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by AR Shih · Cited by 6 — In 2018, the ATS/ERS/JRS/ALAT and Fleischner Society released new diagnostic guidelines for usual interstitial pneumonitis (UIP)/IPF, by CC Thomson · 2019 · Cited by 19 — The first evidence-based guidelines for the diagnosis and treatment of IPF were published in 2011 (2), with the treatment recommendations by V Tzilas · 2022 — The new guideline recommends a diagnostic algorithm in which both UIP and probable UIP HRCT patterns can support an IPF diagnosis in the by G Raghu · 2022 · Cited by 81 — The 2018 guidelines for diagnosis of IPF addressed TBLC in patients with ILD of undetermined type but failed to garner enough agreement to make a consensus Idiopathic pulmonary fibrosis (IPF), a rare and often fatal lung disease whose cause is unknown. The 2018 clinical practice guideline was developed byThe 2018 diagnosis of idiopathic pulmonary fibrosis guidelines: surgical lung Diagnosis of IPF Clinical Practice Guideline: Part 1, Oct. 11, 2018 (Dr. Apr 25, 2022 — Where imaging is performed with clinical suspicion for IPF, but HRCT In 2018 the guidelines were reviewed 5, and the main changes by G Raghu · 2018 · Cited by 2089 — The guideline panel provided recommendations related to the diagnosis of IPF. by J Choe · 2021 — Flow chart of patient inclusion. ILD interstitial lung disease; IPF idiopathic pulmonary fibrosis; UIP usual interstitial pneumonia; NSIP Sep 1, 2018 — Results: The guideline panel updated the diagnostic criteria for IPF. Previously defined patterns of usual interstitial pneumonia (UIP) were
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