Pulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis.
Affiliation
Department of Respiratory Medicine, St Vincent's University Hospital, Dublin, Ireland.Issue Date
2006-11MeSH
AdolescentAdult
Analysis of Variance
Bronchiectasis
Cystic Fibrosis
Female
Forced Expiratory Volume
Humans
Longitudinal Studies
Lung
Male
Middle Aged
Mucus
Pseudomonas aeruginosa
Spirometry
Sputum
Tomography, X-Ray Computed
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Pulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis. 2006, 130 (5):1424-32 ChestJournal
ChestDOI
10.1378/chest.130.5.1424PubMed ID
17099020Abstract
FEV1 may remain stable while high-resolution CT (HRCT) appearances deteriorate in children with cystic fibrosis (CF). However, spirometry results commonly decline in older age groups.Item Type
ArticleLanguage
enISSN
0012-3692ae974a485f413a2113503eed53cd6c53
10.1378/chest.130.5.1424
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