Idiopathic Pulmonary Fibrosis



Idiopathic pulmonary fibrosis (IPF) is a chronic disease. It causes inflammation and fibrosis (scarring) of tissue in the lungs.


Idiopathic means the cause is not known.

Researchers think that IPF is an exaggerated and uncontrolled inflammatory response. This produces the scar tissue. What starts the cycle is not known. Over time, scarring surrounds the thin walled air sacs in the lungs. This makes the tissue thicker and stiffer. As a result, breathing becomes difficult. The lungs gradually lose their ability to pass oxygen to the rest of the body.

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Risk Factors

IPF occurs most often in males and people aged 50 years and older. Other factors that may increase your chance of IPF include:

  • Cigarette smoking
  • Viral infection
  • Occupational exposures to dusts containing wood, metal, silica, bacteria, and animal proteins or to aerosol sprays, gases, and fumes
  • Certain medications
  • Gastroesophageal reflux disease (GERD)
  • Other family members with IPF



Over time, the symptoms get worse. This makes daily activities difficult. People with IPF gradually start to have some or all of these symptoms:

  • Shortness of breath, at first only during or after physical activity, but later also when resting
  • Dry cough
  • Gradual weight loss
  • Fatigue
  • Enlargement of the fingertips or sometimes the toes


You will be asked about your symptoms and medical history. A physical exam will be done.

Your bodily fluids and tissues may be tested. This can be done with:

  • Blood tests
  • Lung biopsy

Images may be taken of your lungs. This can be done with:

  • Chest x-ray
  • CT scan
  • Bronchoscopy

Your lung function may be tested. This can be done with:

  • Pulmonary function tests
  • An exercise text



There is no known cure. The goal of treatment is to improve symptoms and slow the disease process. This is done by reducing inflammation and scarring. The tissue that is already scarred cannot be healed.


Medication is the main form of treatment. It does not work for everyone. Medications are used to:

  • Reduce inflammation
  • Inhibit immune response
  • Slow the progression of the fibrosis

Gastroesophageal Reflux Disease

If present, GERD will need to be treated. This most often involves the use of medication and lifestyle changes.

Supportive Care

  • Some people may need to receive oxygen. This will help them breathe.
  • A pulmonary rehabilitation program may be needed to improve lung function.
  • Get appropriate vaccinations to prevent lung infection, including a flu shot every year and the pneumonia vaccine .
  • A healthy lifestyle may also help slow the disease. This includes:
    • Not smoking
    • Eating a healthy diet
    • Exercising regularly
    • Resting when needed
  • Lung transplantation may be considered for people with advanced IPF who do not respond to other treatments.


There is no proven way to prevent IPF. However, avoiding smoking and wearing masks for work in some occupations may help.

This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.

Edits to original content made by Denver Health.


American Lung Association 

Coalition for Pulmonary Fibrosis 


Health Canada 

The Lung Association 


Explore idiopathic pulmonary fibrosis. National Heart, Lung, and Blood Institute website. Available at: Updated September 20, 2011. Accessed May 9, 2016.

Idiopathic pulmonary fibrosis. American Thoracic Society. Available at: Updated March 2015. Accessed May 9, 2016.

Idiopathic pulmonary fibrosis. EBSCO DynaMed Plus website. Available at:  . Updated September 2, 2016. Accessed September 26, 2016.

Pulmonary fibrosis. American Lung Association website. Available at: Accessed May 9, 2016.