Community Acquired Pneumonia Flashcards

1
Q

Define pneumonia

A

A Lower RTI

Infection of lung parenchyma (bronchioles & alveoli); microbes proliferate in the alveolar level

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2
Q

Describe the pathogenesis of pneumonia

A

1) Aspiration of oropharyngeal secretions
2) Inhalation of aerosols (droplets may contain bacteria)
3) Hematogenous spreading (via bloodstream) from infection @ other body sites

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3
Q

What are the typical signs & symptoms of Pneumonia?

A

1) Cough, chest pains, SOB, hypoxia
2) Fever> 38°C, chills
3) Tachypnea (>22 breaths per min)
4) Tachycardia (>90bpm)
5) Hypotension (SBP< 100)
6) Leukocytosis: WBC < 4x10^9 OR > 10x10^9
7) Fatigue, Change in mental status
8) anorexia (loss of appetite)
9) Nausea

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4
Q

Upon physical examination of a pneumonia patient, what can be observed?

A
  • Diminished breath sounds over the affected area

- Inspiratory crackles during lung expansion

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5
Q

What radiographic findings can be observed in pneumonia patients?

A

dense consolidations/ new infiltrates

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6
Q

What are 2 respiratory samples that can be used for culture?

A

Sputum, Lower RT samples

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7
Q

What is a limitation associated with each of the 2 types of respiratory samples used for culture?

A

Sputum: contaminated by oropharyngeal secretions

Lower RT samples: less contamination but invasive & require sedation (e.g. bronchoalveolar lavage)
**reserved for critically ill/ immunocompromised patients

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8
Q

What organisms do urinary antigen tests test for?

A

Strep pneumo, Legionella pneumophilia

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9
Q

Why are Urinary antigen tests not often used in the diagnosis of pneumonia?

A

1) only indicates exposure to the pathogen; not necessarily infection
2) Despite antibiotic treatment, may remain positive for days~ weeks

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10
Q

Define Community-Acquired Pneumonia

A

Onset of symptoms in community/ <48hrs after hospital admission

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11
Q

What are possible risk factors for CAP?

A

1) old age (>65y/o)
2) previous hospitalisation for CAP
3) Smoking
4) Comorbidities: COPD, DM, Heart Failure
5) immunosuppression/ cancer

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12
Q

How can CAP be prevented?

A

1) smoking cessation
2) Immunization
- Influenza (post-influenza viral pneumonia is a serious complication)
- Pneumococcal (pneumococcus is a common pathogen)

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13
Q

What are the common microbes causing outpatient CAP?

A

1) Strep pneumo
2) H. influenzae
3) Atypicals (Mycoplasma pneumoniae, chlamydophila pneumoniae)

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14
Q

Suggest suitable antibiotic options for outpatient treatment of patients who are generally healthy

A

First line: Amoxicillin

Penicillin Allergy: Resp FQ (Levo/Moxifloxacin)

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15
Q

Why is Respiratory FQ not used as first-line therapy?

A

1) extensive ADRs (e.g. tendonitis, neuropathy, QT prolongation, CNS disturbances etc)
2) Collateral damage; resistance with overuse
3) Preserved for P. aeruginosa coverage (only PO agent for P. aeruginosa) & Pencillin allergy

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16
Q

Which groups of outpatient patients warrant a different antibiotic regimen?

A

Those with weakened immunity:

  • chronic heart/ lung/ liver/ renal disease
  • DM
  • alcoholism
  • malignancy
  • asplenia
17
Q

Suggest suitable antibiotic options for outpatient treatment of patients who have weakened immunity/ comorbidities.

A

First line: β-lactam (Augmentin/ cefuroxime) + Macrolide(C/A)/ Doxycycline

Penicillin allergy: Resp FQ (Levo/Moxifloxacin)

18
Q

What are the common microbes causing non-severe inpatient CAP?

A

1) Strep pneumo
2) Haemophilus influenza
3) Atypicals (Mycoplasma pneumoniae, chlamydophila pneumoniae, Legionella pneumophilia)

19
Q

Suggest suitable empiric therapy for non-severe inpatient CAP

A

First line: (IV; macrolide/doxy given PO if possible)
Augmentin/ Ceftriaxone + Macrolide/Doxycycline

Penicillin Allergy: Resp FQ

20
Q

What are the criteria for deciding if a patient has severe CAP? What are the requirements for severe CAP?

