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A Comparative Study of Variables That Have an Impact on Noncancer End-of-Life Diagnoses

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  • Marjorie Dobratz

    (University of Washington–Tacoma)

Abstract

By way of analysis of variance, this secondary analysis compared three groups of noncancer home hospice patients (AIDS, amyotrophic lateral sclerosis [ALS],and other) for psychological correlates of adaptation and well-being, pain, and physical function, as measured by the Life Closure Scale (LCS), the Affect Balance Scale, the McGill-Melzack Pain Questionnaire Part I, and the Karnofsky Performance Status Scale. The sample included 10 AIDS patients (Group 1), 6 ALS patients (Group 2), and 5 patients with other noncancer, end-stage diseases (Group 3). A significant difference was found between Group 2 (ALS) and Group 3 (other) on the LCS, F(2, 18) = 4.3, p = .03. Scheffe and Duncan range post hoc tests and at test at the p≤.05 level (t9 = 4.1, p = .003) confirmed the finding. No significant group differences were found among the ALS, AIDS, and other groups in measures of psychological well-being, pain, and physical function.

Suggested Citation

  • Marjorie Dobratz, 2004. "A Comparative Study of Variables That Have an Impact on Noncancer End-of-Life Diagnoses," Clinical Nursing Research, , vol. 13(4), pages 309-325, November.
    • Handle: RePEc:sae:clnure:v:13:y:2004:i:4:p:309-325
    DOI: 10.1177/1054773804267730
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    References listed on IDEAS

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    1. Chochinov, Harvey Max & Hack, Thomas & McClement, Susan & Kristjanson, Linda & Harlos, Mike, 2002. "Dignity in the terminally ill: a developing empirical model," Social Science & Medicine, Elsevier, vol. 54(3), pages 433-443, February.
    2. Pakenham, Kenneth I. & Dadds, Mark R. & Terry, Deborah J., 1996. "Adaptive demands along the HIV disease continuum," Social Science & Medicine, Elsevier, vol. 42(2), pages 245-256, January.
    3. McNamara, Beverley & Waddell, Charles & Colvin, Margaret, 1994. "The institutionalization of the good death," Social Science & Medicine, Elsevier, vol. 39(11), pages 1501-1508, December.
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