# Neurodevelopmental outcomes in preschool children with congenital heart defects: A case-control study using Ages & Stages Questionnaire

**Authors:** Simone Hansen, Cathrine Vedel, Jesper Steensberg, Gorm Greisen, Line Rode, Charlotte Kvist Ekelund, Niels Vejlstrup, Karin Sundberg, Olav Bjørn Petersen, Ditte S. Jørgensen, Hany Abo-Haded, Hany Abo-Haded, Hany Abo-Haded

PMC · DOI: 10.1371/journal.pone.0341135 · PLOS One · 2026-03-25

## TL;DR

Preschool children with congenital heart defects had similar overall development scores to healthy children but were more likely to have low scores, especially if their condition was undetected before birth.

## Contribution

Identified increased odds of low neurodevelopmental scores in children with prenatally undetected VSD and TGA.

## Key findings

- Children with CHD had five-fold higher odds of low ASQ scores compared to controls.
- Prenatally undetected VSD was primarily responsible for the increased risk of low scores.
- ASQ scores were lower in TGA cases, especially when undetected prenatally, though not statistically significant.

## Abstract

To investigate neurodevelopmental outcome in preschool children with a CHD (congenital heart defect) requiring surgery compared to healthy controls.

This study includes all Danish children born between 2016–2018 who underwent surgery within the first year for Ventricular Septal Defect (VSD), atrioventricular septal defect, coarctation of the aorta, double outlet right ventricle, tetralogy of fallot, and Transposition of the Great Arteries (TGA). Exclusion criteria: preterm birth (<37 weeks), twins, and genetic aberrations. Cases were matched with two to four healthy controls on age, sex, gestational age at delivery, and region of birth. Neurodevelopmental outcome at 33–60-months was assessed by the Ages & Stages Questionnaire (ASQ). Comparisons were performed by the Mann-Whitney U test and logistic regression analysis and presented as p-values and odds ratios (OR) with 95% confidence intervals (CI).

There were no differences in ASQ score between 105 cases with any CHD (230 (IQR 195–260)) and 179 controls (235 (IQR 205–265)), p = 0.12. Cases had five-fold increased odds of a low score compared to controls after adjusting for maternal educational level and children’s age at ASQ completion (OR 5.02, 95% CI 1.49;16.90). This was primarily driven by cases with prenatally undetected VSD, where 20% scored below −2 standard deviations. No differences were found across individual CHD subgroups. In cases with prenatally undetected TGA, the total ASQ score was 185 (IQR 145–190) compared to 220 (IQR 190–270) in prenatally detected TGA, p = 0.08.

The overall ASQ score in children with surgically corrected CHD was comparable to controls. However, cases had five-fold increased odds of a low score, primarily driven by children with prenatally undetected VSD. Additionally, ASQ scores were lower in TGA cases, especially when undetected prenatally, though not significant. These findings suggest follow-up of all children with a CHD requiring surgery including awareness of potential developmental delays.

## Linked entities

- **Diseases:** congenital heart defect (MONDO:0005453), Ventricular Septal Defect (MONDO:0002070), atrioventricular septal defect (MONDO:0020290), coarctation of the aorta (MONDO:0007345), double outlet right ventricle (MONDO:0018089), tetralogy of fallot (MONDO:0008542), Transposition of the Great Arteries (MONDO:0000153)

## Full-text entities

- **Diseases:** AVSD (MESH:C562831), TGA (MESH:D014188), malformations (MESH:C564254), DORV (MESH:D004310), perimembranous defects (MESH:D000013), genetic (MESH:D030342), abnormal cerebral perfusion (MESH:D014402), VSD (MESH:D006345), Congenital Heart Defects (MESH:D006330), chromosomal abnormalities (MESH:D002869), CoA (MESH:D001017), mental health disorders (OMIM:603663), neurodevelopmental delay (MESH:D006968), DFMD (MESH:D005315), aneuploidies (MESH:D000782), neurodevelopmental (MESH:D008607), adverse neurodevelopment (MESH:D064420), HLHS (MESH:D018636), congenital malformations (OMIM:163000), developmental delays (MESH:D002658), Tetralogy of Fallot (MESH:D013771), UVH (MESH:D000080039), death (MESH:D003643), brain injury (MESH:D001930), preterm birth (MESH:D047928)
- **Chemicals:** PONE-D-25-33159R1 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC13016293/full.md

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Source: https://tomesphere.com/paper/PMC13016293