ILD Flashcards

0
Q

What are the most common identifiable causes of ILD?

A
Exposure to occupational and environmental agents 
- dusts: silica, asbestos, coal
- metals: tin, aluminium, titanium, iron 
Drug induced 
- methotrexate 
- amiodarone
- radiation
- chemotherapy 

Connective tissue diseases
- SLE - RA - SCLERODERMA

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1
Q

What is ILD?

A

A collective number of diseases that injure the lung parenchyma.

Based on injury to tissue and the lungs poor attempt to repair it.

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2
Q

How is ILD classified?

A

Those with identifiable causes and those that are idiopathic.

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3
Q

What are the idiopathic causes of ILD?

A

Sarcoidosis
Cryptogenic pneumonia/Bronchiolitis obliterans organising pneumonia not Bronchiolitis obliterans (different BOOP and BO)
Idiopathic Interstitial pneumonias which is made up of
- idiopathic pulmonary fibrosis
- acute interstitial pneumonia
- desquamative interstitial pneumonia

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4
Q

What is the management of ILD?

A
Identify and treat the cause 
Prednisolone
Stop smoking
Home oxygen 
Pulmonary rehab 

Azathioprine for connective tissue disease? DMARD
Cyclophosphamide decreases immune systems response?
PREDNISOLONE

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5
Q

Clinical presentation of ILD?

A
Progressive SOB on exertion 
Persisting non-productive cough 
History of exposure 
Abnormal CXR 
Restrictive PFTs
Respiratory symptoms in background of connective tissue disease
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6
Q

What is farmers lung?

A

Hypersensitivity pneumonitis from inhalation of hay dust and mold spores and other agricultural products.

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7
Q

What is sarcoidosis?

A

Involves abnormal collections of inflammatory cells (granulomas) that form nodules in organs.

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8
Q

What is the cause of sarcoidosis?

A

Unknown, theory is in genetically susceptible individuals you get an altered immune response after exposure to an enviro, occupational or infectious agent.

Diagnosis of exclusion. Rule out TB with acid-fast bacilli.

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9
Q

What is BOOP?

A

Bronchiolitis obliterans organising pneumonia is a non-infectious pneumonia.

An inflammation of the bronchioles.

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10
Q

What investigations of ILD?

A

LAB:
CBE EUC LFTs

PFTs - restrictive picture
Antibodies for connective tissue disorders - RA (RF, anti-CCP), SLE (ANA +- anti-dsDNA), scleroderma (anti-topoisonerase),

CXR?

HRCT - ground glass appearance in early ILD, honeycomb in late (pulm. Fibrosis)

RHF - ECG, ECHO

BRONCHOALVEOLAR LAVAGE via bronchoscope, if not biopsy

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