Respiratory Medicine Flashcards

1
Q

what are the two main types of intrinsic diseases that damage the lung parenchyma?

A
  1. interstital lung diseases

2. alveolar oedema or haemorrhage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what are the 4 main causes of interstitial lung disease?

A
  1. pneumoconiosis
  2. sarcoidosis
  3. idiopathic pneumonitis
  4. Hypersensitivity pneumonitis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are the three categories, and some examples, of extrapulmonary/extrinsic causes of restrictive lung disease?

A
  1. Pleural disease
    • chronic effusions
    • adhesions
    • PTX
  2. Thoracic deformaties or restrictions
    • kyphoscoliosis
    • obesity
    • ankylosing spondylitis
    • ascites
    • pregnancy
    • pectus excavatum
  3. Neuromuscular weakness
    • ALS
    • GBS
    • myasthenia gravis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what are common symptoms of Restrictive lung disease across all aetiologies?

A
  1. cough
  2. dyspnoea
  3. tachypnoaea
  4. weight loss
  5. Bibasilar, inspiratory crackles or rales on auscultation -> HALLMARK
    Advanced disease
  6. digital clubbing
  7. cyanosis
  8. Loud inspiratory wheeze
  9. symptoms due to underlying cause
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what are the findings on Spirometry for restrictive lung diseases?

A
  • what are the findings on Spirometry for restrictive lung diseases?
    1. reduced TLC
    2. FEV1 and FVC are also often reduced
    3. FEV1/FVC are normal or increased
    4. appearance of spirometry trace in that of a narrowed normal flow volume loop.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What does interstital lung disease look like on CT?

A

ground glass appearance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what are the principles of treatment for restrictive lung diseases?

A
  1. smoking and other irritant inhalation cessation
  2. supportive care
  3. Management specific to cause → bronchodilators, corticosteroids or immune modulators
  4. management for IPF→ antifibrotic agents
  5. Lung transplantation only definitive treatment
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the hallmark presentation for idiopathic pulmonary fibrosis?

A

1) cough
2) dyspnoae
3) FINE, ‘VELRCO’ BIBASILAR CREPS ON END INSPIRATION

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the common causes of finger clubbing?

A

Cardiovascular:

1) Cyanotic congenital heart disease
2) Infective endocarditis

Respiratory:

1) Lung carcinoma
2) Chronic pulmonary suppuration
- Bronchiectasis
- lung abscess
- empyema
3) Idiopathic pulmonary fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are uncommon causes of finger clubbing?

A

Respiratory:

1) CF
2) Asbestosis and mesothelioma

Gastro:

1) cirrhosis -> billiary mainly
2) IBD
3) Coeliac disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the two main categories of TB?

A
  1. Primary tuberculosis
    - initial infection of M.tuberculosis
    - may cause primary progressive disease in immunocompromised people → but usually results in latent infection as immunity develops
  2. Post primary tuberculosis
    - results from either reactivation of a latent primary infection or from the repeat infection of a previously sensitised host
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

how is TB identifies in infected individuals?

A

Ziehl-Neelsen Stain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Describe the pathophysiology of primary TB infection

A
  1. inhaled infectious droplets reach terminal alveoli and are ingested by alveolar macrophages
  2. inhibition of phagolysosome fusion allows M.TB to survive within macrohage as an intracellular infection → replication, lysis and spread
  3. Cell-mediated immune response develops with activation of CD4+ T cells to the focus of infection to stimulate macrophages (via IFNy)
  4. granuloma formation to limit spread of infection → basically and immune focus of caseating necrosis containing macrophages and mycobacteria surrounded by lymphocytes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what are the 3 types of granulomas seen in TB?

A
  1. Ghon focus
    • primary TB granuloma usually in middle or lower lung lobes
  2. Ghon complex
    • Ghon focus + involvement of draining lymphatics and hilar node
  3. Ranke complex
    • evolution of ghon complex resulting from fibrosis and calcification
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the Pulmonary signs and symptoms of primary progressive or reactivation TB infection?

A

Signs

  1. pallor
  2. dullness to percussion of areas of consolidation
  3. Hyperresonance over areas of cavitation
  4. crepitations, bronchial breath sounds

Symptoms

  1. Constitutional symptoms
  2. purulent sputum with occasional haemoptysis
  3. pleuritic chest paun
  4. dysnpoea
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what are the extrapulmonary clinical features of TB?

A
  1. Lymphadenopathy
  2. tuberculosis pleurisy
  3. TB meningitis
  4. Pericardial TB
  5. Adrenal TB → addison’s disease
  6. Miliary or disseminated TB → mulitorgan involvement
17
Q

What is the treatment of latent TB?

A

9 months of Isoniazid

18
Q

What is the treatment for active TB? (RIPE)

A
  1. 2 months of:
    • Rifampicin
    • isoniazid
    • pyrazinamide
    • ethambutol
  2. further 4 months of:
    • Rifampicin and Isoniazid