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Cultural Beliefs About a Patient’s Right Time to Die: An Exploratory Study

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ABSTRACT

BACKGROUND

Generalist physicians must often counsel patients or their families about the right time to die, but feel ill-prepared to do so. Patient beliefs may help guide the discussions.

OBJECTIVE

Because little prior research addresses such beliefs, we investigated them in this exploratory, hypothesis-generating study.

DESIGN AND SUBJECTS

Anticipating culture as a key influence, we interviewed 26 Mexican Americans (MAs), 18 Euro-Americans (EAs), and 14 African Americans (AAs) and content-analyzed their responses.

MAIN RESULTS

Nearly all subjects regardless of ethnic group or gender said God determines (at least partially) a patient’s right time to die, and serious disease signals it. Yet subjects differed by ethnic group over other signals for that time. Patient suffering and dependence on “artificial” life support signaled it for the MAs; patient acceptance of death signaled it for the EAs; and patient suffering and family presence at or before the death signaled it for the AAs. Subjects also differed by gender over other beliefs. In all ethnic groups more men than women said the time of death is unpredictable; but more women than men said the time of death is preset, and family suffering signals it. Furthermore, most MA women—but few others—explicitly declared that family have an important say in determining a patient’s right time to die. No confounding occurred by religion.

CONCLUSIONS

Americans may share some beliefs about the right time to die but differ by ethnic group or gender over other beliefs about that time. Quality end-of-life care requires accommodating such differences whenever reasonable.

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References

  1. Callahan CM, Gramelspacher GP. Death and primary care. J Gen Intern Med. 2004;19:1066–7.

    Article  PubMed  Google Scholar 

  2. Hardwig J. Going to meet death: the art of dying in the early part of the twenty-first century. Hast Cen Rep. 2009;39(4):37–45.

    Article  Google Scholar 

  3. McCormick TR. Patients’ perspectives on dying and on the care of dying patients. West J Med. 1995;163:236–43.

    CAS  PubMed  Google Scholar 

  4. Billings JA, Block S. Palliative care in undergraduate medical education: status report and future directions. JAMA. 1997;278:733–8.

    Article  CAS  PubMed  Google Scholar 

  5. Emanuel EJ, Emanuel LL. The promise of a good death. Lancet. 1998;351(suppl 2): 21–9.

    Google Scholar 

  6. Steinhauser KE, Christakis NA, Clipp EC, McNeilly M, McIntyre L, Tulsky JA. Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA. 2000;284:2476–82.

    Article  CAS  PubMed  Google Scholar 

  7. Crawley LVM, Marshall PA, Lo B, Koenig BA. Strategies for culturally effective end-of-life care. Ann Intern Med. 2002;136:673–9.

    PubMed  Google Scholar 

  8. Baker LM. Information needs at the end of life: a content analysis of one person’s story. J Med Libr Assoc. 2004;92:78–82.

    PubMed  Google Scholar 

  9. Kaldjian LC, Curtis AE, Shinkunas LA, Cannon KT. Goals of care toward the end of life: a structured literature review. Am J Hosp Palliat Med. 2009;25:501–11.

    Article  Google Scholar 

  10. Orr RD, Marshall PA, Osborn J. Cross-cultural considerations in clinical ethics consultations. Arch Fam Med. 1995;4:159–64.

    Article  CAS  PubMed  Google Scholar 

  11. Carrillo JE, Green AR, Betancourt JR. Cross-cultural primary care: a patient-based approach. Ann Intern Med. 1999;130:829–34.

    CAS  PubMed  Google Scholar 

  12. Kagawa-Singer M, Blackhall LJ. Negotiating cross-cultural issues at the end of life: “You got to go where he lives.” JAMA. 2001;286:2993–3001.

    Article  CAS  PubMed  Google Scholar 

  13. Perkins HS. Culture as a useful conceptual tool in clinical ethics consultation. Camb Q Healthc Ethics. 2008;17:164–72.

    Google Scholar 

  14. Koenig BA, Gates-Williams J. Understanding cultural difference in caring for dying patients. West J Med. 1995;163:244–9.

    CAS  Google Scholar 

  15. Hallenbeck JL. Intercultural differences and communication at the end of life. Prim Care. 2001;28:401–13.

    Article  CAS  PubMed  Google Scholar 

  16. Krakauer EL, Crenner C, Fox K. Barriers to optimum end-of-life care for minority patients. J Am Geriatr Soc. 2002;50:182–90.

