Bronchiectasis: Symptoms, Causes, Diagnosis, and Treatment

What Is Bronchiectasis?

What Is Bronchiectasis?
iStock (2); Everyday Health
Bronchiectasis is a chronic lung condition in which your airways, or bronchi, widen permanently and become scarred. It may cause a persistent cough, large daily production of mucus (sputum or phlegm), and shortness of breath. As the damage progresses, the airways lose their ability to clear out mucus, leading to bacteria growing and multiplying. This can cause repeated infections and inflammation of the lungs that worsen bronchiectasis, creating a cycle of disease.

There is no cure for bronchiectasis, but ongoing management with medical treatment and lifestyle adjustments can improve your quality of life and prevent the condition from getting worse.

Types of Bronchiectasis

Bronchiectasis is usually classified based on the extent and location of lung damage. Types of bronchiectasis include:

  • Cylindrical or Tubular Your airways have widened but mostly retain their original shape. This is the mildest and most common type of bronchiectasis.
  • Varicose Your airways have an irregular, stretched appearance.
  • Cystic Your airways develop large, cyst-like sacs filled with mucus. This is the most severe type of bronchiectasis.

Bronchiectasis may also be focal, affecting one or two lung areas, or diffuse, affecting multiple areas.

In some cases, bronchiectasis may result from other lung conditions. For example, fibrotic lung diseases such as interstitial lung disease cause swelling that pulls bronchi open, resulting in bronchiectasis.

Signs and Symptoms of Bronchiectasis

Bronchiectasis symptoms usually develop over many years, typically after a respiratory infection, and get progressively worse.

Common symptoms include:

  • Chronic, daily cough, which may last months or years

  • Large, daily production of sputum (saliva mixed with mucus), which is often coughed up
  • Shortness of breath
  • Frequent, recurrent chest infections or colds, which often worsen symptoms
  • Coughing up blood, or hemoptysis
  • Fever
  • Chest pain
  • Wheezing
  • Fatigue
  • Nail clubbing, in which your nails curve downward because of thickening skin and tissue

  • Bad breath
  • Pale skin

Illustrative graphic titled Signs and Symptoms of Bronchiectasis shows Chronic Daily Cough Large Amounts of Phlegm (Sputum)  Frequent Chest Infections Shortness of Breath Wheezing Chest Pain Fatigue Coughing Up Blood Nail Clubbing. Everyday Health logo.
Everyday Health

Causes and Risk Factors of Bronchiectasis

Bronchiectasis is the result of a cycle of airway damage, inflammation, mucus buildup, and lung infections that lead to irreversible lung changes. Airway damage and the accumulation of bacteria in the lungs can cause inflammation and infections, which widen airways even more.

This cycle of lung damage can be touched off by a wide variety of factors, including genetic conditions, infections, and environmental contaminants. In about 40 percent of cases, the initial cause of bronchiectasis is unknown.

Known causes include:

  • Severe or recurrent respiratory infections
  • Genetic conditions that can affect the lungs, such as cystic fibrosis, primary ciliary dyskinesia, and alpha-1 antitrypsin deficiency

  • Cancers such as leukemia

  • Conditions or medications that weaken the immune system, including HIV and medications used after organ transplants
  • Autoimmune or inflammatory diseases such as rheumatoid arthritis, Sjögren's syndrome, inflammatory bowel disease, and lupus

  • Chronic pulmonary aspiration, the inhalation of substances such as food particles and digestive fluids that inflame the airways

  • Airway obstruction from tumors or foreign objects

  • Allergic bronchopulmonary aspergillosis, an allergic fungal reaction
  • Environmental exposure, including smoke or toxin inhalation
  • Infections with tuberculosis, which can cause severe or repeated lung infections, or other mycobacteria
  • Lung diseases such as chronic obstructive pulmonary disease (COPD) and asthma

How Is Bronchiectasis Diagnosed?

Diagnosing bronchiectasis begins with a thorough review of your symptoms and medical and family history. Your healthcare provider may perform a number of other tests to assist with diagnosis and check for infections, underlying conditions, and immune system function. These may include:

  • Chest X-ray or computed tomography (CT) scans to image your lungs and spot any airway dilation and structural changes
  • Sputum culture to identify bacteria or fungi in your airways
  • Lung function tests to assess your airflow and lung capacity
  • Blood tests to look for infections (including HIV) and evaluate immune function
  • Bronchoscopy, a procedure to look closely at your airways and remove any obstructions using a bronchoscope, a long, flexible tube with a light and camera at the end
  • Specific tests for various immune system and autoimmune disorders and other conditions

Treatment and Medication Options for Bronchiectasis

Bronchiectasis can be treated but not cured.

