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ishadeshpande15

Jul 25

Idiopathic Pulmonary Fibrosis (IPF) is a chronic, progressive lung disease characterized by scarring (fibrosis) of the lung tissue with no known cause. This scarring makes it difficult for the lungs to function properly and progressively worsens over time, leading to breathing difficulties. While there is no cure for IPF, treatment aims to slow disease progression, relieve symptoms, and improve quality of life. Common symptoms include shortness of breath, a dry cough, fatigue, and decreased exercise tolerance. Early diagnosis and management are crucial for better outcomes.

Treatment options for IPF include antifibrotic medications such as pirfenidone and nintedanib, which can help slow the progression of lung damage. Supportive therapies like oxygen supplementation, pulmonary rehabilitation, and vaccinations (e.g., flu and pneumonia shots) are often recommended to manage symptoms and prevent complications. In advanced cases, lung transplantation may be considered for eligible patients. Lifestyle changes, including quitting smoking and maintaining a healthy weight, also play an important role in managing the disease. Regular follow-up with a pulmonologist is essential to monitor disease progression and adjust treatment as needed.