Idiopathic Pulmonary Fibrosis (IPF) is a progressive lung disease that causes scarring of the lung tissue, making it increasingly difficult to breathe. The condition, which affects thousands of people worldwide, remains mysterious in terms of its exact cause, leaving many questions unanswered.
As the disease progresses, the scarring in the lungs worsens, leading to a decline in lung function and ultimately affecting daily activities and quality of life. Diagnosing IPF can be challenging due to its subtle and gradual onset.
Common symptoms include persistent dry cough, shortness of breath, and fatigue, which are often mistaken for other conditions. In this video, Dr Sarthak A Rastogi, Consultant in Respiratory Medicine at Holy Family Hospital, Mumbai, sheds light on the diagnostic approach for Idiopathic Pulmonary Fibrosis.
He outlines the key tests involved, such as high-resolution CT scans, pulmonary function tests, and sometimes lung biopsy, which help doctors accurately diagnose the disease and rule out other conditions.
Dr Rastogi also emphasizes the importance of early diagnosis in managing IPF and improving outcomes for patients.
As this disease progresses rapidly, timely intervention and personalized treatment plans are crucial for slowing its progression and enhancing the patient's quality of life. Watch to learn more from Dr Rastogi's expert insights.