Literature DB >> 29540073

End-of-Life Plans for African American Older Adults With Dementia.

Karen O Moss1, Nancy L Deutsch2, Patricia J Hollen3, Virginia G Rovnyak4, Ishan C Williams4, Karen M Rose5.   

Abstract

African Americans are perceived to be least likely of all racial and ethnic groups to prepare for the end of life. However, verbal plans for the end of life are of particular importance to this population and may help understand why they are less likely to possess a formal end-of-life care planning document. The purpose of this study was to determine the number of formal and/or informal end-of-life care plans that existed among a convenience sample of African American older adults with dementia. For this descriptive study, data were collected from African American family caregivers (N = 65) of older adults with dementia. Descriptive statistics were conducted. Caregivers in this sample reported high rates of formal and/or informal end-of-life plans for their care recipients. Agency forms (power of attorney, health-care surrogate, or guardianship forms) had been obtained by 74% of the care recipients, while 63% of them possessed a formal end-of-life care planning document. All combined, 88% of the caregivers possessed at least 1 document or verbal information concerning end-of-life care for their care recipient or at least there was an assigned surrogate. Although limited, these findings reflect more end-of-life planning in this population than previous studies reported and could improve the quality of end-of-life outcomes in this population by giving health-care providers increased understanding of African American end-of-life planning preferences. This may, in turn, help the providers to inform and educate these care recipients and their family caregivers.

Entities:  

Keywords:  African American; caregivers; dementia; formal end-of-life plans; informal end-of-life plans; older adults

Mesh:

Year:  2018        PMID: 29540073      PMCID: PMC6026577          DOI: 10.1177/1049909118761094

Source DB:  PubMed          Journal:  Am J Hosp Palliat Care        ISSN: 1049-9091            Impact factor:   2.500


  49 in total

1.  Prospective end-of-life treatment decisions and perceived vulnerability: Future time left to live and memory self-efficacy.

Authors:  Jessica Y Allen; Michelle M Hilgeman; Rebecca S Allen
Journal:  Aging Ment Health       Date:  2011-01       Impact factor: 3.658

2.  Promoting advance directives among African Americans: a faith-based model.

Authors:  Karen Bullock
Journal:  J Palliat Med       Date:  2006-02       Impact factor: 2.947

3.  Relationship among Trust in Physicians, Demographics, and End-of-life Treatment Decisions Made by African American Dementia Caregivers.

Authors:  Yashika J Watkins; Gloria J Bonner; Edward Wang; Diana J Wilkie; Carol E Ferrans; Barbara Dancy
Journal:  J Hosp Palliat Nurs       Date:  2012-05-01       Impact factor: 1.918

4.  Preferences for aggressive care in underserved populations with advanced-stage lung cancer: looking beyond race and resuscitation.

Authors:  George Kypriotakis; Linda E Francis; Elizabeth O'Toole; Tanyanika Phillips Towe; Julia Hannum Rose
Journal:  Support Care Cancer       Date:  2013-12-07       Impact factor: 3.603

5.  Regional variation in the association between advance directives and end-of-life Medicare expenditures.

Authors:  Lauren Hersch Nicholas; Kenneth M Langa; Theodore J Iwashyna; David R Weir
Journal:  JAMA       Date:  2011-10-05       Impact factor: 56.272

6.  End-of-life care in black and white: race matters for medical care of dying patients and their families.

Authors:  Lisa C Welch; Joan M Teno; Vincent Mor
Journal:  J Am Geriatr Soc       Date:  2005-07       Impact factor: 5.562

7.  Patient values and preferences for end-of-life treatments: are values better predictors than a living will?

Authors:  Laraine Winter
Journal:  J Palliat Med       Date:  2013-02-26       Impact factor: 2.947

8.  Understanding End-of-Life Decision-Making Terminology Among African American Older Adults.

Authors:  Karen O Moss; Nancy L Deutsch; Patricia J Hollen; Virginia G Rovnyak; Ishan C Williams; Karen M Rose
Journal:  J Gerontol Nurs       Date:  2017-10-09       Impact factor: 1.254

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  4 in total

1.  Missing the Mark: The Complexity of African American Dementia Family Caregiving.

Authors:  Glenna S Brewster; Kalisha Bonds; Susan McLennon; Karen O Moss; Fayron Epps; Ruth Palan Lopez
Journal:  J Fam Nurs       Date:  2020-08-06       Impact factor: 3.818

2.  Attitudes toward advance care planning among persons with dementia and their caregivers.

Authors:  Corinne Pettigrew; Rostislav Brichko; Betty Black; Maureen K O'Connor; Mary Guerriero Austrom; Maisha T Robinson; Allison Lindauer; Raj C Shah; Guerry M Peavy; Kayla Meyer; Frederick A Schmitt; Jennifer H Lingler; Kimiko Domoto-Reilly; Dorothy Farrar-Edwards; Marilyn Albert
Journal:  Int Psychogeriatr       Date:  2019-07-16       Impact factor: 3.878

3.  Development of a Dementia-Focused End-of-Life Planning Tool: The LEAD Guide (Life-Planning in Early Alzheimer's and Dementia).

Authors:  Kara Dassel; Rebecca Utz; Katherine Supiano; Sara Bybee; Eli Iacob
Journal:  Innov Aging       Date:  2019-08-02

Review 4.  Advance Care Planning in Neurodegenerative Disorders: A Scoping Review.

Authors:  Andrea Giordano; Ludovica De Panfilis; Marta Perin; Laura Servidio; Marta Cascioli; Maria Grazia Grasso; Alessandra Lugaresi; Eugenio Pucci; Simone Veronese; Alessandra Solari
Journal:  Int J Environ Res Public Health       Date:  2022-01-12       Impact factor: 3.390

  4 in total

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