C39 BIOMARKERS AND PROGNOSTIC FACTORS IN ILD: Mid-Flow Rates Do Not Predict Mortality In Idiopathic Pulmonary Fibrosis Patients

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, fibrosing interstitial lung disease occurring predominantly in elderly with unknown etiology. Data on baseline demographics, lung function, and survival were collected.

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Bibliographic Details
Published inAmerican journal of respiratory and critical care medicine Vol. 195
Main Authors Nunes, F S, Brown, A W, King, C, Battle, E, Shlobin, O A, Nathan, S D
Format Journal Article
LanguageEnglish
Published New York American Thoracic Society 01.01.2017
Subjects
Medical prognosis
Pulmonary fibrosis
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Summary:Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, fibrosing interstitial lung disease occurring predominantly in elderly with unknown etiology. Data on baseline demographics, lung function, and survival were collected.
ISSN:1073-449X
1535-4970