Resp 7.5 Flashcards
(127 cards)
Group 1 pulmonary HTN
(1ry) idiopathic, familial, or persistent pulm HTN of the newborn
- ass in: collagen vast disease, congenital heart disease with systemic->pulm shunts, HIV, drugs & toxins, sickle cell disease
Group 2 pulmonary HTN
= pulm HTN with left heart disease
- left-sided atrial, ventricular or valvular disease e.g. LV systolic & diastolic dysfunction, mitral stenosis & mitral regurgitation
Group 3 pulmonary hypertension?
= pulm HTN 2ry to lung disease/hypoxia
- COPD, ILD, sleep apnoea, high altitude
Group 4 pulmonary hypertension?
= pulm HTN due to thromboembolic disease
Group 5 pulmonary hypertension?
= miscellaneous conditions
- lymphangiomatosis e.g. 2ry to carcinomatosis/sarcoid
Resp manifestations of rheumatoid arthritis?
- pulm fibrosis
- pleural effusion
- pulm nodules
- bronchiolitis obliterans (obstructive)
- complications of drugs e/g/ MTX pneumonitis
- pleurisy
- Caplan’s syndrome - massive fibrotic nodules with occ coal dust exposure
- infection (may be atypical) 2ry to immunosuppression
%pred of FEV1 in copd?
post-bronchodilator FEV1/FVC <0.7
1 mild >80% WITH SYMPTOMS
2 moderate 50-79%
3 severe 30-49%
4 v severe <30%
Rx for low-severity CAP?
1st Amoxicillin 5/7 (/macrolide/tetracycline)
Rx for mod-high severity CAP?
What to consider in high-severity?
- Dual Abx: Amoxicillin + Macrolide 7-10/7
- beta-lactamase stable penicillin e.g. co-amoxiclav/ceftriaxone/tazocin + macolide in high severity
What is transfer factor?
Rate at which a gas will diffuse from alveoli into blood - CO used to test rate of diffusion
- total gas transfer TLCO or corrected for lung volume transfer coefficient KCO
Conditions that can cause increased KCO with a normal/reduced TLCO?
(KCO also tends to increase with age)
- pneumonectomy/lobectomy
- neuromuscular weakness
- scoliosis/kyphosis
- ankylosis of costovertebral joints
Causes of raised TLCO?
- pulmonary haemorrhage
- asthma
- L->R cardiac shunts
- polycythaemia
- hyperkinetic states, exercise, males
Causes of a lower TLCO?
- fibrosis
- pneumonia
- PE
- pulm oedema
- emphysema
- anaemia
- low cardiac output
Causes of predominantly Upper zone fibrosis?
Coal workers pneumoconiosis Histiocytosis/hypersensitivity pneumonitis/EAA Ank spond (rare) Radiation TB Sarcoid/silicosis
Causes of predominantly lower zone fibrosis?
- idiopathic
- most CT disorders except ank spend
- asbestosis
- drugs: amiodarone, bleomycin, MTX, NSAIDs, nitrofurantoin
Gene ass with bronchiectasis?
HLA-DR1
Causes of bronchiectasis?
- post-infective: TB, pneumonia etc
- CF
- obstruction e.g. cancer/FB
- immune deficiency: selective IgA, hypogammaglobulinaemia
- ABPA
- ciliary dyskinetic syndromes: Kartagener’s syndrome, Young syndrome
- yellow nail syndrome
CXR/CT signs in bronchiectasis?
tramlines/tram-track & signet rings
5 features of Churg-Strauss syndrome? (small-medium vessel vasculitis)
- asthma
- blood eosinophilia >10%
- paranasal sinusitis
- monomeuritis multiplex
- pANCA +ive in 60%
What drugs can precipitate Churg-strauss syndrome?
Leukotriene receptor antagonists e.g. montelukast
Sx of acute mountain sickness?
what may if progress to?
prevention?
Rx?
- headache, nausea, fatigue. Develops gradually over 6-12h and can last a number of days. Starts to occur above 2500-3000m
- HAPE/HACE
- prevent with Acetazolamide (carbonic anhydrase inhibitor), gain no more than 500m/day
- Rx = descent…
Features & Rx of HAPE?
- classic pulm oedema features
- Descend, O2 if available, drugs can help by reducing systolic pulmonary artery pressure e.g. nifedipine, dexamethasone, acetazolamide, phosphodiesterase V inhibitors)
Features & Rx of HACE?
- headache, ataxia, papilloedema
- Descent & Dexamethason
Hypersensitivity pneumonitis = EAA
- what is acute presentation?
- CXR? BAL? FBC? CT?
- SOB, dry cough, fever 4-8h post-exposure
- CXR upper/midzone fibrosis
- BAL: lymphocytosis
- FBC: NO eosinophilia
- CT: centrilobular ground glass nodules