Risk factors for developing asthma
Allergic rhinitis
Food allergies
Obesity
PMH + FHx Atopy
Male
Low BW
Airway hypersensitivity
Pathophysiology of RSV infection
Narrowing distal airways
Sloughed necrotic endothelium
Mucus secretion and mucus plugging
Alveolar hypoxia –> apnoea
Pathophysiology asthma
Variable obstruction to small and mod sized airways
Eosinophilic and neutrophilic inflammation
Contraction of bronchial SM
Airway hypersensitivity and bronchospasm
Causes of interstitial lung disease
Interstitial lung disease on CXR + spirometry
Ground glass shadowing
Restrictive pattern lung function tests
Pathology and presentation of primary ciliary dyskinesia
Defect in structure / function of cilia –> mucus retention
Recessive
- Recurrent sinusitis / otitis media
- Nasal polyps
- +/- Hydrocephalus
- Infertility
- Moist cough –> eventual bronchiectasis
- Situs invertus
- Lung function tests = obstructive / mixed
- Ix: EM / ciliary studies, reduced exhaled NO
Pathophysiology cystic fibrosis
Recessive genetic defect to CFTR gene (Ch 7) –> defective CFTR protein (ATP-regulated channel esp chloride)
–> accumulation of viscous mucus –> organ damage.
Esp delta F508 mutation. More white europeans.
Presentation of CF
LRTI infections
Malabsorption
Raised chloride on sweat test
Restrictive lung function tests
Reduced FEV1 <80% pred.
Reduced FVC <80% pred.
Normal FEV1:FVC
Obstructive lung function tests
Reduced FEV1 <80% pred
Normal FVC
Reduced FEV1:FVC <0.7
Causes of restrictive lung function tests
Pulmonary fibrosis
Pulmonary oedema
Lobectomy
Connective tissue disease
NMD
Skeletal
Obesity
Causes of obstructive lung function tests
Asthma - reversible= >9% response
Bronchiectasis
CF
COPD
Emphysema