IC16: LRTI Flashcards

1
Q

What are the typical causative pathogens for outpatient CAP? State the most common pathogen as well.

A

1) Streptococcus pneumoniae (most common)

2) Haemophilus influenzae

3) Atypical organisms, e.g. Mycoplasma pneumoniae, Chlamydophila pneumoniae, Legionella pneumophilia

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2
Q

What additional pathogens may need to be covered for inpatient non-severe CAP?

A

Based on risk factors for MDROs, consider if need MRSA and Pseudomonas cover

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3
Q

What pathogens need to be covered for inpatient severe CAP?

A

1) Streptococcus pneumoniae

2) Haemophilus influenzae

3) Atypical organisms, e.g. Mycoplasma pneumoniae, Chlamydophila pneumoniae, Legionella pneumophilia

4) S. Aureus (MSSA)

5) Other Gram‐negative bacilli, e.g. Klebsiella pneumonia, Burkholderia pseudomallei

6) Based on risk factors for MDROs, consider if need MRSA and Pseudomonas cover

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4
Q

What other illness should be considered and tested for all inpatients during circulating season?

A

Influenza

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5
Q

What does the risk stratification for CAP determine?

A

1) Location of treatment
* Outpatient versus inpatient (non‐ICU versus ICU)

2) Organisms that need to be covered

3) Empiric antibiotic selection

4) Route of antibiotic administration

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6
Q

What are the risk stratification strategies that can be employed to determine site of treatment for a patient with CAP?

A

1) Pneumonia Severity Index (PSI)

2) CURB-65 + IDSA Criteria for severe CAP

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7
Q

_____ is preferentially recommended over _____ in IDSA CAP guidelines as a risk stratification strategy?

A

Pnemonia Severity Index, CURB 65

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8
Q

How many mortality risk classes are there in PSI and what are the recommendations for location of CAP treatment for each class?

A

Class I and II: Treat in outpatient
Class III: short hospitalisation or observation
Class IV and V: Treat in inpatient

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9
Q

What are the components of CURB-65?

A

1) Confusion (New onset)

2) Urea > 7 mmol/L (Uremia)

3) Respiratory Rate ≥ 30 breaths/min

4) Blood pressure (hypotension; SBP < 90 mmHg or DBP < 60 mmHg)

5) Age ≥ 65 years

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10
Q

Relate the CURB-65 score to location of treatment of CAP

A

Score 0 or 1 = Can be managed in outpatient

Score 2 = manage in inpatient (short term hospitalisation or observation)

Score ≥ 3 = manage in inpatient, consider ICU

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11
Q

What are the major criteria for severe CAP?

A

1) Mechanical ventilation

2) Septic shock requiring vasoactive medications (hemodynamic instability)

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12
Q

How is severe CAP defined by IDSA guidelines?

A

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

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13
Q

What are the minor criteria for severe CAP? (total 8)

A
  • RR ≥ 30 breaths/min
  • PaO2 /FiO2 ratio ≤ 250 (fraction of inspired oxygen; typically need ICU monitoring and mechanical ventilation also)
  • Multilobar infiltrates
  • Confusion/ disorientation (common in elderly)
  • Uremia (urea ≥ 7 mmol/L)
  • Leukopenia (WBC < 4 x 10^9/L) (must not be due to chemotherapy)
  • Hypothermia (core temperature < 36°C)
  • Hypotension requiring aggressive fluid resuscitation
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14
Q

State the possible empiric regimen(s) for CAP for a patient with CURB score 1 and no significant PMH. State the pathogen(s) to be targeted. State anything special about the regimen if any.

A

β-lactam: Amoxicillin 1g q8H (High dose used in case of resistant S. pneumoniae)

If penicillin allergy: Respiratory Fluoroquinolone (Levofloxacin or Moxifloxacin)

Pathogen targeted: S. Pneumonia

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15
Q

State the possible empiric regimen(s) for CAP for a patient with CURB score 1 and with significant PMH of HTN, DM, asthma etc. State the pathogen(s) to be targeted.

A

β-Lactam (Augmentin or Cefuroxime) + Macrolide (Clarithromycin or Azithromycin) OR Doxycycline

Alternative: Levofloxacin or Moxifloxacin (if Penicillin allergy)

Pathogens targeted:
S. pneumoniae, H. influenzae, Atypicals

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16
Q

State the possible empiric regimen(s) for CAP for a patient with CURB score 2 and no significant PMH. State the pathogen(s) to be targeted.

A

β-Lactam (Augmentin or Cefuroxime or Ceftriaxone) + Macrolide (Clarithromycin or Azithromycin) OR Doxycycline

Alternative: Levofloxacin or Moxifloxacin (if Penicillin allergy)

Pathogens targeted:
S. pneumoniae, H. influenzae, Atypicals

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17
Q

State the possible empiric regimen(s) for CAP for a patient with CURB score 2 with risks of Pseudomonas.

