Risk factors and outcome analysis of acinetobacter baumannii complex bacteremia in critical patients

Crit Care Med. 2014 May;42(5):1081-8. doi: 10.1097/CCM.0000000000000125.

Abstract

Objectives: Acinetobacter baumannii complex bacteremia has been identified increasingly in critical patients admitted in ICUs. Notably, A. baumannii complex bacteremia has a high mortality rate, yet the risk factors associated with mortality remain unclear and controversial.

Design: Retrospective study.

Setting: All adult ICUs at a tertiary care medical center.

Patients: All patients with A. baumannii complex bacteremia admitted in 2009-2010.

Interventions: None.

Measurements and main results: Risk factors for mortality were analyzed. Bacterial isolates were identified by 16S-23S ribosomal RNA intergenic spacer region sequencing for genospecies and genotyped by pulsed-field gel electrophoresis. Carbapenemase genes were detected by polymerase chain reaction and sequencing. A total of 298 patients met the inclusion criteria, including 73 (24.5%) infected by imipenem-resistant A. baumannii complex. The overall 30-day mortality was 33.6% (100 of 298). Imipenem-resistant A. baumannii complex bacteremia specifically showed a high mortality (69.9%) and was associated with prior use of broad-spectrum antibiotics for more than 5 days for treating ventilator-associated pneumonia before the occurrence of bacteremia. Mortality was associated with inappropriate initial antimicrobial therapy, which was correlated with imipenem-resistant A. baumannii complex but not with any specific genospecies. ISAba1-blaOXA-23-ISAba1 (Tn2006) was found in most (66.7%, 40 of 68) imipenem-resistant A. baumannii (genospecies 2) and also spread beyond species border to all imipenem-resistant genospecies 3 (2), 13TU (2), and 10 (1).

Conclusions: For critical patients with A. baumannii complex infection, ventilator-associated pneumonia in particular, the selective pressure from prior use of broad-spectrum antibiotics for 5 days or more increased risk of subsequent imipenem-resistant A. baumannii complex bacteremia. To reduce mortality, rapid identification of imipenem-resistant A. baumannii complex and early initiation of appropriate antimicrobial therapy in these high-risk patients are crucial.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acinetobacter Infections / drug therapy
  • Acinetobacter Infections / mortality*
  • Acinetobacter baumannii / drug effects
  • Acinetobacter baumannii / genetics
  • Acinetobacter baumannii / isolation & purification*
  • Anti-Bacterial Agents / therapeutic use*
  • Bacteremia / microbiology*
  • Bacteremia / mortality
  • Bacterial Proteins / genetics*
  • Critical Illness / mortality
  • Electrophoresis, Gel, Pulsed-Field
  • Female
  • Humans
  • Imipenem / therapeutic use*
  • Intensive Care Units
  • Kaplan-Meier Estimate
  • Male
  • Multivariate Analysis
  • Pneumonia, Ventilator-Associated / microbiology
  • Polymerase Chain Reaction
  • RNA, Ribosomal, 16S
  • Retrospective Studies
  • Risk Factors
  • Tertiary Care Centers
  • Treatment Outcome
  • beta-Lactam Resistance / genetics*

Substances

  • Anti-Bacterial Agents
  • Bacterial Proteins
  • RNA, Ribosomal, 16S
  • Imipenem