End-of-life care in the intensive care unit: can we do better?

Everywhere we turn these days, it seems that we are confronted with a new study that reports the dissatisfaction expressed by families with the quality of care received by their loved ones who have died while in the intensive care unit. It is difficult for caregivers to accept this information, which is now commonly reported both in published studies and in the lay press. As clinicians, most of us believe that we truly care about our patients and are trying, as best we can, to act in their best interest. No caregiver wants to hear that he or she does not do a good job when caring for dying patients and their families. It is ironic that clinicians recognize and accept the need for continuing education. Yet many clinicians resent the suggestion that the skills required for end-of-life care might be viewed in the same manner, as a lifelong learning process. It is unusual for physicians to identify end-of-life-care as an area of competency that can be improved or updated. Perhaps this is why end-of-life-care has been so difficult to teach to clinicians in training. Although many medical schools offer courses on the ethics of death and dying, formal training in end-of-life care skills is not routinely given in most postgraduate training programs. Learning these skills is a matter of on-the-job training for most caregivers. Not only have we been unable to measure any beneficial impact from education initiatives for end-of-life care, we have yet to identify clear indicators for end-of-life care. For caregivers, enhancing end-of-life skills may be a matter of improved listening skills, attention to the proper environment for end-of-life discussions, and a willingness to facilitate end-of-life decision-making. Encouraging caregivers to view end-of-life skills as a lifelong educational process, identifying core competencies in end-of-life care, and training clinicians in these skills are the challenges for the future. The quality of care our patients receive at the end of life will depend on our ability to answer these difficult questions.

[1]  N. Molter Needs of relatives of critically ill patients: a descriptive study. , 1979, Heart & lung : the journal of critical care.

[2]  M. Solomon How Physicians Talk about Futility: Making Words Mean Too Many Things , 1993, Journal of Law, Medicine & Ethics.

[3]  J. Garrett,et al.  What Is Wrong With End‐of‐Life Care? Opinions of Bereaved Family Members , 1997, Journal of the American Geriatrics Society.

[4]  J. Ptacek,et al.  Breaking Bad News: A Review of the Literature , 1996 .

[5]  J. Nelson Saving Lives and Saving Deaths , 1999, Annals of Internal Medicine.

[6]  E. Cook,et al.  Relationship between cancer patients' predictions of prognosis and their treatment preferences. , 1998, JAMA.

[7]  D. Gudmundson,et al.  Measuring the ability to meet family needs in an intensive care unit. , 1998, Critical care medicine.

[8]  V. Raveis,et al.  Caregiver burden and unmet patient needs , 1991, Cancer.

[9]  M. Hickey What are the needs of families of critically ill patients? A review of the literature since 1976. , 1990, Heart & lung : the journal of critical care.

[10]  M. Kelner Activists and delegators: elderly patients' preferences about control at the end of life. , 1995, Social science & medicine.

[11]  D. Patrick,et al.  The quality of patient-doctor communication about end-of-life care: a study of patients with advanced AIDS and their primary care clinicians. , 1999, AIDS.

[12]  M. Bott,et al.  The experiences of families with a relative in the intensive care unit. , 1996, Heart & lung : the journal of critical care.

[13]  William A. Knaus,et al.  A controlled trial to improve care for seriously ill hospitalized patients. The study to understand prognoses and preferences for outcomes and risks of treatments (SUPPORT). The SUPPORT Principal Investigators. , 1995, JAMA.

[14]  Albert Wu,et al.  Perceptions by Family Members of the Dying Experience of Older and Seriously Ill Patients , 1997, Annals of Internal Medicine.

[15]  J. Luce,et al.  Increasing incidence of withholding and withdrawal of life support from the critically ill. , 1997, American journal of respiratory and critical care medicine.

[16]  P. Singer,et al.  Quality end-of-life care: patients' perspectives. , 1999, JAMA.

[17]  S. Zisook,et al.  The Psychological and Physical Health of Hospice Caregivers , 2000, Annals of clinical psychiatry : official journal of the American Academy of Clinical Psychiatrists.

[18]  P. Houts,et al.  Unmet needs of persons with cancer in pennsylvania during the period of terminal care , 1988, Cancer.

[19]  J. Kaur Palliative care and hospice programs. , 2000, Mayo Clinic proceedings.

[20]  D. Patrick,et al.  Why don't patients and physicians talk about end-of-life care? Barriers to communication for patients with acquired immunodeficiency syndrome and their primary care clinicians. , 2000, Archives of internal medicine.

[21]  H. Brody,et al.  Withdrawing intensive life-sustaining treatment -- recommendations for compassionate clinical management. , 1997, The New England journal of medicine.

[22]  K. Faber-Langendoen,et al.  A multi-institutional study of care given to patients dying in hospitals. Ethical and practice implications. , 1996, Archives of internal medicine.