Understanding Barriers to Early Intervention Services for Preterm Infants: Lessons From Two States
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Published on: January 12, 2018
Alison A Little1, Karen Kamholz1, Brian K Corwin1
1Center for Policy, Outcomes and Prevention & Division of General Pediatrics, Stanford University School of Medicine, Stanford, CA.
Insights
Barriers in early intervention (EI) for very low birth weight (VLBW) infants hinder access and service. Addressing funding, regulations, and communication gaps is crucial for improving care for these vulnerable children.
Area of Science:
- Neonatal care
- Developmental pediatrics
- Public health
Background:
- Very low birth weight (VLBW) infants (<1500 g) require specialized early intervention (EI) services.
- Existing EI systems face challenges in referral, enrollment, and service provision for VLBW infants.
Purpose of the Study:
- To identify barriers and challenges in the EI system for VLBW infants.
- To explore gaps in EI services from parent and provider perspectives.
Main Methods:
- Conducted 10 focus groups with parents (n=44) and 32 interviews with EI, NICU, and clinic professionals across 6 sites.
- Utilized grounded theory to analyze data and identify themes related to service gaps.
Main Results:
- Parents and providers recognize EI's value but report significant system gaps.
- Barriers include eligibility criteria, referral process failures, family hesitancy, and poor coordination with medical care.
- Inadequate funding, variable evaluations, and limited provider training further impede services.
Conclusions:
- Systemic issues like funding, staffing, regulations, and communication create critical gaps in EI for VLBW infants.
- A chronic care model could integrate EI with medical services for VLBW infants and other vulnerable groups.
Objective:
To explore existing barriers and challenges to Early Intervention (EI) referral, enrollment, and service provision for very low birth weight (VLBW; <1500 g) infants.
Methods:
We conducted 10 focus groups with parents of VLBW children (n = 44) and 32 interviews with key informants from EI (n = 7), neonatal intensive care units (n = 17), and outpatient clinics (n = 8) at 6 sites in 2 states. We used grounded theory to identify themes about gaps in services.
Results:
Both parents and providers found EI helpful. However, they also identified gaps in the current EI system at the levels of eligibility, referral, family receptivity, and service provision and coordination with medical care. Inadequate funding and variable procedures for evaluation may affect children's eligibility. Referrals can be missed as a result of simple oversight or communication failure among hospitals, EI, and families; referral outcomes often are not formally tracked. Families may not be receptive to services as a result of wariness of home visits, social stressors, denial about potential developmental delays, or lack of understanding of the benefits of EI. Once a child is deemed eligible, services may be delayed or terminated early, and EI providers may have little specialized training. Communication and coordination with the child's medical care team is often limited.
Conclusions:
Systemic barriers, including funding and staffing issues, state and federal regulations, and communication with families and medical providers, have led to gaps in the EI system. The chronic care model may serve as a framework for integrating community-based interventions like EI with medical care for VLBW children and other vulnerable populations.
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