Bronchiectasis

The most common cause of bronchiectasis is severe or repeated respiratory infections, which are particularly likely to occur in people who have one or more of the following:

• Cystic fibrosis

• Other hereditary disorders, such as primary ciliary dyskinesia, in which the ability to clear the airways is impaired

• Immunodeficiency disorders

• Certain autoimmune disorders, such as rheumatoid arthritis, ulcerative colitis, or Sjögren syndrome

• Mechanical factors, such as airway blockage caused by an inhaled object, chronically enlarged lymph nodes, changes after lung surgery, or a lung tumor

• Inhaling toxic substances that injure the airways, such as noxious fumes, gases, smoke (including tobacco smoke), and injurious dust (for example, silica and coal dust)

Allergic bronchopulmonary aspergillosis, which affects the larger airways, can cause mucus plugs that block the airways and lead to bronchiectasis. It is an allergic reaction to the fungus Aspergillus and occurs most commonly in people with asthma or cystic fibrosis.

In places where tuberculosis is common, tuberculosis is often the cause of severe or repeated infections that cause bronchiectasis. Poor nutrition and unavailability of vaccines to prevent various respiratory infections can also contribute.

In many people with bronchiectasis, a cause cannot be determined despite a thorough evaluation.

Bronchiectasis can develop at any age. In most people, symptoms begin gradually, usually after a respiratory infection, and tend to worsen over the years. Most people develop a chronic cough that produces thick sputum. The amount and type of sputum depend on the extent of the disease and whether there is a complicating infection (often called a disease flare or exacerbation). Often, people have coughing spells only early in the morning and late in the day.

Coughing up of blood (hemoptysis) is common because the damaged airway walls are fragile and have increased numbers of blood vessels. Hemoptysis may be the first or only symptom.

Recurrent fever or chest pain, with or without frequent bouts of pneumonia, may also occur. People with widespread bronchiectasis may develop wheezing or shortness of breath. People whose bronchiectasis progresses to cor pulmonale or chronic respiratory failure also have fatigue, lethargy, and worsening shortness of breath, particularly during exertion. If bronchiectasis is severe and chronic, people commonly lose weight.

People may have flares (exacerbations) of disease, sometimes with pneumonia. Exacerbations may result from a new or worsening infection. When an exacerbation occurs, people may have more severe cough, increased sputum production, or worsening of breathing difficulties.

• Chest x-ray

• Computed tomography

• Pulmonary function tests

• Specific tests for suspected causes

Doctors may suspect bronchiectasis because of a person’s symptoms or the presence (currently or in the past) of a condition thought to cause bronchiectasis.

Tests are done to

• Confirm the diagnosis

• Assess the extent of the disease

• Identify the cause of the disease

Chest x-rays can often detect the lung changes caused by bronchiectasis. However, occasionally, x-ray results are normal. Computed tomography (CT) is the most accurate test to identify and confirm the diagnosis and to determine the extent and severity of the disease.

Pulmonary function tests are done to assess how well the lungs are working. These tests measure how well the lungs are able to hold air, to move air in and out, and to exchange oxygen and carbon dioxide. Pulmonary function tests do not diagnose bronchiectasis but do help doctors determine how severe the lung disorder is and are useful for monitoring its progression over time.

After bronchiectasis is diagnosed, tests are often done to check for disorders that may be causing or contributing to it. Such tests may include the following:

• Testing for human immunodeficiency virus (HIV) infection and other immune system and autoimmune disorders

• Measuring the salt level in sweat (which is abnormal in people with cystic fibrosis)

• Testing nasal, bronchial, or sputum specimens for evidence of infectious organisms

• Doing other tests to determine if the cilia are structurally or functionally defective

• Testing for allergic bronchopulmonary aspergillosis, tuberculosis, and alpha-1 antitrypsin deficiency

When bronchiectasis is limited to one area—for example, a lung lobe or segment—doctors may do a bronchoscopy to determine whether an inhaled foreign object or lung tumor is the cause.

Sweat chloride tests and genetic testing for cystic fibrosis may be needed when there is a family history, repeated respiratory infections, or other unusual findings in a child or adult, even when other typical features of cystic fibrosis are absent.

Lab Test

Sweat Test for Cystic Fibrosis

Doctors may take a sputum sample and send it to a laboratory to grow (culture) the bacteria to determine which bacteria are present and what antibiotics are most effective against these bacteria. This testing can help determine the best antibiotics to use during flares.

