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Comparative study of three health related quality of life instruments in cystic fibrosis patients

✍ Scribed by M. Cebrián; A. Solé; E. Ansótegui; A. Pastor; J. Pastor; S. Peiró; M. Peña

Book ID
118642820
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
49 KB
Volume
9
Category
Article
ISSN
1569-1993

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The majority of patients with cystic fibrosis (CF) will grow into adulthood. Despite this improvement in survival, the disease is progressive, especially with respect to the decline in pulmonary function, which in turn may have an impact on a patient's quality of life. In this study we evaluated the