The use of parent‐completed questionnaires to investigate developmental outcomes in large populations of children exposed to antiseizure medications in pregnancy

Author:

Bluett‐Duncan Matthew1ORCID,Bullen Philip2,Campbell Ellen3,Clayton‐Smith Jill45,Craig John3,García‐Fiñana Marta6,Hughes David M.6,Ingham Amy4,Irwin Beth3,Jackson Cerian7,Kelly Teresa2,Morrow James3,Rushton Sarah4,Winterbottom Janine8,Wood Amanda G.9,Yates Laura M.10,Bromley Rebecca L.111ORCID

Affiliation:

1. Division of Neuroscience University of Manchester Manchester UK

2. Department of Obstetric and Fetal Medicine, St. Mary's Hospital Manchester University Hospitals NHS Foundation Trust Manchester UK

3. Department of Neurology Belfast Health and Social Care Trust Belfast UK

4. Manchester Centre for Genomic Medicine, St. Mary's Hospital University of Manchester Manchester UK

5. Division of Evolution and Genomic Sciences, School of Biological Sciences University of Manchester Manchester UK

6. Department of Health Data Science, Institute of Population Health University of Liverpool Liverpool UK

7. Department of Neuropsychology Walton Centre for Neurology and Neurosurgery NHS Foundation Trust Liverpool UK

8. Department of Neurology Walton Centre for Neurology and Neurosurgery NHS Foundation Trust Liverpool UK

9. School of Psychology Deakin University Burwood Victoria Australia

10. Department for Clinical Genetics Northern Genetics Service Newcastle UK

11. Royal Manchester Children's Hospital Manchester University Hospitals NHS Foundation Trust and Manchester Academic Health Sciences Centre Manchester UK

Abstract

AbstractObjectiveThis study was undertaken to assess the utility of the Ages and Stages Questionnaire–3rd Edition (ASQ‐3) and the Vineland Adaptive Behavior Scales–2nd Edition (VABS‐II) as neurodevelopmental screening tools for infants exposed to antiseizure medications in utero, and to examine their suitability for use in large‐population signal generation initiatives.MethodsParticipants were women with epilepsy who were recruited from 21 hospitals in England and Northern Ireland during pregnancy between 2014 and 2016. Offspring were assessed at 24 months old using the Bayley Scales of Infant Development–3rd Edition (BSID‐III), the VABS‐II, and the ASQ‐3 (n = 223). The sensitivity and specificity of the ASQ‐3 and VABS‐II to identify developmental delay at 24 months were examined, using the BSID‐III to define cases.ResultsThe ASQ‐3 identified 65 children (29.1%) as at risk of developmental delay at 24 months using standard referral criteria. Using a categorical approach and standard referral criteria to identify delay in the ASQ‐3 and BSID‐III at 24 months, the ASQ‐3 showed excellent sensitivity (90.9%) and moderate specificity (74.1%). Utilizing different cut‐points resulted in improved properties and may be preferred in certain contexts. The VABS‐II exhibited the strongest psychometric properties when borderline impairment (>1 SD below the mean) was compared to BSID‐III referral data (sensitivity = 100.0%, specificity = 96.6%).SignificanceBoth the ASQ‐3 and VABS‐II have good psychometric properties in a sample of children exposed to antiseizure medications when the purpose is the identification of at‐risk groups. These findings identify the ASQ‐3 as a measure that could be used effectively as part of a tiered surveillance system for teratogenic exposure by identifying a subset of individuals for more detailed investigations. Although the VABS‐II has excellent psychometric properties, it is more labor‐intensive for both the research team and participants and is available in fewer languages than the ASQ‐3.

Publisher

Wiley

Reference49 articles.

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