Clinical features and Management of Restrictive Lung Diseases Flashcards

1
Q

What is the physiological definition of restriction?

A

Forced vital capacity of less than 80% of predicted normal

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2
Q

Look

A
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3
Q

What is the marker of restrictino?

A

Vital capacity - spirometry

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4
Q

What are the lung causes of Interstitial lung diseases?

A
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5
Q

What are the possible routes of restriction?

A
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6
Q

What are the pleural causes of restrictive lung disease?

A

Pleural effusion

Pneumothorax

Pleural thickening - asbestos related, pneumonia

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7
Q

What are the skeletal causes of restrictive lung diseases?

A

Kyphoscoliosis

Ankylosing spondylitis

Thoracoplasty

Rib fractures - soreness

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8
Q

What are the muscular casues of restrictive lung disease?

A

Amyotrophic lateral sclerosis

Obesity - sub diaphragmatic - diaphragm can’t fall properly

Pregnancy - sub diaphragmatic

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9
Q

What is the interstitium?

A
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10
Q

What is sarcoidosis?

A

Multisystem granulomatous disease of unknown cause

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11
Q

What is the Histological hallmark of Sarcoidosis?

A

non-caseating granuloma

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12
Q

What are the clinical signs of sarcoidosis?

A

Erythema nodosum - granulomas often locate to scar tissue

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13
Q

Who gets sarcoidosis?

A
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14
Q

How do you investigate sarcoidosis?

A

History and exam

CXR

Bronchoscopy including transbronchial biopsies and endobronchial ultrasound

Pulmonary function tests

Bloods / urinalysis / ECG / TB skin test / eye exam

Surgical Biopsies (Mediastinoscopy, Video assisted thoracoscopic lung biopsy (VATS))

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15
Q

Look at chest x - rays

A

.

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16
Q

Look at the different stages as presented on these chest X-Rays

A
17
Q

When would you provide no treatment for Sarcoidosis?

A

Mild disease, no vital organ involvement, normal lung function, few symptoms

18
Q

When would you treat sarcoidosis with NSAIDS?

A

Erythema nodosum / arthralgia

19
Q

When would you treat sarcoidosis with Topical steroids?

A

Skin lesions / anterior uveitis / cough

20
Q

When would you treat sarcoidosis with Systemic Steroids?

A

Cardiac, neurological, eye disease not responding to topical Rx, hypercalcaemia

21
Q

What is prognosis?

A

Few Caucasian’s die (<1%)

10-20% sustain permanent pulmonary or extra-pulmonary complications

Respiratory

»Progressive respiratory failure

»Bronchiectasis

»Aspergilloma, haemoptysis, pneumothorax

22
Q

What is the typical presentation for idiopathic pulmonary fibrosis?

A
23
Q

How does fibrotic tissue vary in the lung?

A

Usually most prominent in peripheral tissue, central tissue is usually unaffected - worsens as severity of the condition increases

24
Q

What are the options for Idiopathic pulmonary fibrosis?

A
25
Q

What initiates hypersensitivity pneumonitis?

A

Allergens from things like, pigeons, mould, farms etc

26
Q
A