Development of a Dementia-Focused End-of-Life Planning Tool: The LEAD Guide ( L ife-Planning in E arly A lzheimer's and D ementia)

Kara Dassel, Rebecca Utz, Katherine Supiano, Sara Bybee, Eli Iacob, Kara Dassel, Rebecca Utz, Katherine Supiano, Sara Bybee, Eli Iacob

Abstract

Background and objectives: To address the unique characteristics of Alzheimer's disease and related dementias (ADRD) that complicate end-of-life (EOL), we created, refined, and validated a dementia-focused EOL planning instrument for use by healthy adults, those with early-stage dementia, family caregivers, and clinicians to document EOL care preferences and values within the current or future context of cognitive impairment.

Research design and methods: A mixed-method design with four phases guided the development and refinement of the instrument: (1) focus groups with early-stage ADRD and family caregivers developed and confirmed the tool content and comprehensiveness; (2) evaluation by content experts verified its utility in clinical practice; (3) a sample of healthy older adults (n = 153) and adults with early-stage ADRD (n = 38) completed the tool, whose quantitative data were used to describe the psychometrics of the instrument; and (4) focus groups with healthy older adults, family caregivers, and adults with early-stage ADRD informed how the guide should be used by families and in clinical practice.

Results: Qualitative data supported the utility and feasibility of a dementia-focused EOL planning tool; the six scales have high internal consistency (α = 0.66-0.89) and high test-rest reliability (r = .60-.90). On average, both participant groups reported relatively high concern for being a burden to their families, a greater preference for quality over length of life, a desire for collaborative decision-making process, limited interest in pursuing life-prolonging measures, and were mixed in their preference to control the timing of their death. Across disease progression, preferences for location of care changed, whereas preferences for prolonging life remained stable.

Discussion and implications: The LEAD Guide (Life-Planning in Early Alzheimer's and Dementia) has the potential to facilitate discussion and documentation of EOL values and care preferences prior to loss of decisional capacity, and has utility for healthy adults, patients, families, providers, and researchers.

Keywords: Advance care planning; Advance directive; Caregiving; Goals of care discussions; Palliative care.

