How are the ancient cystic fibrosis patients?: Cystic fibrosis diagnosed over 60 years-old

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dc.contributor.author Prados, Concepción
dc.contributor.author Lerín, M.
dc.contributor.author Cabanillas, J. J.
dc.contributor.author Gómez-Carrera, L.
dc.contributor.author Álvarez-Sala, Rodolfo
dc.contributor.author Martinez, M. T.
dc.contributor.author Máiz, L.
dc.contributor.author Girón, R. M.
dc.contributor.author Solé, A.
dc.contributor.author Martínez, M.
dc.contributor.author Quirós, S.
dc.contributor.other UAM. Departamento de Medicina es_ES
dc.contributor.other Instituto de Investigación Sanitaria Hospital Universitario de La Paz (IdiPAZ) es_ES
dc.date.accessioned 2017-11-30T15:25:37Z
dc.date.available 2017-11-30T15:25:37Z
dc.date.issued 2017-01-01
dc.identifier.citation Respiratory Medicine Case Reports 21 (2017): 49-51 en_US
dc.identifier.issn 2213-0071 es_ES
dc.identifier.uri http://hdl.handle.net/10486/680565
dc.description.abstract Background and aims To specify the prevalence of patients diagnosed with CF at age of ≥60 year-old and to analyze their characteristics. Patients and methods Observational study of CF patients which were diagnosed at age ≥60 year-old. The analyzed variables were: age, sex, nationality, lung function parameters, conditions present at diagnosis, microbiological characteristics and genetic findings. Results eight patients were included. 7 patients were female (87.5%) with a mean age of 70.6 years (median 71.5 years, range 60–78 years). The most important findings were: sweat test > 60 mEq/l; heterozygotes F508del; bronchiectasis in CT; methicillin-sensitive Staphylococcus aureus (50%) in sputum. The most patients presented a normal or mild obstructive lung function. Conclusions CF must also be considered a disease diagnosed in adulthood, incorporating the sweat test within the usual techniques of differential diagnosis in patients with different diseases associated with CF, because genetic counselling is esencial. en_US
dc.format.extent 3 pag. es_ES
dc.format.mimetype application/pdf en
dc.language.iso eng en
dc.publisher Elsevier Ltd. en_US
dc.relation.ispartof Respiratory Medicine Case Reports en_US
dc.rights © 2017 The Authors en_US
dc.subject.other Aging en_US
dc.subject.other Cystic fibrosis en_US
dc.title How are the ancient cystic fibrosis patients?: Cystic fibrosis diagnosed over 60 years-old en_US
dc.type article en
dc.subject.eciencia Medicina es_ES
dc.relation.publisherversion http://dx.doi.org/10.1016/j.rmcr.2017.03.015 es_ES
dc.identifier.doi 10.1016/j.rmcr.2017.03.015 es_ES
dc.identifier.publicationfirstpage 49 es_ES
dc.identifier.publicationissue 21 es_ES
dc.identifier.publicationlastpage 51 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion en
dc.rights.cc Reconocimiento – NoComercial – SinObraDerivada es_ES
dc.rights.accessRights openAccess en
dc.authorUAM Álvarez-Sala Walther, Rodolfo (259489)
dc.authorUAM Prados Sánchez, María Concepción (262355)


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