Skip to main content
Log in

Life-sustaining treatments during terminal illness

Who wants what?

  • Original Articles
  • Published:
Journal of General Internal Medicine Aims and scope Submit manuscript

Abstract

Objective: To determine patient characteristics associated with the desire for life-sustaining treatments in the event of terminal illness.

Design: In-person survey from October 1986 to June 1988.

Setting: 13 internal medicine and family practices in North Carolina.

Patients: 2,536 patients (46% of those eligible) aged 65 years and older who were continuing care patients of participating practices, enrolled in Medicare. The patients were slightly older than the 65+ general population, 61% female, and 69% white, and most had one or more chronic illnesses.

Measurements and main results: The authors asked the patients whether they would want each of six different treatments (hospitalization, intensive care, cardiopulmonary resuscitation, surgery, artificial ventilation, or tube feeding) if they were to have a terminal illness. The authors combined responses into three categories ranging from the desire for more treatment to the desire for less treatment. After adjustment for other factors, 53% of women chose less treatment compared with 43% of men; 35%ofblacksvs 15% of whites and 23% of the less well educated vs 15% of the better educated expressed the desire for more treatment. High depression scores also were associated with the desire for more treatment (26% for depressed vs 18% for others).

Conclusion: Patients’ choices for care in the event of terminal illness relate to an intricate set of demographic, educational, and cultural factors. These results should not be used as a shortcut to determine patient preferences for care, but may provide new insights into the basis for patients’ preferences. In discussing choices for future life-sustaining care, physicians need to explore with each individual the basis for his or her choices.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Hastings Center. Guideline on the termination of life-sustaining treatment and the care of the dying. Bloomington, IN: University Press, 1987.

    Google Scholar 

  2. Wolf SM, Boyle T, Callahan D, et al. Sources of concern about the Patient Self-Determination Act. N Engl J Med. 1991;325:1666–71.

    Article  PubMed  CAS  Google Scholar 

  3. Emanuel IX, Barry MJ, Stoeckle JD, Ettelson LM, Emanuel EJ. Advance directives for medical care—a case for greater use. N Engl J Med. 1991;324:889–95.

    Article  PubMed  CAS  Google Scholar 

  4. Gamble ER, McDonald PJ, Lichstein PR. Knowledge, attitudes, and behavior of elderly persons regarding living wills. Arch Intern Med. 1991;515:277–80.

    Article  Google Scholar 

  5. Lo B, McLeod GA, Saika G. Patient attitudes to discussing life-sustaining treatment. Arch Intern Med. 1986;146:1613–5.

    Article  PubMed  CAS  Google Scholar 

  6. Snow RM, Atwood K. Probable death: perspective of the elderly. South Med J. 1985;78:851–3.

    Article  PubMed  CAS  Google Scholar 

  7. Mossey J, Shapiro E. Self-rated health: a predictor of mortality among the elderly. Am J Public Health. 1982;72:800–8.

    PubMed  CAS  Google Scholar 

  8. Kaplan RM, Anderson JP. The general health policy model: an integrated approach. In: Spilker B (ed). Quality of life assessments in clinical trials. New York: Raven Press, 1990;131–49.

    Google Scholar 

  9. Patrick DL, Bush J, Chen M. Toward an operational definition of health. J Health Soc Behav. 1973;14:6–23.

    Article  PubMed  CAS  Google Scholar 

  10. Kaplan RM, Bush JW, Berry CC. Health status: types of validity and the index of well-being. Health Serv Res. 1976;11:478–507.

    PubMed  CAS  Google Scholar 

  11. Danis M, Patrick DL, Southerland LI, et al. Patients’ and families’ preferences for medical intensive care. JAMA. 1988;260:797–802.

    Article  PubMed  CAS  Google Scholar 

  12. Radloff LS. The CES-D scale: a self-report depression scale for research in the general population. Appl Psychol Measurement. 1977;1:385–401.

    Article  Google Scholar 

  13. Fries J. Personal communication, Sept 1991.

  14. Frankl D, Oye RK, Bellamy PE. Attitude of hospitalized patients toward life support: survey of 200 medical inpatients. Am J Med. 1989;86:645–8.

