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Since the early 1980s, the delivery of care near theend of life in the United States has changed dramatically—and improved—often without much no-tice. The rights of persons to refuse all types of medical interventions are well-established and no longer liti-gated. Pain is now the fifth vital sign. Specialized palli-ative care consultative services are available in most U.S. hospitals (1). Increasing numbers of persons in the United States die while receiving hospice care, includ-ing 60 % of those who have died of cancer (2). And new initiatives are increasingly prompting clinicians and pa-tients to engage in advance care planning, such as completing written advance directives. Yet, even with these changes, much has nonethe-less stayed the same. Despite nearly 30 years of effort to get persons in the United States to complete ad-
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Halpern et al. (2014) studied this question.
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