The primary goal of bronchiectasis treatment is to keep the airways clean, thereby reducing the risk of infections, which can lead to worsening lung damage.

Airway Clearance

Clearing mucus from airways is the most commonly recommended preventive treatment, and many people with the condition develop a once- or twice-daily airway clearance ritual. By keeping the airways clear of mucus, you can prevent bacterial infections from developing. Some people will be able to perform airway clearance by themselves using a variety of breathing techniques, while others will need support from professionals or specialized devices. Airway and mucus clearance may involve:

  • Active cycle of breathing technique (ACBT), a type of deep breathing exercise that can be performed at home

  • Forced expiration technique (FET), or huffing, which involves taking a breath and quickly breathing out with an O-shaped mouth as if to fog up a mirror

  • Chest physical therapy, also known as chest physiotherapy and percussion, in which a therapist or trained caregiver taps or gently pounds your chest and back to loosen and drain the mucus from your lungs

  • Postural drainage, which involves huffing while lying with your chest lower than your abdomen

  • Handheld devices, masks, and therapy vests that help loosen mucus with vibration or high-frequency airwaves technologies such as oscillating positive expiratory pressure (PEP) and intrapulmonary percussive ventilation (IPV)

Medication: Treatments for Symptoms and Infections

Various medications can help manage symptoms, infections, and underlying conditions, including:

  • Antibiotics (pills, inhaler, or intravenous), to fight infections
  • Bronchodilators, inhalers to relieve airway narrowing and ease breathing
  • Inhaled corticosteroids that reduce airway inflammation
  • Mucus thinning drugs (mucolytics) and expectorants, often delivered through a nebulizer
  • Macrolides, which treat infections and reduce inflammation

Medication: Disease-Modifying Treatment

There is one medication approved by the U.S. Food and Drug Administration (FDA) to treat bronchiectasis specifically: brensocatib (Brinsupri). It targets enzymes associated with inflammation in people with non-cystic fibrosis bronchiectasis, helping reduce flare-ups and slow disease progression.

For people with cystic fibrosis–related bronchiectasis, long-term macrolide therapy may also help reduce flare-ups and slow lung function decline.

Other Treatments

If you have severe issues from bronchiectasis, you may need more advanced treatments, such as:

  • Oxygen therapy, a treatment providing supplemental oxygen (with an oxygen tank and mask) if you experience low blood oxygen levels

  • Bronchial artery embolization, a technique that uses a catheter to inject a substance that blocks a bleeding blood vessel, if you have significant bleeding with cough
  • Lobectomy, a surgical procedure to remove a section of the lung that is experiencing significant bleeding

  • Lung transplant, which is reserved for end-stage disease, mostly people with advanced cystic fibrosis

Lifestyle Changes for Bronchiectasis

Bronchiectasis is a lifelong condition, but certain lifestyle changes can help reduce symptoms and infections, prevent disease progression, and improve your quality of life.

Infection Prevention and Hygiene

When you have bronchiectasis, preventing respiratory infections can help slow or stop the cycle of disease. It’s also important to avoid exposing your lungs to substances that can potentially cause inflammation, which can damage the airways and perpetuate bronchiectasis. Helpful habits may include:

  • Do not smoke and avoid secondhand smoke.

  • Minimize exposure to fumes and pollution.

  • Stay current on routine vaccinations for infectious respiratory diseases, including influenza, COVID-19, pneumonia, and pertussis (whooping cough).

  • Maintain good hygiene to reduce your risk of infections, such as by frequently washing your hands, especially before eating, and avoiding crowded spaces during cold and flu season.
  • Stay away from people with respiratory infections, including the cold and flu.

  • Don’t use mineral oil or petroleum jelly near your nose to avoid accidentally inhaling the substances into the lungs.

Hydration and Diet

Your hydration and diet can affect the quality of your mucus, your body’s overall levels of inflammation, and your immune system’s ability to fight infections, all of which play a role in bronchiectasis. Ways to stay healthy include:

  • Drink plenty of water to help keep mucus thinner and easier to clear.
  • Consider a diet high in vegetables, fruits, whole grains, or lean proteins and low in sodium, added sugar, saturated fats, and refined grains.
  • Maintain adequate levels of dietary vitamin D through supplements, fish such as salmon and mackerel, mushrooms, and milk; ask your doctor about the right way to get the vitamin D you may need.

