LIFE-SUSTAINING TREATMENTS DURING TERMINAL ILLNESS - WHO WANTS WHAT

被引:216
作者
GARRETT, JM
HARRIS, RP
NORBURN, JK
PATRICK, DL
DANIS, M
机构
[1] Cecil G. Sheps Center for Health Services Research, University of North Carolina, Chapel Hill, 27599-7490, NC, CB# 7590, 725 Airport Road
[2] the Department of Medicine, University of North Carolina, Chapel Hill, North Carolina
[3] the Department of Health Services Research, University of Washington, Seattle, Washington
关键词
TERMINAL ILLNESS; LIFE-SUSTAINING TREATMENT; LIVING WILL; PATIENT PREFERENCES;
D O I
10.1007/BF02600073
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
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% of blacks vs 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.
引用
收藏
页码:361 / 368
页数:8
相关论文
共 28 条
  • [1] Guideline on the termination of life-sustaining treatment and the care of the dying, (1987)
  • [2] Wolf S.M., Boyle T., Callahan D., Et al., Sources of concern about the Patient Self-Determination Act, N Engl J Med, 325, pp. 1666-71, (1991)
  • [3] Emanuel I.X., Barry M.J., Stoeckle J.D., Ettelson L.M., Emanuel E.J., Advance directives for medical care—a case for greater use, N Engl J Med, 324, pp. 889-95, (1991)
  • [4] Gamble E.R., McDonald P.J., Lichstein P.R., Knowledge, attitudes, and behavior of elderly persons regarding living wills, Arch Intern Med, 515, pp. 277-80, (1991)
  • [5] Lo B., McLeod G.A., Saika G., Patient attitudes to discussing life-sustaining treatment, Arch Intern Med, 146, pp. 1613-5, (1986)
  • [6] Snow R.M., Atwood K., Probable death: perspective of the elderly, South Med J, 78, pp. 851-3, (1985)
  • [7] Mossey J., Shapiro E., Self-rated health: a predictor of mortality among the elderly, Am J Public Health, 72, pp. 800-8, (1982)
  • [8] Kaplan R.M., Anderson J.P., The general health policy model: an integrated approach, Quality of life assessments in clinical trials, pp. 131-49, (1990)
  • [9] Patrick D.L., Bush J., Chen M., Toward an operational definition of health, J Health Soc Behav, 14, pp. 6-23, (1973)
  • [10] Kaplan R.M., Bush J.W., Berry C.C., Health status: types of validity and the index of well-being, Health Serv Res, 11, pp. 478-507, (1976)