| | The Landscape of Distress in the Terminally IllAccepted 1 April 2009. published online 27 August 2009. Abstract Understanding the complexities of distress and knowing who is most vulnerable is foundational to the provision of quality, palliative end-of-life care. Although prior studies have examined the prevalence of symptom distress among patients nearing death, these studies have tended to largely focus on physical and, to a lesser extent, psychological challenges. The aim of this study was to use the Patient Dignity Inventory (PDI), a novel, reliable, and validated measure of end-of-life distress, to describe a broad landscape of distress in patients who are terminally ill. The PDI, a 25-item self-report, was administered to 253 patients receiving palliative care. Each PDI item is rated by patients to indicate the degree to which they experience various kinds of end-of-life distress. Palliative care patients reported an average of 5.74 problems (standard deviation, 5.49; range, 0–24), including physical, psychological, existential, and spiritual challenges. Being an inpatient, being educated, and having a partner were associated with certain kinds of end-of-life problems, particularly existential distress. Spirituality, especially its existential or “sense of meaning and purpose” dimension, was associated with less distress for terminally ill patients. A better appreciation for the nature of distress is a critical step toward a fuller understanding of the challenges facing the terminally ill. A clear articulation of the landscape of distress, including insight regarding those who are most at risk, should pave the way toward more effective, dignity-conserving end-of-life care. a Manitoba Palliative Care Research Unit, University of Manitoba, Winnipeg, Manitoba, Canada b Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada c Faculty of Nursing, University of Manitoba, Winnipeg, Manitoba, Canada d Manitoba Palliative Care Research Unit, CancerCare Manitoba, Winnipeg, Manitoba, Canada e Patient and Family Support Services, CancerCare Manitoba, Winnipeg, Manitoba, Canada f Western Australian Centre for Cancer & Palliative Care, Curtin University of Technology, Perth, Australia g St. Boniface General Hospital, Winnipeg, Manitoba, Canada h Tom Baker Cancer Centre, Calgary, Alberta, Canada i Department of Oncology, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada j Calgary Health Region, Calgary, Alberta, Canada Address correspondence to: Harvey Max Chochinov, MD, PhD, Manitoba Palliative Care Research Unit, University of Manitoba, CancerCare Manitoba, Rm. 3021, 675 McDermot Avenue, Winnipeg, Manitoba R3E 0V9, Canada.
The work was supported by a grant from the National Cancer Institute of Canada, with funding from the Canadian Cancer Society. Dr. Chochinov is a Canada Research Chair in Palliative Care, funded by the Canadian Institutes for Health Research. The authors declare no conflicts of interest. PII: S0885-3924(09)00636-8 doi:10.1016/j.jpainsymman.2009.04.021 © 2009 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved. | |
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