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Improving Health System Care Access for Diverse Children and Families at Risk for Developmental Disabilities

Fri, April 9, 11:35am to 1:05pm EDT (11:35am to 1:05pm EDT), Virtual

Session Type: Paper Symposium

Abstract

As many as 1 in 6 children ages 3-17 are at-risk for developmental delays (e.g., speech-language, motor) or neurodevelopmental diagnoses (e.g., ADHD, autism, learning disability, intellectual disability) (Zablotsky, et al., 2019). At elevated risk are children receiving public health insurance or whose families live at <200% of the federal poverty level. This higher risk for developmental delays and disabilities (DD/D) begins at birth, with Non-Hispanic Black and American Indian/Alaskan Native mothers more likely than their White counterparts to give birth early or have low birthweight babies (Ratnasiri, et al., 2018; Ely & Driscoll, 2019). Later, these children’s cognitive performance, academic achievement, and developmental milestones may be significantly affected (Agrawal, et al., 2018; Lampi, et al., 2012; Rabie, et al., 2015). Unfortunately, service disparities for racial and ethnic minority children with DD/D persist across the lifespan and include misdiagnosis (Mandell et al. 2007) and inadequate access to care (Thomas et al. 2007). Embedding psychologists into medical teams is a viable way of increasing access to developmental and behavioral health care services for all children, and ultimately maximizing child outcomes. This symposium will overview three separate studies of such integrated approaches for (a) obstetrics, (b) families, and (c) primary care. Families whose race, ethnicity, language, and/or socioeconomic status may be associated with elevated risk of their children having DD/D are of particular focus across studies. Presenters will discuss future research directions, as well as practice implications.

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