Late onset ventilator-associated pneumonia due to multidrug-resistant Acinetobacter spp.: experience with tigecycline

D Curcio1, F Fernández, J Vergara

  • 1Infectología Institucional SRL, Buenos Aires, Argentina. djcurcio@gmail.com

Insights

Tigecycline shows a 69.86% clinical success rate for treating ventilator-associated pneumonia (VAP) caused by multidrug-resistant Acinetobacter spp. Older age and non-bronchoalveolar lavage sampling predict negative outcomes.

Area of Science:

  • Infectious Diseases
  • Critical Care Medicine
  • Antimicrobial Stewardship

Background:

  • Ventilator-associated pneumonia (VAP) poses a significant challenge, particularly when caused by multidrug-resistant (MDR) Acinetobacter spp.
  • Limited treatment options exist for VAP due to MDR Acinetobacter infections, necessitating evaluation of alternative therapies.

Purpose of the Study:

  • To assess the clinical success rate of tigecycline in treating VAP caused by MDR Acinetobacter spp.
  • To identify predictor variables associated with clinical outcomes in this patient population.

Main Methods:

  • A retrospective study evaluating 73 patients with VAP due to MDR Acinetobacter spp. treated with tigecycline across seven intensive care units.
  • Analysis of clinical success rates and identification of significant predictor variables for treatment outcomes.

Main Results:

  • Overall clinical success rate with tigecycline was 69.86% (51/73 patients).
  • No significant differences in success rates were observed based on carbapenem resistance or prior antibiotic duration.
  • Age over 67 and non-bronchoalveolar lavage (BAL) respiratory sampling were identified as predictors of negative clinical outcomes.

Conclusions:

  • Tigecycline appears to be a viable therapeutic option for VAP caused by MDR Acinetobacter spp.
  • Further evidence from controlled clinical trials is needed to support tigecycline's approval for new indications in VAP treatment.

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