Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis (IPF) is a serious disease that affects the lungs. The lung is composed of small air sacs that expand to accommodate the air we inhale. In IPF, the lung is scarred and the alveoli become more and more difficult to expand. This causes shortness of breath, a dry cough, fatigue, weight loss, loss of appetite, and clubbing of fingers. IPF is usually seen in individuals older than 50 years of age.
Difficulty breathing
Occurs or worsens with exertion
common
Cough with mucus or without mucus
Dry
Occurs or worsens with exertion
Lasting 4 weeks or more
An irritating cough that doesn't go away
common
Fatigue
common
Enlarged feet or ankle
In both feet or ankles
or Swelling in lower leg
In both lower legs
common
Enlargement of the fingertips and downward sloping of nails
common
Weight loss
Poor appetite
Fever
Less than 38°C (100. 4°F)
Muscle pain
or Joint pain
Recurrent
Both sides of the body
At hip, Knees, At wrist, In fingers, Elbows
Smoking
Family history of idiopathic pulmonary fibrosis
If you have Idiopathic Pulmonary Fibrosis, then visit a pulmonologist as soon as possible.
Contact a
Pulmonologist
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