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Fibrosis quística en el adulto: experiencia de un centro de referencia nacional

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dc.contributor.author Fernández, Patricia
dc.contributor.author Labarca, Gonzalo
dc.date.accessioned 2017-05-26T16:00:41Z
dc.date.available 2017-05-26T16:00:41Z
dc.date.issued 2012
dc.identifier.citation Rev Med Chile 2012; 140: 841-846 es_CL
dc.identifier.uri http://dx.doi.org/10.4067/S0034-98872012000700002 es_CL
dc.identifier.uri http://hdl.handle.net/11447/1351
dc.description.abstract Background: Although in most patients the diagnosis of cystic fibrosis (CF) is made during their first years of life, a proportion of patients is diagnosed during adulthood. Aim: To describe the features of adult patients diagnosed with CF. Materials and Methods: Analysis of medical records of patients diagnosed with CF in a public hospital devoted to respiratory diseases. Demographic, clinical, laboratory and microbiological data were recorded. Results: Fifty eight patients aged 25.4 ± 6.5 years were included. In 40% of them, CF was diagnosed after 15 years of age. The most common mutation found was AF508. Among clinical characteristics, lung involvement, mainly bronchiectasis, was found in 93%. The mean forced expiratory volume in the first second (FEV,) was 65,7 ± 27,1%. Fifteen patients were colonized with Pseudomonas aeruginosa. The main complication seen was hemoptysis, in 12% of patients. Five patients died, mostly due to respiratory distress associated with sepsis, while three were subjected to bilateral lung transplantation. Patients in whom the diagnosis of CF was made after 15 years of age, had lower frequency of AF508 mutation, were most commonly women and had a lower rate of pancreatic involvement. Conclusions: CF is a disease that is increasingly reaching adult population. CF must be suspected in adolescents and young adults who suffer chronic lung diseases such as bronchiectasis, particularly when they are colonized by Pseudomonas aeruginosa, or in patients who develop infections by uncommon organisms. es_CL
dc.format.extent 6 es_CL
dc.language.iso spa es_CL
dc.publisher Sociedad Medica de Santiago es_CL
dc.subject Bronchiectasis es_CL
dc.subject Cystic fibrosis es_CL
dc.subject Hemoptysis es_CL
dc.subject Pseudomonas aeruginosa es_CL
dc.title Fibrosis quística en el adulto: experiencia de un centro de referencia nacional es_CL
dc.title.alternative Cystic fibrosis in adults: experience of a national reference center es_CL
dc.type Artículo es_CL


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