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dc.contributor.authorGava Chakr, Valentina C. B.
dc.contributor.authorVendrusculo, Fernanda Maria
dc.contributor.authorTomedi Leites, Gabriela
dc.contributor.authorFagundes Donadio, Márcio Vinícius
dc.contributor.authorFrescura Paim, Taísa
dc.contributor.authorCauduro Marostica, Paulo José
dc.contributor.authorRúbia Silveira, Mara
dc.date.accessioned2022-04-08T15:00:28Z
dc.date.available2022-04-08T15:00:28Z
dc.date.issued2006
dc.identifier.citationGava Chakr, Valentina C. B.; Vendrusculo, Fernanda Maria; Tomedi Leites, Gabriela [et al.]. Descriptive analysis of cystic fibrosis patients followed by the Pediatric Pulmonology Unit of a university hospital in Porto Alegre-RS. Scientia Medica, 2006, 16(3), 103-108. Disponible en: <https://revistaseletronicas.pucrs.br/ojs/index.php/scientiamedica/article/view/1617>. Fecha de acceso: 8 abr. 2022.ca
dc.identifier.issn1980-6108ca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/3220
dc.description.abstractAims: To provide a descriptive analysis of patients followed in a local cystic fibrosis treatment center and compare the collected data with those found in the literature. Methods: Relevant data for clinical follow-up of cystic fibrosis patients were used for analysis and correlation. Results: Twenty six male and twenty two female patients were studied. From 48 patients, 89,6% presented with pancreatic insufficiency and 29,1% had at least one positive culture to Pseudomonas aeruginosa in the last 6 months. The patients colonized by P. aeruginosa and the ones with pancreatic insufficiency presented with worse values for forced expiratory volume in one second (FEV1). The pancreatic insufficiency group (84 versus 112%; p = 0,005) and the patients colonized by P. aeruginosa (75 versus 85%; p = 0,006) had lower pulmonary function parameters. Conclusions: The data from our study show that this group of patients presents in accordance with data available from literature, considering the analysed features of the disease. However, there is a marked exception in the time of diagnosis, which is still very late in Brazil.en
dc.format.extent6ca
dc.language.isoporca
dc.publisherElectronic Journal Publishing Systemca
dc.relation.ispartofScientia Medicaca
dc.relation.ispartofseries16;3
dc.rightsExcept where otherwise specified, material published in this journal is licensed under a Creative Commons Attribution 4.0 International license, which allows unrestricted use, distribution and reproduction in any medium, provided the original publication is correctly cited.en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.otherFibrosi quísticaca
dc.subject.otherDiagnòsticca
dc.subject.otherDietoterapiaca
dc.subject.otherNenca
dc.subject.otherInfantca
dc.subject.otherAdolescentca
dc.subject.otherEspirometriaca
dc.subject.otherFibrosis quísticaes
dc.subject.otherDiagnósticoes
dc.subject.otherDietoterapiaes
dc.subject.otherNiñoes
dc.subject.otherInfantees
dc.subject.otherAdolescentees
dc.subject.otherEspirometríaes
dc.subject.otherCystic fibrosisen
dc.subject.otherDiagnosisen
dc.subject.otherDiet therapyen
dc.subject.otherBoyen
dc.subject.otherInfanten
dc.subject.otherTeenageren
dc.subject.otherSpirometryen
dc.titleDescriptive analysis of cystic fibrosis patients followed by the Pediatric Pulmonology Unit of a university hospital in Porto Alegre-RSen
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc61ca
dc.subject.udc616.2ca


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Except where otherwise specified, material published in this journal is licensed under a Creative Commons Attribution 4.0 International license, which allows unrestricted use, distribution and reproduction in any medium, provided the original publication is correctly cited.
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0/
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