Pneumonia: CAP vs HAP/VAP
Comprehensive empiric therapy summary — Egyptian clinical context
CAP — Community-Acquired Pneumonia
| Setting | Likely Pathogens | Empiric Therapy | Duration |
|---|---|---|---|
| Outpatient (no comorbidities) | S. pneumoniae, H. influenzae, atypicals | Amoxicillin 1 g PO TDS or Doxycycline 100 mg BD or Azithromycin 500 mg day 1 → 250 mg OD × 4 days | 5–7 days |
| Outpatient (with comorbidities) | + Klebsiella, S. aureus | Amox–Clav 1 g PO BD ± Azithro/Doxy or Levofloxacin 500–750 mg PO OD | 7 days |
| Inpatient (non-ICU) | S. pneumoniae, H. influenzae, Legionella | Ceftriaxone 2 g IV OD + Azithro 500 mg IV/PO OD or Levofloxacin 750 mg IV/PO OD | 7 days |
| ICU / severe | S. pneumoniae, Legionella, S. aureus | Ceftriaxone/Cefotaxime + Azithro or Levofloxacin ± Vancomycin/Linezolid (if MRSA) ± Pip-Tazo (if Pseudomonas risk) | 7–10 days |
HAP — Hospital-Acquired Pneumonia
| Type | Likely Pathogens | Empiric Therapy | Duration |
|---|---|---|---|
| HAP (early-onset) | S. pneumoniae, H. influenzae | Ceftriaxone 2 g IV OD or Ampicillin–sulbactam 3 g IV q6h | 7 days |
| HAP (late/MDR risk) | Pseudomonas, Acinetobacter, MRSA | Pip–Tazo 4.5 g IV q6h or Cefepime 2 g IV q8h or Meropenem 1 g IV q8h ± Vancomycin/Linezolid ± Amikacin/Levofloxacin | 7–10 days |
VAP — Ventilator-Associated Pneumonia
| Setting | Likely Pathogens | Empiric Therapy | Duration |
|---|---|---|---|
| Ventilated ICU patients | Pseudomonas, Acinetobacter, MRSA | Same as late HAP (broad-spectrum triple coverage then de-escalate) | 7–10 days |
Risk Factors — MRSA & Pseudomonas
MRSA Risk
- Prior MRSA colonization or infection
- Hospitalization >5 days
- IV antibiotic exposure within 90 days
- Severe ICU illness
Pseudomonas Risk
- Structural lung disease (COPD, bronchiectasis)
- Prolonged ventilation
- Recent broad-spectrum antibiotic use
- High MDR prevalence environment
Clinical Notes & De-escalation
- Obtain cultures before starting antibiotics when possible.
- Reassess after 48–72h for de-escalation based on cultures and clinical response.
- Typical duration: 7 days (extend to 10–14 for complications or slow response).
- Switch to oral therapy when stable and afebrile ≥48h.
Dr. Ahmed Khaled — Drug Information Center
Pneumonia: CAP vs HAP/VAP
Comprehensive empiric therapy summary — Egyptian clinical context
CAP — Community-Acquired Pneumonia
| Setting | Likely Pathogens | Empiric Therapy | Duration |
|---|---|---|---|
| Outpatient (no comorbidities) | S. pneumoniae, H. influenzae, atypicals | Amoxicillin 1 g PO TDS or Doxycycline 100 mg BD or Azithromycin 500 mg day 1 → 250 mg OD × 4 days | 5–7 days |
| Outpatient (with comorbidities) | + Klebsiella, S. aureus | Amox–Clav 1 g PO BD ± Azithro/Doxy or Levofloxacin 500–750 mg PO OD | 7 days |
| Inpatient (non-ICU) | S. pneumoniae, H. influenzae, Legionella | Ceftriaxone 2 g IV OD + Azithro 500 mg IV/PO OD or Levofloxacin 750 mg IV/PO OD | 7 days |
| ICU / severe | S. pneumoniae, Legionella, S. aureus | Ceftriaxone/Cefotaxime + Azithro or Levofloxacin ± Vancomycin/Linezolid (if MRSA) ± Pip-Tazo (if Pseudomonas risk) | 7–10 days |
HAP — Hospital-Acquired Pneumonia
| Type | Likely Pathogens | Empiric Therapy | Duration |
|---|---|---|---|
| HAP (early-onset) | S. pneumoniae, H. influenzae | Ceftriaxone 2 g IV OD or Ampicillin–sulbactam 3 g IV q6h | 7 days |
| HAP (late/MDR risk) | Pseudomonas, Acinetobacter, MRSA | Pip–Tazo 4.5 g IV q6h or Cefepime 2 g IV q8h or Meropenem 1 g IV q8h ± Vancomycin/Linezolid ± Amikacin/Levofloxacin | 7–10 days |
VAP — Ventilator-Associated Pneumonia
| Setting | Likely Pathogens | Empiric Therapy | Duration |
|---|---|---|---|
| Ventilated ICU patients | Pseudomonas, Acinetobacter, MRSA | Same as late HAP (broad-spectrum triple coverage then de-escalate) | 7–10 days |
Risk Factors — MRSA & Pseudomonas
MRSA Risk
- Prior MRSA colonization or infection
- Hospitalization >5 days
- IV antibiotic exposure within 90 days
- Severe ICU illness
Pseudomonas Risk
- Structural lung disease (COPD, bronchiectasis)
- Prolonged ventilation
- Recent broad-spectrum antibiotic use
- High MDR prevalence environment
Clinical Notes & De-escalation
- Obtain cultures before starting antibiotics when possible.
- Reassess after 48–72h for de-escalation based on cultures and clinical response.
- Typical duration: 7 days (extend to 10–14 for complications or slow response).
- Switch to oral therapy when stable and afebrile ≥48h.
Dr. Ahmed Khaled — Drug Information Center