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dc.contributor.authorPaixão, Vilma Almeida-
dc.contributor.authorBarros, Tânia Fraga-
dc.contributor.authorMota, Clélia Maria C-
dc.contributor.authorMoreira, Tamy Fagundes-
dc.contributor.authorSantana, Maria Angélica Pinheiro Santos-
dc.contributor.authorReis, Joice Neves-
dc.creatorPaixão, Vilma Almeida-
dc.creatorBarros, Tânia Fraga-
dc.creatorMota, Clélia Maria C-
dc.creatorMoreira, Tamy Fagundes-
dc.creatorSantana, Maria Angélica Pinheiro Santos-
dc.creatorReis, Joice Neves-
dc.date.accessioned2012-05-03T18:33:40Z-
dc.date.issued2010-
dc.identifier.issn1413-8670-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/5765-
dc.descriptionAcesso restrito: Texto completo. p. 406-409pt_BR
dc.description.abstractRespiratory infection is very common in patients suffering from cystic fibrosis (CF). However, the antimicrobial resistance rate of isolates from CF patients is not often documented. In this study, 279 respiratory specimens of 146 patients were prospectively collected from July to December 2006. Microbiological cultures and antimicrobial susceptibility tests of the most frequently isolated bacteria were performed. Sputum and oropharyngeal swabs were processed for culture. During the study period, 50% of the patients harbored Staphylococcus aureus, 35% Pseudomonas aeruginosa, 4.7% Haemophilus influenzae. Methicillin resistant S. aureus (MRSA) were detected in 8 (6%) patients; ESBL and MBL-producing P. aeruginosa were not identified in these patients. The detection of MRSA in CF patients confirms that antimicrobial resistance patterns should be always kept under surveillance. Moreover, hygiene regulations in CF clinics should prevent a further spread of resistant bacterial strains.pt_BR
dc.language.isoenpt_BR
dc.sourcehttp://dx.doi.org/10.1590/S1413-86702010000400016pt_BR
dc.subjectcystic fibrosispt_BR
dc.subjectantimicrobial resistancept_BR
dc.subjectPseudomonas aeruginosapt_BR
dc.subjectStaphylococcus aureuspt_BR
dc.titlePrevalence and antimicrobial susceptibility of respiratory pathogens in patients with cystic fibrosispt_BR
dc.title.alternativeBrazilian Journal of Infectious Diseasespt_BR
dc.typeArtigo de Periódicopt_BR
dc.description.localpubSalvadorpt_BR
dc.identifier.numberv. 14, n. 4pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (FAR)

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