C101 IPF: CLINICAL STUDIES, THERAPEUTICS, AND MORE II: Bronchoalveolar Lavage Fluid Cytokine Profiles In Idiopathic Pulmonary Fibrosis Patients May Define Distinct Prognostic Groups
While some IPF patients achieve stabilization on treatment, there is a group of patients with unevitable lung functions decline despite treatment. All patients were treated with antifibrotics (pirfenidon or nintedanib according to reimbursement rules of health care provider) and LF were recorded 6 m...
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Veröffentlicht in: | American journal of respiratory and critical care medicine 2017-01, Vol.195 |
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container_title | American journal of respiratory and critical care medicine |
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creator | Sterclova, M Smetakova, M Skibova, J Vasakova, M |
description | While some IPF patients achieve stabilization on treatment, there is a group of patients with unevitable lung functions decline despite treatment. All patients were treated with antifibrotics (pirfenidon or nintedanib according to reimbursement rules of health care provider) and LF were recorded 6 month after IPF diagnosis. |
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identifier | ISSN: 1073-449X |
ispartof | American journal of respiratory and critical care medicine, 2017-01, Vol.195 |
issn | 1073-449X 1535-4970 |
language | eng |
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source | Journals@Ovid Complete; American Thoracic Society (ATS) Journals Online; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Biomarkers Cytokines Medical prognosis Pulmonary fibrosis |
title | C101 IPF: CLINICAL STUDIES, THERAPEUTICS, AND MORE II: Bronchoalveolar Lavage Fluid Cytokine Profiles In Idiopathic Pulmonary Fibrosis Patients May Define Distinct Prognostic Groups |
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