Bronchiectasis



Bronchiectasis involves permanent dilation of the bronchi, the large airways that transport air to the lungs. Sputum collects and organisms grow in the wide tubes, resulting in a chronic cough, continuous sputum production and recurrent infections.

Bronchiectasis results from damage to the airways. Potential causes of this damage include:

  • Idiopathic (no apparent cause)
  • Pneumonia
  • Whooping cough (pertussis)
  • Tuberculosis
  • Alpha-1-antitrypsin deficiency
  • Connective tissue disorders (e.g., rheumatoid arthritis)
  • Cystic fibrosis
  • Yellow nail syndrome

 

TOM TIP: Yellow nail syndrome is characterised by yellow fingernails, bronchiectasis and lymphoedema. Patients are stable and have good clinical signs, making it a good choice for OSCEs. As it is rare, examiners will score high marks if you can combine these features and name the diagnosis.

Symptoms

Key presenting symptoms are:

  • Shortness of breath
  • Chronic productive cough
  • Recurrent chest infections
  • Weight loss

Signs

Signs of bronchiectasis on examination include:

  • Sputum pot by the bedside
  • Oxygen therapy (if needed)
  • Weight loss (cachexia)
  • Finger clubbing
  • Signs of cor pulmonale (e.g., raised JVP and peripheral oedema)
  • Scattered crackles throughout the chest that change or clear with coughing
  • Scattered wheezes and squeaks

Investigations

Sputum culture is used to identify colonising and infective organisms. The most common infective organisms are:

  • Haemophilus influenza 
  • Pseudomonas aeruginosa

 

Chest x-ray findings include:

  • Tram-track opacities (parallel markings of a side-view of the dilated airway)
  • Ring shadows (dilated airways seen end-on)

High-resolution CT (HRCT) is the test of choice for establishing the diagnosis.

 

Management

General management involves:

  • Vaccines (e.g., pneumococcal and influenza)
  • Respiratory physiotherapy to help clear sputum
  • Pulmonary rehabilitation
  • Long-term antibiotics (e.g., azithromycin) for frequent exacerbations (e.g., 3 or more per year)
  • Inhaled colistin for Pseudomonas aeruginosa colonisation
  • Long-acting bronchodilators may be considered for breathlessness
  • Long-term oxygen therapy in patients with reduced oxygen saturation
  • Surgical lung resection may be considered for specific areas of disease
  • Lung transplant is an option for end-stage disease

 

Infective exacerbations require: 

  • Sputum culture (before antibiotics) 
  • Extended courses of antibiotics, usually 7–14 days
  • Ciprofloxacin is the usual choice for exacerbations caused by Pseudomonas aeruginosa

 

TOM TIP: The key features to remember with bronchiectasis are finger clubbing, diagnosis by HRCT, Pseudomonas colonisation and extended courses of 7-14 days of antibiotics for exacerbations. 

 

Last updated September 2023

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