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    Defining dignity in terminally ill cancer patients: A factor-analytic approach

    Access Status
    Fulltext not available
    Authors
    Hack, T.
    Chochinov, H.
    Hassard, T.
    Kristjanson, Linda
    McClement, S.
    Harlos, M.
    Date
    2004
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Hack, Thomas and Chochinov, Harvey and Hassard, Thomas and Kristjanson, Linda and McClement, Susan and Harlos, Mike. 2004. Defining dignity in terminally ill cancer patients: A factor-analytic approach. Psycho-Oncology. 13 (10): pp. 700-708.
    Source Title
    Psycho-Oncology
    DOI
    10.1002/pon.786
    ISSN
    1057-9249
    Faculty
    Faculty of Health Sciences
    Nursing and Midwifery
    Western Australian Centre for Cancer and Palliative Care (WACCP)
    School
    WA Centre for Cancer and Palliative Care (WACCPC)
    Remarks

    Copyright © 2009 John Wiley & Sons, Ltd.

    URI
    http://hdl.handle.net/20.500.11937/11141
    Collection
    • Curtin Research Publications
    Abstract

    The construct of dignity is frequently raised in discussions about quality end of life care for terminal cancer patients, and is invoked by parties on both sides of the euthanasia debate. Lacking in this general debate has been an empirical explication of dignity from the viewpoint of cancer patients themselves. The purpose of the present study was to use factor-analytic and regression methods to analyze dignity data gathered from 213 cancer patients having less than 6 months to live. Patients rated their sense of dignity, and completed measures of symptom distress and psychological well-being. The results showed that although the majority of patients had an intact sense of dignity, there were 99 (46%) patients who reported at least some, or occasional loss of dignity, and 16 (7.5%) patients who indicated that loss of dignity was a significant problem. The exploratory factor analysis yielded six primary factors: (1) Pain; (2) Intimate Dependency; (3) Hopelessness/Depression; (4) Informal Support Network; (5) Formal Support Network; and (6) Quality of Life. Subsequent regression analyses of modifiable factors produced a final two-factor (Hopelessness/Depression and Intimate Dependency) model of statistical significance. These results provide empirical support for the dignity model, and suggest that the provision of end of life care should include methods for treating depression, fostering hope, and facilitating functional independence. Copyright © 2004 John Wiley & Sons, Ltd.

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