ILD Flashcards
What are the most common identifiable causes of ILD?
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
What is ILD?
A collective number of diseases that injure the lung parenchyma.
Based on injury to tissue and the lungs poor attempt to repair it.
How is ILD classified?
Those with identifiable causes and those that are idiopathic.
What are the idiopathic causes of ILD?
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
What is the management of ILD?
Identify and treat the cause Prednisolone Stop smoking Home oxygen Pulmonary rehab
Azathioprine for connective tissue disease? DMARD
Cyclophosphamide decreases immune systems response?
PREDNISOLONE
Clinical presentation of ILD?
Progressive SOB on exertion Persisting non-productive cough History of exposure Abnormal CXR Restrictive PFTs Respiratory symptoms in background of connective tissue disease
What is farmers lung?
Hypersensitivity pneumonitis from inhalation of hay dust and mold spores and other agricultural products.
What is sarcoidosis?
Involves abnormal collections of inflammatory cells (granulomas) that form nodules in organs.
What is the cause of sarcoidosis?
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.
What is BOOP?
Bronchiolitis obliterans organising pneumonia is a non-infectious pneumonia.
An inflammation of the bronchioles.
What investigations of ILD?
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