Treatment for Hospital-Acquired Pneumonia (HAP)
For hospital-acquired pneumonia, empiric antibiotic therapy should be initiated promptly with broad-spectrum coverage for patients with risk factors for multidrug-resistant (MDR) pathogens, while patients without risk factors can receive more targeted therapy. 1
Initial Assessment and Risk Stratification
The key decision in initial empiric therapy is determining whether the patient has risk factors for MDR organisms:
Risk Factors for MDR Pathogens:
- Prior intravenous antibiotic use within 90 days
- Late-onset HAP (≥5 days after hospitalization)
- Septic shock
- Hospitalization in units with high rates of MDR pathogens
- Acute renal replacement therapy
- Structural lung disease
- Previous colonization with MDR pathogens 1
Empiric Antibiotic Therapy
For Patients WITHOUT Risk Factors for MDR Pathogens:
Monotherapy with one of the following:
- Piperacillin-tazobactam 4.5 g IV every 6 hours
- Cefepime 2 g IV every 8 hours
- Levofloxacin 750 mg IV daily
- Ertapenem 1 g IV daily (if Pseudomonas not suspected) 1
For Patients WITH Risk Factors for MDR Pathogens:
Combination therapy with:
- An anti-pseudomonal β-lactam:
PLUS
- Either an aminoglycoside:
OR
- An antipseudomonal fluoroquinolone:
MRSA Coverage:
Add MRSA coverage if risk factors are present or if >25% of S. aureus respiratory isolates in the ICU are MRSA:
- Vancomycin 15-20 mg/kg IV every 8-12 hours (target trough 15-20 μg/mL)
- Linezolid 600 mg IV every 12 hours 2, 1
Special Considerations
For Pseudomonas aeruginosa:
- For confirmed Pseudomonas pneumonia, combination therapy with an antipseudomonal β-lactam plus either an aminoglycoside or a fluoroquinolone is recommended 1
- For nosocomial pneumonia caused by P. aeruginosa, piperacillin-tazobactam should be used in combination with an aminoglycoside 3
For Staphylococcus aureus:
- For confirmed MRSA: Continue vancomycin or linezolid
- For confirmed MSSA: De-escalate to oxacillin, nafcillin, or cefazolin 1
Duration of Therapy and De-escalation
Standard duration: 7-8 days for patients with good clinical response 1
Consider longer durations (10-14 days) for:
- Slow clinical response
- Highly resistant pathogens
- Structural lung disease
- Complications 1
Reassess at 48-72 hours based on clinical response and culture results 1
De-escalate therapy once culture results are available to target the specific pathogens identified 1
Important Caveats
- Delays in appropriate antibiotic therapy increase mortality; therefore, do not delay treatment to obtain cultures in critically ill patients 2, 1
- Lower respiratory tract cultures should be collected from all patients before antibiotic therapy when possible 2
- Use local antibiograms to guide empiric therapy choices, as pathogen prevalence and resistance patterns vary between hospitals 1
- Adjust antibiotic doses based on renal function; for patients with renal impairment (creatinine clearance ≤40 mL/min), reduce doses of piperacillin-tazobactam and other renally cleared antibiotics 3
- Negative lower respiratory tract cultures can be used to stop antibiotic therapy if obtained before antibiotic changes in the previous 72 hours 2