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Bronchiectasis

Updated: Sep 14, 2024


Physical Examination

Surroundings:

  • Presence of purulent sputum in a pot next to the bedside

  • Inhalers by the bedside

On examination:

  • Clubbing of fingers

  • Scarring may be visible

  • Reduced chest expansion

  • Coarse inspiratory crepitations that change in character with coughing

  • Wheezing and inspiratory clicks may be heard

Other positive findings:

  • Signs of bronchiectasis

  • Evidence of complications such as respiratory failure or cor pulmonale or infection

  • Signs of possible underlying causes such as cystic fibrosis, Kartagener’s Syndrome, connective tissue disease, or Yellow Nail Syndrome

  • Signs of treatment such as fever or body mass index included in Bronchiectasis Severity Index

Investigations for Bronchiectasis

Laboratory Tests

  • Full blood count (FBC):

    • Identify anemia or evidence of inflammation.

  • Sputum cultures:

    • Identify causative organisms e.g. Haemophilus influenzae, Pseudomonas aeruginosa.

  • Sputum for acid-fast bacilli (AFB):

    • To rule out tuberculosis as an etiological factor.

  • Serum immunoglobulins:

    • Assess for immunodeficiency, e.g. Common Variable Immunodeficiency.

  • Cystic fibrosis (CF) tests:

    • Sweat chloride test and/or genetic tests to rule out CF.

  • Rheumatoid factor & anti-CCP:

    • Check for rheumatoid arthritis (associated with bronchiectasis).

  • Alpha-1 antitrypsin levels:

    • Rule out Alpha-1 antitrypsin deficiency, especially if early-onset or if there's a coexistent COPD.

Imaging

  • High-resolution computed tomography (HRCT) of the chest:

    • Gold standard to confirm bronchiectasis.

    • Shows dilated and thick-walled bronchi, "tram-line" and "signet ring" appearances.

  • Chest X-ray:

    • Initial imaging; may show bronchial wall thickening and cystic changes, but less sensitive than HRCT.

Invasive tests

  • Bronchoscopy:

    • Inspect airways, rule out obstruction (e.g. tumor), and obtain samples.

  • Lung function tests:

    • Assess severity, with focus on forced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC).

Other tests

  • Allergy testing:

    • Identify allergic bronchopulmonary aspergillosis (ABPA) or other allergic triggers.

  • Serum precipitins:

    • For hypersensitivity pneumonitis or farmer’s lung.

  • Aspergillus IgE & skin prick test:

    • For suspected ABPA.

  • Ciliary function tests and nasal brushings:

    • For suspected primary ciliary dyskinesia.

Management

General Management:

  • Patient education and counseling.

  • Smoking cessation.

  • Pulmonary rehabilitation.

  • Vaccinations: Covid, influenza and pneumococcal vaccinations


Medical Management:

  • Antibiotics: empirical antibiotics based on sputum culture results; long-term, low-dose antibiotics to prevent exacerbations.

  • Airway clearance techniques: postural drainage and percussion, positive expiratory pressure (PEP) therapy, high-frequency chest wall oscillation (HFCWO).

  • Bronchodilators: beta-agonists, anticholinergics.

  • Anti-inflammatory therapy: inhaled corticosteroids and oral corticosteroids for acute exacerbations.


Surgical Management:

  • Surgery may be considered in bronchiectasis cases with localised disease and recurrent infections, lobectomy or lung transplant

Other Management:

  • Management of associated comorbidities such as sinusitis, gastroesophageal reflux disease (GERD), and allergic bronchopulmonary aspergillosis (ABPA).

Causes of Bronchiectasis

  • Cystic fibrosis: A genetic disorder that causes thick, sticky mucus that can lead to bronchiectasis.

  • Primary ciliary dyskinesia (PCD): A rare genetic disorder that affects the cilia in the respiratory tract, leading to impaired mucus clearance and increased risk of bronchiectasis.

  • Immunodeficiency syndromes: Conditions like HIV/AIDS or common variable immunodeficiency (CVID) weaken the immune system, leading to frequent respiratory infections that can cause bronchiectasis.

  • Autoimmune diseases: Disorders such as rheumatoid arthritis, systemic lupus erythematosus (SLE), and Sjögren's syndrome can cause bronchiectasis.

  • Allergic bronchopulmonary aspergillosis (ABPA): A hypersensitivity reaction to Aspergillus fumigatus, a fungus found in the environment, can cause bronchiectasis.

  • Recurrent respiratory infections: Frequent infections like pneumonia or bronchitis can cause permanent damage to the bronchial tubes and lead to bronchiectasis.

  • Obstructive lung diseases: Conditions like chronic obstructive pulmonary disease (COPD) or asthma can lead to bronchiectasis.

  • Environmental factors: Exposure to pollutants like smoke, chemicals, or dust can cause bronchiectasis.

Complications of Bronchiectasis

  • Respiratory failure

  • Hemoptysis

  • Recurrent pneumonia

  • Cor pulmonale

  • Pleural effusion

  • Empyema

  • Lung abscesses

  • Atelectasis

  • Amyloidosis

  • Osteoporosis


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