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Published on: November 3, 2016
Severe Congenital Heart Defects and Cerebral Palsy
Ester Garne1, Shona Goldsmith2, Ingeborg Barisic3
1Department of Pediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
Insights
Children with severe congenital heart defects (sCHD) have a higher prevalence of cerebral palsy (CP). However, CP in these children tends to be milder than in those without congenital anomalies.
Area of Science:
- Pediatric Neurology
- Cardiology
- Developmental Pediatrics
Background:
- Cerebral palsy (CP) is a significant neurodevelopmental disorder.
- Severe congenital heart defects (sCHD) are a known risk factor for adverse neurodevelopmental outcomes.
- Understanding the interplay between sCHD and CP is crucial for early intervention and management.
Purpose of the Study:
- To determine the prevalence of cerebral palsy (CP) in children with severe congenital heart defects (sCHD).
- To describe the outcome and severity of CP in children with sCHD.
- To compare CP characteristics in children with and without sCHD.
Main Methods:
- A population-based data linkage study utilizing CP and congenital anomaly registers.
- Inclusion of data from 4 European and 2 Australian regions (1991-2009).
- Application of the EUROCAT definition for severe CHD (sCHD).
Main Results:
- The prevalence of CP was 2.9 per 1000 births; sCHD prevalence was 2.1 per 1000 births.
- 1.5% of children with sCHD also had CP (n=57).
- Children with CP and sCHD more frequently presented with unilateral spastic CP and intellectual impairments compared to children with CP alone.
Conclusions:
- The proportion of children with CP is significantly higher in those with sCHD compared to the general population.
- CP in children with sCHD appears to be milder in severity than in children with CP without congenital anomalies.
- This highlights the importance of neurodevelopmental surveillance in pediatric cardiology patients.
Objective:
To report the prevalence of cerebral palsy (CP) in children with severe congenital heart defects (sCHD) and the outcome/severity of the CP.
Methods:
Population-based, data linkage study between CP and congenital anomaly registers in Europe and Australia. The EUROCAT definition of severe CHD (sCHD) was used. Linked data from 4 regions in Europe and 2 in Australia were included. All children born in the regions from 1991 through 2009 diagnosed with CP and/or sCHD were included. Linkage was completed locally. Deidentified linked data were pooled for analyses.
Results:
The study sample included 4989 children with CP and 3684 children with sCHD. The total number of livebirths in the population was 1 734 612. The prevalence of CP was 2.9 per 1000 births (95% CI, 2.8-3.0) and the prevalence of sCHD was 2.1 per 1000 births (95% CI, 2.1-2.2). Of children with sCHD, 1.5% (n = 57) had a diagnosis of CP, of which 35 (61%) children had prenatally or perinatally acquired CP (resulting from a brain injury at ≤28 days of life) and 22 (39%) children had a postneonatal cause (a brain injury between 28 days and 2 years). Children with CP and sCHD more often had unilateral spastic CP and more intellectual impairments than children with CP without congenital anomalies.
Conclusions:
In high-income countries, the proportion of children with CP is much higher in children with sCHD than in the background population. The severity of disease in children with CP and sCHD is milder compared with children with CP without congenital anomalies.
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