Bloodstream infection due to Acinetobacter spp: epidemiology, risk factors and impact of multi-drug resistance

D W Wareham1, D C Bean, P Khanna

  • 1Division of Infection, Barts and The London NHS Trust, London, UK. d.w.wareham@qmul.ac.uk

Insights

Acinetobacter infections are rising, with multi-drug resistance a growing concern. Appropriate empirical antimicrobial therapy did not reduce 30-day mortality in Acinetobacter bacteremia cases.

Area of Science:

  • Medical Microbiology
  • Infectious Diseases
  • Clinical Medicine

Background:

  • Acinetobacter species are significant causes of human infections.
  • Increasing multi-drug resistance (MDR) in Acinetobacter complicates treatment.
  • The clinical impact of MDR Acinetobacter infections requires further definition.

Purpose of the Study:

  • To describe Acinetobacter bacteremia episodes in a UK tertiary care center.
  • To assess the impact of antimicrobial resistance and therapy on patient outcomes.
  • To evaluate mortality associated with Acinetobacter bacteremia from 1998-2006.

Main Methods:

  • Retrospective observational study of 399 Acinetobacter bacteremia episodes.
  • Analysis of patient demographics and infecting strain characteristics.
  • Assessment of antimicrobial susceptibility and impact of therapy on 30-day mortality.

Main Results:

  • Acinetobacter baumannii was the most common species identified.
  • Most episodes occurred in critical care settings and were associated with MDR.
  • Carbapenem resistance increased from 0% to 55% between 1998 and 2006.
  • Higher mortality was linked to carbapenem-resistant Acinetobacter and critical care admission.
  • Appropriate empirical antimicrobial therapy did not significantly reduce mortality.

Conclusions:

  • Acinetobacter bacteremia, particularly with MDR strains, is associated with significant mortality.
  • Current empirical antimicrobial strategies may not be sufficient to improve outcomes.
  • Prospective studies are needed to identify effective interventions and patient subgroups.

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