restrictive lung disease Flashcards

1
Q

what are some causes to thoracic restriction?

A

skeletal (kyphoscoliosis, ankylosing spondylisis, rib fracture)
muscle (myopathy, neuropathy, gullian barre, myasthenia gravis)
abdominal obesity/ascites

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2
Q

what does thoracic restriction cause?

A

chronic alveolar underventillation with low oxygen, raised carbon dioxide and reduced lung volumes

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3
Q

how can diffuse parenchymal lung disease (DPLD) be classified?

A

acute, episodic, chronic (occupational or systemic disease), chronic idiopathic

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4
Q

what is DPLD?

A

a disease of the lung parenchyma (i.e alveolar walls & lumen)

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5
Q

what is the pathophysiology of DPLD?

A

impaired gas exchange (alveolar-arteriolar barrier), CO2 exchange normal as ventilation normal

(low oxygen & normal CO2)

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6
Q

what can fluid in the alveolar spaces be caused by?

A

cardiac pulmonary (LVF) & non-cardiac pulmonary oedema (leaky capillaries - sepsis & trauma aka ARDS)

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7
Q

what can cause consolidation of alveolar spaces?

A

pneumonia, infarction, BOOP, rheumatoid disease

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8
Q

what can cause inflammatory infiltrate of alveolar walls (alveolitis)?

A

granulomatous alveolitis, sarcoidosis, drugs (amidarone, methotrexate, gold), toxic fumes (chlorine), fibrosing alveolitis, auto-immune, pneumoconiosis (fibrinogenic e.g asbestosis vs. non-fibronogenic e.g baritosis), neoplasm, eosinophilic (allergic)

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9
Q

what is the general presentation of DPLD?

A

breathlessness on exertion, cough with no wheeze, clubbing, inspiratory crackles, central cyanosis, pulmonary fibrosis

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10
Q

how do we diagnosis DPLD?

A

restrictive spirometry, low TLCO, arteriolar oxygen desaturation (low oxygen), serology, bloods, CXR, ECG, CT, bronchoalveolar lavage/induced sputum, biopsy

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11
Q

how do we treat DPLD?

A

avoidance, immunosuppressives for inflammation, oral steroids, pirfenidone (anti-fibrotic for IPF), acetyl cysteine (anti-oxidant for IPF), oxygen, transplant

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