Bronchiectasis Flashcards
what is bronchiectasis
irreversible abnormal dilation of one or more bronchi, with chronic airway inflammation.
associated with chronic sputum production, recurrent chest infections and airflow obstruction.
bronchiectasis pathophysiology
- Initial insult e.g. infection damages the airways.
- Disordered anatomy leads to 2° bacterial colonization, perpetuating inflammatory change and damaging the mucociliary escalator.
- This prevents bacterial clearance and leads to further airway damage. Major airways and bronchioles are involved, with mucosal oedema, inflammation, and ulceration.
- Terminal bronchioles become obstructed with secretions, leading to volume loss.
- A chronic host inflammatory response ensues, with free radical formation and production of neutrophil elastase, further contributing to inflammation.
- Bronchial neovascularization, with hypertrophy and tortuosity of the bronchial arteries (which are at systemic pressure), may lead to intermittent haemoptysis.
bronchiectasis causes
- usually idiopathic
- cystic fibrosis
- infection, immunodeficiency, airway diseases, toxic and mechanical insults, associated diseases e.g. rheumatoid, sle, ibd.
clinical features
- recurrent chest infections
- confirmed with hrct
investigations
- cxr - ring shadows and tramlines, indicating thickened airways and the gloved finger appearance
- hrct
- spirometry with reversibility testing
- sputum mc&s
- immunoglobulins A, M, G
- RAST for aspergillus, IgE
- CFTR mutation screen and sweat test
Mx
- treat underlying condition
- airway clearance by daily physiotherapy via
- active cycle of breathing technique
- postural or autogenic drainage
- cough augmentation
- exercise regimes
- nebulised saline or hypertonic saline
- reduction of bacterial load and prevention of 2° airway inflammation and damage with antimicrobial chemotherapy
- lung transplant
antimicrobial chemotherapy
- Patients need a higher antibiotic dose and for a longer time period (usually 10–14 d) than people without bronchiectasis
-Treatment response is usually assessed by a fall in sputum volume and change to mucoid from purulent or mucopurulent sputum, with an improvement in systemic symptoms, spirometry, and C-reactive protein (CRP)
-Pseudomonas-colonized patients have more frequent exacerbations, worse CT scan appearances, and a faster decline in lung function.
How to identify bronchiectasis exacerbations
An exacerbation is usually a clinical diagnosis, with an increase in sputum volume and tenacity and with discoloration. It may be associated with chest pain, haemoptysis and wheeze, and systemic upset—fevers, lethargy, and anorexia.