Short Communication
Author Details :
Volume : 7, Issue : 2, Year : 2020
Article Page : 80-85
https://doi.org/10.18231/j.agems.2020.013
Abstract
Idiopathic pulmonary fibrosis (IPF) is an interstitial lung disease characterised by chronic, progressive scarring of the lungs. It is a relatively rare disease, afflicting those 50–70 years of age, slightly more common among men than women, without racial predilection. The most common complaint is progressive shortness of breath. Pulmonary function testing reveals a restrictive Ventilatory defect with a diminished diffusion capacity Despite advances in therapy progress has been challenged by a poor understanding of pathological mechanisms and patient heterogeneity, including variable progression. The outcome of the disease is poor and patients often succumb to mortality in few years.
Keywords: Smoking, Hypersensitivity, Autoimmune, Occupation, Idiopathic pulmonary fibrosis nintedanib, Pirfenidone.
How to cite : Chaudhry S , Focusing on idiopathic pulmonary fibrosis. Ann Geriatr Educ Med Sci 2020;7(2):80-85
This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
Received : 26-11-2020
Accepted : 22-12-2020
Viewed: 1895
PDF Downloaded: 816