Pulmonary Fibrosis

Pulmonary Fibrosis

Pulmonary fibrosis is a progressive lung disease characterized by the formation of scar tissue in the lungs, which stiffens and thickens the lung tissue, making it difficult to breathe. Here are key points about pulmonary fibrosis:

  • Pulmonary fibrosis can develop due to various factors, including environmental exposures, occupational hazards, autoimmune diseases, medications, and genetic predisposition.
  • Symptoms of pulmonary fibrosis may include shortness of breath, persistent dry cough, fatigue, unexplained weight loss, and discomfort in the chest.
  • Diagnosis involves a combination of medical history, physical examination, lung function tests, imaging studies such as chest X-rays and high-resolution CT scans, and sometimes lung biopsy to confirm the presence and extent of fibrosis.
  • Treatment options for pulmonary fibrosis aim to alleviate symptoms, slow disease progression, and improve quality of life through medications such as corticosteroids, immunosuppressants, antifibrotic agents, and oxygen therapy, as well as pulmonary rehabilitation.
  • In advanced cases, lung transplantation may be considered as a treatment option for eligible patients with severe pulmonary fibrosis and significant respiratory impairment. Early diagnosis and intervention are crucial for optimizing outcomes and managing the progression of pulmonary fibrosis.