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Updated: Aug 11, 2026

Murine Fetal Echocardiography
Published on: February 15, 2013
Natural history of isolated ventricular septal defect in the first five years of life
Insights
Most isolated ventricular septal defects (VSD) close spontaneously by age five. Muscular VSDs have better outcomes than perimembranous VSDs, though some require long-term follow-up.
Area of Science:
- Pediatric Cardiology
- Congenital Heart Disease Research
- Echocardiography in Pediatric Cardiology
Background:
- Isolated ventricular septal defect (VSD) is the most common congenital heart defect.
- VSD incidence, prevalence, and outcomes vary geographically.
- Spontaneous VSD closure in children has been documented.
Purpose of the Study:
- To evaluate the natural history of isolated VSD in children during their first five years of life.
- To assess VSD outcomes in the Northeast Tennessee and Southwest Virginia region.
Main Methods:
- Prospective study of 124 infants diagnosed with isolated VSD between December 1998 and October 1990.
- VSD classification using 2D echocardiogram with color flow mapping (muscular, perimembranous, malalignment, subpulmonic).
- Follow-up for at least five years, with cardiac catheterization and angiocardiography for 14 patients.
Main Results:
- Overall VSD spontaneous closure rates were 34% at one year and 67% at five years.
- Muscular VSDs closed spontaneously at twice the rate of perimembranous VSDs.
- Surgery was required for 25% of perimembranous VSDs and 4% of muscular VSDs by age five; 22% of children required follow-up beyond five years.
Conclusions:
- Muscular VSDs demonstrated better clinical outcomes compared to perimembranous VSDs.
- Despite better outcomes, 17% of muscular VSDs remained open at age five, necessitating long-term follow-up.
Background:
Isolated ventricular septal defect (VSD) is the most common congenital heart defect. Incidence, prevalence, and clinical outcomes of VSD have been reported to vary significantly in different geographic areas. Spontaneous closure of VSD, in children, by various methods has been described.
Hypothesis:
This prospective study was undertaken to evaluate natural history of patients with VSD in the first five years of life in the Northeast Tennessee and Southwest Virginia region.
Methods:
Between December 1, 1998 and October 31, 1990, 124 infants were diagnosed clinically with isolated VSD. VSDs were classified as muscular, perimembranous, malalignment, or subpulmonic types by 2-dimensional echocardiogram with color flow mapping. Cardiac catheterization and angiocardiography were performed in 14 patients when clinically indicated. These patients were followed for at least five years.
Results:
Overall spontaneous closure of VSD was 34% at one year and 67% at five years. Twenty-five percent of perimembranous and 4% of muscular VSDs required surgery by five years. The spontaneous closure rate of muscular VSD was twice that of the perimembranous type, though the relative distribution of both types was almost equal. Overall, 22% of children with VSD need follow-up after the fifth year of life.
Conclusion:
The overall clinical outcome of muscular VSD was consistently better than that of the perimembranous type, though 17% of muscular VSDs, irrespective of size, were open at 5 years of age and needed long-term follow-up.
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