Features of the clinical picture and quality of life in patients with idiopathic pulmonary fibrosis and hypersensitivity pneumonitis

Background. Idiopathic pulmonary fibrosis (IPF) and hypersensitivity pneumonitis (HP) are interstitial lung diseases with similar symptoms: dyspnea and cough, which determine disease severity and serve as prognostic markers. Aim. To compare clinical and functional characteristics and their dynami...

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Hlavní autoři:	Olga A. Suvorova, Natalia V. Trushenko, Baina B. Lavginova, Iuliia A. Levina, Zamira M. Merzhoeva, Sergey N. Avdeev
Médium:	Artigo
Jazyk:	Russo
Vydáno:	ZAO "Consilium Medicum" 2025-01-01
Edice:	Consilium Medicum
Témata:	interstitial lung diseases hypersensitivity pneumonitis idiopathic pulmonary fibrosis dyspnea cough
On-line přístup:	https://consilium.orscience.ru/2075-1753/article/viewFile/678792/200410
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