Restrictive Thoracic disease Flashcards

1
Q

What causes outwith the lungs cause restriction?

A
  1. Skeletal (eg spinal curvature/ traumatic multiple rib fracture)
  2. Muscle weakness in Intercostal muscles/diaphragm (myopathy/neuropathy/meylopathy)
  3. Abdominal obesity/ ascites/ pregnancy
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2
Q

What does type II respiratory failure cause?

A

hypo-ventilation
low PaO2
reduced lung volumes

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3
Q

Aa barrier means?

A

Alveolar-arterial barrier

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4
Q

Which gas can be easily passed through the Aa barrier?

A

CO2

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5
Q

DPLD is an example of disease in which lung structure?

A

Alveoli

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6
Q

DPLD does what to partial pressures in the alveoli?

A

decreased PaO2

normal CO2

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7
Q

What is the most common cause of fluid in the alveolar air spaces?

A

Cardiac pulmonary oedema

raised pulmonary venous pressure

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8
Q

Non cardiac pulmonary oedema is due to?

A

leaky pulmonary capillaries

sepsis/trauma

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9
Q

Consolidation is?

A

when alveolar air space becomes filled with infection

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10
Q

What can cause infective consolidation pneumonia?

A

viral
bacterial
fungal
parasites

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11
Q

Pulmonary emboli and vasculitis can cause?

A

Pulmonary Infarction

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12
Q

other causes of BOOP? (broncheolitis oblierans organising pneumonia)

A

rheumatoid disease
drugs
cryptogenic

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13
Q

Extrinsic allergic alveolitis is which type of reaction?

A

IgG mediated type 3 hypersensitivity pneumonitis reaction

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14
Q

farmers lung and avian flu are an example of?

A

Extrinsic- allergic- alveolitis

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15
Q

what are the two branches of granulomatous alveolitis?

A
  1. extrinsic allergic alveolitis

2. sarcoidosis

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16
Q

What is sarcoidosis?

A

multi-system disease
rash on legs
inflammation in eyes/heart/nerves
Granulomatous alveolitis in lungs

17
Q

Drugs that induce alveolitis?

A

amiodarone

bleomycin/methotrexate

18
Q

what is pulmonary fibrosis?

A

An alveolitis that lays down collagen in the alveolar wall (simultanously to neutrophilic response)

19
Q

What conditions are pulmonary fibrosis associated with?

A

idiopathic pulmonary fibrosis

rheumatoid

20
Q

Pneumoconiosis is?

A

dust disease

21
Q

Fibrogenic pneumoconiosis examples?

A

Asbestosis

Silicosis

22
Q

Non-fibrogenic pneumoconiosis examles?

A

siderosis
stanosis
baritosis

23
Q

Cancers associated with carcinomatosis?

A
adenocarcinomas-
bronchus
breast
prostate
colon
stomach
24
Q

where are eosinophils in DPLD?

A

lung tissue

25
Q

clinical symptoms and signs of DPLD?

A
Breathless on exertion
cough-no wheeze
Finger clubbing
Inspiratory lung crackles
Central cyanosis (if hypoxaemic)
Pulmonary fibrosis at end stage
26
Q

Diagnosis of DPLD?

A
History
Reduced lung volumes
(decreased FEV1 and FVC)
Reduced gas diffusion (DLCO)
Arterial oxygen desaturation 
(decreased PaO2 and SaO2)
Presence of specific antibodies
Serum ACE and Ca in sarcoid
Bilateral diffuse alveolar infiltrates on CXR
ECG to diagnose secondary pulmonary hypertension
Bronchoalveolar lavage or induced sputum (exclude pneumocystis/TB etc.)
Transbronchial/ thorascopic lung biopsy
27
Q

treatment DPLD?

A

remove trigger factor
immuno-suppressives for alveolitis (danger of secondart infection)
corticosteroids (higher doeses than asthma)
Anti-fibrotic drugs (pirfenidone, nintedaninb)
O2 if hypoxic
LUNG TRANSPLANT

28
Q

Should inhaled steroids be used for DPLD?

A

NO!

29
Q

what do drugs like pirfenidone and nintedanib do?

A

prevent any further fibrosis of lungs

30
Q

ground glass reversible inflammation can be treated with?

A

corticoteroids