Pulmonary Flashcards

1
Q

Alveolar O2 formula?

Normal A-a gradient?

A

PAO2 = 713*FiO2 - PaCO2/0.8
On room air (21% O2), this is:
PAO2 = 150 - PaCO2/0.8

Normal A-a gradient is <15 mm Hg.
Increases with aging but should always be <30 mm Hg

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2
Q

Light criteria for an exudative effusion

A

At least one of:

  • Pleural fluid protein / serum protein ratio > 0.5
  • Pleural fluid LDH / serum LDH ratio > 0.6
  • Pleural fluid LDH > 2/3 the upper limit of normal for serum LDH
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3
Q

How can the severity of ARDS be graded?

A

PaO2 / FiO2 (P/F) ratio:
<100: Severe
<101-200: Moderate
<201-300: Mild

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4
Q

O2 saturation goal in ARDS

A

88-95% saturation (PaO2 55-80)

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5
Q

Extrapulmonary involvement of sarcoidosis (5)

A
  1. Skin lesions (e.g. erythema nodosum)
  2. Uveitis
  3. Arthralgias
  4. Hypercalcemia
  5. Heart disease
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6
Q

Hypoxia with a petechial rash and neurological signs after trauma

A

Fat embolism from long-bone fracture to lungs

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7
Q

Mechanism of secondary spontaneous pneumothorax

A

Rupture of alveolar blebs due to chronic destruction of alveolar sacks

(seen in chronic lung disease like COPD and CF)

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8
Q

Sensory complication of aspirin-induced respiratory disease

A

Anosmia (due to nasal polyps from chronic rhinosinusitis)

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9
Q

When is long-term suppelemntal oxygen started in COPD?

A

SaO2 < 89% (PaO2 55 mm Hg) ORA in patients with cor pulmonale, right heart failure, or hematocrit >55%

SaO2 <88% (PaO2 <59 mm Hg) ORA in anyone else

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10
Q

Treatment for all acute COPD exacerbations?

Moderate-to-severe? How is this defined?

A
  1. Oxygen (to SpO2 of 88-92%)
  2. Inhaled bronchodilators
  3. Systemic glucocorticoids

Moderate-to-severe: add antibiotics

Moderate-to-severe: at least 2 cardinal symptoms (increased dyspnea, increased sputum volume, incerased sputum purulence) or need for NPPV or intubation

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11
Q

Cardinal symptoms of COPD exacerbation

A
  1. Increased dyspnea
  2. Increased sputum volume
  3. Increased sputum purulence
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12
Q

Cause of panacinar emphysema in a young person?

Manifestation outside the lung

A

Alpha-1-antitrypsin (AAT) deficiency

Also leads to liver disease (e.g. hepatitis, cirrhosis, HCC)

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13
Q

Rare but specific signs of PE on CXR (3)

A

Westermark’s sign: area of hyperlucency distal to a visible pulmonary vessel

Hampton’s hump: peripheral wedge of lung opacity due to infarct

Fleischner sign: enlarged pulmonary artery

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14
Q

Rare but classic sign of PE on EKG

A

S1Q3T3:

  • Deep S wave in I
  • Q wave in III
  • Inverted T wave in III
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15
Q

Rapidly progressing, necrotizing post-influenza pneumonia in a young person

A

Staph aureus

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16
Q

First-line treatment for community acquired pneumonia

A

No recent antibiotics or major comorbidities: macrolide (e.g. azithromycin) or doxycycline

With recent antibiotics or comorbidities: add a beta-lactam (e.g. ceftriaxone), or just use a respiratory fluoroquinolone (e.g. levofloxacin or moxifloxacin)

17
Q

Tool for predicting community-acquired pneumonia severity and management:

A
CURB-65: one point for each of
Confusion
Urea >20
Respirations >30
BP low (systolic <90, diastolic <60)
65 years or older

0: low mortality, outpatient
1-2: Intermediate mortality, likely admission
3 or more: high mortality, urgent admission

18
Q

Treatment options for pneumonia when aspiration suspected

A
  • Amp/sulbactam (IV if inpatient) or amoxicillin/clavulanate (PO if outpatient)
  • Clindamycin
  • Metronidazole + amoxicillin or penicillin
19
Q

Most common organisms for ventilator-associated pnuemonia

A

Gram-negative rods (Pseudomonis, E. coli, Klebsiella pneumonia) or gram positive cocci (Strep and Staph aureus)

20
Q

Pneumonia associated with hyponatremia

A

Legionella (damage to JG cells that secrete renin)

21
Q

Treatment for Legionella

A

Fluoroquinolones (levofloxacin) or macrolides (azithromycin)

22
Q

Specific symptoms of Pancoast tumors

A
  1. Referred shoulder pain
  2. Horner symptom (sympathetic chain invasion)
  3. Brachial plexus invasion leading to arm motor and sensory symptoms
  4. Supraclavicular lymph node
23
Q

Paraneoplastic syndrome(s) associated with lung SCC

A

Hypercalcemia (PTHrp)

24
Q

Paraneoplastic syndrome(s) associated with small cell lung cancer

A
  1. Cushing syndrome (ACTH production)
  2. SIADH
  3. Lam`bert-Eaton myasthenic syndrome (antibodies against NMJ Ca2+ channels)
25
Q

Lung cancer most associated with necrotizing and cavitation on CT

A

SCC