Literature DB >> 12625520

The revised German Cystic Fibrosis Questionnaire: validation of a disease-specific health-related quality of life instrument.

Kerstin Wenninger1, Pierre Aussage, Ulrich Wahn, Doris Staab.   

Abstract

BACKGROUND: The assessment of health related quality of life (HRQOL) has increasingly been recognized as an important adjunct to medical outcome parameters in the monitoring of cystic fibrosis (CF) patients and in clinical studies. The Cystic Fibrosis Questionnaire (CFQ) is a disease-specific HRQOL instrument for CF patients developed in France. Translations are currently being validated in four different countries. The aim of the present study was to validate the German adaptation of the CFQ-14+.
METHOD: On the basis of results from a first dataset (n = 197 CF adolescent and adult patients), revisions were made and retested in a second sample of 103 patients.
RESULTS: The final revised version showed good construct validity. The same nine HRQOL domains as in the French original CFQ-14+ emerged from the analyses as structurally robust scales. The internal consistencies of the HRQOL scales ranged from 0.71 to 0.94. The instrument's clinical validity was supported by severely ill patients reporting lower HRQOL than less severely ill patients on most scales.
CONCLUSION: We conclude that the evidence supports the validity and reliability of the instrument. An important future area of application is the use in comparative multi-center international studies.

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Year:  2003        PMID: 12625520     DOI: 10.1023/a:1022011704399

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  18 in total

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Journal:  Med Care       Date:  1994-09       Impact factor: 2.983

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Journal:  Thorax       Date:  2000-11       Impact factor: 9.139

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Journal:  Thorax       Date:  1996-09       Impact factor: 9.139

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  19 in total

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Journal:  J Behav Med       Date:  2003-02

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Journal:  Med Klin (Munich)       Date:  2009-07-18

Review 3.  Quality of life in children and adolescents with cystic fibrosis: implications for optimizing treatments and clinical trial design.

Authors:  Janice Abbott; Louise Gee
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

4.  Respiratory muscle training for cystic fibrosis.

Authors:  Gemma Stanford; Harrigan Ryan; Arturo Solis-Moya
Journal:  Cochrane Database Syst Rev       Date:  2020-12-17

5.  How about your peers? Cystic fibrosis questionnaire data from healthy children and adolescents.

Authors:  Marijke M Tibosch; Coosje J J C M Sintnicolaas; Jeannette B Peters; Peter J F M Merkus; Jan-Bart L Yntema; Christianne M Verhaak; Jan H Vercoulen
Journal:  BMC Pediatr       Date:  2011-10-11       Impact factor: 2.125

Review 6.  Interventions for promoting physical activity in people with cystic fibrosis.

Authors:  Narelle S Cox; Jennifer A Alison; Anne E Holland
Journal:  Cochrane Database Syst Rev       Date:  2013-12-13

Review 7.  Respiratory muscle training for cystic fibrosis.

Authors:  Nathan Hilton; Arturo Solis-Moya
Journal:  Cochrane Database Syst Rev       Date:  2018-05-24

8.  Cross-sectional validity of the EQ-5D-Y as a generic health outcome instrument in children and adolescents with cystic fibrosis in Germany.

Authors:  Daniela Eidt-Koch; Thomas Mittendorf; Wolfgang Greiner
Journal:  BMC Pediatr       Date:  2009-08-28       Impact factor: 2.125

9.  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
Journal:  Health Qual Life Outcomes       Date:  2009-12-02       Impact factor: 3.186

Review 10.  Antioxidant supplementation for lung disease in cystic fibrosis.

Authors:  Oana Ciofu; Sherie Smith; Jens Lykkesfeldt
Journal:  Cochrane Database Syst Rev       Date:  2019-10-03
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