A fresh look at polymicrobial bloodstream infection in cancer patients

Cristina Royo-Cebrecos1,2, Carlota Gudiol1,2, Carmen Ardanuy3,4

  • 1Department of Infectious Diseases, Hospital Universitari de Bellvitge, IDIBELL (Institut d´Investigació Biomèdica de Bellvitge), University of Barcelona, Barcelona, Spain.

Plos One
|October 25, 2017
PubMed
Abstract

Insights

Polymicrobial bloodstream infections (PBSI) are common in cancer patients and lead to higher mortality. Early identification of risk factors and appropriate antibiotic therapy, including for multidrug-resistant (MDR) strains, are crucial for improving outcomes.

Area of Science:

  • Infectious Diseases
  • Oncology
  • Clinical Microbiology

Background:

  • Polymicrobial bloodstream infection (PBSI) is a significant concern in immunocompromised patients.
  • Understanding the epidemiology and risk factors of PBSI in cancer patients is critical for effective management.

Purpose of the Study:

  • To evaluate the incidence, clinical characteristics, risk factors, etiology, antimicrobial resistance, and outcomes of PBSI in cancer patients.
  • To compare PBSI with monomicrobial bloodstream infection (MBSI) in this population.

Main Methods:

  • Prospective collection and comparison of PBSI and MBSI episodes in hospitalized cancer patients from 2006 to 2015.
  • Analysis of risk factors, causative pathogens, antimicrobial resistance patterns, and case-fatality rates.

Main Results:

  • PBSI occurred in 10.2% of bloodstream infections, with risk factors including cholangitis, biliary stenting, neutropenia, and corticosteroid use.
  • Gram-negative organisms were most frequent, but Enterococcus spp. were common in Gram-positive PBSI. Multidrug-resistant (MDR) organisms were more prevalent in PBSI (20.6%) than MBSI (12.9%).
  • PBSI was associated with significantly higher early (15% vs 1.4%) and overall (32% vs 20.9%) case-fatality rates compared to MBSI.

Conclusions:

  • PBSI is a frequent and high-mortality complication in cancer patients.
  • Identifying patients at risk for PBSI is essential.
  • Empiric antibiotic therapy should target common pathogens, including MDR strains, to improve patient outcomes.