Acute exacerbation of interstitial lung disease in the intensive care unit: Principles of diagnostic evaluation and management

doi:10.5492/wjccm.v12.i3.153

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World Journal of Critical Care Medicine

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2220-3141

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Crit Care Med. Jun 9, 2023; 12(3): 153-164
Published online Jun 9, 2023. doi: 10.5492/wjccm.v12.i3.153

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Figure 1 Classification of interstitial lung disease/diffuse parenchymal lung disease. AIP: Acute interstitial pneumonia; COP: Cryptogenic organizing pneumonia; CTD: Connective tissue disease; DIP: Desquamative interstitial pneumonia; DM: Dermatomyositis; HP: Hypersensitivity pneumonitis; IIP: Idiopathic interstitial pneumonias; IPF: Idiopathic pulmonary fibrosis; LAM: Lymphangioleiomyomatosis; LIP: Lymphoid interstitial pneumonia; MTX: Methotrexate; NSIP: Non-specific interstitial pneumonia; PLCH: Pulmonary Langerhans cell histiocytosis; PM: Polymyositis; PPFE: Pleuroparenchymal fibroelastosis; RA: Rheumatoid arthritis; RB-ILD: Respiratory bronchiolitis-ILD.

Citation: Hayat Syed MK, Bruck O, Kumar A, Surani S. Acute exacerbation of interstitial lung disease in the intensive care unit: Principles of diagnostic evaluation and management. World J Crit Care Med 2023; 12(3): 153-164
URL: https://www.wjgnet.com/2220-3141/full/v12/i3/153.htm
DOI: https://dx.doi.org/10.5492/wjccm.v12.i3.153