What is Idiopathic pulmonary fibrosis ?
Idiopathic pulmonary fibrosis (IPF) is a type of lung disease characterized by the development of scar tissue (fibrosis) in the lungs. This scarring can cause the lungs to become stiff and thickened, making it difficult for oxygen to pass through and reach the bloodstream. As a result, people with IPF may experience shortness of breath, coughing, and fatigue.
Idiopathic pulmonary fibrosis (IPF) is a condition in which the lungs become scarred and breathing becomes increasingly difficult. It’s not clear what causes it, but it usually affects people who are around 70 to 75 years old, and is rare in people under 50.
IPF is classified as a type of interstitial lung disease, meaning it affects the tissues and structures around the air spaces in the lungs. It is considered idiopathic, which means the cause is unknown. It typically occurs in people over the age of 50 and is more common in men than in women. There is no cure for IPF, and treatment is aimed at slowing the progression of the disease and managing symptoms.