    Article  PubMed  Google Scholar 

  17. True G, Phipps EJ, Braitman LE, Harralson T, Harris D, Tester W. Treatment preferences and advance care planning at end of life: the role of ethnicity and spiritual coping in cancer patients. Ann Behav Med. 2005;30:174–9.

    Article  PubMed  Google Scholar 

  18. Barclay JS, Blackhall LJ, Tulsky JA. Communication strategies and cultural issues in the delivery of bad news. J Palliat Med. 2007;10:958–77.

    Article  PubMed  Google Scholar 

  19. O’Connell LJ. Religious dimensions of dying and death. West J Med. 1995;163:231–5.

    PubMed  Google Scholar 

  20. Hallenbeck J, Goldstein MK, Mebane EW. Cultural considerations of death and dying in the United States. Clin Geriatr Med. 1996;12:393–406.

    CAS  PubMed  Google Scholar 

  21. Daaleman TP, VandeCreek L. Placing religion and spirituality in end-of-life care. JAMA. 2000;284:2514–7.

    Article  CAS  PubMed  Google Scholar 

  22. Johnson KS, Elbert-Avila KI, Tulsky JA. The influence of spiritual beliefs and practices on the treatment preferences of African Americans: a review of the literature. J Am Geriatr Soc. 2005;53:711–9.

    Article  PubMed  Google Scholar 

  23. Phelps AC, Maciejewski PK, Nilsson M, et al. Religious coping and use of intensive life-prolonging care near death in patients with advanced cancer. JAMA. 2009;301:1140–7.

    Article  CAS  PubMed  Google Scholar 

  24. McKinley ED, Garrett JM, Evans AT, Danis M. Differences in end-of-life decision making among black and white ambulatory cancer patients. J Gen Intern Med. 1996;11:651–6.

    Article  CAS  PubMed  Google Scholar 

  25. Hanchate A, Kronman AC, Young-Xu Y, Ash AS, Emanuel E. Racial and ethnic differences in end-of-life costs: why do minorities cost more than whites? Arch Intern Med. 2009;169:493–501.

    Article  PubMed  Google Scholar 

  26. Barnato AE, Anthony DL, Skinner J, Gallagher PM, Fisher ES. Racial and ethnic differences in preferences for end-of-life treatment. J Gen Intern Med. 2009;24:695–701.

    Article  PubMed  Google Scholar 

  27. Perkins HS, Geppert MA, Gonzales A, Cortez JD, Hazuda HP. Cross-cultural similarities and differences in attitudes about advance care planning. J Gen Intern Med. 2002;17:48–57.

    Article  PubMed  Google Scholar 

  28. Perkins HS, Cortez JD, Hazuda HP. Advance care planning: does patient gender make a difference? Am J Med Sci. 2004;327:25–32.

    Article  PubMed  Google Scholar 

  29. Perkins HS, Shepherd KJ, Cortez JD, Hazuda HP. Exploring chronically ill seniors’ attitudes about discussing death and postmortem medical procedures. J Am Geriatr Soc. 2005;53:895–900.

    Article  PubMed  Google Scholar 

  30. Arber S, Vandrevala T, Daly T, Hampson S. Understanding gender differences in older people’s attitudes towards life-prolonging medical technologies. J Aging Stud. 2008;22:366–75.

    Article  Google Scholar 

  31. Babbie ER. Survey research methods. Belmont, California: Wadsworth Publishing, Company, Inc. 1973:106–7.

    Google Scholar 

  32. Lincoln YS, Guba EG. Naturalistic inquiry. Newbury Park, California: SAGE Publications, Inc. 1985:199–202.

    Google Scholar 

  33. Wittink MN, Joo JH, Lewis LM, Barg FK. Losing faith and using faith: older African Americans discuss spirituality, religious activities, and depression. J Gen Intern Med. 2009;24:402–7.

    Article  PubMed  Google Scholar 

  34. Hazuda HP, Comeaux PJ, Stern MP, Haffner SM, Rosenthal M. A comparison of three indicators for identifying Mexican Americans in epidemiologic research: methodologic findings in the San Antonio Heart Study. Am J Epidemiol. 1986;123:96–112.

