Respiratory Flashcards
What is A1AT?
Features?
Pathophysiology and inheritance?
Alpha-1 antitrypsin deficiency - AR or co-dominant inhertiance.
Lack of protease inhibitor normally produced by the liver -> panacinar emphysema, esp in lower lobes.
Cirrhosis and hepatocelluar ca in adults, cholestasis in children.
Often misdiagnosed as asthma or COPD.
What would you expect on a blood gas of someone in DKA?
Metabolic acidosis, with increased anion gap (due to ketones)
At what pO2 would you offer someone with COPD long-term O2 therapy?
pO2 <7.3 kPa OR 7.3-8kPa with: - secondary polycythaemia - nocturnal hypoxaemia - peripheral oedema - pulmonary HTN
Varenicline or buproprion are prescribed as nicotine replacement therapy - how do they work?
Varenicline: nicotinic receptor partial agonist
Bupropion: NA and dopamine reuptake inhibitor, nicotinic antagonist
What is the most common sign seen on CXR when a patient has been exposed to asbestos in the past?
Pleural plaques - these are BENIGN and do not undergo malignant change. Generally occur after latent period 20-40 years
What is the most common form of cancer following asbestos exposure?
Bronchial carcinoma (more common than mesothelioma but has other causes)
What are the next steps in management for a patient with COPD that is still breathless despite first-line (SABA or SAMA) use?
How does this differ by FEV1?
FEV1 >50:
- LABA
or
- LAMA
FEV1 <50:
- LABA + ICS combo
or
- LAMA
What is the mx of cor pulmonale?
Loop diuretic for oedema
Consider LT O2.
What if a COPD patient is still breathless despite 2nd line therapy?
What if even this is ineffective? What if people can’t tolerate inhaled therapy?
If taking LABA then switch to LABA + ICS combo
If taking LAMA then add LABA + ICS combo
4: Trial theophylline (reduce dose if macrolide or fluoroquinolone abx co-prescribed)
What would the combination of ENT, respiratory and kidney involvement in a patient suggest?
Granulomatosis with polyangiitis (GPA) - formerly Wegener’s.
What are the features of Granulomatosis with polyangiitis?
(= autoimmune necrotising granulomatous vasculitis)
- URT: Epistaxis, sinusitis, nasal crusting
- LRT: Dyspnoea, haemoptysis
- Rapidly progressive glomerulonephritis
- Saddle-shape nose deformity
- Vasculitic rash, eye involvment, CN lesions
What do cANCA classically relate to?
(cytoplasmic antineutrophil cytoplasmic antibodies)
Granulomatosis with polyangiitis
What do pANCA classically relate to?
(perinuclear antineutrophil cytoplasmic antibodies)
Churg-Strauss
(25% Gran with poly are cANA positive)
What would epithelial crescents in Bowman’s capsule on renal biopsy suggest?
Granulomatosis with polyangiitis
What is the mx of granulomatosis with polyangitis?
-Steroid
- Cyclophosphamide (90% response)
- Plasma exchange
Median survival is 8-9 years