Literature DB >> 15463884

Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults.

Peter H Klijn1, Henk F van Stel, Alexandra L Quittner, Janjaap van der Net, Wytze Doeleman, Cees P van der Schans, Cornelis K van der Ent.   

Abstract

BACKGROUND: This study assesses the reliability and validity of the Dutch version of a disease-specific measure of health-related quality of life (HRQOL) for adolescents and adults with CF (CFQ-14+). The 47-item CFQ-14+ covers nine domains, three symptom scales and one health perception scale.
METHODS: To assess psychometric characteristics of the CFQ-14+, cross-sectional (homogeneity, discriminative and construct validity) and test-retest designs were used. Eighty-four adolescents and adults with CF (mean age: 21.4 years, range 14.0-46.5 years) and a wide range of lung function (mean FEV1: 59.9% predicted, range 15-121%) completed the questionnaire during a routine visit.
RESULTS: Internal consistency was acceptable for most domains of the CFQ-14+ (alpha = 0.43-0.92) and test-retest reliability was high for all domain scores (0.72-0.98). Several domains of the CFQ-14+ were able to differentiate between individuals with varying disease severity and between nourished and malnourished patients. Construct validity of the questionnaire was fair, with moderate to strong correlation between physically orientated domains and pulmonary function (rs = 0.36-0.62).
CONCLUSION: The results demonstrate that the CFQ-14+ questionnaire is a well-validated measure of HRQOL assessment in adolescents and adults with CF.

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Year:  2004        PMID: 15463884     DOI: 10.1016/j.jcf.2003.12.006

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  8 in total

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Journal:  BMC Pediatr       Date:  2011-10-11       Impact factor: 2.125

3.  Training hospital managers for strategic planning and management: a prospective study.

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4.  Factors associated with changes in health-related quality of life in children with cystic fibrosis during 1-year follow-up.

Authors:  Marieke van Horck; Bjorn Winkens; Geertjan Wesseling; Karin de Winter-de Groot; Ilja de Vreede; Quirijn Jöbsis; Edward Dompeling
Journal:  Eur J Pediatr       Date:  2017-06-09       Impact factor: 3.183

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

Authors:  Anne Schmidt; Kerstin Wenninger; Nadja Niemann; Ulrich Wahn; Doris Staab
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6.  Biomarkers in Exhaled Breath Condensate Are Not Predictive for Pulmonary Exacerbations in Children with Cystic Fibrosis: Results of a One-Year Observational Study.

Authors:  Marieke van Horck; Ariel Alonso; Geertjan Wesseling; Karin de Winter-de Groot; Wim van Aalderen; Han Hendriks; Bjorn Winkens; Ger Rijkers; Quirijn Jöbsis; Edward Dompeling
Journal:  PLoS One       Date:  2016-04-06       Impact factor: 3.240

7.  Psychometric evaluation of the Swedish translation of the revised Cystic Fibrosis Questionnaire in adults.

Authors:  Jacek Hochwälder; Agneta Bergsten Brucefors; Lena Hjelte
Journal:  Ups J Med Sci       Date:  2016-09-15       Impact factor: 2.384

8.  Quality of life amongst adolescents and young adults with cystic fibrosis: correlations with clinical outcomes.

Authors:  Daniela W Gancz; Maristela T Cunha; Claudio Leone; Joaquim C Rodrigues; Fabíola V Adde
Journal:  Clinics (Sao Paulo)       Date:  2018-10-18       Impact factor: 2.365

  8 in total

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