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Idiopathic pulmonary fibrosis
Definition Idiopathic pulmonary fibrosis involves scarring or thickening of tissues deep in the lung without a known cause. Alternative Names Idiopathic diffuse interstitial pulmonary fibrosis; IPF; Pulmonary fibrosis; Cryptogenic fibrosing alveolitis; CFA; Fibrosing alveolitis; Usual interstitial pneumonitis; UIP Causes, incidence, and risk factors Idiopathic pulmonary fibrosis is a disease of the lower respiratory tract that damages the air sacs (alveoli) and leads to reduced transfer of oxygen to the blood. It causes widespread scarring of the lung. The condition is believed to result from an inflammatory response to an unknown agent -- "idiopathic" means no cause can be found. The disease occurs most often in people between 50 and 70 years old. Symptoms - Shortness of breath on exertion that lasts for months or years and eventually is present at rest
- Decreased tolerance for activity
- Cough (usually dry)
- Chest pain (occasionally)
Signs and tests The health care provider will perform a physical exam and ask questions about your medical history. Patients with idiopathic pulmonary fibrosis have abnormal breath sounds called crackles. Patients with advanced disease may have blue-colored skin (cyanosis) around the mouth or in the fingernails due to low oxygen. Examination of the fingers and toes may reveal clubbing (abnormal enlargement of the fingernail bases). Tests that help diagnose idiopathic pulmonary fibrosis include the following: - Chest x-ray
- CT - chest
- Pulmonary function tests
- Bronchoscopy with transbronchial lung biopsy
- Lung biopsy
- Measurements of blood oxygen level
- Tests for connective tissue diseases such as rheumatoid arthritis, lupus, or scleroderma
Treatment No known cure exists for idiopathic pulmonary fibrosis. Medications such as corticosteroids and cytotoxic drugs may be given to suppress inflammation, but these treatments are usually unsuccessful. Oxygen is given to patients who have low blood oxygen levels. Lung transplantation may be indicated for some patients with advanced pulmonary fibrosis. Support Groups The stress of illness can often be helped by joining a support group where members share common experiences and problems. See lung disease - support group. Expectations (prognosis) Some patients may improve on treatment with corticosteroids or cytotoxic drugs, but most patients suffer from progressive disease despite treatment. Pulmonary hypertension (high blood pressures in the vessels of the lungs) and respiratory failure is the eventual outcome. Average survival time is 5-6 years, but this varies greatly between patients. Complications - Respiratory failure
- Chronic hypoxemia (low blood oxygen level)
- Pulmonary hypertension
- Cor pulmonale (failure of the right side of the heart)
- Polycythemia (abnormally high levels of red blood cells)
Calling your health care provider Call for an appointment with the health care provider if persistent cough or shortness of breath develops. Prevention Avoiding smoking may help prevent this condition but its cause, and therefore more specific prevention, is not known. Review date: 5/3/2006 Reviewed By: David A. Kaufman, M.D., Assistant Professor, Division of Pulmonary, Critical Care & Sleep Medicine, Mount Sinai School of Medicine, New York, NY. Review provided by VeriMed Healthcare Network.
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