Gastroesophageal Reflux Disease in Idiopathic Pulmonary Fibrosis: Viewer or Actor? To Treat or Not to Treat?

Background: Idiopathic pulmonary fibrosis (IPF) is a rare and severe disease with a median survival of ∼3 years. Several risk factors have been identified, such as age, genetic predisposition, tobacco exposure, and gastro-oesophageal reflux disease (GERD). Prevalence of GERD in IPF is high and may a...

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Detalles Bibliográficos
Autores principales: Ruaro, Barbara, Pozzan, Riccardo, Confalonieri, Paola, Tavano, Stefano, Hughes, Michael, Matucci Cerinic, Marco, Baratella, Elisa, Zanatta, Elisabetta, Lerda, Selene, Geri, Pietro, Confalonieri, Marco, Salton, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9412643/
https://www.ncbi.nlm.nih.gov/pubmed/36015181
http://dx.doi.org/10.3390/ph15081033

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9412643/
https://www.ncbi.nlm.nih.gov/pubmed/36015181
http://dx.doi.org/10.3390/ph15081033

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