Respiratory Flashcards
Causes of airflow obstruction
Asthma (reversible)
COPD (fixed)
Obliterative bronchiolitis (fixed obstruction, can be secondary to pollutants or GvHD)
Investigations for asthma
PEFR and PEFR diary
Bloods for eosinophil and IgE levels
Spirometry
Signs of interstitial lung fibrosis
Finger clubbing
Bilateral fine late inspiratory crackles which do not clear on coughing
May be signs of connective tissue disease (scleroderma, SLE, RA) or AF (amiodarone use)
What drugs can cause IPF?
Nitrofurantoin
Sulfasalazine, methotrexate, NSAIDs
Amiodarone
Bleomycin
What signs of severity might be seen in a patient with IPF?
Crackles becoming widespread and extending more into expiration
Pulmonary hypertension
Hypoxia, central cyanosis, cor pulmonale
What is interstitial pulmonary fibrosis?
The interstitium describes the narrow space between the alveolar epithelium and the capillary endothelium.
The interstitium can become thickened often as a result of the effects of the alveolar transudates or exudates.
This results in fibrosis.
What investigations should you request?
FBC, U&Es, CRP/ESR. Look for eosinophilia
ANA/ANCA/RF
Serum ACE
HIV
ABG
CXR
HRCT
Spirometry
Lung biopsy
Signs of IPF on CXR
Decreased lung volumes
Subpleural reticular or reticulonodular opacities
Bilateral interstitial shadowing
Peripheral migratory air space shadowing
Mediastinal or hilar lymph node enlargement
It may also help to identify a cause.
Causes of apical lung fibrosis
Radiation pneumonitis
ABPA, eosinophilic pneumonia
Pneumonconiosis
Ankylosing spondylitis
Silicosis
TB
Causes of basal lung fibrosis
Rheumatoid arthritis
Asbestosis
Scleroderma
IPF
Spirometry findings for IPF
Reduced FEV1 and reduced FVC
Intact or raised FEV1:FVC
Reduced transfer factor
Features of IPF on HRCT
Ground glass shadowing and honeycombing
Traction bronchiectasis
List some eosinophilic lung diseases
Asthma, ABPA
Drug-induced (nitrofurantoin, sulfasalazine, MTX)
Loeffler’s
Eosinophilic pneumonia
Churg-Strauss (eGPA)
Helminth/parasitic infection
Lung manifestations of rheumatoid arthritis
Pleural effusions
Pulmonary fibrosis
Drug-induced lung fibrosis
Caplan’s syndrome (dust-exposure and RA)
Lung nodules