Annotations only — chart still shows the full chemistry of each drug.
1. Clinical Syndrome
Pneumonia developing ≥48 h after hospital admission (HAP) or ≥48 h after intubation (VAP) — new or progressive infiltrate with clinical signs (fever, leukocytosis, purulent secretions, worsening oxygenation).
Excludes: community-acquired pneumonia (use CAP — different empirics); aspiration pneumonia in community-dwelling (overlapping — defer to v2 with cross-link); tracheobronchitis without infiltrate.
2. Pathogens
Consider the patient: Length of stay (≥5 days raises MDRO risk), prior IV antibiotics ≤90 days, structural lung disease, immunocompromise, ICU vs ward, prior MDRO colonization.
Consider the case: Local antibiogram (unit-specific MRSA / Pseudomonas / MDR-Acinetobacter prevalence drives empirics), severity (vasopressors, bilateral infiltrates), source samples (BAL > tracheal aspirate for VAP).
Common
- Staphylococcus aureus (MRSA)
Empiric coverage often required.
- Staphylococcus aureus (MSSA)
- Pseudomonas aeruginosa
Major MDR concern.
- Klebsiella pneumoniae
- Escherichia coli
- Staphylococcus aureus (MRSA)
3. Empiric Therapy
| Tier | First choice | Alternatives | Duration | Comments |
|---|---|---|---|---|
| Admitted to ward |
|
| 7 days (IDSA/ATS 2016) | HAP without MDRO risk factors and not septic. Single anti-pseudomonal β-lactam. |
| Admitted to ICU |
|
| 7 days | VAP, septic, or HAP with MDRO risk factors. MRSA + Pseudomonas covered empirically. |
| ICU — Pseudomonas risk |
|
| 7 days; longer for non-fermenter or complicated course | ≥5 days hospitalization, prior MDR Pseudomonas, structural lung disease, septic shock. |
Add coverage if:
- Prior MRSA respiratory isolate
- IV antibiotics ≤90 days
- Hospitalization in unit with >20% MRSA prevalence
- Septic shock
Add:
- load + AUC-guided · — · IV
Linezolid 600 mg IV/PO q12h alternative — superior pulmonary penetration, useful in AKI / persistent vanco failure.
MRSA nasal PCR has high NPV in pneumonia — de-escalate vanco/linezolid if negative.
- Prior Pseudomonas respiratory isolate
- Structural lung disease (bronchiectasis, severe COPD, CF)
- Septic shock
- ≥5 days hospitalization
- IV antibiotics ≤90 days
- Recent invasive mechanical ventilation
Add:
- 2 g · q8h · IV
- Tobramycin 5–7 mg/kg · q24h · IV
Add for double-coverage in suspected MDR Pseudomonas; narrow at 48 h.
4. Directed Therapy
De-escalate aggressively at 48 h based on cultures:
- MSSA: cefazolin or nafcillin (link to S. aureus bacteremia syndrome)
- MRSA: continue vancomycin or linezolid
- Susceptible Pseudomonas: narrow to single agent (cefepime, pip-tazo, cipro per susceptibility); consider IV-to-PO if cipro susceptible
- MRSA nasal PCR negative: drop empiric MRSA coverage (high NPV)
- Cultures negative + clinical improvement: consider 5–7 day total course
5. Monitoring
Resolution: defervescence, oxygenation improvement (PaO2/FiO2), repeat imaging at 48–72 h if not improving. Procalcitonin trend can support de-escalation.
Toxicity: vanco AUC + Cr; aminoglycoside levels + Cr + audiometry; cefepime mental status; pip-tazo + vanco AKI (consider switching β-lactam to cefepime per ACORN findings).
Pearls
ACORN trial (JAMA 2023) — cefepime had less AKI than pip-tazo with similar mortality; weigh in patients on vanco. MRSA nasal PCR negative has ~99% NPV for ruling out MRSA pneumonia → de-escalate. 7 days is enough for most HAP/VAP per IDSA 2016 — even Pseudomonas (no benefit from longer course; more antibiotic-resistance selection).
References
- IDSA/ATS HAP/VAP (2016)
- ACORN — Cefepime vs Pip-Tazo (2023)
- IDMP HAP/VAP page