Exercise

Regular physical activity may improve mucus clearing from the airways and shortness of breath and reduce flare-ups. Start slowly and gradually increase activity over time. Your exercise program may include:

  • Aerobic activities such as walking, swimming, dancing, and bike riding
  • Strength-training exercises, including those using hand weights and resistance bands, as well as calisthenics such as push-ups and isometric exercises such as planks
  • Warm-up and cooldown stretches

Prognosis and Outlook for Bronchiectasis

Bronchiectasis damage cannot be reversed, and your prognosis varies depending on its cause, disease severity, your access to medical care, and other medical conditions you may have. When treated early and aggressively, people with bronchiectasis can expect to live a full life with normal life expectancy.

While some research suggests that some people with bronchiectasis may have an increased risk of death from the condition, more long-term, large-scale studies across various populations are needed to understand mortality risks better.

Your prognosis may be more serious because of factors such as:

  • A history of smoking and low lung function
  • Cystic fibrosis
  • Coexisting conditions such as chronic bronchitis or emphysema
  • Complications such as high blood pressure in the arteries of your lungs or enlargement and failure of the right ventricle of your heart
  • Poor access to treatment

Complications of Bronchiectasis

The primary complication of bronchiectasis are the frequent reoccurring respiratory infections that threaten to make the condition worse. If bronchiectasis advances, additional complications may develop.

Your lungs respond to ongoing inflammation and low oxygen levels by growing new, fragile blood vessels along the airway walls, a process called neovascularization. But these vessels rupture easily, causing hemoptysis (coughing up of blood), sometimes in life-threatening amounts.

The same process can also raise blood pressure in the lungs, causing pulmonary hypertension. Over time, pulmonary hypertension can strain the right side of the heart (cor pulmonale), leading to heart failure or respiratory failure in severe cases.

Frequent infections and treatment with antibiotics may lead to antibiotic-resistant bacterial infections.

 When antibiotic-resistant bacteria build up in the airways, the resulting inflammation can cause symptom flare-ups and worsening lung function.

Chronic inflammation from bronchiectasis can also contribute to muscle loss and unintended weight loss over time.

Complications can also develop from having too much mucus in the airways. If the mucus is too thick or blocks the airway, part of the lung may collapse. This condition, called atelectasis, can worsen shortness of breath.

Other potential complications from bronchiectasis include:

  • Pneumonia
  • Lung abscesses
  • Empyema, or pus in the space between the lungs and chest wall
  • Bloodstream infections
  • Recurrent pleurisy, inflammation of the membranes around the lungs
  • Secondary amyloidosis, or abnormal buildup of proteins in tissues and organs

Support for People With Bronchiectasis

Bronchiectasis & NTM Association

This group offers various education materials and resources for people living with bronchiectasis and nontuberculous mycobacteria (NTM). It includes a listing of local support groups, an online community group, and meetup opportunities.

NTM Info & Research (NTMir)

A nonprofit organization serving patients and caregivers dealing with NTM, NTMir offers various ways for people with NTM and bronchiectasis to connect and support one another. The group has online resources and information, virtual and in-person support groups, physician referral lists, and more.

The Takeaway

  • When you have the chronic lung condition bronchiectasis, your airways are permanently widened and scarred, trapping mucus and increasing your risk of infection.
  • Symptoms typically take a while to develop but often occur after a respiratory infection. They may include coughing up blood and sputum, shortness of breath, and fatigue.
  • Bronchiectasis has many different causes, including hereditary conditions, pollutants, and infections. About 40 percent of people with bronchiectasis do not know why they developed it.
  • Although there is no cure for bronchiectasis, clearing airways, taking medications, and lifestyle changes can help you manage its symptoms and stop it from getting worse.

FAQ

Is bronchiectasis the same as COPD?
No, but you can have both chronic lung conditions simultaneously.

Bronchiectasis involves permanent airway widening because of structural damage, whereas COPD involves airflow obstruction from inflammation and tissue damage.
There is no cure for bronchiectasis. The airway damage is permanent and cannot be reversed. Ongoing management with airway clearance, infection treatment, and lifestyle adjustments can help you successfully control symptoms and prevent significant disease progression.

Sometimes. Some underlying causes, such as cystic fibrosis or primary ciliary dyskinesia, are genetic.

