In addition, 85 percent of the children found to be at risk for ASD based on results from the First Year Inventory (FYI), a 63-item questionnaire filled out by their parents, had some other developmental disability or concern by age three, said Grace Baranek, PhD, senior author of the study and an autism researcher with the Program for Early Autism, Research, Leadership and Service (PEARLS) in the Department of Allied Health Sciences at the UNC School of Medicine.
“Identification of children at risk for ASD at 12 months could provide a substantial number of children and their families with access to intervention services months or years before they would otherwise receive a traditional diagnosis.”
Lead author of the study, Lauren Turner-Brown, PhD, also a researcher with PEARLS and the Carolina Institute for Developmental Disabilities said,
The First Year Inventory was developed by Grace Baranek, PhD, Linda Watson, EdD, Elizabeth Crais, PhD and J. Steven Reznick, PhD, who are all researchers with PEARLS. All are also co-authors of the study with Turner-Brown, published online ahead of print on July 10, 2012 by Autism: The International Journal of Research & Practice.
In the study, parents of 699 children who had completed the FYI when their child was 12 months old completed additional screening questionnaires when their child reached age 3. In addition, children who were found to be at risk for ASD based on these measures were invited for in-person diagnostic evaluations.
“These findings are encouraging and suggest promise in the approach of using parent report of infant behaviors as a tool for identifying 12-month-olds who are at risk for an eventual diagnosis of ASD,” Turner-Brown said.
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Story Source:
The above story is reprinted from materials provided by University of North Carolina School of Medicine.Note: Materials may be edited for content and length. For further information, please contact the source cited above.
Journal Reference:
L. M. Turner-Brown, G. T. Baranek, J. S. Reznick, L. R. Watson, E. R. Crais. The First Year Inventory: a longitudinal follow-up of 12-month-old to 3-year-old children. Autism, 2012; DOI: 10.1177/1362361312439633
The FYI is currently only available for research purposes; however, the UNC School of Medicine is in the process of field testing its clinical utility. It has also been translated into several languages including Spanish, Hebrew, Dutch-Flemish, Italian, & Chinese) for use in research studies internationally.
The UNC School of Medicine is currently using research funds from Autism Speaks to develop a new version of the FYI that spans a broader age range and taps additional behaviors indicated by recent research. Scoring for the new FYI will be based on longitudinal data from an extensive cohort of infants whose families participate in the ongoing North Carolina Child Development Survey.
Recent findings published here: Questionnaire completed by parents may help identify 1-year-olds at risk for autism
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