Initial validation of the Argentinean Spanish version of the PedsQL™ 4.0 Generic Core Scales in children and adolescents with chronic diseases: acceptability and comprehensibility in low-income settings

Health and Quality of Life Outcomes - Tập 6 - Trang 1-15 - 2008
Mariana Roizen1, Susana Rodríguez1,2,3, Gabriela Bauer1,3,4, Gabriela Medin5, Silvina Bevilacqua1,6, James W Varni7,8, Veronica Dussel9,10
1Committee on Quality of Life, Hospital de Pediatria Prof. Dr. Juan P Garrahan, Pichincha 1890, Buenos Aires, Argentina
2Department of Research, Hospital de Pediatria Prof. Dr. Juan P Garrahan, Buenos Aires, Argentina
3Department of Neonatology, Hospital de Pediatria Prof. Dr. Juan P Garrahan, Buenos Aires, Argentina
4Department of Pulmonology, Hospital de Pediatria Prof. Dr. Juan P Garrahan, Buenos Aires, Argentina
5Hospital Marañon, Madrid, Spain
6Palliative Care Team, Hospital de Pediatria Prof. Dr. Juan P Garrahan, Buenos Aires, Argentina
7Department of Pediatrics, College of Medicine, Texas A&M University, College Station, USA
8Department of Landscape Architecture and Urban Planning, College of Architecture, Texas A&M University, College Station, USA
9Center for Outcomes and Policy Research and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, USA
10Department of Hematology/Oncology, Children's Hospital, Boston, USA

Tóm tắt

To validate the Argentinean Spanish version of the PedsQL™ 4.0 Generic Core Scales in Argentinean children and adolescents with chronic conditions and to assess the impact of socio-demographic characteristics on the instrument's comprehensibility and acceptability. Reliability, and known-groups, and convergent validity were tested. Consecutive sample of 287 children with chronic conditions and 105 healthy children, ages 2–18, and their parents. Chronically ill children were: (1) attending outpatient clinics and (2) had one of the following diagnoses: stem cell transplant, chronic obstructive pulmonary disease, HIV/AIDS, cancer, end stage renal disease, complex congenital cardiopathy. Patients and adult proxies completed the PedsQL™ 4.0 and an overall health status assessment. Physicians were asked to rate degree of health status impairment. The PedsQL™ 4.0 was feasible (only 9 children, all 5 to 7 year-olds, could not complete the instrument), easy to administer, completed without, or with minimal, help by most children and parents, and required a brief administration time (average 5–6 minutes). People living below the poverty line and/or low literacy needed more help to complete the instrument. Cronbach Alpha's internal consistency values for the total and subscale scores exceeded 0.70 for self-reports of children over 8 years-old and parent-reports of children over 5 years of age. Reliability of proxy-reports of 2–4 year-olds was low but improved when school items were excluded. Internal consistency for 5–7 year-olds was low (α range = 0.28–0.76). Construct validity was good. Child self-report and parent proxy-report PedsQL™ 4.0 scores were moderately but significantly correlated (ρ = 0.39, p < 0.0001) and both significantly correlated with physician's assessment of health impairment and with child self-reported overall health status. The PedsQL™ 4.0 discriminated between healthy and chronically ill children (72.72 and 66.87, for healthy and ill children, respectively, p = 0.01), between different chronic health conditions, and children from lower socioeconomic status. Results suggest that the Argentinean Spanish PedsQL™ 4.0 is suitable for research purposes in the public health setting for children over 8 years old and parents of children over 5 years old. People with low income and low literacy need help to complete the instrument. Steps to expand the use of the Argentinean Spanish PedsQL™ 4.0 include an alternative approach to scoring for the 2–4 year-olds, further understanding of how to increase reliability for the 5–7 year-olds self-report, and confirmation of other aspects of validity.

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