Interstitial Lung Disease Flashcards

1
Q

What is ILD

A

Umbrella term to describe conditions which affect the lung parenchyma causing inflammation and fibrosis

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2
Q

Diagnosis of ILD

A

Combination of clinical features and high resolution CT scan of the thorax

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3
Q

What does a high resolution CT scan show

A

Ground glass appearance with ILD

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4
Q

Management of ILD

A

Poor prognosis and limited management as damage is irreversible

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5
Q

Types of ILD

A

Idiopathic pulmonary fibrosis, drug induced pulmonary fibrosis, secondary pulmonary fibrosis, hypersensitivity penumonitis, cryptogenic organising pneumonia, asbestosis

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6
Q

What is idiopathic pulmonary fibrosis

A

Progressive pulmonary fibrosis with no clear cause

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7
Q

Presentation of idiopathic pulmonary fibrosis

A

Insidious onset SOB and dry cough over more than 3 months

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8
Q

Examination of patient with idiopathic pulmonary fibrosis

A

Bibasal fine inspiratory crackles and finger clubbing

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9
Q

Medications which can slow the progression of idiopathic pulmonary fibrosis

A

Pirfenidone and Nintedanib

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10
Q

Drugs which can cause pulmonary fibrosis

A

Amiodarone, Cyclophosphamide, Methotrexate and Nitrofurantoin

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11
Q

Conditions which can cause secondary pulmonary fibrosis

A

Alpha-1 antitripsin deficiency, rheumatoid arthritis, SLE, systemic sclerosis

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12
Q

What is hypersensitivity pneumonitis

A

Type 3 hypersensitivity reaction to an environmental allegen which causes parenchymal inflammation

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13
Q

What does bronchoalveolar lavage involve

A

Collecting cells from the airways during bronchoscopy by washing the airways with fluid then collecting that fluid for testing

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14
Q

What will bronchoalveolar lavage show

A

Raised lymphocytes and mast cells

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15
Q

Management of hypersensitivity pneumonitis

A

Removing allergen, giving oxygen where necessary and steroids

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16
Q

Examples of specific causes of hypersensitivity pneumonitis

A

Bird-fanciers lung, Farmers lung, Mushroom workers lung, Malt workers lung

17
Q

What is cryptogenic organising pneumonia

A

Focal area of inflammation of the lung tissue.

18
Q

Cause of cryptogenic organising pneumonia

A

Idiopathic or triggered by infection, inflammation disorders, medications, radiation, or environmental toxins or allergens

19
Q

Presentation of cryptogenic organising pneumonia

A

SOB, cough, fever, lethargy, focal consolidation

20
Q

Treatment of cryptogenic organising pneumonia

A

Systemic corticosteroids

21
Q

What problems can asbestos inhalation cause

A

Lung fibrosis, pleural thickening, pleural plaques, adenocarcinoma, mesothelioma

22
Q

Causes of pulmonary fibrosis

A

Lung damage, irritants, diffuse parenchymal lung disease, connective tissue disease, medications and hypersensitivity pneumonitis

23
Q

Symptoms of idiopathic lung fibrosis

A

Dry cough, SOB, fatigue, arthralgia, cyanosis, clubbing, crackles

24
Q

Complications of pulmonary fibrosis

A

Type 2 respiratory failure, increased risk of lung cancer, cor pulmonale, mortality

25
Q

Imaging results of pulmonary fibrosis

A

Bilateral lower zone reticulo-nodular shaddowing, honeycomb lung on CT

26
Q

Management of pulmonary fibrosis

A

Pulmonary rehab, LTOT, antibiotics, control of RHF, long transplant