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      An Official American Thoracic Society/European Respiratory Society Statement: Update of the International Multidisciplinary Classification of the Idiopathic Interstitial Pneumonias

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      , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
      American Journal of Respiratory and Critical Care Medicine
      American Thoracic Society
      idiopathic interstitial pneumonia, usual interstitial pneumonia, nonspecific interstitial pneumonia, respiratory bronchiolitis, desquamative interstitial pneumonia, cryptogenic organizing pneumonia, acute interstitial pneumonia, lymphoid interstitial pneumonia, pleuroparenchymal fibroelastosis, acute fibrinous and organizing pneumonia

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          Abstract

          Background: In 2002 the American Thoracic Society/European Respiratory Society (ATS/ERS) classification of idiopathic interstitial pneumonias (IIPs) defined seven specific entities, and provided standardized terminology and diagnostic criteria. In addition, the historical “gold standard” of histologic diagnosis was replaced by a multidisciplinary approach. Since 2002 many publications have provided new information about IIPs.

          Purpose: The objective of this statement is to update the 2002 ATS/ERS classification of IIPs.

          Methods: An international multidisciplinary panel was formed and developed key questions that were addressed through a review of the literature published between 2000 and 2011.

          Results: Substantial progress has been made in IIPs since the previous classification. Nonspecific interstitial pneumonia is now better defined. Respiratory bronchiolitis–interstitial lung disease is now commonly diagnosed without surgical biopsy. The clinical course of idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia is recognized to be heterogeneous. Acute exacerbation of IIPs is now well defined. A substantial percentage of patients with IIP are difficult to classify, often due to mixed patterns of lung injury. A classification based on observed disease behavior is proposed for patients who are difficult to classify or for entities with heterogeneity in clinical course. A group of rare entities, including pleuroparenchymal fibroelastosis and rare histologic patterns, is introduced. The rapidly evolving field of molecular markers is reviewed with the intent of promoting additional investigations that may help in determining diagnosis, and potentially prognosis and treatment.

          Conclusions: This update is a supplement to the previous 2002 IIP classification document. It outlines advances in the past decade and potential areas for future investigation.

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          Author and article information

          Contributors
          On behalf of : on behalf of the ATS/ERS Committee on Idiopathic Interstitial Pneumonias
          Journal
          Am J Respir Crit Care Med
          Am. J. Respir. Crit. Care Med
          ajrccm
          American Journal of Respiratory and Critical Care Medicine
          American Thoracic Society
          1073-449X
          1535-4970
          15 September 2013
          15 September 2013
          15 September 2013
          : 188
          : 6
          : 733-748
          Article
          PMC5803655 PMC5803655 5803655 201308-1483ST
          10.1164/rccm.201308-1483ST
          5803655
          24032382
          600cd7af-8d41-47f8-b185-5aeb91d12904
          Copyright © 2013 by the American Thoracic Society
          History
          Page count
          Figures: 9, Tables: 4, Pages: 16
          Categories
          American Thoracic Society Documents

          cryptogenic organizing pneumonia,desquamative interstitial pneumonia,respiratory bronchiolitis,idiopathic interstitial pneumonia,usual interstitial pneumonia,nonspecific interstitial pneumonia,acute interstitial pneumonia,lymphoid interstitial pneumonia,pleuroparenchymal fibroelastosis,acute fibrinous and organizing pneumonia

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