References

    1. Alzheimer’s Association (2018) What is Alzheimer’s? Retrieved from
    1. Alzheimer’s Association (2019). 2019 Alzheimer’s disease facts and figures. Alzheimer’s & Dementia, 15, 321–387. doi:10.1016/j.alz.2019.01.010
    1. Beatty P. C., & Willis G. B (2007). The practice of cognitive interviewing. Public Opinion Quarterly, 71, 287–311. doi:10.1093/poq/nfm006
    1. Carr D. (2011). Racial differences in end-of-life planning: Why don’t Blacks and Latinos prepare for the inevitable? Omega, 63, 1–20. doi:10.2190/OM.63.1.a
    1. Carr D., & Khodyakov D (2007). End-of-life health care planning among young-old adults: An assessment of psychosocial influences. The Journals of Gerontology, Series B: Psychological Sciences and Social Sciences, 62, S135–S141. doi:10.1093/geronb/62.2.s135
    1. Carr D., & Luth E. A (2017). Advance care planning: Contemporary issues and future directions. Innovation in Aging, 1, igx012. doi:10.1093/geroni/igx012
    1. Carr D., & Moorman S. M (2009). End-of-life treatment preferences among older adults: An assessment of psychosocial influences. Sociological Forum (Randolph, N.J.), 24, 754–778. doi:10.1111/j.1573-7861.2009.01135.x
    1. Dassel K. B., Utz R., Supiano K., McGee N., & Latimer S (2018). The influence of hypothetical death scenarios on multidimensional end-of-life care preferences. The American Journal of Hospice & Palliative Care, 35, 52–59. doi:10.1177/1049909116680990
    1. Davis T. C., & Wolf M. S (2004). Health literacy: Implications for family medicine. Family Medicine, 36, 595–598.
    1. DeVellis R. F. (2012). Scale development: Theory and applications (pp. 109–110). Los Angeles, CA: Sage.
    1. Dixon J., Karagiannidou M., & Knapp M (2018). The effectiveness of advance care planning in improving end-of-life outcomes for people with dementia and their carers: A systematic review and critical discussion. Journal of Pain and Symptom Management, 55, 132–150.e1. doi:10.1016/j.jpainsymman.2017.04.009
    1. Flesch R. F. (1979). How to write plain English. New York, NY: Harper & Row.
    1. Gaster B., Larson E. B., & Curtis J. R (2017). Advance directives for dementia: Meeting a unique challenge. JAMA, 318, 2175–2176. doi:10.1001/jama.2017.16473
    1. Gundersen L. (2003). Dispositional theories of knowledge. London, UK: Routledge.
    1. Harris P. A., Taylor R., Thielke R., Payne J., Gonzalez N., & Conde J. G (2009). Research electronic data capture (redcap)–a metadata-driven methodology and workflow process for providing translational research informatics support. Journal of Biomedical Informatics, 42, 377–381. doi:10.1016/j.jbi.2008.08.010
    1. Howard M., Day A. G., Bernard C., Tan A., You J., Klein D., & Heyland D. K (2018). Development and psychometric properties of a survey to assess barriers to implementing advance care planning in primary care. Journal of Pain and Symptom Management, 55, 12–21. doi:10.1016/j.jpainsymman.2017.08.003
    1. IBM Corp (2016). IBM SPSS statistics for windows, version 24.0. Armonk, NY: IBM Corp.
    1. Jennings L. A., Turner M., Keebler C., Burton C. H., Romero T., Wenger N. S., & Reuben D. B (2019). The effect of a comprehensive dementia care management program on end-of-life care. Journal of the American Geriatrics Society, 67, 443–448. doi:10.1111/jgs.15769
    1. Institute for Healthcare Improvement (2019). The conversation project: Your conversation starter kit Retrieved from
    1. Institute of Medicine (IOM) (2014). Dying in America: Improving quality and honoring individual preferences near the end of life. Washington, DC: The National Academies.
    1. Kline P. (2000). The handbook of psychological testing (2nd ed.). London: Routledge; pp. 7–8.
    1. Krueger R. A. (1998). Moderating focus groups. In Morgan D. L. & Krueger R. A. (Eds.), The focus group kit (Vol. 4). Thousand Oaks, CA: Sage Publications.
    1. Matthews K. A., Xu W., Gaglioti A. H., Holt J. B., Croft J. B., Mack D., & McGuire L. C (2019). Racial and ethnic estimates of Alzheimer’s disease and related dementias in the United States (2015–2060) in adults aged ≥65 years. Alzheimer’s & Dementia, 15, 17–24. doi:10.1016/j.jalz.2018.06.3063
    1. Mitchell S. L., Teno J. M., Roy J., Kabumoto G., & Mor V (2003). Clinical and organizational factors associated with feeding tube use among nursing home residents with advanced cognitive impairment. JAMA, 290, 73–80. doi:10.1001/jama.290.1.73
    1. Morgan D. L. (1997). Focus groups as qualitative research. Thousand Oaks, CA: Sage Publications.
    1. Moss K. O., Deutsch N. L., Hollen P. J., Rovnyak V. G., Williams I. C., & Rose K. M (2018). End-of-life plans for African American older adults with dementia. The American Journal of Hospice & Palliative Care, 35, 1314–1322. doi:10.1177/1049909118761094
    1. Poole M., Bamford C., McLellan E., Lee R. P., Exley C., Hughes J. C.,…Robinson L (2018). End-of-life care: A qualitative study comparing the views of people with dementia and family carers. Palliative Medicine, 32, 631–642. doi:10.1177/0269216317736033
    1. Portanova J., Ailshire J., Perez C., Rahman A., & Enguidanos S (2017). Ethnic differences in advance directive completion and care preferences: What has changed in a decade? Journal of the American Geriatrics Society, 65, 1352–1357. doi:10.1111/jgs.14800
    1. Prendergast T. J. (2001). Advance care planning: Pitfalls, progress, promise. Critical Care Medicine, 29, N34–N39.
    1. President’s Council on Bioethics (2005). Taking care: Ethical caregiving in our aging society. Washington, DC: Government Printing Office.
    1. Prince M., Wimo A., Guerchet M., Ali G. C., Wu Y. T., & Prina M (2015). World Alzheimer’s report 2015: The global impact of dementia: An analysis of prevalence, incidence, cost, and trends. London, England: Alzheimer’s Disease International.
    1. Singer P. A., & Siegler M (1992). Advancing the cause of advance directives. Archives of Internal Medicine, 152, 22–24.
    1. Supiano K. P., McGee N., Dassel K. B., & Utz R (2019). A comparison of the influence of anticipated death trajectory and personal values on end-of-life care preferences: A qualitative analysis. Clinical Gerontologist, 42, 247–258. doi:10.1080/07317115.2017.1365796
    1. Thomas J. D., Sanchez-Reilly S., Bernacki R., O’Neill L., Morrison L. J., Kapo J.,…Carey E. C (2018). Advance care planning in cognitively impaired older adults. Journal of the American Geriatrics Society, 66, 1469–1474. doi:10.1111/jgs.15471
    1. Towsley G. L., Beck S. L., Ellington L., & Wong B (2018). Me & my wishes: Lessons learned from prototyping resident centered videos about care preferences. Journal of Applied Gerontology, 37, 1037–1049. doi:10.1177/0733464816657473
    1. Unroe K. T., & Meier D. E (2013). Quality of hospice care for individuals with dementia. Journal of the American Geriatrics Society, 61, 1212–1214. doi:10.1111/jgs.12318
    1. Wendler D., & Rid A (2011). Systematic review: The effect on surrogates of making treatment decisions for others. Annals of Internal Medicine, 154, 336–346. doi:10.7326/0003-4819-154-5-201103010-00008. Retrieved from
    1. Willis G. B. (2005). Cognitive interviewing. Thousand Oaks, CA: Sage Publications.
    1. Winter L. (2013). Patient values and preferences for end-of-life treatments: Are values better predictors than a living will? Journal of Palliative Medicine, 16, 362–368. doi:10.1089/jpm.2012.0303

Source: PubMed

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