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Suicide-Risk Identification Across Developmental and Behavioral Pediatric Practices: A DBPNet Study.

Kate E Wallis1, Sarah N Wozniak-Kelly2, Jaclyn Cacia3

  • 1PolicyLab (KE Wallis, SN Wozniak-Kelly, and KK Wu), The Children's Hospital of Philadelphia, Philadelphia, Pa; Division of Developmental and Behavioral Pediatrics (KE Wallis and J Cacia), Children's Hospital of Philadelphia, Philadelphia, Pa; Center for Autism Research (KE Wallis and SN Wozniak-Kelly), Children's Hospital of Philadelphia, Philadelphia, Pa; Perelman School of Medicine (KE Wallis), University of Pennsylvania, Philadelphia, Pa.

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Summary

Suicide screening for children with intellectual and developmental disabilities (IDD) varies widely in pediatric settings. Standardizing procedures and addressing system-level barriers are crucial for effective identification and response to suicide risk.

Keywords:
autismdepressionintellectual and developmental disabilitiesscreeningsuicide

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Area of Science:

  • Pediatric Health
  • Developmental Pediatrics
  • Behavioral Health

Background:

  • Universal suicide screening is recommended for children and adolescents.
  • Children with intellectual and developmental disabilities (IDD) are a vulnerable population requiring tailored screening approaches.
  • Existing practices for suicide screening in pediatric developmental and behavioral health settings show significant variation.

Purpose of the Study:

  • To identify variations in universal suicide screening practices for children and adolescents with IDD.
  • To explore facilitators and barriers to implementing universal suicide screening in these settings.

Main Methods:

  • Utilized the Developmental Behavioral Pediatrics Research Network (DBPNet).
  • Collected data through surveys from 34 respondents and semi-structured interviews with 21 representatives across various clinics (developmental-behavioral pediatrics, psychology, psychiatry).
  • Employed descriptive statistics for surveys and thematic analysis for interviews.

Main Results:

  • Only 44.1% of practices reported universal suicide screening, with significant procedural variations.
  • Facilitators included standardized procedures, staff training, and dedicated response personnel.
  • Barriers encompass patient, family, provider, and system-level factors, including inadequate mental health systems and lack of IDD-specific support.

Conclusions:

  • Despite regulatory requirements and expertise, suicide screening implementation and positive screen management for youth with IDD are inconsistent.
  • Opportunities exist to standardize procedures to improve suicide risk identification and response for this population.