Miller Pneumonia and ARDS Flashcards

1
Q

What are the most frequent pathogens for HAP and VAP?

A

P. aeruginosa and S. aureus

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2
Q

In aspiration pneumonia, what is the common pathogen?

A

Gram negative bacilli such as E.coli K. pneumonia and P.aeruginosa

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3
Q

Clinical presnetation of pneumonia?

A
  • Cough
  • Breathlessness
  • Chest pain
  • Sputum
  • Fatigue
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4
Q

With pneumonia, what two symptoms can predict outcome?

A
  • Delirium has an increased risk of mortality
  • Pleuritic chest pain has increased risk of pleural effusion
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5
Q

Diagnosis of pneumonia?

A
  • LRTI with acute onset
  • New infiltrates on CXR
  • ID cause if admitted to hospital
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6
Q

Treatment of non severe CAP Pneumonia?

A
  • Beta lactam + Macrolide
  • or respiratory fluoroquinolone alone
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7
Q

Treatment of severe CAP?

A
  • Beta lactam + Macrolide
  • Beta lactam + respiratory fluoroquinolone
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8
Q

If a patient has severe CAP and are recently hospitalized and have a risk for MRSA, what should be added to their treatment?

A

Vancomycin

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9
Q

If patient with severe CAP is hospitalized nd at risk of psuedomonas what should be added?

A

Piperacillin-tazobactam

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10
Q

If aspiration is a worry in a patient with severe CAP and have poor dentition, what should be added to their treatment?

A

Broad coverage beta lactam such as ampicillin-sulbactam or quinolone

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11
Q

Adjunctive therapies for cap?

A
  • Corticosteroids restricted to patients with severe CAP
    • must rule out flu
  • Oxygen
  • Non invasive ventilation if needed
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12
Q

Complications of pneumonia?

A
  • increased short term and long term risk of cardiovascular disease
  • decline in cognition and functional status
  • Increased susceptibility for infection
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13
Q

How do we prevent pneumonia?

A

Pneumococcal and influenza vaccines

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14
Q

Most common conditiosn with pleural effusion?

A
  • HF
  • Bacterial pneumonia
  • Pulmonary embolism
  • Malignancy
  • Viral disease
  • Post cardiac surgery

all are exudative except heart failure

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15
Q

What is sensitive and specific for diagnosing effusion?

A

Dullness to percussion

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16
Q

How do you treat pleural effusions?

A
  • Thoracentesis
17
Q

What is light’s criteria?

A
  • 99.5% sensitive for diagnosing exudative effusion and differentiates exudative from transudative effusions
  • Pleural fluid protien to serum protein ratio >0.5
  • pleural fluid LDH to serum LDH >0.6
  • Pleural LDH >0.67 upper limit normal for serum LDH
  • If fluid is below it is transudate
  • If fluid levels are above its exudate
18
Q

Risks for ARDS?

A
  • Old age
  • Alcohol abuse
  • Cigarettes
  • Air pollution
  • Hypoalbuminemia
  • Trauma
  • Men > Women
  • Black/latino > white
19
Q

What is happening with ARDS?

A
  • Increase permeability of capillaries and lung tissue
  • Leads to interstitial edema which moves to alveolil
  • more dead space in the lung and decreased compliance due to inflammatory debris
  • Proliferative phase (healing)
  • Fibrotic phase (some enter)
20
Q

Clinical presentation of ARDS?

A
  • Dyspnea
  • Moderate or severe respiratory distress
  • Elevated RR tachy decreased O2
  • Differentiate from HF, Pneumonia, IPF
21
Q

How do you treat ARDS?

A
  • Supportive
  • Diagnose and tx infection
  • respiratory support
  • fluid management
  • rescue therapies such as ECMO, NO, glucocorticoids
22
Q

Complications of ARDS?

A
  • Most recover near normal pulmonary function within 6-12 months
  • decrement in physical function
  • neurocognitive and mood disorders
  • PTSD