    CAS  PubMed  Google Scholar 

  35. Lo B, Quill T, Tulsky J. Discussing palliative care with patients. Ann Intern Med. 1999;130:744–9.

    CAS  PubMed  Google Scholar 

  36. Puchalski CM. Spirituality and end-of-life care: a time for listening and caring. J Palliat Med. 2002;5:289–94.

    Article  PubMed  Google Scholar 

  37. Bullock K. Promoting advance directives among African Americans: a faith-based model. J Palliat Med. 2006;9:183–95.

    Article  PubMed  Google Scholar 

  38. Branch WT, Torke A, Brown-Haithco RC. The importance of spirituality in African Americans’ end-of-life experience. J Gen Intern Med. 2006;21:1203–5.

    Article  PubMed  Google Scholar 

  39. Copp G. A review of current theories of death and dying. J Adv Nurs. 1998;28:382–90.

    Article  CAS  PubMed  Google Scholar 

  40. Ganzini L, Goy ER, Dobscha SK. Oregonians’ reasons for requesting physician aid in dying. Arch Intern Med. 2009;169:489–92.

    Article  PubMed  Google Scholar 

  41. Heeren O, Menon AS, Raskin A, Ruskin P. Religion and end of life treatment preferences among geriatric patients. Int J Geriatr Psychiatry. 2001;16:203–8.

    Article  CAS  PubMed  Google Scholar 

  42. Carrese JA, Perkins HS. Ethics consultation in a culturally diverse society. Public Affairs Q. 2003;17:97–120.

    Google Scholar 

  43. Silvestri GA, Knittig S, Zoller JS, Nietert PJ. Importance of faith on medical decisions regarding cancer care. J Clin Oncol. 2003;21:1379–82.

    Article  PubMed  Google Scholar 

  44. Fins JJ, Miller FG, Acres CA, Bacchetta MD, Huzzard LL, Rapkin BD. End-of-life decision-making in the hospital: current practice and future prospects. J Pain Symptom Manage. 1999;17:6–15.

    Article  CAS  PubMed  Google Scholar 

  45. Teno JM, Fisher E, Hamel MB, et al. Decision-making and outcomes of prolonged ICU stays in seriously ill patients. J Am Geriatr Soc. 2000;48:S70–4.

    CAS  PubMed  Google Scholar 

  46. Teno J, Clarridge BR, Casey V, et al. Family perspectives on end-of-life care at the last place of care. JAMA. 2004;291:88–93.

    Article  CAS  PubMed  Google Scholar 

  47. Lorenz KA, Lynn J, Dy SM, et al. Evidence for improving palliative care at the end of life: a systematic review. Ann Intern Med. 2008;148:147–59.

    PubMed  Google Scholar 

  48. Pearlman RA, Cain KC, Patrick DL, et al. Insights pertaining to patient assessments of states worse than death. J Clin Ethics. 1993;4:33–41.

    CAS  PubMed  Google Scholar 

  49. Singer PA, Martin DK, Kelner M. Quality end-of-life care: patients’ perspectives. JAMA. 1999;281:163–8.

    Article  CAS  PubMed  Google Scholar 

  50. Steinhauser KE, Clipp EC, McNeilly M, Christakis NA, McIntyre LM, Tulsky JA. In search of a good death: observations of patients, families, and providers. Ann Intern Med. 2000;132:825–32.

    CAS  PubMed  Google Scholar 

  51. Ganzini L, Goy ER, Dobscha SK. Why Oregon patients request assisted death: family members’ views. J Gen Intern Med. 2007;23:154–7.

    Article  PubMed  Google Scholar 

  52. Carrese JA, Rhodes LA. Bridging cultural differences in medical practice: the case of discussing negative information with Navajo patients. J Gen Intern Med. 2000;15:92–6.

    Article  CAS  PubMed  Google Scholar 

  53. Morrison R. Patients’ sense of completion. BMJ. 1994;308:1722.

    PubMed  Google Scholar 

  54. Larson DG, Tobin DR. End-of-life conversations: evolving practice and theory. JAMA. 2000;284:1573–8.

    Article  CAS  PubMed  Google Scholar 

  55. Curtis JR, Patrick DL. Barriers to communication about end-of-life care in AIDS patients. J Gen Intern Med. 1997;12:736–41.

