Restrictive Thoracic disease Flashcards

1
Q

What is ILD? (DPLD)

A

(Interstitial lung disease) A general terms that includes many different conditions which affect a part of the lungs.

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2
Q

Name some restrictions to the thoracx due to causes out with the lungs? And what does it lead to?

A

Skeletal - curvature, ribs etc, cause restriction on the lungs to expand
Muscular - diaphragm paralysed, nerves not working etc
Abdominal obesity/Ascietes - compression of the thoracic contents.

Results in chronic alveolar under ventilation with low PaO2 and raised PaCO2 and reduced lung volumes

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3
Q

Name some restrictions to the thoracx due to causes within the lungs?

A

Acute DPLD - diffuse parenchymal lung disease
Chronic DPLD - due to occupational or environmental drugs/agents
Chronic DPLD - with evidence of systemic disease
Chronic DPLD - with no evidence of systemic disease

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4
Q

Describe DPLD? And its pathophysiology?

A

Diffuse parenchymal lung disease
Disease of the alveolar structures - alveolar wall/lumen (parenchyma)

It causes impaired alveolar gas exchange
Co2 exchanged unimpaired as alveolar ventilation normal
PaO2 decreases
PaCO2 stays the same

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5
Q

What is the aetiology of DPLD?

- fluid in the alveolar air spaces

A

Cardiac pulmonary oedema in the alveolar walls and lumen due to a raised pulmonary venous pressure = LVF

Non cardiac pulmonary oedema - normally pulmonary venous pressure, with leaky pulmonary capillaries, due to sepsis/trauma

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6
Q

What is the aetiology of DPLD?

- Consolidation of alveolar air spaces

A

Infective pneumonia - viral, bacterial, fungal
Infarction - PE, vasculitis
Other causes (BOOP) - rhematoid disease, drugs, idiopathic

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7
Q

What is the aetiology of DPLD?

- Inflam Infiltrate of alveolar walls (ie Alveolitis): Granulomatous-alveolitis

A

Extrinsic - allergic alveolitis - famers lung, pigeons lung
Sarcoidosis - Multi system disorder, erythema nodosum
Drug induced alveoli’s - amiodarone, methotrexate
Toxic gas/fumes - chlorine
Fibrosisng alveoli’s - Rheumatoid
Autoimmune (multi-system) - SLE, Wegners, Churg-strauss

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8
Q

What is the aetiology of DPLD?

- dust disease (Pneumoconiosis)

A

Fibrogenic - asbestosis, silicosis

Non-fibrogenic - Iron etc

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9
Q

What is the aetiology of DPLD?

- carcinomatosis

A

Lympathic/blood spread

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10
Q

What is the aetiology of DPLD?

- eosinophilic

A

(type 3 allergic response)

Drugs, fungal, parasites

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11
Q

What is the clinical syndrome of DPLD?

A
Breathless on exertion
Cough but no wheeze
Finger clubbing
Inspiratory Lung crackles
Central cyanosis (if hypoxaemic)
Pulmonary fibrosis occurs as end stage response to chronic inflammation
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12
Q

What is the diagnosis of DPLD?

A
History 
Reduced lung volumes 
Reduced gas diffusion 
PaO2 decreased SaO2 decreased
Bilateral diffuse alveolar infiltrates on CXR
Ground glass appearance .... etc
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13
Q

Treatment of DPLD?

A

Remove trigger
Treat inflammation - i.e. ground glass appearance on HRTC immunosuppressants
Drugs….
Lung transplant for end stage

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14
Q

What is Alveolitis?

A

inflammation of the air sacs of the lungs.

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15
Q

What is pneuomonitis?

A

inflammation of the walls of the alveoli (air sacs) in the lungs.

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