Bronchiectasis

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• Vaccination to prevent infections that cause or worsen bronchiectasis

• Antibiotics to treat infections that cause or worsen bronchiectasis

• Drainage of airway secretions with therapies that promote cough (such as, chest physical therapy, regular exercise, other techniques

• Inhaled medications that help thin or loosen thick mucus so it can be more easily coughed out

• Inhaled bronchodilators and sometimes inhaled corticosteroids

• Sometimes, oral or inhaled antibiotics to suppress certain bacteria and prevent recurring infections

• Rarely, surgical removal of part of lung

• Oxygen therapy, if needed

Treatment of bronchiectasis is directed toward reducing the frequency of infections when possible, preventing certain infections with vaccines and sometimes antibiotics, decreasing the buildup of mucus, decreasing inflammation, and relieving airway blockage. Early, effective treatment can reduce complications such as hemoptysis, low oxygen levels in the blood, respiratory failure, and cor pulmonale. Treatment of underlying conditions that cause or contribute to flares is also needed.

Flares (exacerbations) are treated with antibiotics, bronchodilators, and chest physiotherapy to promote drainage of secretions and mucus. Chest physiotherapy includes such techniques as postural drainage and chest percussion. Sometimes antibiotics are given for a long period to prevent recurring infections, especially in people who have frequent flares or cystic fibrosis. Most people with cystic fibrosis benefit from treatment with a cystic fibrosis transmembrane regulator (CFTR) modulator, which can decrease exacerbations.

Inflammation and the buildup of mucus may be helped by humidification of the air and inhaling an aerosolized salt water solution. Medications that thin the thick sputum (mucolytics) may also be given to people who have cystic fibrosis. In other people, the effectiveness of mucolytics is uncertain.

Bronchial blockage can be detected and treated by bronchoscopy before severe damage occurs.

Significant bleeding with cough is sometimes treated with a technique called embolization instead of surgery. In embolization, doctors use a catheter to inject a substance that blocks the vessel that is bleeding.

Low blood oxygen levels are treated with oxygen therapy. Appropriate use of oxygen may help prevent complications such as cor pulmonale. If people have wheezing or shortness of breath, bronchodilators and sometimes inhaled corticosteroids often help. If a person has a flare, usually these medications and an antibiotic are given, and oral corticosteroids are added in some cases. Respiratory failure, if present, should be treated.

Rarely, part of a lung needs to be surgically removed. Such surgery usually is an option only if the disease is confined to one lung or, preferably, to one lung lobe or segment. Surgery may be considered for people who have recurrent infections despite treatment or who cough up large amounts of blood.

Advanced bronchiectasis in some people—mostly those who also have advanced cystic fibrosis—can be treated with lung transplantation. Pulmonary function (as measured by the amount of air in the lungs and the rate and amount of air moving in and out of the lungs with each breath) usually improves within 6 months, and the improvement may be sustained for at least 5 years.

Prognosis for people with bronchiectasis depends on its cause and on how well infections and other complications are prevented or controlled. People with coexisting conditions, such as chronic bronchitis or emphysema, and people who have complications, such as pulmonary hypertension or cor pulmonale, tend to have a worse prognosis.

Early identification and treatment of conditions that tend to cause bronchiectasis may prevent its development or reduce its severity. More than half the cases of bronchiectasis in children can be accurately diagnosed and promptly treated.

Childhood immunizations against measles and pertussis (whooping cough), improved living conditions, and better nutrition have markedly reduced the number of people who develop bronchiectasis. Pneumococcal vaccination, COVID-19 vaccination, annual influenza vaccination, and use of appropriate antibiotics early in the course of lung infections help to prevent bronchiectasis or reduce its severity.

Other specific steps that can be taken include the following:

• Receiving immunoglobulin for an immunoglobulin deficiency syndrome may prevent recurring infections.

• Giving the enzyme alpha-1 antitrypsin to people with alpha-1 antitrypsin deficiency may help prevent the disorder from becoming more severe.

• Avoiding toxic fumes, gases, smoke, and injurious dusts also helps prevent bronchiectasis or reduce its severity.

• Watching what children put in their mouth can help prevent them from inhaling foreign objects into the airways.

• Avoiding oversedation due to medication, illicit drugs, or alcohol and seeking medical care for neurologic symptoms (such as impaired consciousness) or gastrointestinal symptoms (such as difficulty in swallowing and regurgitation or coughing after eating) may help to prevent aspiration.

• Avoiding use of mineral oil or petroleum jelly in the nose may prevent accidental inhalation of these substances into the lungs.

The following English-language resources may be useful. Please note that THE MANUAL is not responsible for the content of these resources.

1. American Lung Association: Bronchiectasis: Complete discussion of symptoms, diagnosis, and treatment, and tips on questions to discuss with the doctor

2. National Heart. Lung, and Blood Institute: Bronchiectasis: Complete discussion of symptoms, diagnosis, and treatment, and tips on questions to discuss with the doctor