ch 23 Flashcards

1
Q

Main feature of restrictive pulmonary disorders?

A

Decreased lung expansion.

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2
Q

Four classifications of restrictive disorders?

A

Lung parenchyma, pleura, chest wall, neuromuscular function.

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3
Q

PFT finding in restrictive disease?

A

Decreased vital capacity, TLC, diffusion capacity.

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4
Q

ABG findings in restrictive disease?

A

Low PaO2, normal/low PaCO2, increased pH.

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5
Q

Severity of disease linked to?

A

Degree of lung volume decrease.

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6
Q

Interstitial lung disease feature?

A

Thickened alveolar walls with fibrosis.

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7
Q

Untreated interstitial lung disease leads to?

A

Irreversible fibrosis.

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8
Q

Diffuse interstitial lung disease feature?

A

Alveolar wall thickening.

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9
Q

Diffuse interstitial lung disease pathogenesis?

A

Injury, inflammation, fibrosis, destruction.

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10
Q

Honeycomb lung?

A

Cystic air spaces from fibrosis.

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11
Q

Clinical signs of diffuse interstitial lung disease?

A

Progressive dyspnea, dry cough, clubbing.

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12
Q

Diffuse interstitial lung disease diagnosis?

A

PFTs, chest X-ray, biopsy.

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13
Q

Diffuse interstitial lung disease treatment?

A

Avoid cause, corticosteroids, immunosuppressants.

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14
Q

Sarcoidosis etiology?

A

Unknown, idiopathic granulomatous disease.

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15
Q

Acute vs chronic sarcoidosis?

A

Acute self-resolves; chronic progressive.

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16
Q

Sarcoidosis pathogenesis?

A

Immune granuloma formation in lungs/lymph nodes.

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17
Q

Sarcoidosis clinical signs?

A

Erythema nodosum, eye issues, cough, dyspnea.

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18
Q

Sarcoidosis diagnosis?

A

Chest X-ray, biopsy: noncaseating granulomas.

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19
Q

Sarcoidosis treatment?

A

Corticosteroids, immunosuppressants if needed.

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20
Q

ARDS meaning?

A

Acute respiratory distress syndrome.

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21
Q

ARDS key features?

A

Alveolar-capillary damage, severe hypoxemia.

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22
Q

ARDS causes?

A

Sepsis, trauma, pneumonia, aspiration.

23
Q

ARDS pathogenesis?

A

Inflammation, protein leakage, atelectasis.

24
Q

ARDS early signs?

A

Rapid breathing, dyspnea, low PaO2.

25
ARDS late signs?
Hypoxemia refractory to oxygen, crackles.
26
ARDS chest X-ray finding?
Diffuse white-out appearance.
27
ARDS treatment?
Mechanical ventilation with PEEP, treat cause.
28
Poliomyelitis virus attacks?
Motor neurons in spinal cord/brainstem.
29
US cases of polio yearly?
0 due to vaccination.
30
Polio clinical signs?
Fever, fatigue, paralysis.
31
ALS gender ratio?
Male > female.
32
ALS disease type?
Degenerative motor neuron disease.
33
ALS motor neuron targets?
Upper and lower motor neurons.
34
ALS progression?
Muscle weakness and wasting.
35
Duchenne muscular dystrophy?
X-linked hereditary muscle disorder.
36
Duchenne first muscle weakness?
Pelvic and shoulder muscles.
37
Respiratory involvement in Duchenne?
Occurs in 20s-30s, leads to failure.
38
Guillain-Barre syndrome feature?
Demyelination of peripheral nerves.
39
Guillain-Barre trigger?
Viral infection.
40
Guillain-Barre signs?
Ascending paralysis, respiratory weakness.
41
Myasthenia gravis hallmark?
Weakness of voluntary muscles.
42
Myasthenia worsens with?
Activity.
43
Myasthenia improves with?
Rest.
44
Myasthenia cause of failure?
Respiratory muscle weakness.
45
Pneumonia site?
Lung parenchyma infection.
46
Pneumonia causes?
Bacteria, viruses, fungi, aspiration.
47
Nosocomial pneumonia?
Hospital-acquired lung infection.
48
High-risk pneumonia groups?
Elderly, chronically ill, hospitalized.
49
Pneumonia pathogenesis?
Inflammation, alveolar filling.
50
Pneumonia type without exudate?
Viral pneumonia.
51
Pneumonia symptoms?
Cough, fever, dyspnea, chest pain.
52
Pneumonia diagnosis?
Chest X-ray, sputum culture, CURB-65 score.
53
CURB-65 used for?
Assessing pneumonia severity.
54
Pneumonia treatment?
Antibiotics, oxygen, fluids.