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Brazilian guidelines for the pharmacological treatment of idiopathic pulmonary fibrosis. Official document of the Brazilian Thoracic Association based on the GRADE methodology

Idiopathic pulmonary fibrosis (IPF) is a form of chronic interstitial lung disease of unknown cause, which predominantly affects elderly men who are current or former smokers. Even though it is an uncommon disease, it is of great importance because of its severity and poor prognosis. In recent decad...

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Podrobná bibliografie
Vydáno v:J Bras Pneumol
Hlavní autoři: Baddini-Martinez, José, Ferreira, Juliana, Tanni, Suzana, Alves, Luis Renato, Cabral, Benedito Francisco, Carvalho, Carlos Roberto Ribeiro, Cezare, Talita Jacon, da Costa, Claudia Henrique, Gazzana, Marcelo Basso, Jezler, Sérgio, Kairalla, Ronaldo Adib, Kawano-Dourado, Leticia, Lima, Mariana Silva, Mancuzo, Eliane, Moreira, Maria Auxiliadora Carmo, Rodrigues, Marcelo Palmeira, Rodrigues, Silvia Carla Sousa, Rubin, Adalberto Sperb, Rufino, Rogério Lopes, Steidle, Leila John Marques, Storrer, Karin, Baldi, Bruno Guedes
Médium: Artigo
Jazyk:Inglês
Vydáno: Sociedade Brasileira de Pneumologia e Tisiologia 2020
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7462709/
https://ncbi.nlm.nih.gov/pubmed/32130337
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.36416/1806-3756/e20190423
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