Advance Directives among Nursing Home Residents with Mild, Moderate, and Advanced Dementia

TitleAdvance Directives among Nursing Home Residents with Mild, Moderate, and Advanced Dementia
Publication TypeJournal Article
Year of Publication2018
AuthorsTjia J., Dharmawardene M., Givens J.L
JournalJ Palliat Med
Volume21
Issue1
Pagination16-21
Date PublishedJan
ISBN Number1557-7740
Accession Number28772095
Keywords*Advance Directives, *dementia, *nursing home
Abstract

OBJECTIVE: To describe prevalence and content of AD documentation among NH residents by dementia stage. BACKGROUND: The prevalence of advance directives (ADs) among nursing home (NH) residents with mild, moderate, and advanced dementia remains unclear. METHODS: Population-based, cross-sectional study of all licensed NHs in five U.S. states. Subjects included all long-stay (>90 day) NH residents with dementia, aged >/=65 years, and a Cognitive Performance Scale (CPS) score >/=1 from the 2007 to 2008 Minimum Data Set 2.0 (n = 180,621). Dementia severity was classified as follows: mild (CPS 1-2), moderate (CPS 3-4), and advanced (CPS 5-6). MEASUREMENTS: ADs were defined as the presence of a living will, do-not-resuscitate order, do-not-hospitalize order, medication restriction, or feeding restriction). RESULTS: Overall, 59% of residents had any AD and 17% had a living will. Prevalence of any AD increased by dementia severity: mild (51.2%), moderate (58.2%), and advanced (61.5%) (p < 0.001). In adjusted analysis, resident characteristics associated with any AD documentation included older age, female gender, being white, and having more severe dementia. Having a living will was associated with higher education (>/=high school graduate vs. some high school or less) and being married. DISCUSSION: While dementia severity was associated with greater likelihood of having documented any AD, almost 4 in 10 residents with dementia lacked any AD. Effective outreach may focus efforts on subgroups with lower odds of any AD or living wills, including non-white, less educated, and unmarried NH residents. A greater understanding of how such factors impact care planning will help to address barriers to patient-centered care for this population.

URLhttps://www.liebertpub.com/doi/pdf/10.1089/jpm.2016.0473
DOI10.1089/jpm.2016.0473
Alternate JournalJournal of palliative medicine