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Prenatal Substance Exposure and Positive Developmental Delay Screening Among Patients in Foster Care
Lauren Q Malthaner1,2, Jill D McLeigh3, Gregory Knell4
1Department of Epidemiology, University of Texas Health Science Center School of Public Health, Dallas, TX.
Insights
Children in foster care with prenatal substance exposure (PSE) face higher risks of developmental delays. Those with PSE and prematurity experience the greatest risk, highlighting the need for targeted screening.
Area of Science:
- Pediatrics
- Developmental Psychology
- Public Health
Background:
- Prenatal substance exposure (PSE) is linked to adverse birth and neurodevelopmental outcomes.
- Children in foster care exhibit higher rates of PSE and developmental delays than the general population.
Purpose of the Study:
- To investigate developmental delay screening differences in foster care children with and without PSE.
- To identify specific risk factors, including prematurity, interacting with PSE.
Main Methods:
- Retrospective analysis of medical records for 975 foster care children (2018-2021).
- Cox proportional hazards regression used for developmental delay screening analysis.
- Controlled for sex, race, ethnicity, prematurity, and caregiver type; examined PSE interactions.
Main Results:
- 60.4% of children had PSE; 62.6% screened positive for developmental delay.
- PSE without prematurity increased delay screening hazard by 1.14 times.
- PSE with prematurity increased delay screening hazard by 2.01 times.
Conclusions:
- Foster care children with PSE are at increased risk for developmental delays.
- The combination of PSE and prematurity significantly elevates this risk.
- Consideration of PSE and prematurity interaction is crucial for effective developmental delay screening.
Objective:
Prenatal substance exposure (PSE) is a known risk factor for negative birth outcomes and long-term health outcomes like neurodevelopmental problems. Children in foster care have increased exposure to PSE and higher proportions of developmental delay compared with the general population. It is unclear whether differences still exist among developmental delay screening among children in foster care with and without PSE.
Methods:
Data were extracted from patient medical records of a primary care clinic for children in foster care between January 1, 2018, and December 31, 2021. Cox proportional hazards regression generated hazard of positive developmental delay screening using the Ages and Stages Questionnaire-3 among those who with and without PSE controlling for sex, race, ethnicity, prematurity, caregiver type, as well as interaction between PSE and prematurity and PSE and race.
Results:
The sample included 975 patients. 60.4% had PSE, and 62.6% had a positive developmental delay screening at least once. 52.9% were male, and 45.5% were White. Those who had PSE but were nonpremature had 1.14 (95% confidence interval, 1.01-1.29) times the hazard of positive developmental delay screening compared with those without PSE and prematurity. However, those with PSE and prematurity had 2.01 times the hazard of positive developmental delay screening than those without either condition.
Conclusion:
Children in foster care with PSE are at risk for positive developmental delay screening compared with those without; however, those with both PSE and prematurity are at extra risk. This interaction should be considered when making inferences regarding developmental delay screening in this population.
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