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Changes in management of idiopathic pulmonary fibrosis: impact on disease severity and mortality
BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a serious interstitial lung disease (ILD) with a median survival of 3-5 years. The aim of the present study was to evaluate disease severity and survival in patients diagnosed with IPF in the era of antifibrotic therapies compared with an earlier IP...
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| Publicado en: | Eur Clin Respir J |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Taylor & Francis
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7480407/ https://ncbi.nlm.nih.gov/pubmed/32944203 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/20018525.2020.1807682 |
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