Interstitial Lung Disease Flashcards

(23 cards)

1
Q

What is interstitial lung disease?

A

Group of diseases which all cause inflammation and eventually fibrosis of pulmonary interstitium

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2
Q

What is the pulmonary interstiitum?

A

Thin tissue surrounding alveoli

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3
Q

Symptoms of interstital lung disease?

A

Chronic dry cough
SOB
Fatigue

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4
Q

Examples of interstitial lung disease?

A

Idiopathic pulmonary fibrosis

Secondary pulmonary fibrosis

Hypersensitivity pneumonitis

Cryptogenic organising pneumonia

Asbestosis

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5
Q

What are the most common forms of interstitial lung disease?

A

Idiopathic pulmonary fibrosis (most common)

Hypersensitivity pneumonitis (2nd common)

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6
Q

What conditions are associated with ILD?

A

Connective tissue disorders, e.g. systemic sclerosis

Rheumatoid arthritis

Alpha 1 antitrypsin deficiency

Sarcoidosis

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7
Q

Diagnosis for ILD?

What are the findings?

A

Spirometry - normal, OR restrictive pattern of FEV1/FVC ratio greater than 0.7

HRCT (GOLD STANDARD) - ground glass appearance, traction bronchiectasis

CXR - nodular and reticular shadowing

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8
Q

General management of all interstitial lung disease?

A

Treat the underlying cause

Home oxygen

Stop smoking

Physiotherapy and pulmonary rehabilitation

Pneumococcal and flu vaccine
Advanced care planning and palliative care

Lung transplant

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9
Q

What is idiopathic pulmonary fibrosis?

Who is it more common in?

Symptoms of IPF?

Prognosis?

A

Progressive fibrotic lung disease of unknown origin

Older patients (mean: 74) and smokers

Insidious onset of cough and SOB > 3 months
Bibasal end inspiratory FINE crackles
Clubbing

2-5 year survival rate from diagnosis

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10
Q

What drugs can cause secondary pulmonary fibrosis?

A

Amiodarone (also causes grey/blue skin)
Cyclophosphamide
Methotrexate
Nitrofurantoin

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11
Q

Characteristic finding on HRCT for idiopathic pulmonary fibrosis?

A

Peripheral basal honeycombing

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12
Q

Management of idiopathic pulmonary fibrosis?

A

Pirfenidone
Nintedanib

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13
Q

MoA of nintedanib in treating IPF?

A

tyrosine kinase inhibitor

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14
Q

If HRCT or spirometry don’t show a clear diagnosis for ILD what other investigations can you do?

A

Lung biopsy
Bronchoalveolar lavage

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15
Q

What is hypersensitivity pneumonitis?
What hypersensitivity reaction is it?

A

Type III and IV hypersensitivity reaction to an inhaled allergen, leading to inflammation and damage to lung tissue

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16
Q

Investigation for hypersensitivity pneumonitis?

Management?

A

Bronchoalveolar lavage - airways washed with saline and fluid analysed for presence of lymphocytes

Remove allergen, oxygen, steroids

17
Q

Examples of hypersensitivity pneumonitis?

A

Bird-fancier’s lung - bird droppings

Farmer’s lung - mouldy spores in hay

Mushroom worker’s lung - specific mushroom antigens

Malt worker’s lung - mould on barley

18
Q

What is Cryptogenic Organising Pneumonia?

Signs and symptoms of it?

Findings on CXR?

Definitive diagnosis?

Management?

A

Focal lung inflammation - idiopathic or infection/inflammation/medications/radiation/environmental triggers

Symptoms and CXR findings same as pneumonia

Lung biopsy- definitive diagnosis

Management - corticosteroids

19
Q

What is asbestosis?

A

Lung fibrosis related to asbestos exposure. It is oncogenic (causes cancer)

20
Q

Complications of asbestosis

A

Fibrosis
Pleural thickening and plaques
Adenocarcinoma
Mesothelioma

21
Q

What must happen to all deceased patients with asbestosis?

A

Referred to the coroner

Patients are eligible for compensation.

22
Q

Causes of upper zone lung fibrosis?

A

Coal workers pneumoconiosis
Hypersensitivity pneumonitis
Ankylosing spondyliytis
Radiation
Tuberculosis
Sarcoidosis/Silicosis

CHARTS mnenomic

23
Q

What are the spirometry findings for ILD vs Asthma? (TLCO, FEV1/FVC)

A

ILD
FEV1/FVC ratio > 0.7
TLCO decreased

Asthma
FEV1/FVC ratio < 0.7
TLCO increased/normal