학술논문
Maintaining normal lung function in children with cystic fibrosis is possible with aggressive treatment regardless of Pseudomonas aeruginosa infections.
Document Type
Article
Author
Source
Subject
*PSEUDOMONAS aeruginosa infections
*CYSTIC fibrosis
*PULMONARY fibrosis
*LUNGS
*CHILD patients
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Language
ISSN
0803-5253
Abstract
Both studies only included CF patients with pancreatic insufficiency, while patients with lung transplant or patients who received shared care were excluded. Cystic fibrosis (CF) is an orphan disease with increased morbidity and mortality, mainly due to chronic pulmonary infections. [Extracted from the article]