A24 IPF: CLINICAL STUDIES, THERAPEUTICS, AND MORE I: Baseline Characteristics Of The Initial 200 Participants In The Pulmonary Fibrosis Foundation Registry

Introduction/Rationale: Detailed understanding of patient demographics and longitudinal assessments (including response to therapy and applicable biomarkers) for interstitial lung diseases (ILD) in usual care, real-world settings are lacking. Information from baseline medical history, physical exami...

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Published in:American journal of respiratory and critical care medicine 2017-01, Vol.195
Main Authors: Flaherty, K R, de Andrade, J A, Chou, W, Lancaster, L H, Lindell, K O, Nathan, S D, Raghu, G, Spino, C, Stauffer, J L, Tuomey, P, Wolters, P J, Cosgrove, G P
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Language:English
Subjects:
Biopsy
Enrollments
Family medical history
Pulmonary fibrosis
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container_title American journal of respiratory and critical care medicine
container_volume 195
creator Flaherty, K R
de Andrade, J A
Chou, W
Lancaster, L H
Lindell, K O
Nathan, S D
Raghu, G
Spino, C
Stauffer, J L
Tuomey, P
Wolters, P J
Cosgrove, G P
description Introduction/Rationale: Detailed understanding of patient demographics and longitudinal assessments (including response to therapy and applicable biomarkers) for interstitial lung diseases (ILD) in usual care, real-world settings are lacking. Information from baseline medical history, physical examination, pulmonary function testing, and chest CT images obtained as part of usual care are collected.
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source Freely Accessible Science Journals; EZB Free E-Journals
subjects Biopsy
Enrollments
Family medical history
Pulmonary fibrosis
title A24 IPF: CLINICAL STUDIES, THERAPEUTICS, AND MORE I: Baseline Characteristics Of The Initial 200 Participants In The Pulmonary Fibrosis Foundation Registry
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