Pneumology Flashcards

(42 cards)

1
Q

What’s Bupropion?

A

Norepinephrine-dopamine reuptake inhibitor and nicotinic antagonist

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2
Q

What’s Varenicline?

A

Nicotinic receptor partial agonist

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3
Q

What gene mutation is associated with bronchiectasis?

A

HLA-DR1

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4
Q

Asthma or cystic fibrosis+signs of asthma +proximal bronchiectasis+upper/mid zones fibrosis+eosinophilia+high IgE(<1000)+positive RAST+IgG precipitins positive=

A

Allergic bronchopulmonary aspergillosis

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5
Q

Treatment of Allergic bronchopulmonary aspergillosis?

A

1st line: Oral corticosteroids
2nd line: Itraconazole

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6
Q

Major criteria for the diagnosis of Allergic bronchopulmonary aspergillosis?

A
  • Clinical features of asthma
  • Proximal bronchiectasis
  • Blood eosinophilia
  • Immediate skin reactivity to Aspergillus antigen
  • Increased serum IgE (>1000 IU/ml)
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7
Q

What type of allergic hypersensitivity is involved in Allergic Bronchopulmonary Aspergillosis?

A

Type II Hypersensitivity

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8
Q

Causes of Extrinsinc allergic alveolitis?

A
  • Farmer’s lung: spores of Saccharopolyspora rectivirgula → Contaminated hay ++
  • Malt workers’ lung: ASPERGILLUS CLAVATUS
  • Wood workers
  • Bird fanciers
  • Cheese worker’s lung: Inhalation of mold spores in cheese factories
  • Humidifier lung: Exposure to contaminated water reservoirs or air conditioning systems.
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9
Q

Upper/mid fibrosis + lymphocytosis in bronchoalveolar lavage + NO EOSINOPHILIA + ground glass appearance in high-resolution CT?

A

Extrinsic allergic alveolitis

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10
Q

Management of extrinsic allergic alveolitis?

A

Avoid exposure to allergen + oral corticosteroids

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11
Q

Mode of inheritance of Alpha-1 antitrypsin deficiency?

A

Autosomal recessive / co-dominant fashion

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12
Q

Features of A1AD?

A

Panacinar emphysema mostly marked in the lower lobes in young patients who do not smoke (picture of COPD in young patient)
Liver cirrhosis and hepatocellular carcinoma in adults, cholestasis in children

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13
Q

Management of A1AD?

A

No smoking + supportive treatment with bronchodilators and physiotherapy
- Intravenous alpha1-antitrypsin protein concentrates
- Surgery: lung volume reduction surgery, lung transplantation

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14
Q

Genotypes of A1AD?

A

(Chromosome 14)
Alleles classified by their electrophoretic mobility - M for normal, S for slow, and Z for very slow
- normal: PiMM
- heterozygous: PiMZ
evidence base is conflicting re: risk of emphsema
however, if non-smoker low risk of developing emphsema but may pass on A1AT gene to children
- homozygous PiSS: 50% normal A1AT levels
- homozygous PiZZ: 10% normal A1AT levels

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15
Q

What is the role of Alpha-1 antitrypsin?

A

It’s a protease inhibitor that protects the body from neutrophil elastase, a protein that can degrade elastin and other structural protein in liver and lungs

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16
Q

In A1AD, PiZZ phenotype equals what percentage of A1A level?

A

10% (10% off your PiZZa)

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17
Q

Management and prophylaxis of HACE and HAPE?

A

HACE: Dexamethasone
HAPE: Nifedipine
Prophylaxis for both: Acetazolamide

18
Q

Cause of occupational asthma?

A

ISOCYANATES - the most common cause: spray painting and foam moulding using adhesives
BYSSINOSIS - rare, caused by cotton bacteria endotoxins (EXAM QUESTION)
- platinum salts
-soldering flux resin
-glutaraldehyde
-flour
-epoxy resins
-proteolytic enzymes

19
Q

Diagnosis of occupational asthma?

A

Serial measurements of peak expiratory flow in and out of work

20
Q

Severe pneumonia (CURB 3) management?

A

IV co-amoxiclav + clarithromycin

21
Q

SOB + cough + fever + malaise in 5th or 6th decade of life + bilateral patchy or consolidative or ground glass opacities + raised CRP and ESR + poor responsiveness to ATB

A

Cryptogenic organizing pneumonia

22
Q

Management of cryptogenic organizing pneumonia?

A

Watch and wait or high dose oral steroids if severe

23
Q

Lower lobe fibrosis (interstitial shadowing/ground glass opacities later turning into honeycomb) + restrictive picture in spirometry + low transfer factor TLCO?

A

Idiopathic pulmonary fibrosis

24
Q

Diagnosis of idiopathis pulmonary fibrosis?

A

High-resolution CT scan.

25
Management of idiopathic pulmonary fibrosis?
Pulmonary rehabilitation, supplemental oxygen and eventual lung transplant. Pirfenidone might be used in select patients. Poor prognosis - death in 3-4 years
26
Sarcoidosis X-ray classification?
Stage 0 = normal Stage 1 = bilateral hilar lymphadenopathy (BHL) Stage 2 = BHL + interstitial infiltrates Stage 3 = diffuse interstitial infiltrates only Stage 4 = diffuse fibrosis
27
What test to request before starting a patient on Azithromycin?
ECG - due to risk of prolonged QT-interval and baseline LFTs
28
What's the classic CXR finding in chronic silicosis?
Upper lung fibrosis + egg-shell calcification of peri-hilar lymph nodes
29
Causes of upper zone lung fibrosis?
CHARTS Coal worker's pneumoconiosis Histiocytosis/hypersensitivity pneumonitis Ankylosing spondylitis Radiation Tuberculosis Silicosis
30
Recurrent chest infections + subfertility
Primary ciliary dyskinesia aka Kartagener's syndrome (no malabsorption)
31
BiPAP settings in COPD?
IPAP 10 cm H2O - EPAP 5 cm H2o
32
Asthma, mononeuritis and eosinophilia + positive pANCA (may be unmasked by leukotriene receptor antagonist MONTELUKAST) =
Churg-Strauss syndrome
33
Old age + cough + haemoptysis + weight loss + hypertension, hyperglycaemia, hypokalaemia, alkalosis and muscle weakness
Small cell lung cancer secreting ACTH (also ADH and Lambert-Eaton syndrome)
34
Which type of hypersensitivity reaction predominates in the acute phase of extrinsic allergic alveolitis?
Predominantly type III, then IV is delayed
35
Which metric is most important in considering placement of a chest drain in pleural efflusion?
pH of pleural fluid
36
Best parameter to monitor COPD?
FEV1
37
Hypercalcaemia + bilateral hilar lymphadenopathy = ?
Sarcoidosis
38
Most common organism in COPD exacerbation?
Haemophilus influenzae
39
Middle-aged man + alcoholism + cavitating lesion/abcess formation in mid/upper lobes = which organism?
Klebsiella (Friedlander's pneumonia)
40
What are the contraindications to lung surgery?
FEV1<1.5L SVC obstruction Vocal cords paralysis Malignant pleural effusion
41
Cystic fibrosis is due to a defect in Cystic Fibrosis Transmembrane conductance Regulator. On what chromosome is it located?
Chromosome 7
42