Idiopathic pulmonary fibrosis: state of the art for 2023

AJ Podolanczuk, CC Thomson… - European …, 2023 - Eur Respiratory Soc
Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease characterised by
worsening respiratory symptoms and physiological impairment. Increasing awareness of the …

Hypersensitivity pneumonitis

U Costabel, Y Miyazaki, A Pardo, D Koschel… - Nature Reviews …, 2020 - nature.com
Hypersensitivity pneumonitis (HP) is a complex syndrome caused by the inhalation of a
variety of antigens in susceptible and sensitized individuals. These antigens are found in the …

Inspiratory muscle training enhances recovery post-COVID-19: a randomised controlled trial

MA McNarry, RMG Berg, J Shelley… - European …, 2022 - Eur Respiratory Soc
Background Many people recovering from coronavirus disease 2019 (COVID-19)
experience prolonged symptoms, particularly breathlessness. We urgently need to identify …

[HTML][HTML] Nintedanib in progressive fibrosing interstitial lung diseases

KR Flaherty, AU Wells, V Cottin… - … England Journal of …, 2019 - Mass Medical Soc
Background Preclinical data have suggested that nintedanib, an intracellular inhibitor of
tyrosine kinases, inhibits processes involved in the progression of lung fibrosis. Although the …

Nintedanib in patients with autoimmune disease–related progressive fibrosing interstitial lung diseases: subgroup analysis of the INBUILD trial

EL Matteson, C Kelly, JHW Distler… - Arthritis & …, 2022 - Wiley Online Library
Objective To analyze the efficacy and safety of nintedanib in patients with fibrosing
autoimmune disease–related interstitial lung diseases (ILDs) with a progressive phenotype …

Design of the PF-ILD trial: a double-blind, randomised, placebo-controlled phase III trial of nintedanib in patients with progressive fibrosing interstitial lung disease

KR Flaherty, KK Brown, AU Wells… - BMJ open …, 2017 - bmjopenrespres.bmj.com
600 patients aged≥ 18 years will be randomised in a 1: 1 ratio to nintedanib or placebo.
Patients with diagnosis of IPF will be excluded. The study population will be enriched with …

Effect of ambulatory oxygen on quality of life for patients with fibrotic lung disease (AmbOx): a prospective, open-label, mixed-method, crossover randomised …

D Visca, L Mori, V Tsipouri, S Fleming… - The Lancet …, 2018 - thelancet.com
Background In fibrotic interstitial lung diseases, exertional breathlessness is strongly linked
to health-related quality of life (HRQOL). Breathlessness is often associated with oxygen …

Palliative care early in the care continuum among patients with serious respiratory illness: an official ATS/AAHPM/HPNA/SWHPN policy statement

DR Sullivan, AS Iyer, S Enguidanos… - American Journal of …, 2022 - atsjournals.org
Background: Patients with serious respiratory illness and their caregivers suffer
considerable burdens, and palliative care is a fundamental right for anyone who needs it …

High-dose versus low-dose prednisolone in symptomatic patients with post-COVID-19 diffuse parenchymal lung abnormalities: an open-label, randomised trial (the …

S Dhooria, S Chaudhary, IS Sehgal… - European …, 2022 - Eur Respiratory Soc
In some patients, respiratory symptoms and imaging abnormalities persist after acute
coronavirus disease 2019 (COVID-19) pneumonia [1–3]. Chest computed tomography (CT) …

Health related quality of life in patients with idiopathic pulmonary fibrosis in clinical practice: insights-IPF registry

M Kreuter, J Swigris, D Pittrow, S Geier, J Klotsche… - Respiratory …, 2017 - Springer
Abstract Background The INSIGHTS-IPF registry provides one of the largest data sets of
clinical data and self-reported patient related outcomes including health related quality of life …