Literature DB >> 9060565

Value of caregiver ratings in evaluating the quality of life of patients with cancer.

K C Sneeuw1, N K Aaronson, M A Sprangers, S B Detmar, L D Wever, J H Schornagel.   

Abstract

PURPOSE: To evaluate the usefulness of caregiver ratings of cancer patients' quality of life (QL), we examined the following: (1) the comparability of responses to a brief standardized QL questionnaire provided by patients, physicians, and informal caregivers; and (2) the relative validity of these ratings.
METHODS: The study sample included cancer patients receiving chemotherapy, their treating physicians, and significant others involved closely in the (informal) care of the patients. During an early phase of treatment and 3 months later, patients and caregivers completed independently the COOP/WONCA charts, covering seven QL domains. At baseline, all sources of information were available for 295 of 320 participating patients (92%). Complete follow-up data were obtained for 189 patient-caregiver triads.
RESULTS: Comparison of mean scores on the COOP/WONCA charts revealed close agreement between patient and caregiver ratings. At the individual patient level, exact or global agreement was observed in the majority of cases (73% to 91%). Corrected for chance agreement, moderate intraclass correlations (ICC) were noted (0.32 to 0.72). Patient, physician, and informal caregiver COOP/WONCA scores were all responsive to changes over time in specific QL domains, but differed in their relative performance. Relative to the patients, the physicians were more efficient in detecting changes over time in physical fitness and overall health, but less so in relation to social function and pain.
CONCLUSION: For studies among patient populations at risk of deteriorating self-report capabilities, physicians and informal caregivers can be useful as alternative or complementary sources of information on cancer patients' QL.

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Year:  1997        PMID: 9060565     DOI: 10.1200/JCO.1997.15.3.1206

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  35 in total

1.  Proxy reliability: health-related quality of life (HRQoL) measures for people with disability.

Authors:  E M Andresen; V J Vahle; D Lollar
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2.  Who should measure quality of life?

Authors:  J Addington-Hall; L Kalra
Journal:  BMJ       Date:  2001-06-09

3.  The SIP68: an abbreviated sickness impact profile for disability outcomes research.

Authors:  Upasana Nanda; Patricia M McLendon; Elena M Andresen; Eric Armbrecht
Journal:  Qual Life Res       Date:  2003-08       Impact factor: 4.147

4.  Dialysis Facility Transplant Philosophy and Access to Kidney Transplantation in the Southeast.

Authors:  Jennifer Gander; Teri Browne; Laura Plantinga; Stephen O Pastan; Leighann Sauls; Jenna Krisher; Rachel E Patzer
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Review 5.  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

6.  Health status in patients with Alzheimer's disease: an investigation of inter-rater agreement.

Authors:  J L Novella; F Boyer; C Jochum; N Jovenin; I Morrone; D Jolly; S Bakchine; F Blanchard
Journal:  Qual Life Res       Date:  2006-06       Impact factor: 4.147

7.  Perceived mental health status of drug users with HIV: concordance between caregivers and care recipient reports and associations with caregiving burden and reciprocity.

Authors:  Mary M Mitchell; Allysha C Robinson; Jennifer L Wolff; Amy R Knowlton
Journal:  AIDS Behav       Date:  2014-06

8.  Symptom burden in palliative care patients: perspectives of patients, their family caregivers, and their attending physicians.

Authors:  Karin Oechsle; Kathrin Goerth; Carsten Bokemeyer; Anja Mehnert
Journal:  Support Care Cancer       Date:  2013-02-21       Impact factor: 3.603

Review 9.  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

10.  Concordance of patient and caregiver reports in evaluating quality of life in patients with malignant gliomas and an assessment of caregiver burden.

Authors:  Daniel I Jacobs; Priya Kumthekar; Becky V Stell; Sean A Grimm; Alfred W Rademaker; Laurie Rice; James P Chandler; Kenji Muro; MaryAnne Marymont; Irene B Helenowski; Lynne I Wagner; Jeffrey J Raizer
Journal:  Neurooncol Pract       Date:  2014-05-05
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