Clinical Predictive Model of Multidrug Resistance in Neutropenic Cancer Patients with Bloodstream Infection Due to

C Gudiol1,2,3, A Albasanz-Puig4,3, J Laporte-Amargós4

  • 1Infectious Diseases Department, Bellvitge University Hospital, IDIBELL, University of Barcelona, Barcelona, Spain cgudiol@iconcologia.net jcarratala@bellvitgehospital.cat.

Insights

Multidrug-resistant Pseudomonas aeruginosa bloodstream infections (BSIs) are increasing in neutropenic cancer patients. Prior antibiotic exposure and urinary catheter use predict these infections, aiding early targeted treatment.

Area of Science:

  • Infectious Diseases
  • Oncology
  • Clinical Microbiology

Background:

  • Neutropenic cancer patients are highly susceptible to bloodstream infections (BSIs).
  • Multidrug-resistant (MDR) Pseudomonas aeruginosa poses a significant threat in immunocompromised populations.
  • Understanding risk factors for MDR P. aeruginosa BSIs is crucial for effective management.

Purpose of the Study:

  • To determine the incidence of MDR P. aeruginosa BSIs in neutropenic cancer patients.
  • To identify predictors of MDR P. aeruginosa BSIs.
  • To develop a model for predicting high-risk patients.

Main Methods:

  • Multicenter, retrospective cohort study.
  • Inclusion of oncohematological neutropenic patients with P. aeruginosa BSI across 34 centers in 12 countries (2006-2018).
  • Mixed logistic regression analysis to identify predictive factors for MDR.

Main Results:

  • 25.4% of P. aeruginosa BSIs were caused by MDR strains.
  • MDR rates significantly increased over the study period.
  • Predictors of MDR P. aeruginosa BSI included prior piperacillin-tazobactam, carbapenem use, fluoroquinolone prophylaxis, hematological disease, and urinary catheter. Older age was protective.

Conclusions:

  • A predictive model for MDR P. aeruginosa BSI in neutropenic patients was developed.
  • The model demonstrates good discrimination and calibration.
  • Early identification of high-risk patients can guide targeted antibiotic therapy and optimize resource utilization.