scholarly journals P196 Healthcare utilisation by patients with Idiopathic Pulmonary Fibrosis; observations from the UK pirfenidone Named Patient Programme

Thorax ◽  
2013 ◽  
Vol 68 (Suppl 3) ◽  
pp. A164.3-A165 ◽  
Author(s):  
H Parfrey ◽  
C Leonard ◽  
MA Gibbons ◽  
E Armstrong ◽  
E Harris ◽  
...  
Thorax ◽  
2016 ◽  
Vol 71 (Suppl 3) ◽  
pp. A236.1-A236 ◽  
Author(s):  
N Snell ◽  
D Strachan ◽  
R Hubbard ◽  
J Gibson ◽  
T Maher ◽  
...  

Thorax ◽  
2012 ◽  
Vol 67 (Suppl 2) ◽  
pp. A48.2-A49 ◽  
Author(s):  
H Parfrey ◽  
C Leonard ◽  
MA Gibbons ◽  
E Harris ◽  
R Frank ◽  
...  

2016 ◽  
Vol 19 (7) ◽  
pp. A553 ◽  
Author(s):  
C Rinciog ◽  
M Watkins ◽  
S Chang ◽  
T Maher ◽  
C LeReun ◽  
...  

2021 ◽  
Vol 30 (6) ◽  
pp. 359-366
Author(s):  
Penny Tremayne ◽  
Samuel John Clark

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive incurable lung disease that affects a significant amount of people in the UK. Many health professionals have a limited understanding of IPF, which can result in a delayed diagnosis and inadequate care for individuals and their families. This article aims to provide an overview of IPF and help to enhance health professionals' understanding of the disease, thus contributing towards improving the care that IPF sufferers receive. This article provides a definition of IPF and explores its pathophysiology. It discusses the causes and risk factors for developing the condition, examines how IPF is diagnosed and details the treatment options available for IPF patients.


2018 ◽  
Vol 27 (150) ◽  
pp. 180078 ◽  
Author(s):  
Colin Holtze ◽  
Kevin Flaherty ◽  
Michael Kreuter ◽  
Fabrizio Luppi ◽  
Teng Moua ◽  
...  

There are over 200 interstitial lung diseases (ILDs). In addition to patients with idiopathic pulmonary fibrosis (IPF), a percentage of patients with other ILDs also develop progressive fibrosis of the lung during their disease course. Patients with progressive-fibrosing ILDs may show limited response to immunomodulatory therapy, worsening symptoms and lung function and, ultimately, early mortality. There are few data for ILDs that may present a progressive fibrosing phenotype specifically, but we believe the burden and healthcare costs associated with these conditions may be comparable to those reported in IPF. This review discusses the burden of ILDs that may present a progressive fibrosing phenotype and the factors impacting healthcare utilisation.


Thorax ◽  
2014 ◽  
Vol 69 (12) ◽  
pp. 1136-1140 ◽  
Author(s):  
David R Thickett ◽  
Clare Kendall ◽  
Lisa G Spencer ◽  
Nick Screaton ◽  
William A Wallace ◽  
...  

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