Idiopathic pulmonary fibrosis is scarring or thickening of the lungs without a known cause.
Idiopathic diffuse interstitial pulmonary fibrosis; IPF; Pulmonary fibrosis; Cryptogenic fibrosing alveolitis; CFA; Fibrosing alveolitis; Usual interstitial pneumonitis; UIP
Doctors do not know what causes idiopathic pulmonary fibrosis (IPF) or why some people get it. Idiopathic means the cause is not known. The condition may be due to the lungs responding to an unknown substance or injury. Genes may play a role in developing IPF. The disease occurs most often in people between 50 and 70 years old.
When you have IPF, your lungs become scarred and stiffened. This makes it hard for you to breathe. In some people, IPF gets worse quickly over months or a few years. In others, IPF worsens over a much longer time.
Chest pain(occasionally) Cough(usually dry)
- Decreased tolerance for activity
Shortness of breathduring activity (this symptom lasts for months or years, and over time may also occur when at rest)
Exams and Tests
The health care provider will perform a physical exam and ask about your medical history. You will be asked whether you have been exposed to asbestos and if you have been a smoker.
The physical exam may find that you have:
- Abnormal breath sounds called crackles
- Blue-colored skin (cyanosis) around the mouth or fingernails due to low oxygen (with advanced disease)
- Enlargement of the fingernail bases, called clubbing (with advanced disease)
Patients with idiopathic pulmonary fibrosis have abnormal breath sounds called crackles. Patients with advanced disease may have blue-colored skin (
Examination of the fingers and toes may show abnormal enlargement of the fingernail bases (
Tests that help diagnose idiopathic pulmonary fibrosis include the following:
Bronchoscopy Chest CT scan Chest x-ray
- Measurements of blood oxygen level
Pulmonary function tests
- Six-minute walk test
- Tests for connective tissue diseases such as
rheumatoid arthritis, lupus, or scleroderma
- Open lung (surgical) lung biopsy
There is no known cure exists for IPF.
Treatment is aimed at relieving symptoms:
Medicines such as corticosteroids may help reduce swelling (inflammation) inside the lungs.
Patients with low blood oxygen levels may need
oxygen supportat home.
Lung rehabilitation will not cure the disease. But it can help maintain the ability to exercise without breathing difficulty.
Some patients with advanced pulmonary fibrosis may need a lung transplant.
You can ease the stress of illness by joining a support group. Sharing with others who have common experiences and problems can help you not feel alone.
These organizations are good resources for information on lung disease:
- American Lung Association |
- National Heart, Lung, and Blood Institute |
Some patients may improve or stay stable for a long time with or without treatment. Most people get worse, even with treatment.
When breathing symptoms become more severe, you and your doctor should discuss
- Abnormally high levels of red blood cells due to low blood oxygen levels
Collapsed lung High blood pressure in the arteries of the lungs Respiratoryfailure
When to Contact a Medical Professional
Call your health care provider promptly if you have any of the following::
- Your breathing is getting harder, faster, or shallow (are unable to take a deep breath)
- Need to lean forward when sitting to breathe comfortably.
- Frequent headaches
- Feel sleepy or confused
- Coughing up dark mucus
- Fingertips or the skin around your fingernails is blue
Related:Using oxygen at home, Respiratory