Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper.
By D. Lynch, N. Sverzellati, W. Travis, K. Brown, T. Colby, J. Galvin, J. Goldin, D. Hansell, Y. Inoue, T. Johkoh and 7 more. The Lancet Respiratory Medicine, 2017
873 citations recorded by the source corpus.
Subfields: Physiology, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/b41e33768702a882bdbc7eb3dadebc01029cee4b
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In Physiology
In Pulmonary and Respiratory Medicine
Citations in the corpus
- Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline (2018, methodology): “It is based on these 2018 guidelines and the 2011 guidelines (2) and similar to that suggested by a task force sponsored by the Fleischner Society (82).”
- Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults: An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline (2022, background): “There were several reasons that merging the UIP and probable UIP categories was considered: 1) there is increasing evidence that patients with the probable UIP pattern and UIP pattern on HRCT have similar disease behavior and clinical courses (19–21); 2) the likelihood of histologic confirmation of ”
- Diagnosis of Hypersensitivity Pneumonitis in Adults. An Official ATS/JRS/ALAT Clinical Practice Guideline (2020, background): “Fibrotic HP. Coexisting lung fi brosis and signs of bronchiolar obstruction are highly suggestive of fi brotic HP (Table 6) (7, 40, 121, 127, 128).”