Interstitial Lung Disease Flashcards

1
Q

How is interstitial lung disease diagnosed?

A

High res CT- ground glass

Biopsy

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2
Q

What is generalised management of Interstitial lung disease?

A
Remove cause
Home O2 when needed
Stop smoking
Physio and pulmonary rehab
Pneumococcal and flu vaccines
Advanced care planning
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3
Q

What is IPF?

A

Idiopathic Pulmonary fibrosis
Progressive fibrosis with no clear cause
Presents wih SOB and cough for 3 months

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4
Q

What is seen on examination with IPF?

A

Finger clubbing

Bibasal crackles

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5
Q

What slows IPF progression?

A

Pirfenidine (anti inflammatory)

Nintedanib (monoclonal ab)

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6
Q

Which drugs cause drug induced lung fibrosis?

A

Amiodarone
Cyclophosphamide
Methotrexate
Nitrofurantoin

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7
Q

What can pulmonary fibrosis occur secondary to?

A

A1ATD
RA
SLE
SS

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8
Q

What is hypersensitivity Pneumonitis?

A

Type 3 hypersensitivity
Parenchymal inflammation in those sensitive to allergen
Bronchoalveolar lavage shows raised lymphocytes an dmast cells

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9
Q

How is hypersensitivity pneumonitis managed?

A

Remove cause
Oxygen
Steroids

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10
Q

What are specific causes of hypersensitivity pneumonitis?

A

Bird fanciers lung
Farmers lung
Malt workers lung

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11
Q

Why would you test serum ACE?

A

Sarcoid

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12
Q

How would you test for Wegeners?

A

ANCA

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13
Q

What causes lesions in the upper lobe on CT?

A

Sarcoid, EAA, Silicosis

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14
Q

WHat causes lesions in the lower lobe on CT?

A

IPF, DIP, Asbestososis

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15
Q

What causes central lesions on CT?

A

Sarcoid

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16
Q

What is the morphological appearance of IPF?

A

linear and reticular

Honeycomb lung

17
Q

How would you treat rheumatoid lung disease?

A

Cyclophosphamide

Rituximab

18
Q

When do you treat sarcoid and with what/

A

Late

Prednisolone