Skip to main content
Social Sci LibreTexts

10.R: Death and Dying (References)

  • Page ID
    10797
  • American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders (5th ed.). Washington, DC: Author.

    Archer, J. (1999). The nature of grief: The evolution and psychology of reactions to loss. London and New York: Routledge.

    Batts, J. (2004). Death and grief in the family: Tips for parents. Retrieved from https://www.nasponline.org/search/search-results?keywords=death+and+grief+in+the+family

    Bell, K. W. (2010). Living at the end of life. New York: Sterling Ethos.

    Berger, J. T. (1998). Cultural discrimination in mechanisms for health decisions: A view from New York. Journal of Clinical Ethics, 9, 127-131.

    Brannely, T. (2011). Sustaining citizenship: People with dementia and the phenomenon of social death. Nursing Ethics, 18(5), 662-671. Doi:10.1177/0969733011408049

    Broad, J. B., Gott, M., Kim, H., Boyd, M., Chen, H., & Connolly, J. M. (2013). Where do people die? An international comparison of the percentage of deaths occurring in hospital and residential aged care settings in 45 populations, using published and available statistics. International Journal of Public Health, 58(2), 257-267.

    Candib, L. M. (2002). Truth telling and advanced planning at end of life: problems with autonomy in a multicultural world. Family System Health, 20, 213-228.

    Casarett, D., Kutner, J. S., & Abrahm, J. (2001). Life after death: a practical approach to grief and bereavement. Annals of Internal Medicine, 134(3), 208-15.

    Centers for Disease Control (2015). Leading causes of death by age group 2013. Retrieved from https://www.cdc.gov/injury/wisqars/p...oup_2013-a.pdf

    Centers for Disease Control. (2016). Leading causes of death. Retrieved from https://www.cdc.gov/nchs/fastats/leading-causes-of-death.htm

    Coolen, P. R. (2012). Cultural relevance in end-of-life care. EthnoMed, University of Washington. Retrieved from https://ethnomed.org/clinical/end-of...d-of-life-care

    Doka, K. (1989). Disenfranchised grief. Lexington, MA: Lexington Books.

    Dresser, N. & Wasserman, F. (2010). Saying goodbye to someone you love. New York: Demos Medical Publishing.

    Ellis, J., Dowrick, C., & Lloyd-Williams, M. (2013). The long-term impact of early parental death: Lessons from a narrative study. The Journal of the Royal Society of Medicine, 106(2), 57-67.

    Erber, J. T., & Szuchman, L. T. (2015). Great myths of aging. West Sussex, UK: Wiley & Sons.

    Fox, E. (1997). Predominance of the curative model of medical care: A residual problem. Journal of the American Medical Association, 278(9), 761-764. Retrieved from: http://www.fammed.washington.edu/pal...9/PCvCC.htm#11

    Friedman, R., & James, J. W. (2008). The myth of the stages of loss, death, and grief. Skeptic Magazine, 14(2), 37-41. Glaser, B. G., & Strauss, A. L. (1966). Awareness of dying. London: Weidenfeld and Nicholson.

    Hall, M. J., Levant, S., & DeFrances, C. J. (2013). Trends in in-patient hospital deaths: National hospital discharge survey (2000-2010). CDC: National Centers for Health Statistics. Retrieved from https://www.cdc.gov/nchs/data/databriefs/db118.pdf

    Herndon, E., & Joyce, L. (2004). Getting the most from language interpreters. Family Practice Management, 11, 37-40. Holland, J. L., Geary, N., Marchini, A., & Tross, S. (1987). An international survey of physician attitudes and practices in regard to revealing the diagnosis of cancer. Cancer Investigation, 5, 151-154.

    Institute of Medicine. (1997). Approaching death: Improving care at the end of life. M. J. Field & C. K. Cassel (eds). Washington (DC): National Academies Press Retrieved from: https://www.ncbi.nlm.nih.gov/books/NBK233601/

    Institute of Medicine. (2015). Dying in America: Improving quality and honoring individual preferences near end of life. Washington, DC: The National Academies Press.

    Kaufert, J. M., & Putsch, R. W., (1997). Communication through interpreters in healthcare: Ethical dilemmas arising from differences in class, culture, language, and power. Journal of Clinical Ethics, 8, 71-87.

    Kübler-Ross, E. (1969). On death and dying. New York: Macmillan.

    Kübler-Ross, E. (1975). Death; The final stage of growth. Englewood Cliffs, N. J.: Prentice-Hall. Kübler-Ross,

    E., & Kessler, D. (2005). On grief and grieving. New York: Schribner.

    Lipka, M. (2014). 5 facts about Americans’ views on life and death issues. Pew Research Institute. Retrieved from http://www.pewresearch.org/fact-tank...-death-issues/

    Lynn, J., & Harrold, J. (2011). Handbook for mortals (2nd ed.). New York: Oxford University Press.

    Maciejewski, P. K., Zhang, B., Block, S. D., & Prigerson, H. G. (2007). An empirical examination of the stage theory of grief. Journal of the American Medical Association, 297(7), 716-723.

