Literature DB >> 11176400

Comparison of patient and spouse assessments of health related quality of life in men with metastatic prostate cancer.

K C Sneeuw1, P C Albertsen, N K Aaronson.   

Abstract

PURPOSE: We examined the extent of agreement in health related quality of life ratings provided by patients with metastatic prostate cancer and their spouses. This agreement is important for determining the feasibility of using spouses as potential proxy raters in quality of life studies in this patient population.
MATERIALS AND METHODS: The study sample consisted of 72 pairs of patients with metastatic prostate cancer in remission or progression and their spouses. Patients and spouses independently completed the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-C30 and a prostate cancer specific questionnaire module. Together the 2 questionnaires assess a wide range of symptoms and functional limitations for a total of 21 quality of life outcomes.
RESULTS: For 5 of the 21 patient-proxy comparisons we noted systematic differences in the mean score with spouses rating more impairment in patients than patients indicated. Most patient-proxy correlations were 0.40 to 0.75, indicating moderate to good agreement in patient and spouse ratings. A low patient-proxy correlation of less than 0.40 was noted only for the 2 measures of sexual function.
CONCLUSIONS: Our findings suggest that the spouses of men with metastatic prostate cancer evaluate with a fair degree of accuracy how patients experience physical and psychosocial functioning, symptoms and overall quality of life. However, caution should be exercised when relying on proxy raters for assessing sexual functioning and satisfaction.

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Mesh:

Year:  2001        PMID: 11176400     DOI: 10.1097/00005392-200102000-00029

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  6 in total

Review 1.  Proxy evaluation of health-related quality of life: a conceptual framework for understanding multiple proxy perspectives.

Authors:  A Simon Pickard; Sara J Knight
Journal:  Med Care       Date:  2005-05       Impact factor: 2.983

Review 2.  Systematic review of caregiver responses for patient health-related quality of life in adult cancer care.

Authors:  Jessica K Roydhouse; Ira B Wilson
Journal:  Qual Life Res       Date:  2017-03-14       Impact factor: 4.147

3.  Understanding the psychosocial issues of African American couples surviving prostate cancer.

Authors:  Brian M Rivers; Euna M August; Gwendolyn P Quinn; Clement K Gwede; Julio M Pow-Sang; B Lee Green; Paul B Jacobsen
Journal:  J Cancer Educ       Date:  2012-06       Impact factor: 2.037

4.  Proxy assessment of quality of life in patients with prostate cancer: how accurate are partners and urologists?

Authors:  R Pearcy; D Waldron; C O'Boyle; R MacDonagh
Journal:  J R Soc Med       Date:  2008-03       Impact factor: 5.344

5.  How well do parents know their children? Implications for proxy reporting of child health-related quality of life.

Authors:  A Jokovic; D Locker; G Guyatt
Journal:  Qual Life Res       Date:  2004-09       Impact factor: 4.147

6.  Do Cohabitants Reliably Complete Questionnaires for Patients in a Terminal Cancer Stage when Assessing Quality of Life, Pain, Depression, and Anxiety?

Authors:  Olivier Q Groot; Nuno Rui Paulino Pereira; Michiel E R Bongers; Paul T Ogink; Erik T Newman; Jorrit-Jan Verlaan; Kevin A Raskin; Santiago A Lozano-Calderon; Joseph H Schwab
Journal:  Clin Orthop Relat Res       Date:  2021-04-01       Impact factor: 4.176

  6 in total

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