Literature DB >> 10679874

The Pediatric Cancer Quality of Life Inventory: a modular approach to measuring health-related quality of life in children with cancer.

M Seid1, J W Varni, C A Rode, E R Katz.   

Abstract

Measurement of pediatric cancer patients' health-related quality of life (HRQL) in phase III randomized, controlled clinical trials is being recognized increasingly as an essential component in evaluating the comprehensive health outcomes of modern anti-neoplastic treatment protocols. Use of a brief core measure of HRQL plus disease-specific symptom modules is a way to assess specific HRQL outcomes with a minimum of subject burden. Demonstrating a measure's feasibility, reliability and validity also represents children's ability to provide reliable and valid responses to HRQL questions. The Pediatric Cancer Quality of Life Inventory (PCQL) Modular Approach consists of a 15-item core measure of HRQL and 2 specific symptom modules: pain and nausea. To validate a patient-report form and a parent-report form, the PCQL was administered to 291 pediatric cancer patients and to their parents. Feasibility and range of measurement, as well as patient-parent concordance, were assessed. Internal consistency reliability was assessed via Cronbach's alpha. Validity was determined by the known-groups approach and by correlating PCQL scores with days missed from school. Patients had minimal missing data, and the range of measurement for the items was good. Patient-parent concordance was large but not perfect. For both patient and parent forms, internal consistency reliability of the PCQL core scale (0.83 and 0. 86, respectively) was strong. The internal consistency reliabilities of the 2 symptom modules for both patient and parent forms were in the acceptable range for group comparisons. Regarding clinical validity, the core scale and the 2 symptom modules distinguished between patients on and off treatment for both patient and parent reports. Further, both patient and parent reports correlated with days of missed school in the past 6 and 12 months. The PCQL Modular Approach has demonstrated acceptable internal consistency reliability and clinical validity for both patient-report and parent-report forms. By implication, children are capable of providing reliable and valid responses to these HRQL questions. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10679874     DOI: 10.1002/(sici)1097-0215(1999)83:12+<71::aid-ijc13>3.0.co;2-5

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


  19 in total

1.  Quality of life as conveyed by pediatric patients with cancer.

Authors:  P S Hinds; J S Gattuso; A Fletcher; E Baker; B Coleman; T Jackson; A Jacobs-Levine; D June; S N Rai; S Lensing; C H Pui
Journal:  Qual Life Res       Date:  2004-05       Impact factor: 4.147

Review 2.  Measuring the psychosocial health of adolescent and young adult (AYA) cancer survivors: a critical review.

Authors:  Tara Clinton-McHarg; Mariko Carey; Rob Sanson-Fisher; Anthony Shakeshaft; Kathy Rainbird
Journal:  Health Qual Life Outcomes       Date:  2010-03-06       Impact factor: 3.186

3.  The associations among economic hardship, caregiver psychological distress, disease activity, and health-related quality of life in children with juvenile idiopathic arthritis.

Authors:  Karine Toupin April; Sabrina Cavallo; Debbie Ehrmann Feldman; Andy Ni
Journal:  Qual Life Res       Date:  2011-10-11       Impact factor: 4.147

Review 4.  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

5.  Optimizing the measurement of health-related quality of life in adolescents and young adults with cancer.

Authors:  John M Salsman; Suzanne C Danhauer; Justin B Moore; Mollie R Canzona; David E Victorson; Bradley J Zebrack; Bryce B Reeve
Journal:  Cancer       Date:  2020-09-10       Impact factor: 6.860

6.  Improving the care of children with advanced cancer by using an electronic patient-reported feedback intervention: results from the PediQUEST randomized controlled trial.

Authors:  Joanne Wolfe; Liliana Orellana; E Francis Cook; Christina Ullrich; Tammy Kang; Jeffrey Russell Geyer; Chris Feudtner; Jane C Weeks; Veronica Dussel
Journal:  J Clin Oncol       Date:  2014-03-10       Impact factor: 44.544

Review 7.  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

8.  Recruitment of representative samples for low incidence cancer populations: do registries deliver?

Authors:  Tara Clinton-McHarg; Mariko Carey; Rob Sanson-Fisher; Elizabeth Tracey
Journal:  BMC Med Res Methodol       Date:  2011-01-16       Impact factor: 4.615

Review 9.  Quality of life questionnaires for children with cancer and childhood cancer survivors: a review of the development of available measures.

Authors:  Anne F Klassen; Sonya J Strohm; Heleen Maurice-Stam; Martha A Grootenhuis
Journal:  Support Care Cancer       Date:  2009-10-16       Impact factor: 3.603

10.  Generic and diabetes-specific parent-child behaviors and quality of life among youth with type 1 diabetes.

Authors:  Jill Weissberg-Benchell; Tonja Nansel; Grayson Holmbeck; Rusan Chen; Barbara Anderson; Tim Wysocki; Lori Laffel
Journal:  J Pediatr Psychol       Date:  2009-03-06
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