Child characteristics and early intervention referral and receipt of services: a retrospective cohort study
Beth M McManus1, Zachary Richardson2, Margaret Schenkman3
1Department of Health Systems, Management and Policy, Colorado School of Public Health, 13001 E 17th Place, MS B119, Aurora, Colorado, 80045, USA. Beth.mcmanus@ucdenver.edu.
Insights
Early Intervention (EI) referral and access rates are low, especially for minority children. Improvements in integrated care systems are needed to address these gaps in service use.
Area of Science:
- Pediatric primary care
- Developmental disabilities
- Public health systems
Background:
- Early Intervention (EI) is a federally mandated system for children under three with developmental delays.
- Significant gaps exist in accessing EI services through pediatric primary care, disproportionately affecting minority and low-income children.
- This study is the first to use linked health system and EI data to longitudinally track EI service use gaps.
Purpose of the Study:
- To examine child characteristics associated with gaps in EI referral, access, and service use.
- To identify factors influencing the transition from EI referral to service utilization.
- To understand disparities in EI service access within a safety-net population.
Main Methods:
- Retrospective cohort design analyzing 14,710 children with developmental delays or disabilities.
- Linked pediatric primary care records from a safety-net health system with EI program data (2014-2016).
- Used adjusted marginal effects to estimate gaps in EI referral, access, and specific therapies (PT, OT, ST, DI), controlling for child characteristics.
Main Results:
- Only 18.7% of eligible children received an EI referral, and only 5% ultimately enrolled in services.
- Children with severe developmental conditions were more likely to be referred and receive services.
- Black, non-Hispanic children and those with diagnosed conditions were less likely to be referred; higher income was linked to PT/OT receipt.
Conclusions:
- Significant gaps in EI referral, access, and service use were identified in an urban safety-net population.
- Interventions are necessary to enhance integrated care systems and coordination between primary care and EI.
- Addressing these systemic issues is crucial for equitable access to developmental services for all children.
Background:
Early Intervention (EI) is a federally mandated, state-administered system of care for children with developmental delays and disabilities under the age of three. Gaps exist in the process of accessing EI through pediatric primary care, and low rates of EI access are well documented and disproportionately affect poor and minority children. The aims of this paper are to examine child characteristics associated with gaps in EI (1) referral, (2) access and (3) service use. To our knowledge, this is the first study to leverage linked safety net health system pediatric primary care and EI records data to follow EI-referred children longitudinally to understand EI service use gaps from EI referral to EI service utilization.
Methods:
In a retrospective cohort design (14,710 children with developmental disability or delay), we linked pediatric primary care records between a large, integrated safety net health system in metro Denver and its corresponding EI program (2014-2016). Using adjusted marginal effects [ME, (95% CI)], we estimated gaps in EI referral, access, and service type (i.e., physical [PT], occupational [OT], speech therapy [ST] and developmental intervention [DI]). Analyses accounted for child characteristics including socio-demographics, diagnosis, condition severity, and baseline function.
Results:
Only 18.7% of EI-eligible children (N = 2726) received a referral; 26% of those (N = 722) received services for a net enrollment rate of 5% among EI-eligible children. Having the most severe developmental condition was positively associated with EI referral [ME = 0.334 [0.249, 0.420]) and Individualized Family Services Plan (IFSP) receipt [ME = 0.156 [0.088, 0.223]). Children less likely to be EI-referred were Black, non-Hispanic (BNH) [ME = -0.029 (- 0.054, - 0.004)] and had a diagnosed condition ([ME = - 0.046 (- 0.087, - 0.005)]. Children with a diagnosis and those with higher income were more likely to receive PT or OT. Higher baseline cognitive and adaptive skills were associated with lower likelihood of PT [ME = -0.029 (- 0.054, - 0.004)], OT [ME = -0.029 (- 0.054, - 0.004)], and ST [ME = -0.029 (- 0.054, - 0.004)].
Conclusions:
We identified and characterized gaps in EI referral, access, and service use in an urban safety-net population of children with high rates of developmental delay. Interventions are needed to improve integrated systems of care affecting primary care and EI processes and coordination.
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