Idiopathic pulmonary fibrosis (IPF) is a serious, but rare lung infection that causes fibrosis buildup and leads to difficulty in breathing. The cause of this disease is unclear, so it’s called idiopathic, which means unknown. This condition mostly causes breathing difficulty, however, it changes from case to case. Nearly 1,00,000 people are affected by Idiopathic pulmonary fibrosis around the world. Whereas in the U.S. approximately 100,000 people are primarily affected by the condition. Read on to know more about Idiopathic pulmonary fibrosis causes, symptoms and cure.
The main cause of IPF is damaged or scarred alveoli. Alveoli is a tiny air sac that helps lungs and blood exchange oxygen and carbon dioxide while breathing in and breathing out. Damaged or scarred alveoli cause stiff lungs and make it difficult for the lungs to function. Idiopathic pulmonary fibrosis mostly affects people around 70 to 75 years of age.
This condition can be linked to –
Symptoms
Idiopathic pulmonary fibrosis signs include the following-
How to Diagnose Idiopathic Pulmonary Fibrosis?
IPF can be diagnosed by-
Stages
There are four stages of pulmonary fibrosis prognosis: Mild, moderate, severe, and very severe.
Treatment of Idiopathic Pulmonary Fibrosis
At present, there is no treatment for IPF. But if you have IPF, do the following to stay healthy-
Facts About Pulmonary Fibrosis Prognosis and Life Expectancy
Here are some facts that you need to know about pulmonary fibrosis-
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