Results 11 to 20 of about 765,049 (358)

Nintedanib for Systemic Sclerosis-Associated Interstitial Lung Disease. [PDF]

open access: yesNew England Journal of Medicine, 2019
BACKGROUND Interstitial lung disease (ILD) is a common manifestation of systemic sclerosis and a leading cause of systemic sclerosis-related death. Nintedanib, a tyrosine kinase inhibitor, has been shown to have antifibrotic and antiinflammatory effects ...
O. Distler   +14 more
semanticscholar   +5 more sources

Differentiating interstitial lung diseases from other respiratory diseases using electronic nose technology

open access: yesRespiratory Research, 2023
Introduction Interstitial lung disease (ILD) may be difficult to distinguish from other respiratory diseases due to overlapping clinical presentation. Recognition of ILD is often late, causing delay which has been associated with worse clinical outcome ...
Iris G. van der Sar   +6 more
doaj   +1 more source

Rheumatoid arthritis-interstitial lung disease: manifestations and current concepts in pathogenesis and management

open access: yesEuropean Respiratory Review, 2021
Rheumatoid arthritis (RA) is a systemic inflammatory disorder, with the most common extra-articular manifestation of RA being lung involvement. While essentially any of the lung compartments can be affected and manifest as interstitial lung disease (ILD),
S. Kadura, G. Raghu
semanticscholar   +1 more source

Nintedanib in Patients With Autoimmune Disease–Related Progressive Fibrosing Interstitial Lung Diseases: Subgroup Analysis of the INBUILD Trial

open access: yesArthritis & Rheumatology, 2022
To analyze the efficacy and safety of nintedanib in patients with fibrosing autoimmune disease–related interstitial lung diseases (ILDs) with a progressive phenotype.
E. Matteson   +14 more
semanticscholar   +1 more source

Predictors and changes of physical activity in idiopathic pulmonary fibrosis

open access: yesBMC Pulmonary Medicine, 2022
Background Different clinical predictors of physical activity (PA) have been described in idiopathic pulmonary fibrosis (IPF), but studies are lacking evaluating the potential role of muscle strength and anxiety and depression symptoms in PA limitation ...
Diana Badenes-Bonet   +15 more
doaj   +1 more source

Immunomodulatory treatment of interstitial lung disease

open access: yesTherapeutic Advances in Respiratory Disease, 2022
Interstitial lung diseases (ILDs) other than idiopathic pulmonary fibrosis (IPF) have an array of immunomodulatory treatment options compared with IPF, due to their inflammatory component.
L. van den Bosch   +3 more
semanticscholar   +1 more source

Variability in Global Prevalence of Interstitial Lung Disease

open access: yesFrontiers in Medicine, 2021
There are limited epidemiologic studies describing the global burden and geographic heterogeneity of interstitial lung disease (ILD) subtypes. We found that among seventeen methodologically heterogenous studies that examined the incidence, prevalence and
B. Kaul   +3 more
semanticscholar   +1 more source

Clinicoserological features of antisynthetase syndrome (ASyS)-associated interstitial lung disease presenting to respiratory services: comparison with idiopathic pulmonary fibrosis and ASyS diagnosed in rheumatology services

open access: yesBMJ Open Respiratory Research, 2021
Introduction Antisynthetase syndrome (ASyS) is a rare autoimmune connective tissue disease (CTD), associated with autoantibodies targeting tRNA synthetase enzymes, that can present to respiratory (interstitial lung disease (ILD)) or rheumatology ...
Harsha Gunawardena   +7 more
doaj   +1 more source

In-hospital mortality following surgical lung biopsy for interstitial lung disease in the USA: 2000-2011 [PDF]

open access: yes, 2016
Rationale: Surgical lung biopsy can help to determine a specific diagnosis in interstitial lung disease, but has associated risks. Most currently available mortality data are derived from case series and may not be generalizable to broader populations.
Fogarty, Andrew W.   +3 more
core   +1 more source

Lung function trajectory in progressive fibrosing interstitial lung disease

open access: yesEuropean Respiratory Journal, 2021
Background Proposed criteria for progressive fibrosing interstitial lung disease (PF-ILD) have been linked to increased mortality risk, but lung function trajectory after satisfying individual criteria remains unknown. Because survival is rarely employed
J. Oldham   +15 more
semanticscholar   +1 more source

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