What is Idiopathic Pulmonary Fibrosis (IPF)?

Idiopathic pulmonary fibrosis (IPF) is a progressive lung condition characterized by scarring of lung tissue, leading to breathlessness and a persistent dry cough. The exact cause is unknown, but potential triggers include viral infections, smoking, and heartburn. Diagnosis involves tests like CT scans and bronchoscopy. While there is no cure, treatments can alleviate symptoms and slow progression. Management includes medications, pulmonary rehabilitation, and possibly lung transplants. Support groups and lifestyle changes, such as quitting smoking and maintaining a healthy diet, are crucial for coping with IPF.

What does the term 'idiopathic' mean in the context of idiopathic pulmonary fibrosis?

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What are some potential triggers that may cause the scarring process in IPF?

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Describe the main symptoms of idiopathic pulmonary fibrosis.

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What diagnostic tests are commonly used to investigate suspected cases of IPF?

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What lifestyle changes can help individuals with IPF manage their condition?

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