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Frequency of cardiac death in children with idiopathic dilated cardiomyopathy
V Vivian Dimas1, Susan W Denfield, Richard A Friedman
1Department of Pediatrics, Division of Cardiology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Insights
Idiopathic dilated cardiomyopathy (IDC) in children has a poor prognosis. However, sudden cardiac death (SCD) is rare in pediatric IDC patients, suggesting implantable cardioverter-defibrillators may not be needed for primary prevention.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Research
- Clinical Pediatrics
Background:
- Idiopathic dilated cardiomyopathy (IDC) in children carries a guarded prognosis with significant mortality.
- Risk factors for sudden cardiac death (SCD) in adult IDC, such as ventricular tachycardia and poor left ventricular function, are not well-established in pediatric populations.
Purpose of the Study:
- To investigate the incidence of SCD and identify risk factors in children diagnosed with IDC.
- To evaluate the potential role of implantable cardioverter-defibrillators (ICDs) for primary prevention in this cohort.
Main Methods:
- A retrospective review of 85 pediatric patients diagnosed with IDC between 1990 and 2004.
- Analysis of patient demographics, left ventricular ejection fraction, and occurrence of arrhythmias at presentation and during follow-up.
- Assessment of cumulative survival rates and incidence of SCD.
Main Results:
- The study included 85 children with a median age of 3.8 years and a mean ejection fraction of 25%.
- Arrhythmias, including nonsustained ventricular tachycardia, were observed, but only one episode of SCD occurred during a mean follow-up of 6.2 years.
- The cumulative survival rate was 40%.
Conclusions:
- Despite low ejection fraction and ventricular arrhythmias, SCD is infrequent in pediatric IDC.
- The low incidence of SCD (1%) suggests that routine primary prevention with ICDs may not be indicated in children with IDC.
Abstract:
The prognosis in children with idiopathic dilated cardiomyopathy (IDC) is guarded, with the 5-year mortality rate ranging from 14% to 50%, owing to sudden cardiac death (SCD) or pump failure. The risk factors for SCD in adults with IDC include asymptomatic nonsustained ventricular tachycardia and poor left ventricular function. It is unclear whether these findings can be extrapolated to the pediatric population. A retrospective review of all patients with the diagnosis of IDC seen at a single institution from 1990 to 2004 was performed. A total of 85 patients (46 males), with a median age of 3.8 years (0 days to 17.3 years) were studied. The mean left ventricular ejection fraction was 25 +/- 12% (median 23%, range 45% to 45%) at presentation. The following arrhythmias occurred at presentation or during the initial hospitalization: nonsustained ventricular tachycardia in 6, sustained ventricular tachycardia or fibrillation in 1, supraventricular arrhythmias in 6, and both atrial and ventricular arrhythmias in 1. During a subsequent hospitalization or outpatient follow-up, 7 patients had the following arrhythmias: supraventricular arrhythmias in 2, nonsustained ventricular tachycardia in 4, and both atrial and ventricular arrhythmias in 1. The cumulative survival rate was 40% at a mean follow-up of 6.2 years (95% confidence interval 4.4 to 8.1). One single episode of SCD occurred in 1 patient without a history of sustained arrhythmias. In conclusion, in children with IDC, despite the low left ventricular ejection fraction and presence of ventricular arrhythmias, only one episode of SCD occurred in this group of patients. Given the 1% incidence of SCD in this cohort, the use of implantable cardioverter-defibrillators as primary prevention in children with IDC might not be indicated.
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