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Published on: June 6, 2020
Emergency medical services providers' perspective of end-of-life decision making for people with intellectual
Jacqueline McGinley1, Deborah P Waldrop1, Brian Clemency2
1School of Social Work, University at Buffalo, Buffalo, NY, USA.
Background:
Emergency medical services (EMS) providers are often called to rapidly determine and act upon patients' wishes for end-of-life care. People with intellectual disabilities are living increasingly longer with complex conditions leading to international calls for person-centred advance care planning. Yet, best estimates suggest that very few people with intellectual disabilities document their wishes.
Methods:
This exploratory-descriptive study incorporated mixed methods to analyse data collected consecutively (surveys, n = 239; interviews, n = 48) with EMS providers from five agencies. Data were subjected to a sequential quantitative-qualitative analysis applying a critical discourse analysis framework.
Results:
Findings indicate that 62.7% had treated a person with intellectual disability who had medical orders directing end-of-life care. Three themes (provider familiarity, organizational processes, sociocultural context) offer insights about how medical orders inform EMS providers during calls involving people with intellectual disabilities.
Conclusion:
Multiple contexts influence how wishes are documented and care provided to people with intellectual disabilities near life's end.
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