    Article  CAS  PubMed  Google Scholar 

  56. Quill TE. Initiating end-of-life discussions with seriously ill patients: addressing the “elephant in the room.” JAMA. 2000;284:2502–7.

    Article  CAS  PubMed  Google Scholar 

  57. Ressler AB. Aesthetic expression: an existential examination of healthcare ethics. Int J Human Caring. 2006;10:61–7.

    Google Scholar 

  58. Back AL, Young JP, McCown E, et al. Abandonment at the end of life from patient, caregiver, nurse, and physician perspectives: loss of continuity and lack of closure. Arch Intern Med. 2009;169:474–9.

    Article  PubMed  Google Scholar 

  59. Perkins HS. Controlling death: the false promise of advance directives. Ann Intern Med. 2007;147:51–7.

    PubMed  Google Scholar 

  60. Pantilat SZ. Communicating with seriously ill patients: better words to say. JAMA. 2009;301:1279–81.

    Article  CAS  PubMed  Google Scholar 

  61. Zier LS, Burack JH, Micco G, et al. Doubt and belief in physicians’ ability to prognosticate during critical illness: the perspective of surrogate decision makers. Crit Care Med. 2008;36:2341–7.

    Article  PubMed  Google Scholar 

  62. Carr D. A “good death” for whom? Quality of a spouse’s death and psychological distress among older widowed persons. J Health Soc Behav. 2003;44:215–32.

    Article  PubMed  Google Scholar 

  63. Seymour JE. Negotiating natural death in intensive care. Soc Sci Med. 2000;51:1241–52.

    Article  CAS  PubMed  Google Scholar 

  64. Maciejewski PK, Zhang B, Block SD, Prigerson HG. An empirical examination of the stage theory of grief. JAMA. 2007;297:716–23.

    Article  CAS  PubMed  Google Scholar 

  65. Hauser JM, Kleefield SF, Brennan TA, Fischbach RL. Minority populations and advance directives: insights from a focus group methodology. Camb Q Healthc Ethics. 1997;6:58–71.

    CAS  Google Scholar 

  66. Block SD. Psychological considerations, growth, and transcendence at the end of life: the art of the possible. JAMA. 2001;285:2898–2905.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

Others besides the authors made important contributions to this manuscript. Sarah Piper McMahon, M.D.; Caroline McGee-Jones, M.D.; and Alisa Meny, M.D., helped analyze the data. Drs. Piper McMahon and McGee-Jones were students at The University of Texas Health Science Center at San Antonio, and Dr. Meny was a student at Harvard University when they participated in the study. Charles Cavazos from the Intercultural Development Research Association provided computer support. Susan Bagby made editorial suggestions about early drafts of the manuscript.

The John A. Hartford Foundation; the American Federation on Aging Research; and the Mexican-American Medical Treatment Effectiveness Research Center, the Aging Research and Education Center, and the Medical Dean’s Office at The University of Texas Health Science Center at San Antonio all contributed funds for this research. The authors thank all these people and funders for their help.

Authors’ Conflict of Interest Statement

Henry Perkins, Josie Cortez, and Helen Hazuda collaboratively conceived and designed this study, analyzed and interpreted its data, and prepared the manuscript reporting the results. The authors have no conflicts of interest to disclose.

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Correspondence to Henry S. Perkins M.D..

Additional information

Presentations at professional meetings: The results we report here were presented at the Eighth Annual David C. Thomasma, Ph.D., International Bioethics Retreat, Freije Universitat, Amsterdam, the Netherlands, 24 June 2006; and at the annual meeting of the Southern Region, Society of General Internal Medicine, Atlanta, Georgia, 04 March 2006. The results were also accepted for presentation at the national meeting, Society of General Internal Medicine, Los Angeles, California, 26–9 April 2006.

Grant Support: The John A. Hartford Foundation; the American Federation on Aging Research; and the Mexican-American Medical Treatment Effectiveness Research Center, the Aging Research and Education Center, and the Medical Dean’s Office at The University of Texas Health Science Center at San Antonio all contributed funds for this research. The sponsors played no role in any part of the study.

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Perkins, H.S., Cortez, J.D. & Hazuda, H.P. Cultural Beliefs About a Patient’s Right Time to Die: An Exploratory Study. J GEN INTERN MED 24, 1240–1247 (2009). https://doi.org/10.1007/s11606-009-1115-5

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