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Update on diagnosis and treatment of idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis is a type of chronic fibrosing interstitial pneumonia, of unknown etiology, which is associated with a progressive decrease in pulmonary function and with high mortality rates. Interest in and knowledge of this disorder have grown substantially in recent years. In this...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Pneumologia e Tisiologia
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635093/ https://www.ncbi.nlm.nih.gov/pubmed/26578138 http://dx.doi.org/10.1590/S1806-37132015000000152 |
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author | Baddini-Martinez, José Baldi, Bruno Guedes da Costa, Cláudia Henrique Jezler, Sérgio Lima, Mariana Silva Rufino, Rogério |
author_facet | Baddini-Martinez, José Baldi, Bruno Guedes da Costa, Cláudia Henrique Jezler, Sérgio Lima, Mariana Silva Rufino, Rogério |
author_sort | Baddini-Martinez, José |
collection | PubMed |
description | Idiopathic pulmonary fibrosis is a type of chronic fibrosing interstitial pneumonia, of unknown etiology, which is associated with a progressive decrease in pulmonary function and with high mortality rates. Interest in and knowledge of this disorder have grown substantially in recent years. In this review article, we broadly discuss distinct aspects related to the diagnosis and treatment of idiopathic pulmonary fibrosis. We list the current diagnostic criteria and describe the therapeutic approaches currently available, symptomatic treatments, the action of new drugs that are effective in slowing the decline in pulmonary function, and indications for lung transplantation. |
format | Online Article Text |
id | pubmed-4635093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Sociedade Brasileira de Pneumologia e Tisiologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-46350932015-11-18 Update on diagnosis and treatment of idiopathic pulmonary fibrosis Baddini-Martinez, José Baldi, Bruno Guedes da Costa, Cláudia Henrique Jezler, Sérgio Lima, Mariana Silva Rufino, Rogério J Bras Pneumol Review Article Idiopathic pulmonary fibrosis is a type of chronic fibrosing interstitial pneumonia, of unknown etiology, which is associated with a progressive decrease in pulmonary function and with high mortality rates. Interest in and knowledge of this disorder have grown substantially in recent years. In this review article, we broadly discuss distinct aspects related to the diagnosis and treatment of idiopathic pulmonary fibrosis. We list the current diagnostic criteria and describe the therapeutic approaches currently available, symptomatic treatments, the action of new drugs that are effective in slowing the decline in pulmonary function, and indications for lung transplantation. Sociedade Brasileira de Pneumologia e Tisiologia 2015 /pmc/articles/PMC4635093/ /pubmed/26578138 http://dx.doi.org/10.1590/S1806-37132015000000152 Text en http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License |
spellingShingle | Review Article Baddini-Martinez, José Baldi, Bruno Guedes da Costa, Cláudia Henrique Jezler, Sérgio Lima, Mariana Silva Rufino, Rogério Update on diagnosis and treatment of idiopathic pulmonary fibrosis |
title | Update on diagnosis and treatment of idiopathic pulmonary fibrosis |
title_full | Update on diagnosis and treatment of idiopathic pulmonary fibrosis |
title_fullStr | Update on diagnosis and treatment of idiopathic pulmonary fibrosis |
title_full_unstemmed | Update on diagnosis and treatment of idiopathic pulmonary fibrosis |
title_short | Update on diagnosis and treatment of idiopathic pulmonary fibrosis |
title_sort | update on diagnosis and treatment of idiopathic pulmonary fibrosis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635093/ https://www.ncbi.nlm.nih.gov/pubmed/26578138 http://dx.doi.org/10.1590/S1806-37132015000000152 |
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