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State Variability in Diagnosed Conditions for IDEA Part C Eligibility
Brian Barger1, Jane Squires1, Maureen Greer1
1Center for Leadership in Disability, School of Public Health, Georgia State University, Atlanta (Dr Barger); Disability Research and Dissemination Center, Arnold School of Public Health, University of South Carolina, Columbia (Dr Barger); Center on Human Development, University of Oregon, Eugene (Dr Squires and Ms Twombly); Infant & Toddler Coordinators Association, Indianapolis, Indiana (Ms Greer); Office of Special Education Programs (Dr Noyes-Grosser and Ms Martin Eile) and Office of General Counsel (Dr Surprenant), US Department of Education, Washington, District of Columbia; Department of Psychiatry and Behavioral Sciences (Dr Rice) and Emory School of Public Health (Ms London), Emory University, Atlanta, Georgia; Frank Porter Graham Child Development Institute, University of North Carolina at Chapel Hill (Ms Shaw); Carter Consulting, Inc, Atlanta, Georgia (Dr Zubler); and National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia (Drs Rice and Zubler and Mss London and Wolf).
State definitions for early intervention services vary widely, with no single condition recognized by all. This heterogeneity may create access imbalances for children needing developmental support.
Area of Science:
- Pediatrics
- Public Health
- Special Education
Background:
- Part C of the Individuals with Disabilities Education Improvement Act mandates early intervention services for infants and toddlers with diagnosed conditions likely to cause developmental delay.
- The criteria for initiating these services, specifically the list of qualifying diagnosed conditions, differ significantly among states.
Purpose of the Study:
- To analyze the heterogeneity in diagnosed conditions used by states to initiate Part C early intervention services.
- To identify potential disparities in access to early intervention services based on state-specific condition lists.
Main Methods:
- A descriptive analysis was conducted using lists of diagnosed conditions obtained from state Part C websites and Part C coordinators.
- Data were collected from 49 states, the District of Columbia, and 4 territories.
Main Results:
- A total of 620 unique conditions were compiled, with no single condition listed by all jurisdictions.
- Hearing impairment (38 states) and fetal alcohol syndrome (34 states) were the most frequently listed conditions.
- The vast majority of listed conditions (89%) were identified by fewer than 10 states, highlighting significant variation.
Conclusions:
- The wide variation in diagnosed conditions across states may lead to inequities in children's access to Part C evaluations and services.
- Standardizing or improving access to these condition lists could help facilitate service access for eligible children nationwide.
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