Literature DB >> 16224322

Evaluating quality of life in children with cancer using children's self-reports and parent-proxy reports.

Chao-Hsing Yeh1, Chi-Wen Chang, Pi-Chen Chang.   

Abstract

BACKGROUND: Assessment of quality of life (QOL) of children is complex due to the developmental differences in understanding the content being measured. The validity of parent-proxy reports versus children's self-reports remains to be clarified.
OBJECTIVES: To examine the agreement on QOL measures between children's self-reports and parent-proxy reports at different points in time, including at baseline and at 6-month follow up, as well as the change in scores between 6-month follow up and baseline.
METHOD: A longitudinal study of QOL assessment of children with cancer for parents and children was conducted. At baseline assessment, 126 children with cancer and at least one of their parents participated (n = 252). Forty boys, 25 girls, and their parents (n = 130) completed the 6-month follow up assessment.
RESULTS: Parents tended to report better QOL than did the children at both baseline and 6-month follow up assessments in both the on- and off-treatment groups. Agreement on QOL measure between children and parent proxies varied as a result of the following factors: treatment status (on and off treatment), time (at baseline vs. at 6-month follow up), and changes in score between the time of the baseline assessment and the 6-month follow up. The effects of time, age, gender, and severity of illness had different degrees of significance as predictors on various subscales. DISCUSSION: The predictors of agreement between patients' reports and parent-proxy reports, including the passage of time (from baseline to 6-month follow up), gender, age, and illness severity, have not been conclusively determined. Further studies are needed to examine patient-proxy agreement during a longer follow up period at more than two points in time and using the same patients through the stages of confirmation of diagnosis, acceptance of diagnosis, treatment, and after treatment.

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Mesh:

Year:  2005        PMID: 16224322     DOI: 10.1097/00006199-200509000-00010

Source DB:  PubMed          Journal:  Nurs Res        ISSN: 0029-6562            Impact factor:   2.381


  22 in total

Review 1.  Self-report of symptoms in children with cancer younger than 8 years of age: a systematic review.

Authors:  D Tomlinson; L Tigelaar; S Hyslop; T Lazor; L L Dupuis; K Griener; J Oliveria; L Sung
Journal:  Support Care Cancer       Date:  2017-05-12       Impact factor: 3.603

2.  Psychometric properties and gender invariance of the Chinese version of the self-report Pediatric Quality of Life Inventory version 4.0: short form is acceptable.

Authors:  Chung-Ying Lin; Wei-Ming Luh; Ai-Lun Yang; Chia-Ting Su; Jung-Der Wang; Hui-Ing Ma
Journal:  Qual Life Res       Date:  2011-05-15       Impact factor: 4.147

Review 3.  Child and adolescent self-report symptom measurement in pediatric oncology research: a systematic literature review.

Authors:  Laura C Pinheiro; Molly McFatrich; Nicole Lucas; Jennifer S Walker; Janice S Withycombe; Pamela S Hinds; Lillian Sung; Deborah Tomlinson; David R Freyer; Jennifer W Mack; Justin N Baker; Bryce B Reeve
Journal:  Qual Life Res       Date:  2017-09-06       Impact factor: 4.147

4.  The effect of parental mental health on proxy reports of health-related quality of life in children with sickle cell disease.

Authors:  Julie A Panepinto; Raymond G Hoffmann; Nicholas M Pajewski
Journal:  Pediatr Blood Cancer       Date:  2010-10       Impact factor: 3.167

5.  Reliability and validity of the PedsQL™ Multidimensional Fatigue Scale in Japan.

Authors:  Kyoko Kobayashi; Yoshiyuki Okano; Naohiro Hohashi
Journal:  Qual Life Res       Date:  2011-01-12       Impact factor: 4.147

Review 6.  Considering quality of life for children with cancer: a systematic review of patient-reported outcome measures and the development of a conceptual model.

Authors:  Samantha J Anthony; Enid Selkirk; Lillian Sung; Robert J Klaassen; David Dix; Katrin Scheinemann; Anne F Klassen
Journal:  Qual Life Res       Date:  2013-08-02       Impact factor: 4.147

7.  PedsQL relates to function and behavior in very low and normal birth weight 2- and 3-year-olds from a regional cohort.

Authors:  Mari Palta; Mona Sadek-Badawi
Journal:  Qual Life Res       Date:  2008-05-06       Impact factor: 4.147

8.  Reliability in the ratings of quality of life between parents and their children of school age with cerebral palsy.

Authors:  Annette Majnemer; Michael Shevell; Mary Law; Chantal Poulin; Peter Rosenbaum
Journal:  Qual Life Res       Date:  2008-09-27       Impact factor: 4.147

9.  Development of the Japanese version of the Pediatric Quality of Life Inventory Brain Tumor Module.

Authors:  Iori Sato; Akiko Higuchi; Takaaki Yanagisawa; Akitake Mukasa; Kohmei Ida; Yutaka Sawamura; Kazuhiko Sugiyama; Nobuhito Saito; Toshihiro Kumabe; Mizuhiko Terasaki; Ryo Nishikawa; Yasushi Ishida; Kiyoko Kamibeppu
Journal:  Health Qual Life Outcomes       Date:  2010-04-14       Impact factor: 3.186

10.  Impact of music on pediatric oncology outpatients.

Authors:  Kathi J Kemper; Craig A Hamilton; Thomas W McLean; James Lovato
Journal:  Pediatr Res       Date:  2008-07       Impact factor: 3.756

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