PNEUMONIA 2 Flashcards

1
Q

Risk Stratification: Low Risk CAP

Therapy: W/o Comorbid illness

A

Amoxicillin or

Extended macrolides: azithromycin or clarithromycin

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2
Q

Risk Stratification: Low Risk CAP

Therapy: W/ stable Comorbid illness

A
  • B-lactam combination or
    2nd gen cephalosporin +/- extended macrolides
  • Co amoxiclav or sultamicillin or
    Cefuroxime axetil +/- azithromycin or clarithromycin
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3
Q

Risk Stratification: Moderate Risk CAP

Therapy:

A
  • IV non-antipseudomonal β-lactamd (BLIC, cephalosporin)
    + extended macrolidesa
    or
    respiratory fluoroquinolonese (PO)
- Ampicillin-Sulbactam IV OR
Cefuroxime IV OR
Ceftriaxone  OD 
\+
Azithromycin PO OR
Clarithromycin BID PO OR
Levofloxacin PO OR
Moxifloxacin OD PO
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4
Q

Risk Stratification: Moderate Risk CAP
If aspiration pneumonia is suspected.
Therapy:

A

A regimen containing ampicillin-sulbactam and/or moxifloxacin is used,

there is no need to add another antibiotic for additional anaerobic coverage.

If another combination is used may add clindamycin to the regimen to cover microaerophilic streptococci.

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5
Q

Risk Stratification: High Risk CAP

Therapy: No risk for P. aeruginosa

A
  • IV non-antipseudomonal β-lactam
    + IV extended macrolidesa
    or
    IV respiratory fluoroquinolonese
  • Ceftriaxone OD OR
    Ertapenem OD + Azithromycin dihydrate OD IV OR
    Levofloxacin OD IV OR
    Moxifloxacin OD IV
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6
Q

Risk Stratification: High Risk CAP

Therapy: Risk for P. aeruginosa

A
  • IV antipneumococcal antipseudomonal β-lactam (BLIC, cephalosporin or carbapenem) + IV extended macrolidesa
    + aminoglycoside Piperacillin-tazobactam
    OR
    Cefepime 8-12h
    OR
    Meropenem q8h + Azithromycin dihydrate OD IV + Gentamicin OD OR
    Amikacin OD
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7
Q

Risk Stratification: High Risk CAP

Therapy: MRSA pneumonia is suspected

A
Vancomycin q8-12 h
OR
Linezolid q12h IV
OR
Clindamycin q8h IV
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8
Q

Indications For Streamlining of Antibiotic Therapy

  1. Resolution of ___ for > 24 hours
  2. Less ___ & resolution of respiratory distress (normalization of respiratory rate)
  3. Improving ____, no bacteremia.
  4. Etiologic agent is not a ___ (virulent/resistant) pathogen e.g. Legionella, S. aureus or Gram-negative enteric bacilli
  5. No _____ such as myocardial infarction, congestive heart failure, complete heart block, new atrial fibrillation, supraventricular tachycardia, etc.
  6. No sign of organ dysfunction such as ____
  7. Patient is clinically ___, taking oral fluids and is
    able to take oral medications
A
  1. fever
  2. cough
  3. white blood cell count
  4. high-risk
  5. unstable comorbid condition or life-threatening complication
  6. hypotension, acute mental changes, BUN to creatinine ratio of >10:1, hypoxemia, and metabolic acidosis
  7. hydrated
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9
Q
A significant pleural effusion should be tapped if
– fluid pH
– glucose level 
– lactate dehydrogenase concentration  
– bacteria
A

– fluid has a pH of <7
– glucose level of <2.2 mmol/L
– lactate dehydrogenase concentration of >1000 U/L
– bacteria are seen or cultured

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10
Q

During the 24 hours before discharge, the patient should have the following characteristics (unless this represents the baseline status):

  1. Temperature
  2. Pulse
  3. Respiratory rate
  4. Systolic BP
  5. Blood oxygen saturation
  6. gastrointestinal tract
A
  1. Temperature of 36-37.5C
  2. Pulse < 100/min
  3. Respiratory rate between 16-24/minute
  4. Systolic BP >90 mmHg
  5. Blood oxygen saturation >90%
  6. Functioning gastrointestinal tract
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11
Q

FOLLOW-UP
■ Fever and leukocytosis usually resolve
■ Chest radiographic abnormalities are slowest to resolve
■ Follow-up radiograph

A

■ Fever and leukocytosis usually resolve within 2–4 days
■ Chest radiographic abnormalities are slowest to resolve (4–12 weeks)
■ Follow-up radiograph ~4–6 weeks later is recommended.

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12
Q
Follow Up CPG:
■ 1 week:  
■ 4 weeks: 
■ 6 weeks: 
■ 3 months: 
■ 6 months:
A

■ 1 week: fever should have resolved
■ 4 weeks: chest pain and sputum production should have substantially reduced
■ 6 weeks: cough and breathlessness should have substantially reduced
■ 3 months: most symptoms should have resolved but fatigue may still be present
■ 6 months: most people will feel back to normal.

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13
Q

Prevention of CAP

A

■ pneumococcal polysaccharide vaccine (PPSV23)
– contains capsular material from 23 pneumococcal serotypes
■ protein conjugate pneumococcal vaccine (PCV13)
– produces T cell–dependent antigens that result in long-term immunologic memory
■ Influenza vaccine
– available in an inactivated or recombinant form

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14
Q

MDR Pathogens/ Microbiologic Causes of Ventilator- Associated Pneumonia

A
  • P. aeruginosa
  • MRSA
  • Acinetobacter spp.
  • ARE (Antibiotic-resistant Enterobacteriaceae
    ESBL-positive strains an Carbapenem-resistant strains
  • Legionella pneumophila
  • Burkholderia cepacia
  • Aspergillus spp.
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15
Q

Three factors are critical in the pathogenesis of VAP:

A

– colonization of the oropharynx with pathogenic microorganisms,
– aspiration of these organisms from the oropharynx into the lower respiratory tract,
– compromise of normal host defense mechanisms.

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16
Q

Complications of VAP

A

■ Prolongation of mechanical ventilation, with corresponding increases in the duration of ICU stay and hospitalization
■ Necrotizing pneumonia
■ Death

17
Q

Prognosis of VAP

A

■ crude mortality rates as high as 50–70%
■ MDR pathogens are associated with significantly greater attributable mortality than
non-MDR pathogens.

18
Q

Prevention of VAP

A

■ Most important preventive intervention is to avoid intubation or minimize its duration.
■ Daily holding of sedation and formal weaning protocols
■ Minimizing microaspiration around the endotracheal tube cuff
– Elevating the head of the bed (at least 30° above horizontal but preferably 45°)
■ Specially modified endotracheal tubes that allow removal of the secretions pooled above the cuff

19
Q

in non-intubated patients—both inside and outside the ICU—is similar to VAP
■ Higher frequency of non-MDR pathogens and the generally better underlying host immunity in
non-intubated patients

A

HOSPITAL-ACQUIRED PNEUMONIA

20
Q

the only pathogens that may be more common in the non-VAP population
– Specific therapy targeting it probably is not needed since many of the recommended antibiotics are active against it

A

Anaerobes