Respiratory Flashcards

1
Q

How long should an unprovoked PE be treated for?

A

6 months

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2
Q

What can happen as a result of prolonged intubation?

A

physical communication between the trachea and oesophagus due to proximity of structures and inflammation around the tube in the trachea. Knows as a tracheooesophageal fistula

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3
Q

What is Barrett’s oesophagus?

A

Metaplasia of the lower oesophageal mucosa, with the usual squamous epithelium being replaced by columnar epithelium

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4
Q

Where is an inhaled foreign body most likely to be found?

A

Right main bronchus

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5
Q

what are contraindications to insertion of a chest drain?

A

INR >1,3
platelet count < 75
Pulmonary bullae
Pleural adhesions

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6
Q

what are indications for inserting a chest drain?

A

pleural effusion
pneumothorax
empyema
haemothorax
hemopneumothorax
chylothorax
in some cases of penetrating chest wall injury in ventilated patients

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7
Q

How should patients with suspected PE be treated?

A

DOAC i.e. apixaban or rivaroxaban

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8
Q

What are characteristic features of streptococcal pneumonia?

A

rapid onseet
high fever
pleuritic chest pain
herpes labialis (cold sores)

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9
Q

what antibiotic is given in non-severe community acquired pneumonia that can be managed as an outpatient?

A

oral amoxicillin

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10
Q

what investigation should be done to confirm SIADH?

A

paired urine and plasma osmolalities

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11
Q

what is allergic bronchopulmonary aspergillosis?

A

complex hypersensitivity reaction often in patients with asthma or cystic fibrosis that occurs when bronchi become colonized by Aspergillus species
Repeated episodes of bronchial obstruction, inflammation and mucoid impaction can lead to bronchiectasis, fibrosis and respiratory compromise

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12
Q

what is allergic bronchopulmonary aspergillosis?

A

complex hypersensitivity reaction often in patients with asthma or cystic fibrosis that occurs when bronchi become colonized by Aspergillus species
Repeated episodes of bronchial obstruction, inflammation and mucoid impaction can lead to bronchiectasis, fibrosis and respiratory compromise

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13
Q

what are the features of allergic bronchopulmonary aspergillosis?

A

bronchoconstriction: wheeze, cough, dyspnoea
bronchiectasis - proximal

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14
Q

What is seen on investigation in allergic bronchopulmonary aspergillosis?

A
  • eosinophilia
  • flitting CXR changes
  • positive RAST test to aspergillosis
  • positive IgG precipitins
  • raised IgE
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15
Q

What is the management of allergic bronchopulmonary aspergillosis?

A

oral glucocorticoids
itraconazole sometimes introduced second-line

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16
Q

What are the signs of life-threatening asthma?

A

PEFR < 33% Best or predicted
oxygen sats < 92%
normal PCO2
silent chest, cyanosis or feeble respiratory effort
bradycardia, dysrhythmia, hypotension
exhaustion, confusion, coma

17
Q

How is pneumocystic jirovecci treated?

A

co-trimoxazole

18
Q

what are the CURB65 criteria?

A

C = confusion
U = urea > 7mmol/L
R = respiration rate >/= 30
BP = systolic </=90 and/or diastolic </=60
65

19
Q

what is a transudative effusion and what could cause it?

A

<30g/L protein:
- heart failure - most common transudate cause
- hypalbuminaemia - liver disease, nephrotic syndrome, malabsorption
- hypothyroidism

20
Q

what is an exudative effusion and what could cause it?

A

> 30g/L protein:
- infection: pneumonia - most common exudate cause, TB
- connective tissue disease - RA, SLE
- neoplasia - lung cancer, mesothelioma, metastases
- pancreatitis
- pulmonary embolism
- Dressler’s syndrome

21
Q

What are the features of carcinoma on needle biopsy?

A

nuclear enlargement, hyperchromasia, pleomorphism

22
Q

what should you do if you have a strong suspicion of PE but there is a delay in performing a scan?

A

start patient on treatment dose apixaban whilst awaiting scan

23
Q

what are pleural plaques?

A

change that can be seen on CXR in people with asbestos exposure
pleural plaques are benign and do not undergo malignant change - therefore don’t require any follow-up

24
Q

what are the indications for BIPAP/NIV in patients with COPD?

A
  • COPD with resp. acidosis pH 7.25-7.35
  • type II respiratory failure 2ndary to chest wall deformity, neuromuscular disease or OSA
  • cardiogenic pulmonary oedema unresponsive to CPAP
  • weaning from tracheal intubation
24
Q

what are the indications for BIPAP/NIV in patients with COPD?

A
  • COPD with resp. acidosis pH 7.25-7.35
  • type II respiratory failure 2ndary to chest wall deformity, neuromuscular disease or OSA
  • cardiogenic pulmonary oedema unresponsive to CPAP
  • weaning from tracheal intubation
25
Q

diagnostic testing of asthma?

A

patients >/= 17 - patients should be asked if symptoms are better on days away from work/during holidays, if so, patients should be referred to a specialist as possible occupational asthma, all patients should have spirometry with a bronchodilator reversibility test, all patients should have an FeNO test
children 5-16 years: all children should have spirometry with bronchodilator reversibility testing, FeNO should be requested if normal spirometry
patients < 5 years: diagnosis should be made on clinical judgement

26
Q

How is an acute exacerbation of COPD treated?

A
  • increase frequency of bronchodilator use and consider giving nebs
  • give prednisolone 30mg daily for 5 days
  • oral abx are recommended if sputum is purulent or there are clinical signs of pneumonia
  • BNF recommends one of following oral antibiotics first line: amoxicillin/clarithromycin/doxycycline
27
Q

in what cancer are ‘cavitating lesions’ most commonly seen?

A

squamous cell lung cancer

28
Q

what is flail chest?

A

chest wall disconnects from thoracic cage
multiple rib fractures - at least 2 fractures per rib in at least 2 ribs
associated with pulmonary contusion
abnormal chest motion
avoid over hydration and fluid overload

29
Q

what is flail chest?

A

chest wall disconnects from thoracic cage
multiple rib fractures - at least 2 fractures per rib in at least 2 ribs
associated with pulmonary contusion
abnormal chest motion
avoid over hydration and fluid overload

30
Q

what is the long-term management of COPD?

A

1: short-acting bronchodilators - salbutmaol/terbutaline or short acting antimuscarinics (ipratropium)
2a: if they do not have asthmatic or steroid responsive features they should have a combined LABA and LAMA
2B: if they have asthmatic or steroid responsive features they should have a combined LABA and ICS - e.g. fostair/symbicort - if this does not work they can be stepped up to a LABA,LAMA and ICS - “trimbo”
3. In more severe cases additional options are:
- nebulisers (salbutamol and/or ipratropium)
- oral theophylline
- oral mucolytic therapy to break down sputum
- long term prophylactic antibiotics
- long term oxygen therapy at home - used for severe COPD that is causing problems such as chronic hypoxia, polcythaemia, cyanosis or heart failure secondary to pulmonary hypertension (cor pulmonale)