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Bisoprolol in Patients With Chronic Obstructive Pulmonary Disease at High Risk of Exacerbation: The BICS Randomized Clinical Trial | Chronic Obstructive Pulmonary Disease | JAMA

High-resolution CT phenotypes in pulmonary sarcoidosis: a multinational Delphi consensus study

High-resolution CT phenotypes in pulmonary sarcoidosis: a multinational Delphi consensus study
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Those Who Smoke Heavily Have High Incidence of Undiagnosed COPD

About a third of participants in the COPDGene trial with a history of heavy smoking had undiagnosed COPD or abnormal spirometry warranting medication.

Usual interstitial pneumonia as a stand-alone diagnostic entity: the case for a paradigm shift?

Usual interstitial pneumonia (UIP) is characterised by a distinctive morphological and radiological appearance that was considered the pathognomonic hallmark of idiopathic pulmonary fibrosis (IPF). However, this peculiar lung remodelling pattern is also seen in other fibrotic interstitial lung diseases, including hypersensitivity pneumonitis, and connective tissue diseases. In this Personal View, we advocate the designation of a UIP pattern as a single, discrete diagnostic entity, amalgamating its primary form and secondary processes in disorders such as hypersensitivity pneumonitis (hypersensitivity pneumonitis with UIP), rheumatoid arthritis (rheumatoid arthritis with UIP), and others.

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