Literature DB >> 28990634

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

Karen O Moss, Nancy L Deutsch, Patricia J Hollen, Virginia G Rovnyak, Ishan C Williams, Karen M Rose.   

Abstract

The purpose of the current study was to examine understanding of end-of-life (EOL) decision-making terminology among family caregivers of African American older adults with dementia. This qualitative descriptive study was part of a larger mixed-methods study from which a subset of caregivers (n = 18) completed interviews. Data were analyzed using descriptive statistics and content analyses guided by methods of qualitative analysis. Caregiver interpretation of EOL decision-making terminology varied between associations before and/or after death. EOL decision making was most often a family decision, based on past experiences, and included reliance on resources such as faith or spirituality and health care providers. Patients and families attach meaning to health care terms that should be aligned with health care providers' understanding of those terms. Results provide insight to improve EOL decision making in this population via tailored interventions for patients, families, and health care providers. [Journal of Gerontological Nursing, 44(2), 33-40.]. Copyright 2018, SLACK Incorporated.

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Year:  2017        PMID: 28990634      PMCID: PMC5884144          DOI: 10.3928/00989134-20171002-02

Source DB:  PubMed          Journal:  J Gerontol Nurs        ISSN: 0098-9134            Impact factor:   1.254


  28 in total

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2.  Culture care theory: a major contribution to advance transcultural nursing knowledge and practices.

Authors:  Madeleine Leininger
Journal:  J Transcult Nurs       Date:  2002-07       Impact factor: 1.959

3.  Hospice utilization and end-of-life care decision making of African Americans.

Authors:  Polly M Mazanec; Barbara J Daly; Aloen Townsend
Journal:  Am J Hosp Palliat Care       Date:  2010-12       Impact factor: 2.500

4.  A place called LIFE: exploring the advance care planning of African-American PACE enrollees.

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Journal:  Soc Work Health Care       Date:  2008

5.  Racial differences in self-reported exposure to information about hospice care.

Authors:  Kimberly S Johnson; Maragatha Kuchibhatla; James A Tulsky
Journal:  J Palliat Med       Date:  2009-10       Impact factor: 2.947

Review 6.  Overview of the theory of culture care with the ethnonursing research method.

Authors:  M Leininger
Journal:  J Transcult Nurs       Date:  1997 Jan-Jun       Impact factor: 1.959

7.  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

8.  Voices of African American, Caucasian, and Hispanic surrogates on the burdens of end-of-life decision making.

Authors:  Ursula K Braun; Rebecca J Beyth; Marvella E Ford; Laurence B McCullough
Journal:  J Gen Intern Med       Date:  2008-01-03       Impact factor: 5.128

9.  Relationships and communication in minority participation in research: multidimensional and multidirectional.

Authors:  Giselle Corbie-Smith; Ishan Canty Williams; Connie Blumenthal; Jessica Dorrance; Sue E Estroff; Gail Henderson
Journal:  J Natl Med Assoc       Date:  2007-05       Impact factor: 1.798

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  8 in total

1.  The Effect of the "Great Village" on Psychological Outcomes, Burden, and Mastery in African American Caregivers of Persons Living With Dementia.

Authors:  Glenna S Brewster; Fayron Epps; Clinton E Dye; Kenneth Hepburn; Melinda K Higgins; Monica L Parker
Journal:  J Appl Gerontol       Date:  2019-09-19

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

Authors:  Karen O Moss; Nancy L Deutsch; Patricia J Hollen; Virginia G Rovnyak; Ishan C Williams; Karen M Rose
Journal:  Am J Hosp Palliat Care       Date:  2018-03-14       Impact factor: 2.500

3.  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

4.  A Review of Qualitative Research of Perception and Experiences of Dementia Among Adults From Black, African, and Caribbean Background: What and Whom Are We Researching?

Authors:  Moïse Roche; Paul Higgs; Jesutofunmi Aworinde; Claudia Cooper
Journal:  Gerontologist       Date:  2021-07-13

5.  Understanding of Health-related Decision-making Terminology Among Cancer Caregivers.

Authors:  Karen O Moss; Sara L Douglas; Amy R Lipson; Eric Blackstone; Dionne Williams; Siobhan Aaron; Celia E Wills
Journal:  West J Nurs Res       Date:  2020-10-16       Impact factor: 1.774

Review 6.  Disparities in Palliative and Hospice Care and Completion of Advance Care Planning and Directives Among Non-Hispanic Blacks: A Scoping Review of Recent Literature.

Authors:  Mohsen Bazargan; Shahrzad Bazargan-Hejazi
Journal:  Am J Hosp Palliat Care       Date:  2020-12-08       Impact factor: 2.500

7.  Actual and Missed Opportunities for End-of-Life Care Discussions With Oncology Patients: A Qualitative Study.

Authors:  Kristin E Knutzen; Olivia A Sacks; Olivia C Brody-Bizar; Genevra F Murray; Raina H Jain; Lindsay A Holdcroft; Shama S Alam; Matthew A Liu; Kathryn I Pollak; James A Tulsky; Amber E Barnato
Journal:  JAMA Netw Open       Date:  2021-06-01

8.  Perspectives of elders and their adult children of Black and minority ethnic heritage on end-of-life conversations: A meta-ethnography.

Authors:  Joanna De Souza; Karen Gillett; Katherine Froggatt; Catherine Walshe
Journal:  Palliat Med       Date:  2020-01-22       Impact factor: 4.762

  8 in total

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