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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...

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Autores principales: Baddini-Martinez, José, Baldi, Bruno Guedes, da Costa, Cláudia Henrique, Jezler, Sérgio, Lima, Mariana Silva, Rufino, Rogério
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Pneumologia e Tisiologia 2015
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.
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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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