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Pediatric Social Risk Screening: Leveraging Research to Ensure Equity

Video Published 2022-07-27 Updated 2024-02-10

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Topic Overview

Review of social risk screening practices in pediatrics reveals potential ineffectiveness and equity concerns, including low concordance between screening results and resource utilization, patient discomfort, and racial biases in screening frequency. Authors propose five evidence-based improvements: population-level needs assessment, community partnerships, universal resource offerings, tiered support systems, and patient feedback integration.

Key Takeaways

  • Current social risk screening shows low concordance between identified needs and families actually requesting resources.
  • Screening may introduce racial bias, with non-white patients screened more frequently, potentially worsening health inequities.
  • Families may withhold information due to fear of downstream consequences from disclosing social vulnerabilities.
  • Universal resource offering may be more effective than selective screening based on risk assessment results.
  • Community partnerships and tiered support levels can better align screening practices with actual population needs.

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