Bronchiectasis and Fibrotic lung disease Flashcards

1
Q

What is bronchiectasis

A
  • This is chronic inflammation of the bronchi and bronchioles that leads to a permanent dilatation and thinning of these airways
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2
Q

What are the main organisms that cause bronchiectasis

A
  • H.influenzae
  • Strep.pneumoniae
  • Staph.aureus
  • Pseudomonas aeruginosa
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3
Q

What are the common causes of bronchiectasis

A

Congenital

  • Cystic fibrosis
  • young’s syndrome
  • primary colliery dyskinesia
  • Kartagener’s syndrome

Post infection

  • measles
  • pertussis
  • bronchiolitis
  • pneumonia
  • TB
  • HIV

Other

  • bronchial obstruction
  • allergic bronchopulmonary aspergillosis
  • rheumatoid arthritis
  • ulcerative colitis
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4
Q

What are the symptoms of bronchiectasis

A
  • persistent cough
  • large amounts of purulent sputum
  • intermittent haemoptysis
  • breathlessness occurs as disease progression
  • infection characterised by increase sputum volume and purulence
  • pleuritic chest pain
  • coarse crackles can occur
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5
Q

What are the signs of bronchiectasis

A
  • finger clubbing
  • coarse inspiratory crepitations
  • wheeze
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6
Q

What are the complications of bronchiectasis

A
  • pneumonia
  • pleural effusion
  • pneumothorax
  • haemoptysis
  • cerebral abscess
  • amyloidosis
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7
Q

What investigations do you use to diagnose bronchiectasis

A
  • HRCT scanning
  • Sputum culture
  • CXR
  • spirometry
  • bronchoscopy
  • serum immunoglobulins
  • CF - Sweat test
  • skin prick test
  • aspergillus precipitins
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8
Q

What differences do you observe on an CXR to diagnose bronchiectasis with

A
  • cystic shadows

- thickened bronchial walls

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9
Q

What does spirometry show in bronchiectasis

A
  • obstruction pattern

- reversibility should be assessed

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10
Q

What is the global leading cause of bronchiectasis

A

TB

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11
Q

describe the pathophysiology of bronchiectasis

A
  • abnormal and permanently dilated airways
  • characterised by a vicious circle of neutrophilic inflammation, recurrent infection and damage to the airways
  • this impairs mucociliary clearance and persistent inflammation which leads to the impairment of immunity
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12
Q

What is the management for bronchiectasis

A
  • airway clearance
  • anti-inflammatories
  • antibiotics
  • bronchodilators
  • ## corticosteroids
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13
Q

Describe how you would use airway clearance in bronchiectasis

A
  • airway clearance techniques and mucolytics

- chest physiotherapy and devices such as a flutter valve can help sputum expectoration and mucus drainage

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14
Q

Why are anti-inflammatories sued in bronchiectasis

A
  • long term azithromycin has an immunomodulatory effect and has been demonstrated to reduce exacerbation
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15
Q

When should antibiotics be prescribed in bronchiectasis and what antibiotics should be prescribed

A
  • Should be prescribed according to bacterial sensitivities
  • patients known to culture pseudomonas aeruginosa require either oral ciprofloxacin
  • if you have more than or equal to 3 exacerbations a year long term antibiotic should be considered
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16
Q

Why is P.aeruginosa important to isolate in bronchiectasis

A

patients with P. aeruginosa experience an accelerated decline in lung function and more frequent exacerbations
- increases morbidity

17
Q

What are the differential diagnosis of a cough with sputum

A
  • infection
  • COPD
  • cystic fibrosis
  • pneumonia
  • lung abscess
  • pulmonary edema
18
Q

Name the similarities and differences between COPD and Bronchiectasis

A

COPD

  • caused by smoking or environmental causes
  • corticosteroid and LABA/LAMA treatment

Bronchiectasis

  • consistent infection
  • excess mucus
  • treatment involves airway clearance and antibiotics to treat infection

Both have similar symptoms

19
Q

What is the pathophysiology of fibrotic lung disease

A
  • there is fibrosis and remodelling of the interstitium
  • chronic inflammation
  • hyperplasia of type II epithelial cells
  • type II pneumocytes
20
Q

What are the common causes of fibrotic lung disease

A

known cause

  • occupation
  • drugs
  • hypersensitivity reactions
  • infections

Systemic disorders

  • sarcoidosis
  • rheumatoid arthritis
  • SLE
  • ulcerative colitis, renal tubular acidosis, autoimmune thyroid diseases

Idiopathic

  • idiopathic pulmonary fibrosis
  • cryptogenic organising pneumonia
  • non-specific interstitial pneumonitis
21
Q

What are the symptoms of fibrotic lung disease

A
  • dyspnoea on exertion
  • non productive paroxysmal cough
  • abnormal breath sounds
22
Q

What are the signs of fibrotic lung disease

A
  • abnormal CXR
  • restrictive pulmonary spirometry
  • decrease DLCO
23
Q

What investigations are used to confirm the diagnosis of fibrotic lung disease

A
  • CXR
  • Spirometry
  • DLCO
24
Q

What causes fibrotic shadowing in the upper zone of a CXR

A
  • TB hypersensitivity pneumonitis
  • ankylosing spondylitis
  • radiotherapy
  • progressive massive fibrosis
25
Q

What causes fibrotic shadowing in the mid zone of a CXR

A
  • sarcoidosis

- histoplasmosis

26
Q

What causes fibrotic shadowing in the lower zone of a CXR

A
  • idiopathic pulmonary fibrosis

- asbestosis

27
Q

How do you manage fibrotic disease

A
  • corticosteroids
  • oxygen support
  • pulmonary rehabilitation
  • lung transplant