Literature DB >> 15877572

Exploring chronically ill seniors' attitudes about discussing death and postmortem medical procedures.

Henry S Perkins1, Krysten J Shepherd, Josie D Cortez, Helen P Hazuda.   

Abstract

Proxy decisions about postmortem medical procedures must consider the dead patient's likely preferences. Ethnic- and sex-based attitudes surely underlie such preferences but lack sufficient characterization to guide decisions. Therefore, this exploratory study interviewed Mexican-American, Euroamerican, and African-American seniors in San Antonio, Texas, for their attitudes about discussing death before it occurs and about organ donation, autopsy, and practice on cadavers. A rigorous content analysis identified themes. Majority attitudes of an ethnic group or sex subgroup here may characterize the group generally. Attitudes about discussing death differed only by ethnic group. Mexican Americans and Euroamericans favored such discussions, but African Americans did not. Attitudes about the postmortem procedures differed by ethnic group and sex. Overall, Mexican Americans viewed the procedures most favorably; Euroamericans, less so; and African Americans, least so. Men and women differed further within ethnic groups. Mexican-American men and women split evenly over organ donation, the men expressed no majority preference about autopsies and the women agreed to them, and the men refused and the women agreed to practice on their cadavers. Euroamerican men expressed no majority preferences, but Euroamerican women agreed to organ donation, had no majority preference about autopsies, and refused practice on their cadavers. African-American men expressed no majority preferences, and African-American women expressed none about organ donation or autopsies but refused practice on their cadavers. If confirmed, these ethnic- and sex-based attitudes can help health professionals tailor postmortem care to individual patients' preferences.

Entities:  

Keywords:  Biomedical and Behavioral Research; Death and Euthanasia; Empirical Approach; Health Care and Public Health

Mesh:

Year:  2005        PMID: 15877572     DOI: 10.1111/j.1532-5415.2005.53274.x

Source DB:  PubMed          Journal:  J Am Geriatr Soc        ISSN: 0002-8614            Impact factor:   5.562


  4 in total

1.  Comments on Shrank et al., focus group findings about the influence of culture on communication preferences in end-of-life care.

Authors:  Henry S Perkins; Emi Ponce De Souza; Josie D Cortez; Helen P Hazuda
Journal:  J Gen Intern Med       Date:  2005-12-22       Impact factor: 5.128

2.  Surrogate decision-makers' perspectives on discussing prognosis in the face of uncertainty.

Authors:  Leah R Evans; Elizabeth A Boyd; Grace Malvar; Latifat Apatira; John M Luce; Bernard Lo; Douglas B White
Journal:  Am J Respir Crit Care Med       Date:  2008-10-17       Impact factor: 21.405

3.  Using the medical record to evaluate the quality of end-of-life care in the intensive care unit.

Authors:  Bradford J Glavan; Ruth A Engelberg; Lois Downey; J Randall Curtis
Journal:  Crit Care Med       Date:  2008-04       Impact factor: 7.598

4.  Cultural beliefs about a patient's right time to die: an exploratory study.

Authors:  Henry S Perkins; Josie D Cortez; Helen P Hazuda
Journal:  J Gen Intern Med       Date:  2009-10-02       Impact factor: 5.128

  4 in total

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