
Bronchiectasis
Causes
Common: Childhood pneumonia, cystic fibrosis, severe infections, asthma, COPD
Less Common: RA, GORD/aspiration, ABPA, non-TB mycobacteria, immunodeficiency, primary ciliary dyskinesia
Rare: Alpha-1 antitrypsin deficiency, yellow nail syndrome, foreign body
Presentation
Chronic productive cough, recurrent infections
Purulent ± bloodstained sputum, fatigue, dyspnoea, pleuritic pain
Coarse crackles, clubbing (<5%)
Investigations
HRCT: Gold standard (bronchial diameter > adjacent vessel)
Spirometry: Obstructive pattern
Sputum Culture: Key for pathogens (e.g. Pseudomonas, Haemophilus)
Consider:
FBC, immunoglobulins (IgG, IgA, IgM)
Autoimmune markers (e.g., RF, ANA)
CF sweat test (esp. children)
Aspergillus-specific IgE or skin-prick testing
Diagnosis
Clinical features + HRCT: Persistent symptoms despite treatment
Refer If:
Wet cough >4 weeks, recurrent pneumonia, parenchymal changes
Consider bronchoscopy for obstruction or foreign body
Management
General:
Airway clearance with physiotherapy
Regular exercise (30 min/day)
Annual pneumococcal and influenza vaccination
Smoking cessation, optimise nutrition
Stable Disease:
Pulmonary rehabilitation
Bronchodilators for sx relief in select cases (e.g., severe breathlessness)
Written action plan for exacerbations
Macrolides (e.g. azithromycin) for frequent exacerbations
Inhaled antibiotics (e.g. tobramycin) for chronic Pseudomonas
Exacerbations:
Mild: Oral antibiotics if signs of bacterial infection (e.g., increased sputum purulence) (e.g. doxycycline 100 mg BD for 14 days)
Severe: Hospital admission, IV antibiotics
If Pseudomonas colonisation: Ciprofloxacin 750 mg BD for 14 days
If no colonisation: Amoxicillin 1 g TDS or doxycycline 100 mg BD for 14 days
Haemoptysis:
Massive: Urgent hospital transfer (embolisation/surgery)
Recurrent: Specialist referral
Bookmark Failed!
Bookmark Saved!