
Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS…
For patients with newly detected ILD of apparently unknown cause who are clinically suspected of having IPF and have an HRCT pattern of probable UIP, indeterminate for UIP, or an alternative diagnosis, we suggest cellular analysis of their BAL fluid (conditional recommendation, very low quality of evidence).
Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS…
Background: 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.
Diagnostic HRCT criteria for usual interstitial pneumonia (UIP) …
2024年6月19日 · The importance of this guideline is that (definite) UIP pattern on chest HRCT precludes the need for tissue diagnosis 1,2,5. However, unfortunately up to 20% of inconsistent with UIP group (or actually atypical UIP) can be UIP on biopsy or progress clinically to a diagnosis of idiopathic pulmonary fibrosis (IPF). UIP pattern
American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Latin American Thoracic Association (ALAT) Evidence-Based Guidelines for Diagnosis and Management of Idiopathic Pulmonary Fibrosis (IPF). This pocket guide was complied by Ganesh Raghu, MD and Bridget Collins, MD, University of Washington,
American Journal of Respiratory and Critical Care Medicine
Idiopathic pulmonary fibrosis (IPF) is a chronic, fibrosing interstitial pneumonia of unknown cause that is associated with radiological and histologic features of usual interstitial pneumonia (UIP). It occurs primarily in older adults, is characterized by progressive worsening of dyspnea and lung function, and has a poor prognosis.
Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS…
2018年9月1日 · For patients with newly detected interstitial lung disease (ILD) who have a high-resolution computed tomography scan pattern of probable UIP, indeterminate, or an alternative diagnosis, conditional recommendations were made for performing BAL and surgical lung biopsy; because of lack of evidence, no recommendation was made for or against ...
2022 update on clinical practice guidelines for idiopathic …
2022年6月24日 · The 2022 update on guidelines for idiopathic pulmonary fibrosis (IPF) by ATS/ERS/JRS/ALAT1 consists of two parts. The first part is an update on the diagnosis and treatment of IPF and the second deals with the important issue …
An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary …
Idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic, progressive fibrosing interstitial pneumonia of unknown cause, occurring primarily in older adults, and limited to the lungs. It is characterized by progressive worsening of dyspnea and lung function and is associated with a poor prognosis.
Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline. Background: This document provides clinical recommendations for the diagnosis of idiopathic pulmonary fibrosis (IPF).
Practical application and validation of the 2018 ATS/ERS/JRS/ALAT …
2021年4月26日 · In 2018, the ATS/ERS/JRS/ALAT and Fleischner Society released new diagnostic guidelines for usual interstitial pneumonitis (UIP)/IPF, adding Probable UIP as a CT category based on prior studies demonstrating this category had relatively high positive predictive value (PPV) for histopathologic UIP/Probable UIP.