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      Role of imaging in progressive-fibrosing interstitial lung diseases

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          Abstract

          Imaging techniques are an essential component of the diagnostic process for interstitial lung diseases (ILDs). Chest radiography is frequently the initial indicator of an ILD, and comparison of radiographs taken at different time points can show the rate of disease progression. However, radiography provides only limited specificity and sensitivity and is primarily used to rule out other diseases, such as left heart failure. High-resolution computed tomography (HRCT) is a more sensitive method and is considered central in the diagnosis of ILDs. Abnormalities observed on HRCT can help identify specific ILDs. HRCT also can be used to evaluate the patient's prognosis, while disease progression can be assessed through serial imaging. Other imaging techniques such as positron emission tomography-computed tomography and magnetic resonance imaging have been investigated, but they are not commonly used to assess patients with ILDs. Disease severity may potentially be estimated using quantitative methods, as well as visual analysis of images. For example, comprehensive assessment of disease staging and progression in patients with ILDs requires visual analysis of pulmonary features that can be performed in parallel with quantitative analysis of the extent of fibrosis. New approaches to image analysis, including the application of machine learning, are being developed.

          Abstract

          Imaging techniques, particularly HRCT, are the cornerstone for ILD diagnosis and new approaches to analysing HRCT images, including machine-learning technology, are being developed http://ow.ly/1R1e30mOqhn

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          Most cited references73

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          An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management

          American Journal of Respiratory and Critical Care Medicine, 183(6), 788-824
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            Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline

            This document provides clinical recommendations for the diagnosis of idiopathic pulmonary fibrosis (IPF). It represents a collaborative effort between the American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Latin American Thoracic Society.
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              Fleischner Society: glossary of terms for thoracic imaging.

              Members of the Fleischner Society compiled a glossary of terms for thoracic imaging that replaces previous glossaries published in 1984 and 1996 for thoracic radiography and computed tomography (CT), respectively. The need to update the previous versions came from the recognition that new words have emerged, others have become obsolete, and the meaning of some terms has changed. Brief descriptions of some diseases are included, and pictorial examples (chest radiographs and CT scans) are provided for the majority of terms. (c) RSNA, 2008.
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                Author and article information

                Journal
                Eur Respir Rev
                Eur Respir Rev
                ERR
                errev
                European Respiratory Review
                European Respiratory Society
                0905-9180
                1600-0617
                31 December 2018
                21 December 2018
                : 27
                : 150
                : 180073
                Affiliations
                [1 ]Dept of Radiology, King's College NHS Foundation Trust, London, UK
                [2 ]Dept of Radiology, Royal Brompton & Harefield Hospital, London, UK
                [3 ]División Neumonología, Hospital de Clínicas José de San Martín, Universidad de Buenos Aires, Fundación Funef, Buenos Aires, Argentina
                [4 ]Dept of Respiratory Medicine, Respiratory Center, Toranomon Hospital, Tokyo, Japan
                [5 ]Facultad de Ciencias de la Salud, Universidad Autónoma de Chile, Talca, Chile
                [6 ]Division of Pulmonary, Allergy, and Critical Care Medicine, Columbia University College of Physicians and Surgeons, New York, NY, USA
                [7 ]Pulmonary, Allergy & Critical Care Division, University of Pennsylvania, Philadelphia, PA, USA
                [8 ]Pulmonology Dept, Hospital Universitario de La Princesa, Madrid, Spain
                [9 ]Regional Referral Centre for Rare Lung Diseases, University Hospital “Policlinico”, Dept of Clinical and Respiratory Medicine, University of Catania, Catania, Italy
                [10 ]Both authors contributed equally
                Author notes
                Simon L.F. Walsh, Dept of Radiology, King's College NHS Foundation Trust, Kings College London, Denmark Hill, Brixton, London, SE5 9RS, UK. E-mail: slfwalsh@ 123456gmail.com
                Article
                ERR-0073-2018
                10.1183/16000617.0073-2018
                9488692
                30578332
                672a029d-f24e-4b6f-a978-192f86b2714f
                Copyright ©ERS 2018.

                ERR articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.

                History
                : 14 August 2018
                : 01 November 2018
                Categories
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