Barriers and facilitators to improving health care for adults with intellectual and developmental disabilities: what do staff tell us?

Avra Selick, Janet Durbin, Ian Casson, Jacques Lee, Yona Lunsky
Author Information
  1. Avra Selick: Provincial System Support Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
  2. Janet Durbin: Provincial System Support Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
  3. Ian Casson: Department of Family Medicine, Queen's University, Kingston, Ontario, Canada.
  4. Jacques Lee: Sunnybrook Research Institute, Toronto, Ontario, Canada.
  5. Yona Lunsky: Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.

Abstract

INTRODUCTION: Adults with intellectual and developmental disabilities (IDD) have high rates of morbidity and are less likely to receive preventive care. Emergency departments and primary care clinics are important entry points into the health care system. Improving care in these settings can lead to increased prevention activities, early disease identification, and ongoing management. We studied barriers and facilitators to improving the care of patients with IDD in three primary and three emergency care sites in Ontario.
METHODS: Data sources included structured implementation logs at each site, focus groups (n = 5) and interviews (n = 8). Barriers and facilitators were coded deductively based on the Consolidated Framework for Implementation Research (CFIR). Synthesis to higher level themes was achieved through review and discussion by the research team. Focus was given to differences between higher and lower implementing sites.
RESULTS: All sites were challenged to prioritize care improvement for a small, complex population and varied levels of implementation were achieved. Having national guidelines, using local data to demonstrate need and sharing evidence on value were important engagement strategies. Factors present at higher implementing sites included strong champions, alignment with site mandate, and use of electronic prompts/reminders. Lower implementing sites showed more passive endorsement of the innovation and had lower capacity to implement.
CONCLUSION: Providing effective care for small, complex groups, such as adults with IDD, is critical to improving long-term health outcomes but is challenging to achieve. At a systemic level, funding incentives, access to expertise and improved electronic record systems may enhance capacity.

Keywords

References

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MeSH Term

Adult
Attitude of Health Personnel
Developmental Disabilities
Electronic Health Records
Emergency Service, Hospital
Evidence-Based Medicine
Focus Groups
Humans
Intellectual Disability
Interviews as Topic
Leadership
Ontario
Primary Health Care
Process Assessment, Health Care
Quality Improvement

Word Cloud

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