Literature DB >> 12569925

End of life care and reactions to death in African-American and white family caregivers of relatives with Alzheimer's disease.

J E Owen1, K T Goode, W E Haley.   

Abstract

Family caregivers for relatives with Alzheimer's Disease (AD) often experience significant stress-related problems in mental and physical health. Patients with AD often survive for protracted periods of time, placing an extensive burden of care on the caregiver prior to the patient's death. The present study addresses ethnic differences in the experience of AD caregivers around the time of their loved one's death, including life-sustaining treatment decisions and reactions to death. The results showed that, in our sample, more patients died in their homes than has been reported for deaths in the United States. African-American and White caregivers differed substantially in their reports of end of life care and subjective reactions to the death. Compared with White caregivers, African-American caregivers were less likely to make a decision to withhold treatment at the time of death, less likely to have their relative die in a nursing home, and reported less acceptance of the relative's death and greater perceived loss. Results suggest that death after AD caregiving deserves further study, and that ethnic differences in end of life care and bereavement may be of particular importance.

Entities:  

Keywords:  Death and Euthanasia; Empirical Approach

Mesh:

Year:  2001        PMID: 12569925     DOI: 10.2190/YH2B-8VVE-LA5A-02R2

Source DB:  PubMed          Journal:  Omega (Westport)        ISSN: 0030-2228


  11 in total

1.  End-of-life decision-making confidence in surrogates of African-American dialysis patients is overly optimistic.

Authors:  Mi-Kyung Song; Sandra E Ward; Feng-Chang Lin
Journal:  J Palliat Med       Date:  2012-04-02       Impact factor: 2.947

2.  The Meanings African American Caregivers Ascribe to Dementia-Related Changes: The Paradox of Hanging on to Loss.

Authors:  Allison Lindauer; Theresa A Harvath; Patricia H Berry; Peggy Wros
Journal:  Gerontologist       Date:  2015-04-09

3.  Measuring change in perceived well-being of family caregivers: validation of the Spanish version of the Perceived Change Index (PCI-S) in Chilean dementia caregivers.

Authors:  José M Aravena; Cecilia Albala; Laura N Gitlin
Journal:  Int J Geriatr Psychiatry       Date:  2017-05-16       Impact factor: 3.485

4.  End-of Life Issues in the Context of Alzheimer's Disease.

Authors:  Rebecca S Allen; Jung Kwak; Kristine L Lokken; William E Haley
Journal:  Alzheimers Care Q       Date:  2003-10-01

5.  Achieving Health Equity in Embedded Pragmatic Trials for People Living with Dementia and Their Family Caregivers.

Authors:  Ana R Quiñones; Susan L Mitchell; Jonathan D Jackson; María P Aranda; Peggye Dilworth-Anderson; Ellen P McCarthy; Ladson Hinton
Journal:  J Am Geriatr Soc       Date:  2020-07       Impact factor: 5.562

6.  Association of Nursing Home Organizational Culture and Staff Perspectives With Variability in Advanced Dementia Care: The ADVANCE Study.

Authors:  Ruth Palan Lopez; Meghan Hendricksen; Ellen P McCarthy; Kathleen M Mazor; Ashley Roach; Anita Hendrix Rogers; Fayron Epps; Kimberly S Johnson; Harriet Akunor; Susan L Mitchell
Journal:  JAMA Intern Med       Date:  2022-03-01       Impact factor: 21.873

7.  Anxiety, Depression, Quality of Life, Caregiver Burden, and Perceptions of Caregiver-Centered Communication among Black and White Hospice Family Caregivers.

Authors:  Lauren T Starr; Karen Bullock; Karla Washington; Subhash Aryal; Debra Parker Oliver; George Demiris
Journal:  J Palliat Med       Date:  2021-11-18       Impact factor: 2.947

8.  Racial Differences in Outcomes of an Advance Care Planning Intervention for Dialysis Patients and Their Surrogates.

Authors:  Mi-Kyung Song; Sandra E Ward; Feng-Chang Lin; Jill B Hamilton; Laura C Hanson; Gerald A Hladik; Jason P Fine
Journal:  J Palliat Med       Date:  2016-02       Impact factor: 2.947

9.  ADVANCE: Methodology of a qualitative study.

Authors:  Ruth Palan Lopez; Ellen P McCarthy; Kathleen M Mazor; Meghan Hendricksen; Susan McLennon; Kimberly S Johnson; Susan L Mitchell
Journal:  J Am Geriatr Soc       Date:  2021-05-10       Impact factor: 7.538

Review 10.  The Grief and Bereavement Experiences of Informal Caregivers: A Scoping Review of the North American Literature.

Authors:  Neerjah Skantharajah; Carol Barrie; Sharon Baxter; M Carolina Borja; Anica Butters; Deborah Dudgeon; Ayeshah Haque; Iqra Mahmood; Mehrnoush Mirhosseini; Raza M Mirza; Ankita Ankita; Carly Thrower; Christina Vadeboncoeur; Andrew Wan; Christopher A Klinger
Journal:  J Palliat Care       Date:  2021-12-03       Impact factor: 1.980

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