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- W2000668325 abstract "Cystic fibrosis is the most common and best known genetic disease involving a defect in transepithelial Cl- transport by mutations in the CF gene on chromosome 7, which codes for the cystic fibrosis transmembrane conductance regulator protein (CFTR). The most serious symptoms are observed in the lungs, augmenting the risk of bacterial infection. The objective of this review was to describe the bacterial pathogens colonizing patients with cystic fibrosis. A systematic search was conducted using the international bibliographic databanks SCIELO, HIGHWIRE, PUBMED, SCIRUS and LILACS to provide a useful and practical review for healthcare workers to make them aware of these microorganisms. Today, B. cepacia, P. aeruginosa and S. aureus are the most important infectious agents in cystic fibrosis patients. However, healthcare professionals must pay attention to emerging infectious agents in these patients, because they represent a potentially serious future problem. Therefore, these pathogens should be pointed out as a risk to these patients, and hospitals all over the world must be prepared to detect and combat these bacteria." @default.
- W2000668325 created "2016-06-24" @default.
- W2000668325 creator A5032285188 @default.
- W2000668325 creator A5039188189 @default.
- W2000668325 creator A5057305681 @default.
- W2000668325 date "2008-01-01" @default.
- W2000668325 modified "2023-10-18" @default.
- W2000668325 title "Pulmonary bacterial pathogens in cystic fibrosis patients and antibiotic therapy: a tool for the health workers" @default.
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- W2000668325 doi "https://doi.org/10.1186/1755-7682-1-24" @default.
- W2000668325 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2586015" @default.
- W2000668325 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18992146" @default.
- W2000668325 hasPublicationYear "2008" @default.
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