Artigo Acesso aberto Revisado por pares

Does ambulatory oxygen improve quality of life in patients with fibrotic lung disease? Results from the AmbOx trial

2019; European Respiratory Society; Volume: 15; Issue: 2 Linguagem: Inglês

10.1183/20734735.0002-2019

ISSN

2073-4735

Autores

Andrew Creamer, Shaney Barratt,

Tópico(s)

Respiratory and Cough-Related Research

Resumo

The fibrotic interstitial lung diseases (ILDs) encompass a heterogenous group of conditions affecting the lung parenchyma, resulting in progressive, irreversible scarring. While prognosis varies between conditions, they commonly have a significant adverse impact both on health-related quality of life (HRQoL) and on survival. For idiopathic pulmonary fibrosis (IPF), the most common and fatal ILD, antifibrotic therapies (nintedanib [1] and pirfenidone [2]) have been shown to slow rate of progression, but the disease remains incurable. Management of all fibrotic ILDs therefore requires symptomatic and supportive care as well as interventions aimed at modifying the disease course [3]. The AmbOx trial provides RCT evidence for ambulatory oxygen therapy improving HRQoL in patients with fibrotic ILD

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