    Article  CAS  Google Scholar 

  15. Danis M, Mutran E, Fitzsimmons J. Attitudes associated with the desire for life-sustaining treatment in elderly patients. Clin Res. 1991;39(2):624A.

    Google Scholar 

  16. Wenger NS, Oye RK, Teno JM, et al. Patient age, race and perceived health status are associated with preferences for “comfort care.” Clin Res. 1992;40(2):620A.

    Google Scholar 

  17. Miles SH, August A. Courts, gender and “the right to die”. Law Med Health Care. 1990;19(1–2):85–95.

    Google Scholar 

  18. Strogatz DS. Use of medical care for chest pain: differences between blacks and whites. Am J Public Health. 1990;80:290–4.

    PubMed  CAS  Google Scholar 

  19. Kessler RC, Neighbors HW. A new perspective on the relationships among race, social class, and psychological distress. J Health Soc Behav. 1986;27:107.

    Article  PubMed  CAS  Google Scholar 

  20. Kasiske BL, Neylan JF, Riggio RR, et al. The effects of race on access and outcome in transplantation. N Engl J Med. 1991;324:302–7.

    Article  PubMed  CAS  Google Scholar 

  21. Wenneker MB, Epstein AM. Racial inequalities in the use of procedures for patients with ischemic heart disease in Massachusetts. JAMA. 1989;261:253–7.

    Article  PubMed  CAS  Google Scholar 

  22. James SA, Wagner EH, Strogatz DS, et al. The Edgecombe County (NC) high blood pressure control program: II. Barriers to the use of medical care among hypertensives. Am J Public Health. 1985;74:468–72.

    Article  Google Scholar 

  23. Gemson DH, Elinson J, Messeri P. Differences in physician prevention practice patterns for white and minority patients. Community Health. 1988;13(1):53–64.

    Article  CAS  Google Scholar 

  24. Blendon RJ, Aiken LH, Freeman HE, Corey CR. Access to medical care for black and white Americans. JAMA. 1989;261:278–81.

    Article  PubMed  CAS  Google Scholar 

  25. Sehgal A, Galbraith A, Chesney M, Schoenfeld P, Charles G, Lo B. How strictly do dialysis patients want their advance directives followed: JAMA. 1992;267:59–63.

    Article  PubMed  CAS  Google Scholar 

  26. Meehan PJ, Saltzman LE, Sattin RW. Suicides among older United States residents: epidemiologic characteristics and trends. Am J Public Health. 1991;81:1198–200.

    PubMed  CAS  Google Scholar 

  27. Lund J. Personal communication, Sept 1991.

  28. National Center for Health Statistics. Health, United States, 1990. Hyattsville, MD: Public Health Service, 1991.

    Google Scholar 

  29. Kalish RA, Reynolds DK. Death and ethnicity: a psychocultural study. Los Angeles, CA: Ethyl Percy Andrus Gerontology Center, University of Southern California, 1976.

    Google Scholar 

  30. Blendon JR, Szalay VS, Knox RA. Should physicians aid their patients in dying? JAMA. 1992;267:2658–62.

    Article  PubMed  CAS  Google Scholar 

  31. President’s Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research. Deciding to forego life-sustaining treatment. Washington, DC: U.S. Government Printing Office, 1983.

    Google Scholar 

  32. Wanzer SH, Federman DD, Adelstein SJ, et al. The physician’s responsibility toward hopelessly ill patients: a second look. N Engl J Med. 1989;320:844–9.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported in part by a cooperative research agreement (95-C-98516/4) between the Health Care Financing Administration and the Department of Social Medicine, School of Medicine, in collaboration with the Cecil G. Sheps Center for Health Services Research, at the University of North Carolina at Chapel Hill (Joseph P. Morrissey, PhD, principal investigator).

The views expressed are those of the authors and do not necessarily reflect the opinions of HCFA.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Garrett, J.M., Harris, R.P., Norburn, J.K. et al. Life-sustaining treatments during terminal illness. J Gen Intern Med 8, 361–368 (1993). https://doi.org/10.1007/BF02600073

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02600073

Key words

Navigation