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Monitoring quality of life in outpatients with cystic fibrosis: Feasibility and longitudinal results

✍ Scribed by Lutz Goldbeck; Sven Zerrer; Tim G. Schmitz


Book ID
119288508
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
203 KB
Volume
6
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