2012
DOI: 10.5812/jcp.6944
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Microbial Colonization and Drug Resistance in Patients with Cystic Fibrosis

Abstract: Background: Cystic fibrosis (CF) is a genetic disease with an autosomal recessive pattern of inheritance. CF caused by a mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and characterized by impaired transport of chloride ions across the cell membrane. Staphylococcus aureus, Pseudomonas aeruginosa, and Burkholderia cepacia have been identified in the cultures of respiratory secretions of CF patients, and infections of these microorganisms are associated with high rates of morbidi… Show more

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Cited by 2 publications
(3 citation statements)
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“…Based on the molecular investigation, P. aeruginosa was the most frequent species in the sputum of CF patients in our study. Keating (19). The results of these three studies are comparable to the findings of the current study.…”
Section: Discussionsupporting
confidence: 88%
“…Based on the molecular investigation, P. aeruginosa was the most frequent species in the sputum of CF patients in our study. Keating (19). The results of these three studies are comparable to the findings of the current study.…”
Section: Discussionsupporting
confidence: 88%
“…P. aeruginosa is the main cause of chronic airway infection in this complex inherited disease, as confirmed by an interesting study of one of your articles published in this journal (1). This bacterium is also difficult to eradicate (since the chronic infection is established) and the development of resistance to the antibiotic treatment is also frequent.…”
Section: Dear Editormentioning
confidence: 92%
“…Some studies reported that using inhaled drugs for prophylaxis may decrease some complications in these patients (1,4). In our recent published review, we reported some data about the use of anti-pseudomonal inhaled antibiotics in the eradication of early and chronic infection, to treat acute exacerbations or for prophylaxis.…”
Section: Dear Editormentioning
confidence: 99%