults with heart failure, several dyssynchrony parameters have been shown to be a valuable predictor of clinical outcome.
Methods:
This multicenter, prospective study included 75 children with DCM and 75 healthy age-matched controls. Using STE, quantitative (time to global peak strain and parameters describing intraventricular time differences) and qualitative dyssynchrony parameters (pattern analysis) of the apical four-chamber, three-chamber, two-chamber views, and the short axis of the left ventricle were assessed. Cox regression was used to identify risk factors for the primary endpoints of death or heart transplantation. Inter-observer and intra-observer variability were described.
Results:
During a median of 21 months follow-up, 10 patients (13%) reached an endpoint. Although quantitative dyssynchrony measures were higher in patients as compared to controls, the inter-observer and intra-observer variability were high. Pattern analysis showed mainly reduced strain, instead of dyssynchronous patterns.
Conclusions:
In this study, quantitative dyssynchrony parameters were not reproducible, precluding their use in children. Qualitative pattern analysis showed predominantly reduced strain, suggesting that in children with DCM dyssynchrony may be a minor problem.
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