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Early Diagnosis and Treatment of Idiopathic Pulmonary Fibrosis: A Narrative Review

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrosing interstitial lung disease of unknown aetiology. Patients typically present with symptoms of chronic dyspnoea and cough over a period of months to years. IPF has a poor prognosis, with an average life expectancy of 3–5 years from...

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Detalles Bibliográficos
Autores principales: Alsomali, Hana, Palmer, Evelyn, Aujayeb, Avinash, Funston, Wendy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203082/
https://www.ncbi.nlm.nih.gov/pubmed/36773130
http://dx.doi.org/10.1007/s41030-023-00216-0

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