Risk Factors and Outcomes of Multidrug-resistant Pseudomonas aeruginosa in Kelantan, Malaysia: A Multicenter

Siti Norfairuz Md Salim1,2, Nurul Izzah Md Din3, Rosnita Rashid4

  • 1Department of Medical Microbiology and Parasitology, Universiti Sains Malaysia Health Campus, Kota Bharu, Malaysia.

Abstract

Insights

Multidrug-resistant Pseudomonas aeruginosa (MDR-PA) is a growing threat. This study identified risk factors like age and catheters for MDR-PA acquisition, linked to treatment failure and mortality.

Area of Science:

  • Clinical microbiology
  • Infectious diseases
  • Epidemiology

Background:

  • Multidrug-resistant Pseudomonas aeruginosa (MDR-PA) poses a significant challenge in healthcare settings.
  • The increasing prevalence of MDR-PA necessitates understanding its risk factors and resistance patterns.

Purpose of the Study:

  • To investigate the risk factors and outcomes associated with MDR-PA acquisition in Kelantan, Malaysia.
  • To analyze the susceptibility patterns and identify common resistance genes in MDR-PA isolates.

Main Methods:

  • Retrospective review of clinical data from patients with MDR-PA and susceptible-PA.
  • Susceptibility testing and identification of resistance genes (e.g., blaNDM-1, blaOXA-48) in MDR-PA isolates.
  • Comparative analysis of risk factors and outcomes between MDR-PA and susceptible-PA groups.

Main Results:

  • Ceftolozane-tazobactam showed susceptibility in 41.3% of MDR-PA, significantly higher than other beta-lactams.
  • The blaNDM-1 gene was present in 46% of MDR-PA isolates; blaOXA-48 was absent.
  • Independent risk factors for MDR-PA acquisition included advanced age, genitourinary disorders, and central venous catheter use.
  • MDR-PA acquisition was associated with increased antimicrobial treatment failure (41.1% vs. 25.0%) and mortality (40.0% vs. 6.0%).

Conclusions:

  • The blaNDM-1 gene, prevalent in Kelantan hospitals, poses a risk for outbreaks due to its transmissibility.
  • A notable proportion of MDR-PA isolates remain susceptible to ceftolozane-tazobactam, offering a potential treatment option.

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