'No control whatsoever': end-of-life care on a medical teaching unit from the perspective of family members.

BACKGROUND In our institution, about one third of annual deaths occur on the general medical teaching unit. (MTU) The average patient dies on the MTU from non-malignant disease after 4 weeks in hospital, and approximately 20% of available beds on the MTU at any time are occupied by patients who will not survive to discharge, but quality of end-of-life care on the MTU is not routinely assessed. AIM To identify areas for improvement in delivering high quality end-of-life care on the medical teaching unit. DESIGN Qualitative study using semi-structured interviews. METHODS Six months after the death of the patient, next of kin were sent a letter inviting participation; 75 family members were screened and 50 invitations were mailed out. Interviews were conducted in the home. Eliciting narratives and direct questioning about important aspects of end-of-life care were used. RESULTS Six next of kin agreed to participate. All patients were described as seriously and chronically ill. None died of cancer. Deaths were not described as 'good', and some comments suggested that death was unexpected and not inevitable. There were few concerns about pain control or unnecessary suffering. Proactive efforts to provide prognostic information or end-of-life care were not described. Survival, not palliation, was of central importance. Consistent with this priority, satisfaction with care provided in the intensive care unit was high. Follow-up after death was desired, especially if autopsy results were available. DISCUSSION Earlier discussions about treatment failure and end-of-life care, and the need for palliation, appear to be central to improving the quality of end-of-life care for patients dying on our medical teaching unit. Our results are consistent with other studies in this area.

[1]  B. Souweine,et al.  A communication strategy and brochure for relatives of patients dying in the ICU. , 2007, The New England journal of medicine.

[2]  A. Gafni,et al.  What matters most in end-of-life care: perceptions of seriously ill patients and their family members , 2006, Canadian Medical Association Journal.

[3]  Amber E Barnato,et al.  Use of intensive care at the end of life in the United States: An epidemiologic study* , 2004, Critical care medicine.

[4]  J. O’Leary,et al.  Prognosis Communication in Serious Illness: Perceptions of Older Patients, Caregivers, and Clinicians , 2003, Journal of the American Geriatrics Society.

[5]  Jocalyn P Clark Patient centred death , 2003, BMJ : British Medical Journal.

[6]  M. L. van der Lee,et al.  Effects of euthanasia on the bereaved family and friends: a cross sectional study , 2003, BMJ : British Medical Journal.

[7]  P. Edmonds,et al.  'If only someone had told me . . .' A review of the care of patients dying in hospital. , 2003, Clinical medicine.

[8]  A. Gafni,et al.  The seriously ill hospitalized patient: preferred role in end-of-life decision making? , 2003, Journal of critical care.

[9]  J. D. Armstrong,et al.  Would you be surprised if this patient died?: Preliminary exploration of first and second year residents' approach to care decisions in critically ill patients , 2003, BMC palliative care.

[10]  Scott A Murray,et al.  Dying of lung cancer or cardiac failure: prospective qualitative interview study of patients and their carers in the community , 2002, BMJ : British Medical Journal.

[11]  G. Crelinsten,et al.  Routine advance directive and organ donation questioning on admission to hospital. , 2002, Annals.

[12]  Roger B. Davis,et al.  The Last Six Months of Life for Patients with Congestive Heart Failure , 2000, Journal of the American Geriatrics Society.

[13]  Richard Smith A good death , 2000, BMJ.

[14]  T. Nilstun,et al.  Not if, but how: one way to talk with patients about forgoing life support , 2000, Postgraduate medical journal.

[15]  W. Baile,et al.  Discussing disease progression and end-of-life decisions. , 1999, Oncology.

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

[17]  M. Field,et al.  Measuring quality of care at the end of life. , 1998, Archives of internal medicine.

[18]  J. Martínez-Alier,et al.  Series Editor: , 2007 .