A

1) Piperacillin/ tazobactam (+ Macrolide/ Doxy for atypical cover)

2) Ceftazidime (does not cover S. pneumoniae -> cannot use on it’s own)

3) Cefepime (+ Macrolide/ Doxy; for atypical cover)

4) Meropenem (+ Macrolide/ Doxy; for atypical cover)

5) Levofloxacin (can monotherapy if not targeting S. Aureus, need combination if targeting S. Aureus)

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18
Q

Which antibiotics are used to target Burkholderia Pseudomallei

A

Ceftazidime or Meropenem

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19
Q

Which antibiotic cannot be used for severe CAP although it can be used for all other less severe CAP and why?

A

Doxycycline (No easily accessible IV formulation)

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20
Q

Which of the FQs have anaerobic cover?

A

Moxifloxacin

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21
Q

Which of the FQs does not cover Pseudomonas?

A

Moxifloxacin

22
Q

When will anaerobic cover be needed for CAP?

A

Presence of Lung abscess or Empyema

23
Q

Which antibiotic regimens already includes cover for anaerobes?

A

1) Augmentin (covers the anaerobes) + Ceftazidime + Macrolide

2) Moxifloxacin (covers anaerobes) + Ceftazidime

24
Q

Which antibiotics are added on if regimen has no anaerobic coverage?

A

Metronidazole IV/PO OR Clindamycin IV/ PO

25
Q

When is adjunctive corticosteroids indicated in CAP?

A

Add if shock refractory to fluid resuscitation and vasopressor support (more for ICU patients)

26
Q

How to de-escalate therapy in CAP patients with no positive culture?

Which pathogens are still covered after de-escalation?

A

Empiric cover for MRSA, Pseudomonas aeruginosa or Burkholderia pseudomallei can be stopped in 48 hours if pathogen not isolated and patient is improving

Still have to cover S. pneumonia, H. influenzae and atypicals

27
Q

State the minimum treatment duration of CAP, when longer treatment durations are warranted and their durations.

A

Minimum 5 days.

Longer durations if:
1) MRSA or Pseudomonas: treat for 7 days

2) Presence of complications/other infections (e.g meningitis, lung abscess): treat for 2-3 weeks

3) Presence of other rare pathogens (Bulkholderia, fungi, Mycobacterium tuberculosis): treat for 3-6 weeks

4) Not clinically stable after 5 days (e.g still cannot eat, not at baseline mental status, continued presence of vital sign abnormalities)

28
Q

What should/should not be done during monitoring for Pneumonia?

A

Should:
1) Monitor for clinical stability [resolution of vital sign abnormalities, ability to maintain oral intake, return to baseline mental status (except VAP)] usually within 2-3 days

2) ADR of antibiotics

Should NOT:
1) Repeat radiographic test to document resolution (only repeat if significant clinical deterioriation)

2) Repeat microbiological tests to document resolution (only repeat if culture comes back negative and patient not improving)

3) Escalate treatment within first 72 hours (unless culture returns and empiric antibiotics not effective or significant clinical deterioriation)

29
Q

Which antibiotic is effective against MRSA but not used in Pneumonia?

A

Daptomycin

30
Q

What are the prevention measures for CAP?

A

1) Stop smoking
2) Vaccinations (e.g Influenza, Pneumococcal)

31
Q

Risk factors for CAP

A

1) History of Pneumonia

2) Smoking

3) Chronic lung conditions

4) Immune suppression

5) Concurrent bacteremia

6) Swallowing impairment

32
Q

Describe the radiographic finding that suggests pneumonia.

A

Evidence of a new infiltrates or dense consolidations that are usually unilateral

33
Q

Urinary antigen tests detect presence of antigen against which 2 bacteria?

A

1) Streptococcus pneumonia (most common for CAP)

2) Legionella pneumophilia

34
Q

When is urinary antigen test recommended to be carried out and what is the limitation of UAT?

A

Recommended only for severe CAP or hospitalized patients (due to limitations); usually not done in outpatient diagnosis of pneumonia

Limitation: Remains positive for days to weeks despite antibiotic treatment (only indicate prior exposure to the organism)

35
Q

IDSA Guidelines recommends obtaining pre-treatment blood and respiratory gram stain and cultures for which group of patients? (2)

A

1) Severe CAP

2) Have risk factor for drug resistant pathogens (e.g Pseudomonas, MRSA) -> basically all HAP/VAP patients

The risk factors are:
o Being empirically treated for MRSA or P. aeruginosa
o Were previously infected with MRSA or P. aeruginosa in the last 1 year
o Were hospitalised or received parenteral antibiotics in the last 90 days

36
Q

What should not be present in well-collected sputum culture?

A

Epithelial cells (indicates contamination by saliva)

37
Q

State + Compare and contrast the sources of respiratory samples

A

Sputum: easier to collect (less invasive) but high contamination rate

Lower respi tract sample: more invasive (need trained personnel) but less contamination

38
Q

Define hospital-acquired pneumonia (HAP).

