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. 2009 Dec 2:7:97.
doi: 10.1186/1477-7525-7-97.

Health-related quality of life in children with cystic fibrosis: validation of the German CFQ-R

Affiliations

Health-related quality of life in children with cystic fibrosis: validation of the German CFQ-R

Anne Schmidt et al. Health Qual Life Outcomes. .

Abstract

Background: This study evaluates the psychometric properties of the Child and Parent versions of the German CFQ-R (Cystic Fibrosis Questionnaire Revised), a disease-specific measure of Health-Related Quality of Life (HRQoL) in children with cystic fibrosis (CF). Self-Rating is combined with proxy-rating by parents in the use of the questionnaire.

Methods: 136 children with CF (6 - 13 years) and their parents were recruited to evaluate internal consistency (Cronbach's alpha) and validity, 20 children and parents to examine reproducibility (ICC).

Results: Cronbach's alpha is high in all but two dimensions of the Child version (alpha = 0.23-0.77) and for all dimensions of the Parent version (alpha = 0.69-0.89). For both questionnaires, reproducibility is moderate to high (ICC = 0.50-0.94). Factor analysis shows loadings of >0.4 in the majority of items. Higher HRQoL is reported by children with mild disease compared to those with moderate/severe disease and by boys compared to girls. Convergence between self-rating and proxy-rating depends on the dimension.

Conclusion: The German CFQ-R, Child and Parent versions, are reliable and valid measures of HRQoL. They should be administered in combination as both, child and parent, provide important information. The measure offers a new patient-reported outcome for clinical purposes as well as for national and international studies in schoolchildren.

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Figures

Figure 1
Figure 1
Convergent validity of the German CFQ-R, Child and Parent versions. The blue bars represent mean values of the CFQ-R Child version, the brown bars represent those of the CFQ-R Parent version. ICC values show convergence between self- and proxy rating.

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