But the cause may be another condition or may be unknown.

Yes. Though breathing difficulties can make exercise seem uncomfortable, experts recommend that you exercise when you can to clear mucus, improve your breathing, and boost your overall fitness.

Resources We Trust

EDITORIAL SOURCES
Everyday Health follows strict sourcing guidelines to ensure the accuracy of its content, outlined in our editorial policy. We use only trustworthy sources, including peer-reviewed studies, board-certified medical experts, patients with lived experience, and information from top institutions.
Resources
  1. Learn About Bronchiectasis. American Lung Association. January 20, 2026.
  2. Bronchiectasis. Cleveland Clinic. August 6, 2022.
  3. Bronchiectasis. Penn Medicine.
  4. Steinbach T. Bronchiectasis. MSD Manual Consumer Version. April 2025.
  5. Bronchiectasis. Johns Hopkins Medicine.
  6. Bronchiectasis Symptoms and Diagnosis. American Lung Association. January 20, 2026.
  7. What Is Bronchiectasis? American Thoracic Society. October 2022.
  8. Bronchiectasis Causes and Risk Factors. National Heart, Lung, and Blood Institute. October 29, 2023.
  9. What Is Bronchiectasis? National Heart, Lung, and Blood Institute. October 2023.
  10. Bird K et al. Bronchiectasis. StatPearls. May 22, 2023.
  11. Active Cycle of Breathing Technique (ACBT). Cystic Fibrosis Foundation.
  12. Treating and Managing Bronchiectasis. American Lung Association. January 20, 2026.
  13. Bronchiectasis Treatment. National Heart, Lung, and Blood Institute. October 29, 2023.
  14. Vaccines that Protect Against Infectious Respiratory Diseases. American Lung Association. January 23, 2026.
  15. Bronchiectasis. National Health Service. June 11, 2025.
  16. Nutrition. Bronchiectasis & NTM Association.
  17. Exercise. Bronchiectasis & NTM Association.
  18. Sin S et al. Mortality Risk and Causes of Death in Patients With Non-Cystic Fibrosis Bronchiectasis. Respiratory Research. December 3, 2019.
  19. Nigro M et al. Epidemiology of Bronchiectasis. European Respiratory Review. October 9, 2024.
  20. Pendkar C et al. Nonpharmacologic Care of Bronchiectasis: Addressing Frailty with Nutrition and Physical Activity. Pulmonary Therapy. October 30, 2025.
  21. Bronchiectasis: Living With. National Heart, Lung, and Blood Institute. October 29, 2023.

David Mannino, MD

Medical Reviewer

David Mannino, MD, is the chief medical officer at the COPD Foundation. He has a long history of research and engagement in respiratory health.

After completing medical training as a pulmonary care specialist, Dr. Mannino joined the Centers for Disease Control and Prevention (CDC) Air Pollution and Respiratory Health Branch. While at CDC, he helped to develop the National Asthma Program and led efforts on the Surveillance Reports that described the U.S. burden of asthma (1998) and COPD (2002).

After his retirement from CDC in 2004, Mannino joined the faculty at the University of Kentucky, where he was involved both clinically in the College of Medicine and as a teacher, researcher, and administrator in the College of Public Health. He served as professor and chair in the department of preventive medicine and environmental health from 2012 to 2017, with a joint appointment in the department of epidemiology.

In 2004, Mannino helped to launch the COPD Foundation, where he served as a board member from 2004 through 2015, chairman of the Medical and Scientific Advisory Committee from 2010 through 2015, and chief scientific officer from 2015 to 2017.

Mannino has over 350 publications and serves as an associate editor or editorial board member for the following journals: American Journal of Respiratory and Critical Care Medicine, Chest, Thorax, European Respiratory Journal, and the Journal of the COPD Foundation. He was also a coauthor of the Surgeon General’s Report on Tobacco in 2008 and 2014.

Joseph Bennington-Castro

Author

Joseph Bennington-Castro is a science writer based in Hawaii. He has written well over a thousand articles for the general public on a wide range topics, including health, astronomy, archaeology, renewable energy, biomaterials, conservation, history, animal behavior, artificial intelligence, and many others.

In addition to writing for Everyday Health, Bennington-Castro has also written for publications such as Scientific American, National Geographic online, USA Today, Materials Research Society, Wired UK, Men's Journal, Live Science, Space.com, NBC News Mach, NOAA Fisheries, io9.com, and Discover.