Idiopathic pulmonary fibrosis

• Illustrations
• Alternative names
• Definition
• Causes, incidence, and risk factors
• Symptoms
• Signs and tests

• Treatment
• Support Groups
• Expectations (prognosis)
• Complications
• Calling your health care provider
• Prevention

Alternative names    Return to top

Definition    Return to top

Idiopathic pulmonary fibrosis involves scarring or thickening of tissues deep in the lung without a known cause.

Causes, incidence, and risk factors    Return to top

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    Return to top

• 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    Return to top

In addition to a physical examination, your health care provider will take a careful history in order to exlude other similar diseases.

Patients with idiopathic pulmonary fibrosis have dry, Velcro-like breath sounds called crackles. Patients with advanced disease may have cyanosis (blueness 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
• High-resolution CT scan of the chest
• Pulmonary function tests
• Bronchoscopy with transbronchial lung biopsy
• Surgical lung biopsy
• Measurement of blood oxygen level at rest or during exertion
• Tests for connective tissue diseases such as rheumatoid arthritis, lupus, or scleroderma

Treatment    Return to top

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.

Recently, interferon-gamma-1B has shown some promise in treating this disease, but more research is necessary to demonstrate that this drug is beneficial.

Lung transplantation may be indicated for some patients with advanced pulmonary fibrosis.

Support Groups    Return to top

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)    Return to top

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    Return to top

• 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    Return to top

Call for an appointment with the health care provider if persistent cough or shortness of breath develops.

Prevention    Return to top

Avoiding smoking may help prevent this condition but its cause, and therefore more specific prevention, is not known.