AbstractVulnerable populations in the United States experience disparities in access to advance care planning and may have significant unmet health care needs at the end of life, including unrelieved suffering. People who are homeless have increased morbidity and mortality risks, yet lack opportunities to communicate end‐of‐life preferences. This paper includes a narrative literature review of advance care planning interventions and qualitative investigations into end‐of‐life concerns among people experiencing homelessness. Trials of clinician‐guided interventions with homeless individuals demonstrated effectiveness in achieving advance directive completion and surrogate decision‐maker designation. End‐of‐life concerns among homeless persons included fears of dying alone, dying unnoticed, or remaining unidentified after death. Research participants also reported concerns regarding burial and notification of family members. Public health practitioners should facilitate advance care planning for people who are homeless by providing opportunities for education and discussion on care options and advance directives.
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