Bronchiectasis and CF Flashcards
1
Q
What is bronchiectasis?
A
- Permanent dilatation of the airways
- Secondary to chronic infection or inflammation
- Wide variety of causes
2
Q
What are congenital causes of bronchiectasis?
A
- Cystic fibrosis → most common
- Kartagener’s syndrome
- Young’s syndrome
3
Q
What are post-infective causes of bronchiectasis?
A
- Measles
- Pertussis
- TB
- Pneumonia
- Bronchiolitis
Other causes → UC / RA / bronchial obstruction
4
Q
What are the clinical features of bronchiectasis?
A
- Persistent cough
- Copioid purulent sputum
- Intermittent haemoptysis
- Signs → clubbing / coarse insp creps / wheeze
5
Q
What are complications of bronchiectasis?
A
- Pneumonia
- Pleural effusion
- Pneumothorax
- Amyloidosis
6
Q
What may sputum culture show for bronchiectasis?
A
- Single or multiple pathogens present
- Most common (25%) = gram-negative → pseudomonas aeruginosa
7
Q
What other investigations are done for bronchiectasis?
A
- CXR → cystic shadows / thickened bronchial walls
- CT → extent + distribution / dilated bronchus wider than accompanying pulm artery + resemble signet ring
- Spirometry → obstructive pattern
- Bronchoscopy → site of haemoptysis / exclude obstruction / obtain culture samples
- Other tests → serum Igs / CF sweat test / Aspergillus preceiptans or skin-prick test RAST + total IgE
8
Q
What is the management of bronchiectasis?
A
- Airway clearance → chest physio / flutter valve
- ABx → known pseudomonas: oral ciprofloxacin or suitable IV abx
- Bronchodilators → useful in asthma, COPD, CF, ABPA
- Corticosteroids → prednisolone and itraconazole for ABPA
- Surgery → indicated in localised disease or to control severe haemoptysis