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
Hauptverfasser: Sterclova, M, Smetakova, M, Skibova, J, Vasakova, M
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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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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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