P. aeruginosa bloodstream infections among hematological patients: an old or new question?

Chiara Cattaneo1, F Antoniazzi, S Casari

  • 1Dept. of Haematology, Spedali Civili, Piazza Spedali Civili, 25100 Brescia, Italy. chiara.cattaneo@libero.it

Annals of Hematology
|February 22, 2012
PubMed

Insights

Pseudomonas aeruginosa bloodstream infections (BSI) are increasing in hematological patients. Multiresistant P. aeruginosa significantly raises mortality, highlighting the need for effective empiric antibiotic therapy.

Area of Science:

  • Infectious Diseases
  • Hematology
  • Epidemiology

Background:

  • Pseudomonas aeruginosa is a significant pathogen causing severe infections in hematological patients.
  • An increasing trend of P. aeruginosa bloodstream infections (BSI) was observed in a Hematology Unit.
  • These infections pose a substantial threat to patient outcomes.

Purpose of the Study:

  • To analyze the impact of P. aeruginosa BSI on patient outcomes and antibiotic susceptibility.
  • To identify risk factors associated with increased mortality in hematological patients with BSI.
  • To evaluate the effectiveness of empiric antibiotic therapy against P. aeruginosa.

Main Methods:

  • Prospective epidemiological surveillance over a 70-month period.
  • Evaluation of 441 bloodstream infections (BSI).
  • Correlation analysis of pathogen type, disease status, neutropenia, prior antibiotics, resistance, and outcomes. Multivariate analysis was performed.

Main Results:

  • P. aeruginosa accounted for a significant proportion of Gram-negative BSI.
  • Multiresistant P. aeruginosa (MR P. aeruginosa) BSI showed a 30-day mortality of 36.4%.
  • Active hematological disease and P. aeruginosa BSI were independently associated with increased mortality. Empiric therapy including an active antibiotic against MR P. aeruginosa significantly reduced mortality (83.3% vs. 18.8%).

Conclusions:

  • The emergence of P. aeruginosa BSI, especially multiresistant strains, increases mortality in hematological patients.
  • Active hematological disease is a key factor in mortality risk.
  • Revising empiric antibiotic strategies for neutropenic fever is crucial to improve outcomes.

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