Respiratory Flashcards

(31 cards)

1
Q

Cryptogenic organising pneumonia

A
  • Diffuse interstitial lung disease
  • M = F; presents in 5th-6th decade
  • No association with smoking
  • Symptoms: fever, malaise, cough, SOB
  • No response to antibiotics
  • Bloods: leukocytosis, high ESR / CRP
  • Imaging: bilateral patchy, diffuse consolidative, ground glass opacities
  • Lung function tests restrictive (but sometimes obstructive / normal)
  • Reduced transfer factor
  • Mx: sometimes steroids
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2
Q

Yellow nail syndrome

A
  • yellow, clubbed nails
  • bronchiectasis
  • pleural effusions
  • congenital lymphoedema
  • recurrent sinusitis
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3
Q

Lung cancer surgery indications and contraindiactions

A

Indications

  • stage 1 or 2 disease
  • FEV1 > 60% predicted

Contraindications

  • FEV1 < 1.5 litres (lobectomy)
  • FEV1 < 2L (pneumonectomy)
  • malignant pleural effusion
  • tumour near hilum
  • vocal cord paralysis
  • SVC obstruction
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4
Q

Non-small cell lung cancer types

A

Squamous cell: central, PTHrP secretion
Adenocarcinoma: non-smokers, peripheral
Large cell: aggressive, BhCG secretion

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5
Q

Non-small cell lung ca mx

A

1) Surgery: stage 1-2
2) Curative / palliative radiotherapy
Poor response to chemotherapy

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6
Q

Pneumonia cause in cases associated with cold sores

A

Strep pneumoniae

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7
Q

Cavitating pneumonia associated with alcoholics

A

Klebsiella

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8
Q

Bug that can cause IECOPD

A

Haemophilus influenzae

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9
Q

Post influenza pneumonia bug

A

S Aureus

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10
Q

How to assess suitability for lung cancer surgery

A
  • combined PET / CT gives an idea on LN involvement
  • FEV1 < 1.5 litres is considered a general cut-off point for lobectomy ( <2L for pneumonectomy)

Other general contraindications

  • malignant pleural effusion
  • tumour near hilum
  • vocal cord paralysis
  • SVC obstruction
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11
Q

Best long-term intervention for sleep apnoea

A
Weight loss 
(CPAP may be needed in the interim as well)
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12
Q

Small cell lung cancer paraneoplastic syndromes

A
  • SIADH
  • ACTH secretion
  • Lambert-Eaton
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13
Q

Squamous cell carcinoma paraneoplastic syndromes

A
  • PTHrP
  • clubbing
  • hypertrophic pulmonary osteoarthropathy
  • ectopic TSH -> hyperthyroidism
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14
Q

Adenocarcinoma paraneoplastic syndromes

A
  • gynaecomastia

- hypertrophic pulmonary osteoarthropathy

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15
Q

Chronic asthma treatment ladder

A

1) SABA
2) SABA + low dose ICS
3) SABA + low dose ICS + montelukast
4) SABA + low dose ICS + LABA (+/- montelukast if it had any effect)
5) SABA (+/- montelukast) & maintenance and reliever LABA/ICS combo
6) Increase steroid dose
7) Increase steroid dose further OR add LAMA OR theophylline

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16
Q

FVC threshold for ventilatory support in neuromuscular disease

17
Q

Chronic COPD treatment ladder

A

1) SABA / SAMA
2) LABA + ICS (if asthmatic features)
OR LABA + LAMA (if no asthmatic features)
3) LABA + LAMA + ICS
4) Roflumilast (>2 exacerbations in a year, despite triple inhaled therapy, where FEV1 is less than 50% of predicted)

Others

  • oral theophylline
  • mucolytics
  • lung volume reduction surgery
18
Q

Secondary pneumothorax management

A

Definition: significant respiratory co-morbidity OR over 50 and smoker

<1cm: oxygen, admit for observation

1-2cm and asymptomatic: aspiration -> chest drain if residual >1cm

> 2cm or symptomatic: chest drain

19
Q

Primary pneumothorax management

A

<2cm and asymptomatic: consider discharge

> 2cm or symptomatic: aspiration -> chest drain if residual >2cm

20
Q

Pneumocystis pneumonia prophylaxis

A

Co-trimoxazole OR nebulised pentamidine

21
Q

Management of severe pneumocystis pneumonia

A

IV clindamycin & primaquine
OR
IV pentamidine

AND prednisolone (if PO2 <9.3)

22
Q

Symptoms of extrinsic allergic alveolitis

A

E.g. bird fancier’s lung, farmer’s lung, malt worker’s lung
Acute: 4-8 hrs after exposure, SOB, dry cough, fever
Chronic: fibrosis (upper lobe predominant)

23
Q

Pulmonary alveolar proteinosis

A
  • Rare diffuse lung disease where alveolar sacs become filled with protein rich fluid
  • primary or secondary e.g. PCP / atypical mycobacteria as cause
  • fluid typically stains for PAS
  • ages 20-60
  • crazy paving pattern on CT
  • spirometry: restrictive, reduced TLC, reduced KCO
  • mx: washing alveoli with saline during bronchoscopy
24
Q

Bronchial carcinoid

A
  • flushing etc and diarrhoea when hepatic mets occur (carcinoid syndrome)
  • symptoms unrelated to smoking
  • ix: imaging and 5-IHAA
  • mx: surgery if no mets
25
Yellow nail syndrome
Triad: primary lymphoediema, recurrent pleural effusions, dystrophic nails (lymphatic system abnormality as root cause) - associated with bronchiectasis and siusitis - pleural fluid typically clear exudate with lymphocytic predominace
26
Allergic bronchopulmonary aspergillosis
- DDx for raised blood eosinophilia (along with Churg-Straus and asthma) - Pulmonary infiltrates on CXR OR lobar collapse - Asthma - Blood & sputum eosinophilia - aspergillus precipitins - positive RAST - raised total IgE - may see aspergillus fumigatus hyphae on microscopy of sputum - Mx 1) steroids PO 2) itraconazole
27
SVC obstruction mx
Dexamethasone may alleviate some symptoms Endovascular stenting is likely to be needed asap Treat the cause if possible
28
Management of invasive bronchopulmonary aspergillosis
1) voriconazole | 2) amphotericin B (less effective, also has more side effects)
29
Aspergilloma mx
Voriconazole / itraconazole | Surgical resection
30
Haemoptysis in CF patients
- consider bronchial artery aneurysm -> CTPA to investigate | - tranexamic acid
31
Nitrogen air embolism in diving
- arises from venous blood | - if then presents with CVA, need echo to exclude ASD