    Marks, N. F., Jun, H., & Song, J. (2007). Death of parents and adult psychological and physical well-being: A prospective U. S. national study. Journal of Family Issues, 28(12), 1611-1638.

    Morrison, R. S., Zayas, L. H., Mulvihill, M., Baskin, S. A., & Meier, D. E. (1998). Barriers to completion of healthcare proxy forms: A qualitative analysis of ethnic differences. Journal of Clinical Ethics, 9, 118-126.

    Moss, M. S., & Moss, S. Z. (1995). Death and bereavement. In R. Blieszner and V. H. Bedford (Eds.), Handbook of aging and the family (pp.422-439). Westport, CT: Greenwood.

    National Institute on Health. (2007). Hospitals Embrace the Hospice Model. Retrieved from http://www.nlm.nih.gov/medlineplus/n...ory_43523.html

    National Hospice and Palliative Care Organization. (2013). NHPCO’s facts and figures: Hospice care in America 2013 edition. Retrieved from http://www.nhpco.org/sites/default/f...ts_Figures.pdf

    National Hospice and Palliative Care Organization. (2014). NHPCO’s facts and figures: Hospice care in America 2014 edition. Retrieved from http://www.nhpco.org/sites/default/f...ts_Figures.pdf

    Newson, R. S., Boelen, P. A., Hek, K., Hofman, A., & Tiemeier, H. (2011). The prevalence and characteristics of complicated grief in older adults. Journal of Affective Disorders, 132(1-2), 231-238.

    Narayan, C. (2016). First child dies by euthanasia in Belgium. Retrieved from http://www.cnn.com/2016/09/17/health/belgium-minor-euthanasia/

    National Cancer Institute. (2013). Grief, bereavement, and coping with loss. Retrieved from https://www.cancer.gov/about-cancer/advanced-cancer/caregivers/planning/bereavement-pdq#section/_62

    Oregon Public Health Division. (2016). Oregon Death with Dignity Act: 2015 data summary. Retrieved from https://public.health.oregon.gov/Pro...nts/year18.pdf

    Parkes, C. M., & Prigerson, H. G. (2010). Bereavement: Studies of grief in adult life. New York: Routledge.

    Pattison, E. M. (1977). The experience of dying. Englewood Cliffs, N. J.: Prentice-Hall.

    Pew Research Center. (2013). Views on end-of-life medical treatment. Retrieved from http://www.pewforum.org/2013/11/21/v...al-treatments/

    ProCon.org. (2016). State-by-state guide to physician-assisted suicide. Retrieved from http://euthanasia.procon.org/view.re...ourceID=000132

    Redfoot, D., Feinberg, L., & Houser, A. (2013). The aging of the baby boom and the growing care gap: A look at future declines in the availability of family caregivers. AARP. Retrieved from http://www.aarp.org/content/dam/aarp...RP-ppi-ltc.pdf

    Schechter, H. (2009). The whole death catalog. New York: Ballantine Books.

    Searight, H. R., & Gafford, J. (2005a). Cultural diversity at end of life: Issues and guidelines for family physicians. American Family Physician, 71(3), 515-522.

    Searight, H. R., & Gafford, J. (2005b). “It’s like playing with your destiny”: Bosnian immigrants’ views of advance directives and end-of-life decision-making. Journal or Immigrant Health, 7(3), 195-203.

    Shannon, J. B. (2006). Death and dying sourcebook. Detroit, MI: Omnigraphics.

    Stroebe, M. S., & Schut, H. (2001). Meaning making in the duel process model of coping with bereavement. In R. A. Neimeyer (Ed.), Meaning, reconstruction and the experience of loss (pp. 55-73). Washington, DC: American Psychological Association.

    Stroebe, M. S., Schut, H., & Stroebe, W. (2005). Attachment in coping with bereavement: A theoretical integration. Review of General Psychology, 9, 48-66.

    Sweeting, H., & Gilhooly, M. (1997). Dementia and the phenomenon of social death. Sociology of Health and Illness, 19, 93– 117.

    Taylor, S. E., Kemeny, M. E., Reed, G. M., Bower, J. E., & Gruenewald, T. L. (2000). Psychological resources, positive illusions, and health. American Psychologist, 55(1), 99-109.

    Telford, K., Kralik, D., & Koch, T. (2006). Acceptance and Denial: Implications for People Adapting to chronic illness: Literature review. Journal of Advanced Nursing, 55, 457-464.

    Uniform Law Commissioners. (1980). Defining death: medical, legal and ethical issues in the definition of death. Washington, DC: US Government Printing Office, 1981159–166.166

    Weitz, R. (2007). The sociology of health, illness, and health care: A critical approach (4th ed.). Belmont, CA: Thomson/Wadsworth.

    Worden, J. W. (2002). Children and grief: When a parent dies. London: Guilford Press.

    Worden, J. W. (2008). Grief counseling and grief therapy: A handbook for the mental health practitioner (4th ed.). New York: Springer Publishing company.

    World Health Organization. (2016). The top ten causes of death. Retrieved from http://www.who.int/mediacentre/facts...en/index2.html

    Youdin, R. (2016). Psychology of aging 101. New York: Springer Publishing Company.