Researchers outline new policies for earlier detection of autism in children

The earlier that autism is diagnosed and treated in children, the better outcomes they will experience for future relationships and careers. However, most children aren’t detected and diagnosed with Autism Spectrum Disorder (ASD) until around age four, with children from economically disadvantaged or minority backgrounds detected and diagnosed up to two years later, on average. For all autistic children to get the care they need, researchers  as well as the American Academy of Pediatrics recommend that children be universally screened for ASD at 18 months and again at 24 months, among other strategies. A review of research and public health ramifications  was published today in Policy Insights from the Behavioral and Brain Sciences, a Federation of Associations in Behavioral & Brain Sciences (FABBS) journal published in partnership with SAGE Publishing.

In order to successfully diagnose all children who are at risk of ASD, researchers Fein et al. recommend using a combination of strategies, such as:

• Regular universal screening in the doctor’s office: ASD screening should become a routine part of pediatric care. Doctors should not wait for a child to exhibit signs of ASD or for parents to express concern.
•  Screening in other settings: screening should also take place in settings other than the doctor’s office, such as day care, child care, churches, and other community settings in order to help reduce disparities—as many children do not receive consistent healthcare and may miss doctor appointments.
• Better dialogue between doctor and parent about developmental concerns: screening tools, such as questionnaires, should be routinely used in doctor offices. They can serve as ice-breakers for parents who may not raise concerns on their own and for doctors who may be concerned about upsetting parents.

The researchers also recommend that government policy not continue funding early intervention using local property taxes, which results in children from wealthy states and communities receiving more access to treatment than children in poorer areas.

They concluded: “The cost of effective early intervention is significant; however, the impact of failing to provide this intervention in long-term costs and unrealized human potential is much greater.”

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The article, “Optimizing Outcome in Autism Spectrum Disorders,” by Fein et al, in Policy Insights from the Behavioral and Brain Sciences is free to access for a limited time. Read the article. 

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Sara Miller McCune founded SAGE Publishing in 1965 to support the dissemination of usable knowledge and educate a global community. SAGE is a leading international provider of innovative, high-quality content publishing more than 1,000 journals and over 800 new books each year, spanning a wide range of subject areas. Our growing selection of library products includes archives, data, case studies and video. SAGE remains majority owned by our founder and after her lifetime will become owned by a charitable trust that secures the company’s continued independence. Principal offices are located in Los Angeles, London, New Delhi, Singapore, Washington DC and Melbourne. www.sagepublishing.com 

Policy Insights from the Behavioral and Brain Sciences is a publication of the Federation of Associations in Behavioral and Brain Sciences (FABBS) that presents original research and scientific reviews relevant to public policy. This allows scientists to share research that can help build sound policies, allows policymakers to provide feedback to the scientific community regarding research that could address societal challenges, and encourages the scientific community to build models that seriously consider implementation to address the needs of society. journals.sagepub.com/home/bbs