Literature DB >> 19807237

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

Kimberly S Johnson1, Maragatha Kuchibhatla, James A Tulsky.   

Abstract

BACKGROUND: Previous research suggests that lack of knowledge of hospice is a barrier to the use of hospice care by African Americans. However, there is little data examining racial differences in exposure to hospice information.
OBJECTIVES: Examine racial differences in self-reported exposure to hospice information and determine how this exposure impacts beliefs about hospice care.
METHODS: We surveyed 200 community-dwelling older adults (65 or older). We used Spearman's correlations to examine the relationship between responses to individual items on the Hospice Beliefs and Attitudes Scale (HBAS) and self-reported exposure to hospice information (never heard of hospice, heard a little, or heard a lot). We used multivariate analyses to examine predictors of exposure to hospice information and beliefs about hospice care (total score on HBAS).
RESULTS: Compared to whites (n = 95), African Americans (n = 105) reported significantly less exposure to hospice information (p = 0.0004). Nineteen percent of African Americans and 4% of whites had never heard of hospice; 47.6% of African Americans and 71.6% of whites had heard a lot about hospice. In multivariate analysis controlling for demographics and health status, African Americans had a two times higher odds of reporting that they had never heard of hospice or heard only a little about hospice versus heard a lot about hospice (odds ratio [OR] = 2.24 [1.17, 4.27]. Greater exposure to hospice information was associated with more favorable beliefs about hospice care (outcome: total score on HBAS; parameter estimate 1.34, standard error 0.44, p = 002).
CONCLUSIONS: African Americans reported less exposure to information about hospice than whites. Greater exposure to hospice information was associated with more favorable beliefs about some aspects of hospice care. Because knowledge is power, educational programs targeting older African Americans are needed to dispel myths about hospice and to provide minorities with the tools to make informed choices about end-of-life care.

Mesh:

Year:  2009        PMID: 19807237      PMCID: PMC2904186          DOI: 10.1089/jpm.2009.0066

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  26 in total

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2.  How do surrogate decision makers describe hospice? Does it matter?

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3.  Access to hospice for African Americans: are they informed about the option of hospice?

Authors:  Ramona L Rhodes; Joan M Teno; Lisa C Welch
Journal:  J Palliat Med       Date:  2006-04       Impact factor: 2.947

4.  Racial differences in the willingness to use hospice services.

Authors:  Robert L Ludke; Douglas R Smucker
Journal:  J Palliat Med       Date:  2007-12       Impact factor: 2.947

5.  Are there racial differences in attitudes toward hospice care? A study of hospice-eligible patients at the Visiting Nurse Service of New York.

Authors:  Peri Rosenfeld; Jeanne Dennis; Suzanne Hanen; Ernesto Henriquez; Theresa M Schwartz; Lyla Correoso; Christopher M Murtaugh; Alan Fleishman
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6.  Geographic variation in hospice use in the United States in 2002.

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9.  Racial disparity in hospice use in the United States in 2002.

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10.  What explains racial differences in the use of advance directives and attitudes toward hospice care?

Authors:  Kimberly S Johnson; Maragatha Kuchibhatla; James A Tulsky
Journal:  J Am Geriatr Soc       Date:  2008-09-02       Impact factor: 5.562

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  27 in total

1.  Geographic access to hospice in the United States.

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Journal:  J Palliat Med       Date:  2010-10-27       Impact factor: 2.947

2.  Is public communication about end-of-life care helping to inform all? Cancer news coverage in African American versus mainstream media.

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3.  What are Hospice Providers in the Carolinas Doing to Reach African Americans in Their Service Area?

Authors:  Kimberly S Johnson; Richard Payne; Maragatha N Kuchibhatla
Journal:  J Palliat Med       Date:  2016-02       Impact factor: 2.947

4.  End-of-Life Decision Making and Communication of Bereaved Family Members of African Americans with Serious Illness.

Authors:  Esther R Smith-Howell; Susan E Hickman; Salimah H Meghani; Susan M Perkins; Susan M Rawl
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5.  Awareness and Misperceptions of Hospice and Palliative Care: A Population-Based Survey Study.

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6.  Racial and ethnic disparities in palliative care.

Authors:  Kimberly S Johnson
Journal:  J Palliat Med       Date:  2013-09-27       Impact factor: 2.947

7.  Association of Sensory and Cognitive Impairment With Healthcare Utilization and Cost in Older Adults.

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8.  Utilization of supportive and palliative care services among oncology outpatients at one academic cancer center: determinants of use and barriers to access.

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9.  Psychosocial, cultural, and spiritual health disparities in end-of-life and palliative care: where we are and where we need to go.

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