Literature DB >> 10679881

Cross-cultural adaptation of a health status classification system in children with cancer. First results of the French adaptation of the Health Utilities Index Marks 2 and 3.

C Le Galès1, N Costet, J C Gentet, C Kalifa, D Frappaz, C Edan, E Sariban, D Plantaz, F Doz.   

Abstract

Our objective was to adapt and validate the Health Utilities Index Mark 2 (HUI 2) and HUI 3 health status classification systems self-report questionnaire in a population of children with cancer, a group of 42 children already included in a multi-centre database designed by the Group on Brain Tumors in Children of the French Society for Pediatric Oncology. Children were recruited during a routine consultation. Most of them had completed treatment. The version of the questionnaire for French adults was adapted linguistically for children. Open-ended queries by children about the comprehensiveness of the questions and very low non-response rates showed a good acceptability of the questionnaire. The main psychometric properties of the HUI 2 and HUI 3 classification systems were assessed in 3 groups of raters (child, parent, physician): construct validity was tested against the rating of the child's health state on a Likert scale and through comparison with clinical data, and internal consistency was determined through multi-trait analysis. Weighted and unweighted kappa values were used to measure the inter-rater agreement between the child's, parent's and physician's assessment of the child's health state. The convergent validity was satisfactory, with better results when the physician's assessment was used. The most affected attributes were the expected ones (i.e., cognition, pain and emotion). Disagreement was observed between the 3 raters, more often in the same direction: taking the child's assessment as the reference, the parents tended to under-estimate the health status while physicians tended to over-estimate it. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10679881

Source DB:  PubMed          Journal:  Int J Cancer Suppl        ISSN: 0898-6924


  13 in total

1.  Are nurses and physicians able to assess which strategies adolescents recently diagnosed with cancer use to cope with disease- and treatment-related distress?

Authors:  Gunn Engvall; Inger Skolin; Elisabet Mattsson; Mariann Hedström; Louise von Essen
Journal:  Support Care Cancer       Date:  2010-03-27       Impact factor: 3.603

Review 2.  Identifying determinants of quality of life of children with cancer and childhood cancer survivors: a systematic review.

Authors:  Anne F Klassen; Samantha J Anthony; Aalia Khan; Lillian Sung; Robert Klaassen
Journal:  Support Care Cancer       Date:  2011-05-25       Impact factor: 3.603

3.  Proxy assessment of quality of life in pediatric clinical trials: application of the Health Utilities Index 3.

Authors:  Cheryl L Cox; Shelly Lensing; Shesh N Rai; Pam Hinds; Elizabeth Burghen; Ching-Hon Pui
Journal:  Qual Life Res       Date:  2005-05       Impact factor: 4.147

Review 4.  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

Review 5.  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

6.  Development of a preference-weighted health status classification system in France: the Health Utilities Index 3.

Authors:  Galès Catherine Le; Catherine Buron; Nathalie Costet; Sophia Rosman; P R Gérard Slama
Journal:  Health Care Manag Sci       Date:  2002-02

7.  Quality of life in chronic illness: perceptions of parents and paediatricians.

Authors:  A J Janse; G Sinnema; C S P M Uiterwaal; J L L Kimpen; R J B J Gemke
Journal:  Arch Dis Child       Date:  2005-05       Impact factor: 3.791

Review 8.  Evaluating health-related quality-of-life studies in paediatric populations: some conceptual, methodological and developmental considerations and recent applications.

Authors:  Mirella De Civita; Dean Regier; Abul H Alamgir; Aslam H Anis; Mark J Fitzgerald; Carlo A Marra
Journal:  Pharmacoeconomics       Date:  2005       Impact factor: 4.981

9.  Eliciting the child's voice in adverse event reporting in oncology trials: Cognitive interview findings from the Pediatric Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events initiative.

Authors:  Bryce B Reeve; Molly McFatrich; Laura C Pinheiro; Meaghann S Weaver; Lillian Sung; Janice S Withycombe; Justin N Baker; Jennifer W Mack; Mia K Waldron; Deborah Gibson; Deborah Tomlinson; David R Freyer; Catriona Mowbray; Shana Jacobs; Diana Palma; Christa E Martens; Stuart H Gold; Kathryn D Jackson; Pamela S Hinds
Journal:  Pediatr Blood Cancer       Date:  2016-09-21       Impact factor: 3.167

10.  From childhood to adulthood: long-term outcome of medulloblastoma patients. The Institut Curie experience (1980-2000).

Authors:  P Frange; C Alapetite; G Gaboriaud; D Bours; J M Zucker; M Zerah; H Brisse; M Chevignard; V Mosseri; E Bouffet; F Doz
Journal:  J Neurooncol       Date:  2009-06-12       Impact factor: 4.130

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