Abstract
Background Children born extremely preterm are at high risk for intellectual disability, learning disabilities, executive dysfunction and special educational needs, but little is understood about the comorbidity of intellectual and learning disabilities in this population. Aims This study explored comorbidity in intellectual disability (ID) and learning disabilities (LD) in children born extremely preterm (EP; < 26+ 0 weeks’ gestation). Subjects and study design A UK national cohort of 161 EP children and 153 term-born controls without neurosensory impairments was assessed at 11 years of age (the EPICure Study). Outcome measures IQ, mathematics and reading attainment, executive function, visuospatial processing and sensorimotor skills were assessed using standardised tests, and curriculum-based attainment and special educational needs (SEN) using teacher reports. Results Overall, 75 (47%) EP children and 7 (4.6%) controls had ID or LD (RR 10.12; 95% CI 4.81, 21.27). Comorbidity in ID/LD was more common among EP children than controls (24% vs. 0%). EP children with comorbid ID/LD had significantly poorer neuropsychological abilities and curriculum-based attainment than EP children with an isolated disability or no disabilities. LD were associated with a 3 times increased risk for SEN. However, EP children with ID alone had poorer neuropsychological abilities and curriculum-based attainment than children with no disabilities, yet there was no increase in SEN provision among this group. Conclusions EP children are at high risk for comorbid intellectual and learning disabilities. Education professionals should be aware of the complex nature of EP children's difficulties and the need for multi-domain assessments to guide intervention.
Originalsprog | Engelsk |
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Tidsskrift | Early Human Development |
Vol/bind | 103 |
Sider (fra-til) | 69-75 |
Antal sider | 7 |
ISSN | 0378-3782 |
DOI | |
Status | Udgivet - 1 dec. 2016 |
Udgivet eksternt | Ja |
Bibliografisk note
Funding Information:The EPICure Studies were funded by the Medical Research Council (MRC) UK and the work conducted for this manuscript was supported by a project grant from The Nuffield Foundation ( EDU/40442 ). Neil Marlow receives a proportion of funding from the Department of Health’s NIHR Biomedical Research Centres funding scheme at UCLH/UCL. Dr Gilmore is supported by a Royal Society Dorothy Hodgkin Fellowship .
Publisher Copyright:
© 2016 Elsevier Ireland Ltd