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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

This study examines whether the addition of bisoprolol to treatment of people with chronic obstructive pulmonary disease (COPD) at high risk of ....

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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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Grifols Meets Enrollment Target in Phase 3 Study of Two Dose Regimens of Prolastin®-C in Patients with Emphysema Due to Alpha-1-Antitrypsin Deficiency

Grifols Meets Enrollment Target in Phase 3 Study of Two Dose Regimens of Prolastin®-C in Patients with Emphysema Due to Alpha-1-Antitrypsin Deficiency
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Comunidad Autonoma De Cataluna , United States , Grifol Prolastin , Grifols Prolastin , Sandra Camprubi , Blood Institute , Spanish Stock Exchange , Investors Relations Department Sustainability , National Heart , European Respiratory Society , American Thoracic Society European Respiratory , American Thoracic Society , Home Genetic Health Risk Service Alpha , Media Press Office , Meets Enrollment Target , Two Dose Regimens , Emphysema Due , Proteinase Inhibitor , Prolastinc Randomized Therapy , Grifols Senior Director Clinical , Product Characteristics , North America , Middle East , Mercado Continuo , Royal Legislative Decree , Securities Market Law ,

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. ....

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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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