Psychometric evaluation of the EORTC QLQ-PR25 questionnaire in assessing health-related quality of life in prostate cancer survivors: a curate’s egg
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  • 作者:Eamonn O’Leary ; Frances J. Drummond ; Anna Gavin
  • 关键词:Health ; related quality of life ; Prostate cancer ; Survivors ; QLQ ; PR25
  • 刊名:Quality of Life Research
  • 出版年:2015
  • 出版时间:September 2015
  • 年:2015
  • 卷:24
  • 期:9
  • 页码:2219-2230
  • 全文大小:402 KB
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  • 作者单位:Eamonn O’Leary (1)
    Frances J. Drummond (1)
    Anna Gavin (2)
    Heather Kinnear (2)
    Linda Sharp (1) (3)

    1. National Cancer Registry, Cork, Ireland
    2. Northern Ireland Cancer Registry, Belfast, UK
    3. Institute of Health and Society, Newcastle University, Baddiley-Clark Building, Richmond Road, Newcastle upon Tyne, NE2 4AX, UK
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Quality of Life Research
    Sociology
    Public Health
  • 出版者:Springer Netherlands
  • ISSN:1573-2649
文摘
Purpose The EORTC QLQ-PR25 was primarily developed to measure disease-specific health-related quality of life (HRQoL) of prostate cancer (PCa) patients undergoing active treatment. The growing number of cancer survivors has focussed interest on assessing survivors-HRQoL. We evaluated psychometric properties of the EORTC QLQ-PR25 questionnaire amongst PCa survivors. Methods A postal questionnaire, including the QLQ-PR25, was administered to 6559 PCa survivors 2-8?years post-diagnosis, identified through population-based cancer registries in Ireland; 3348 participated. The QLQ-PR25 has been suggested to have five multi-item subscales measuring urinary (US), bowel (BS) and hormone treatment-related symptoms (TS), sexual activity (SA) and sexual functioning (SF), and a single item measuring bother due to using incontinence aids (IA). Reliability analysis, divergent validity, discriminant validity (compared to EORTC QLQ-C30, DASS-21 and EuroQoL EQ-5D-5L), and exploratory and confirmatory factor analysis (EFA, CFA) were undertaken. Results The percentage of survivors completing QLQ-PR25 subscales was: US-79?%; IA-20?%; BS-83?%; TS-86?%; SA-87?%; and SF-26?%. Reliability was acceptable (Cronbach’s α?>?0.7) for three subscales (US, SA, SF). The instrument discriminated well between clinically distinct groups, especially those defined by primary treatment(s) and stage at diagnosis. The SA and SF subscales showed good discriminant validity compared to QLQ-C30, DASS-21 and EQ-5D-5L; other subscales did not. EFA reproduced a near fit to the proposed factor structure. CFA confirmed this. Conclusion This is the largest ever QLQ-PR25 validation study. When used in PCa survivors, although the proposed factor structure was confirmed, some of the subscales (e.g. BS and TS) showed poor reliability, a lack of discriminant validity and moderate levels of item non-response.

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