What is the treatment for Hospital-Acquired Pneumonia (HAP)?

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Last updated: September 30, 2025View editorial policy

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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:

  1. An anti-pseudomonal β-lactam:
    • Piperacillin-tazobactam 4.5 g IV every 6 hours
    • Cefepime 1-2 g IV every 8 hours
    • Ceftazidime 2 g IV every 8 hours
    • Imipenem 500 mg IV every 6 hours or 1 g every 8 hours
    • Meropenem 1 g IV every 8 hours 2, 1

PLUS

  1. Either an aminoglycoside:
    • Amikacin 15-20 mg/kg IV daily
    • Gentamicin 5-7 mg/kg IV daily
    • Tobramycin 5-7 mg/kg IV daily 2, 1

OR

  1. An antipseudomonal fluoroquinolone:
    • Ciprofloxacin 400 mg IV every 8 hours
    • Levofloxacin 750 mg IV daily 2, 1

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

References

Guideline

Hospital-Acquired Pneumonia Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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