Antibiogram Surveillance to Determine Appropriate Initial Empiric Antibiotic Therapy for Ventilator-Associated

Andrew J Kerwin1, G Christopher Wood2, Saskya Byerly1

  • 1Department of Surgery, Division of Trauma and Surgical Critical Care, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Surgical Infections
|February 24, 2025
PubMed

Insights

Antibiotic therapy for ventilator-associated pneumonia (VAP) is often inappropriate due to changing pathogen sensitivities. Continuous monitoring of local antibiograms is crucial for effective VAP treatment protocols.

Area of Science:

  • Critical Care Medicine
  • Infectious Diseases
  • Clinical Microbiology

Background:

  • Protocolized empiric antibiotic therapy for ventilator-associated pneumonia (VAP) is guided by local antibiograms.
  • Inappropriate empiric antibiotic therapy (IEAT) for VAP occurs approximately 15% of the time.
  • Changes in pathogen sensitivity patterns may necessitate adjustments to VAP treatment protocols.

Purpose of the Study:

  • To review the trauma intensive care unit (TICU) antibiogram for changing sensitivity patterns.
  • To determine if current VAP treatment protocols require adjustment based on evolving resistance.
  • To evaluate trends in IEAT and antimicrobial use over time.

Main Methods:

  • Retrospective review of TICU patients diagnosed with VAP between 2017 and 2022.
  • Analysis of bronchoalveolar lavage cultures (≥100,000 CFU/mL) to identify pathogens and their sensitivities.
  • Assessment of IEAT percentages and changes in antimicrobial days per 1,000 days present (2018-2022).

Main Results:

  • An increasing trend in IEAT was observed starting in 2017.
  • Early VAP showed increased gram-negative isolates (7%-24%), notably *Pseudomonas* (3%-10%), with decreased *Streptococcus* and *Haemophilus influenzae*.
  • Late VAP demonstrated increased *Stenotrophomonas* (3%-5%) and *Acinetobacter* (4%-10%) isolates.
  • Antimicrobial use shifted, with increased rates for cefazolin, vancomycin, cefepime, and meropenem, and decreased rates for ampicillin/sulbactam and piperacillin/tazobactam.

Conclusions:

  • Shifting pathogen prevalence and increasing IEAT underscore the need for ongoing antibiogram surveillance.
  • Local antibiogram data is essential for refining VAP empiric antibiotic therapy protocols.
  • Continuous monitoring can guide timely adjustments to antimicrobial stewardship and treatment efficacy.

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