Battin, M. P. (1994). The politics of dying. In The least worst death: Essays in bioethics on the end of life (pp. 1-29). New York: Oxford University Press.
2.
Block, S. D. (2000). Assessing and managing depression in the terminally ill patient. Annals of Internal Medicine, 132, 209-218.
3.
Breitbart, W. , Rosenfeld, B., Pessin, H., Kaim, M., Funesti-Esch, J., Galietta, M., et al. (2000). Depression, hopelessness, and desire for hastened death in terminally ill patients with cancer. Journal of the American Medical Association, 284, 2907-2911.
4.
Christakis, N. A. , & Iwashyna, T. J. (2000). The impact of individual and market factors on the timing of initiation of hospice terminal care. Medical Care, 38, 528-541.
5.
Cruzan v. Director, Missouri Department of Health, 497 U.S. 261 (1990).
6.
Farberman, R. K. (1997). Terminal illness and hastened death requests: The important role of the mental health professional. Professional Psychology: Research and Practice, 28, 544-547.
7.
Field, M. J. , & Cassel, C. K. (Eds.). (1997). Approaching death: Improving care at the end of life. Washington, DC: National Academy Press.
8.
General Accounting Office . (1995). Patient Self-Determination Act: Providers offer information on advance directives but effectiveness uncertain (Publication No. GAO/HEHS-95-135). Washington, DC: Government Printing Office.
9.
General Accounting Office . (2000). Medicare: More beneficiaries use hospice; many factors contribute to shorter periods of use (Publication No. GAO/HEHS-00-201). Washington, DC: Government Printing Office.
10.
Jackson, A. (2000). Observations on the first year: A commentary. Psychology, Public Policy, and Law, 6, 322-330.
11.
Leggat, J. E. , Swartz, R. D., & Port, F. K. (1997). Withdrawal from dialysis: A review with an emphasis on the Black experience. Advances in Renal Replacement Therapy, 4, 22-29.
12.
Magaziner, J. , Zimmerman, S. I., German, P. S., Kuhn, K., May, C., Hooper, F., et al. (1996). Ascertaining dementia by expert panel in epidemiologic studies of nursing home residents. Annals of Epidemiology, 6, 431-437.
13.
Marwit, S. J. (1997). Professional psychology's role in hospice care. Professional Psychology: Research and Practice, 28, 457-463.
14.
Meisel, A. (1995). The right to die (2nd ed.). New York: John Wiley.
15.
Moss, M. S. (2001). End of life in nursing homes. In M. P. Lawton (Ed.), Annual review of gerontology and geriatrics, Vol. 20, the end of life: Scientific and social issues (pp. 224-258). New York: Springer.
16.
National Association of Social Workers . (1994). Client self-determination in end-of-life decisions. In Social work speaks (3rd ed., pp. 58-61). Washington, DC: NASW Press.
17.
Schulz, R. , & Heckhausen, J. (1996). A life span model of successful aging. American Psychologist, 51, 702-714.
18.
Singer, P. A. , Martin, D. K., & Kelner, M. (1999). Quality end-of-life care: Patients' perspectives. Journal of the American Medical Association, 281, 163-168.
19.
Smith, D. (2001). Increasing psychology's voice on end-of-life issues. Monitor on Psychology, 32(1), 61.
20.
Steinberg, M. D. , & Youngner, S. J. (Eds.). (1998). End-of-life decisions: A psychosocial perspective. Washington, DC: American Psychiatric Press.
21.
Steinhauser, K. E. , Christakis, N. A., Clipp, E. C., McNeilly, M., McIntyre, L., & Tulsky, J. A. (2000). Factors considered important at the end of life by patients, family, physicians, and other care providers. Journal of the American Medical Association, 284, 2476-2482.
22.
SUPPORT Principal Investigators . (1995). A controlled trial to improve care for seriously ill hospitalized patients: The Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatment (SUPPORT). Journal of the American Medical Association, 274, 1591-1598.
23.
Thomas, J. (2001). Assisted suicide debate divides APA council meeting. National Psychologist, 10(2), 1, 3.
24.
Tomes, H. (2000). The heaviness of end-of-life issues. Monitor on Psychology, 31(11), 68-69.
25.
Vacco v. Quill, 117 S.Ct. 2293 (1997).
26.
Washington v. Glucksberg, 117 S.Ct. 2258 (1997).
27.
Werth, J. L., Jr. , & Gordon, J. R. (2002). Amicus curiae brief for the United States Supreme Court on mental health issues associated with “physician-assisted suicide.”Journal of Counseling and Development, 80, 160-172.
28.
Werth, J. L., Jr. , Gordon, J. R., & Johnson, R. (in press). Psychosocial issues near the end of life. Aging and Mental Health.
29.
Wilson, K. G. , Viola, R. A., Scott, J. F., & Chater, S. (1998, April). Talking to the terminally ill about euthanasia and physician-assisted suicide. Canadian Journal of Clinical Medicine, 68-74.
30.
Working Group on Assisted Suicide and End-of-Life Decisions. (2000). Report to the board of directors of the American Psychological Association. Retrieved May 31, 2002, from http://www.apa.org/pi/aseolf.html