A

Onset of pneumonia >/= 48h after hospital admission

39
Q

Define ventilator-associated pneumonia (VAP).

A

Onset of pneumonia >/= 48h after mechanical ventilation

40
Q

List out some of the risk factors associated with HAP and VAP.

A

Patient-related factors:
- Elderly
- Smoking
- COPD, cancer, immunosuppression
- Prolonged hospitalization
- Coma, impaired consciousness
- Malnutrition

Infection control-related factors:
- Lack of hand hygiene
- Contaminated respiratory care devices (e.g. oxygen masks)

Healthcare-related factors:
- Prior antibiotic use
- Sedatives
- Opioid analgesics
- Mechanical ventilation
- Supine position

41
Q

What are some preventive measures for HAP/VAP?

A
  • Practise consistent hand hygiene
  • Judicious use of antibiotics and medications with sedative effects
  • (VAP) Limit duration of mechanical ventilation
  • (VAP) Minimize duration and deep levels of sedation
  • (VAP) Elevate head of bed by 30 degrees
42
Q

List out the common causative pathogens for HAP/VAP.

A
  • Non-fermenting Gram-negative bacilli (Pseudomonas, Acinetobacter spp)
  • Enteric Gram-negative bacilli (Enterobacter spp, Klebsiella spp, E. coli)
  • S. aureus
  • Stenotrophomonas maltophilia
43
Q

State the possible empiric regimens for a person with HAP/VAP, with no significant PMH, and no MRSA or MDRO risk factors.

A

Cover MSSA and Pseudomonas (single agent since no risk factor for MDRO)

  • Anti-pseudomonal beta-lactam (Pip-tazo/ cefepime/ ceftazidime/ meropenem/ imipenem)
    AND/OR
  • Anti-pseudomonal FQs (levofloxacin/ciprofloxacin)
    OR
  • Aminoglycoside (amikacin, gentamicin)

*Avoid ceftazidime and ciprofloxacin if MRSA cover is omitted (don’t cover S. aureus)
**Avoid use of AGs as sole anti-pseudomonal agent

44
Q

List out some of the criteria for MRSA coverage in HAP/VAP.

A

Either of the following:
- Prior IV antibiotic use within 90d
- Isolation of MRSA in last 1 yr
- Hospitalization in unit where >20% of S. aureus are MRSA
- Prevalence of MRSA not known, but patient is at high risk for mortality (need ventilatory support due to HAP; septic shock)

45
Q

List out some of the criteria for double-anti-pseudomonal use in HAP/VAP. (3)

A

Either of the following:
- Risk factor for AMR (prior IV antibiotic use within 90d; acute RRT prior to VAP onset; isolation of Pseudomonas in last 1 yr)
- Hospitalization in unit where >10% of Pseudomonas isolates are resistant to agent considered for monotherapy
- Prevalence of PA unknown, but patient at high risk of mortality

46
Q

Describe how de-escalation or IV-to-PO conversion is conducted for HAP/VAP

A
  • IV to PO conversion: Carried out when pt is hemodynamically stable, improving clinically, able to ingest PO meds

Positive culture:
- Use AST to guide selection of narrower-spectrum (possibly PO) antibiotics
- Single anti-pseudomonal agent (for Pseudomonas)
- Take out MRSA cover if MRSA-negative

No positive culture:
- Maintain coverage according to local HAP/VAP antibiogram
- If biogram not available, maintain coverage for Pseudomonas, enteric GNR and MSSA
- Might still need to keep IV antibiotics for patients with high MDRO risk
- IV-to-PO conversion (ciprofloxacin + augmentin; levofloxacin)

47
Q

State the minimum treatment duration for HAP/VAP, when longer treatment durations are warranted and their durations

A
  • Recommend treatment for 7 days, regardless of pathogen
  • Longer courses (~2-3w) of antibiotic therapy for pneumonia complicated with other deep-seated infections (e.g. meningitis, lung abscess)
48
Q

Which antibiotic is effective against Acinetobacter and Stenotrophomonas Maltophilia?

A

Polymyxin or Levofloxacin

49
Q

Which organisms must minimally be covered for HAP/VAP

A

Pseudomonas and MSSA

50
Q

What is the clinical presentation of Pneumonia?

A

o General systemic presentations of infection:
- Fever, chills, malaise, change in mental status (especially in elderly), tachycardia, hypotension
o Localised symptoms:
- Cough
- Pleuritic chest pains (sharp chest pain when breathing in deeply)
- Shortness of breath
- Tachypnoea (>24 breath/min)
- Hypoxia (<95% Oxygen; patient often will need supplemental oxygen)
- Increased sputum production
o Physical examination (lung auscultation)
- Diminished breath sounds over the affected area (due to decreased air entry)
- Inspiratory crackles during lung expansion

51
Q

What is the clinical presentation of acute bronchitis?

A

Acute cough < 3 weeks