Impact of anatomic closure on somatic growth among small, asymptomatic children with secundum atrial septal defect
E K Rhee1, J K Evangelista, D J Nigrin
1Department of Cardiology, Children's Hospital, Boston, MA 02115, USA.
Insights
Children with atrial septal defect (ASD) who were underweight or short showed improved growth after surgical repair. Early ASD repair is recommended for children with poor growth.
Area of Science:
- Pediatric Cardiology
- Growth and Development
- Congenital Heart Disease
Background:
- Children with isolated secundum atrial septal defect (ASD) often present with growth deficits.
- Preoperative growth parameters are crucial for assessing the impact of ASD on a child's development.
Purpose of the Study:
- To evaluate the effect of surgical repair of ASD on the growth of undersized children.
- To determine if early surgical intervention improves height and weight z scores in pediatric patients with ASD.
Main Methods:
- Retrospective analysis of 92 children aged ≤9 years with isolated ASD and preoperative low height or weight (z score ≤1.0).
- Comparison of growth improvement between low-weight/low-height groups and age-, gender-, and size-matched controls post-ASD repair.
- Univariate and multivariate analyses to assess factors influencing growth improvement.
Main Results:
- 50% of low-weight patients achieved a +0.5 SD weight improvement in 2.6 years vs. 5.6 years for controls (p=0.02).
- 50% of low-height patients achieved a +0.5 SD height improvement in 1.7 years vs. 11.6 years for controls (p<0.001).
- Repair offered significant benefits for height (RR 5.11) and weight (RR 2.35) improvement; older age and higher weight at repair were associated with less growth improvement.
Conclusions:
- Surgical repair of ASD significantly enhances growth in undersized children.
- Poor growth in children with ASD should be considered a relative indication for early surgical intervention.
Abstract:
We retrospectively identified 92 children aged =9 years with isolated secundum atrial septal defect (ASD) with preoperative height or weight z score < or =1.0 (16th percentile), respectively. Children with additional cardiac malformations, chromosomal abnormalities, recognized syndromes, pulmonary hypertension, heart failure, prematurity (<34 weeks' gestation), or use of cardiac medications were excluded from further analysis. After exclusion, 24 low-weight and 25 low-height children were compared with 48 and 50 age-, gender-, and size-matched normal controls, respectively. Univariate and multivariate analyses were performed separately for height and weight groups for achieving an end point of improvement in height or weight z score by +0.5 after repair. There were no significant preoperative demographic differences. After repair, 50% of low-weight patients improved +0.5 SD in weight within 2.6 years versus 5.6 years for controls (p = 0.02). Similarly, 50% of low-height patients improved +0.5 SD in height within 1.7 years versus 11.6 years for controls (p <0.001). Multivariate analysis also indicated a benefit of repair with relative risks of 2.35 (95% confidence interval 1.20 to 4.62; p = 0.01) and 5.11 (95% confidence interval 2.45 to 10.65; p <0.0001), respectively, for improving height or weight by +0.5 SD in patients with ASD relative to controls. Furthermore, children heavier at repair were less likely to improve in weight (relative risk 0.56 [0.34, 0.92] per 1.0 z [p = 0.02]). Likewise, children older at repair were less likely to improve in height (relative risk 0.77 [0.64, 0.92] per year of age [p = 0.003]). We conclude that undersized children with ASD exhibit improved growth after repair. Poor growth should be considered a relative indication for early ASD repair.