A

Major:

  • Mech ventilation
  • Septic shock

Minor:

1) RR ≥30 breaths per min
2) PaO2/FiO2 ≤ 250
3) Multilobal infiltrates
4) Confusion/ disorientation
5) Urea > 7 mmol/L
6) WBC < 4x10^9 /L (leukopenia)
7) Temp < 36°C (hypothermia)
8) Hypotension req aggressive fluid resuscitation (SBP<90 or DBP≤60)

Severe CAP = ≥1 major criteria OR ≥3 minor criteria

21
Q

What are the common microbes causing severe inpatient CAP?

A

1) Strep pneumo
2) Haemophilus influenza
3) Atypicals (Mycoplasma pneumoniae, chlamydophila pneumoniae, Legionella pneumophilia)
4) MRSA
5) Gram neg bacilli:
Klebsiella,
Burkholderia pseudomallei (found in contaminated soil; causes melioidosis; pneumonia is a common presentation)

22
Q

Suggest suitable empiric therapy for severe inpatient CAP

A

First-line (IV):
Augmentin/ Ceftazidime + Macrolide/ Doxy

Alternative: Resp FQ + ceftazidime (Burkholderia coverage)
** if patient has severe penicillin allergy, may remove ceftazidime

23
Q

When is anaerobic coverage indicated in inpatient CAP?

A

Presence of lung abscess/ empyema (pus in pleural space)

24
Q

What are the common anaerobes involved in inpatient CAP?

A
  1. Bacteroides fragilis
  2. Prevotella
  3. Porphyromonas
  4. Fusobacterium
25
Suggest appropriate modifications to the inpatient treatment regimen to account for anaerobic coverage
If std regimen does NOT HAVE ANAEROBIC COVERAGE, Add: Clinda PO/IV or Metronidazole PO/IV **Augmentin & moxifloxacin have anaerobic coverage
26
When is MRSA coverage indicated in inpatient CAP?
1) Prior MRSA in the lung in last 1 year | 2) For SEVERE CAP: hospitalization & IV antibiotics in last 90 days
27
Suggest appropriate modifications to the inpatient treatment regimen to account for MRSA coverage
Add: IV Vanco; or PO/IV Linezolid
28
When is pseudomonal coverage indicated in inpatient CAP?
Prior respiratory isolate of pseudomonas in last 1 year
29
Suggest appropriate modifications to the inpatient treatment regimen to account for pseudomonal coverage
Modify standard regimen to include one of: 1) IV Pip/Tazo 2) IV Ceftazidime 3) IV cefepime 4) IV meropenem 5) PO/IV Levofloxacin
30
Adjunctive corticosteroid therapy is recommended for patients with CAP a) True b) False
False; any impact (e.g. reduction in lung inflammation) is small and outweighed by the risk of hyperglycemia
31
When is the clinical improvement of CAP symptoms to be expected?
48~72 hrs (hence X immediately adjust therapy if no response in first 1~2 days; allow time for response); elderly/ those with multiple comorbidities may take longer
32
When can empiric MRSA & pseudomonal coverage be stopped?
Stopped within 48 hrs if the patient has improved/ is improving + X MRSA/ P. aeruginosa in culture
33
If the patient is initially given IV antibiotics, under what conditions can they be stepped down to PO antibiotics?
When ALL criteria are met: 1) Hemodynamically stable (normal BP) 2) Clinically improved/ improving 3) Afebrile for ≥ 24 hrs 4) Able to tolerate PO medication (normal GI function)
34
How is a PO regimen selected when stepping down from IV?
1) Choose PO formulation of IV drugs (if available) | 2) otherwise: choose PO option in the same class as the initial antibiotic
35
Suggest a suitable antibiotic given that a patient is suitable for step down from IV Ceftazidime
PO cefuroxime
36
How long should CAP patients be treated for?
Until clinical stability is achieved & for AT LEAST 5 DAYS
37
If a patient has MRSA/ P. aeruginosa, how long should treatment duration be?
~7 days
38
If a patient has Burkholderia Pseudomallei (from culture findings), how long should treatment duration be?
3~6 mths