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The medical information on this site is provided as an information resource only, and is not to be used or relied on for any diagnostic or treatment purposes. This information is not intended to be patient education, does not create any patient-physician relationship, and should not be used as a substitute for professional diagnosis and treatment.

Bronchiectasis

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Overview

Type of Disease: Genetic, autosomal dominant

Bronchiectasis is common in those who have cystic fibrosis and those who are long term smokers. It can also be caused by immune system problems, inflammatory bowel disease, HIV, or other lung diseases like COPD (chronic obstructive pulmonary disease). Exposure to smoking, polluted air, and chemicals may increase risk of getting bronchiectasis.

Bronchiectasis is diagnosed with a range of tests including chest x-ray or CT scans, tests of lung function, and the collection of mucus to check for growth of bacteria. Treatment focuses on improving lung function and managing infections, usually through the use of antibiotics to kill bacteria. This condition is chronic and can be life long; needing to be managed over many years.

If you or a family member has been diagnosed with bronchiectasis, talk to your doctor about the most current treatment options. Support groups are also a good source of information.


Description Last Updated: Aug 29, 2018

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Genetic & Rare Diseases Information Center (GARD) GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.

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Bronchiectasis and NTM Research Registry
Added By: COPD Foundation
Added On: Mar 21, 2013
Category: General
The Bronchiectasis and NTM Research Registry is a consolidated database of non-Cystic Fibrosis (non-CF) Bronchiectasis and/or NTM patients from multiple clinical institutions across the United States.