Lower respiratory tract diseases - BRONCHIECTASIS Flashcards

1
Q

what is bronchiectasis?

A

= abnormal and PERMANENTLY DILATED airways

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2
Q

who most commonly gets bronchiectasis?

A

median age is 50 years

  • however, patients often had symptoms for over 10-20 years
  • most cases (60%) occur inn women
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3
Q

what 3 things are characteristic of bronchiectasis?

A

1) neutrophilic inflammation
2) recurrent infection
3) damage to the airway

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4
Q

what effect do these 3 things have on mucous clearance and immunity?

A
  • impairs mucociliary clearance

- impaired immunity caused by persistent inflammation

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5
Q

what causes bronchiectasis?

A

1) congenital causes
- deficiency of bronchial wall

2) bronchial obstruction
- foreign body
- mucus
- post TB stenosis
- tumour
- lymph node

3) post-infection bronchial damage

4 ) granuloma
- Tuberculosis, sarcoidosis

5) mucociliary clearance defects
- cystic fibrosis
- primary ciliary dyskinesia
- young’s syndrome

6) immune deficiency
- HIV & malignancy
- SELECTIVE IMMUNOGLOBULIN DEFICIENCIES (IgA & IgG)

7) immunological over-response
- allergic broncho-pulmonary aspergillosis
- post-lung transplant

8) diffuse diseases of lung parenchyma
- idiopathic pulmonary fibrosis

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6
Q

symptoms of bronchiectasis?

A
  • COUGH
  • chronic daily SPUTUM PRODUCTION (large amounts of it)
  • breathlessness if the disease progresses
  • minor haemoptysis (usually a sign of infection)
  • pleuritic chest pain & severe & systemic upset can be signs of infection
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7
Q

on examination what could be expected?

A
  • coarse crackles on auscultation but examination can be normal
  • clubbing can occur, especially in cystic fibrosis
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8
Q

how would you investigate bronchiectasis?

A

1) chest X-ray
2) high resolution CT scan
3) sputum examination
4) immune assessment
5) sweat tests & cystic fibrosis genetic assessment
6) nasal nitric oxide
7) total IgE & aspergillus specific IgE or aspergillus skin prick testing

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9
Q

what would a chest X-ray show in a patient with bronchiectasis?

A
  • most often will be normal
  • but may show bronchial wall thickening
  • ring shadows
  • tramlines
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10
Q

what would a high resolution CT scan show?

A
  • tram-track airways

- increased bronchoarterial ratio

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11
Q

what would the immune assessment look at?

A
  • immunoglobulins and responses to;
  • haemophilus influenza b
  • tetanus
  • pneumococcal vaccines as a baseline test
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12
Q

what type of patient should sweat tests & cystic fibrosis genetic assessment be carried out?

A
  • patients under the age of 40
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13
Q

what is nasal nitric oxide a useful test for?

A
  • for screening for primary ciliary dyskinesia (PCD)
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14
Q

why should total IgE & aspergillus specific IgE or aspergillus skin prick testing be done?

A

to exclude allergic broncho-pulmonary aspergillosis

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15
Q

name 3 ways to manage bronchiectasis?

A

1) airway clearance
2) anti-inflammatories
3) treatment of infection

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16
Q

give examples of airway clearance mechanisms?

A
  • activated cycle of breathing technique
  • autogenic (self)-drainage
  • postural drainage
  • nebulised hypertonic saline works as a muco-active agent
17
Q

name a drug used for anti-inflammatory

A

azithromycin, is a long term immunomodulator

18
Q

what does azithromycin do?

A
  • reduces exacerbation frequency

- reduces inflammation

19
Q

when treating infections caused by the bacteria pseudomonas aeruginosa what type of therapy should be used and why?

A
  • DUAL therapy should be used

- due to multi-resistant pathogens

20
Q

what drug/(s) should be used to treat pseudomonas haemophilus influenzae?

A
  • high dose ciprofloxacin (oral drug)

- amoxicillin
- co-amoxiclav
- doxycycline
all oral antibiotics

21
Q

what do multi-resistant species need to be treated?

A

intravenous cephalosporin treatment