Epidemiology of Carbapenem Resistance among Multi-drug Resistant Enterobacteriaceae in Uganda

Lucas M Ampaire1, Victoria Katawera2, Dan Nyehangane3

  • 1Department of Medical Laboratory Sciences, Mbarara University of Science and Technology, Mbarara, Uganda.

British Microbiology Research Journal
|November 26, 2015
PubMed
Abstract

Insights

Multi-drug resistant Carbapenemase-producing Enterobacteriaceae (MDR-CPE) are a growing threat. This study found a significant prevalence of MDR-CPE in South Western Uganda, highlighting the need for enhanced infection control.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Public Health

Background:

  • Multi-drug resistant (MDR) Enterobacteriaceae, particularly Carbapenemase-producing Enterobacteriaceae (CPE), pose a significant global health challenge.
  • Data on MDR-CPE prevalence in resource-limited settings is scarce, hindering effective patient management and control strategies.

Purpose of the Study:

  • To investigate the epidemiology of MDR-CPE in clinical isolates from South Western Uganda.
  • To assess the prevalence and characteristics of carbapenem resistance among Enterobacteriaceae in the region.

Main Methods:

  • A laboratory-based cross-sectional study was conducted from September 2013 to June 2014.
  • Enterobacteriaceae isolates from Mbarara Regional Referral Hospital were screened for MDR.
  • Carbapenem resistance was evaluated phenotypically (disc diffusion) and genetically (multiplex real-time PCR).

Main Results:

  • Out of 658 Enterobacteriaceae strains, 183 (27.8%) were MDR.
  • Of the MDR isolates, 68 (37.15%) showed carbapenem resistance.
  • Eleven MDR-CPE isolates (6.01%) exhibited both phenotypic and genotypic resistance, with *bla*VIM and *bla*OXA-48 genes detected.

Conclusions:

  • The high prevalence of MDR-CPE in this resource-limited setting necessitates urgent implementation of robust infection control and prevention strategies.
  • Reinforcing hand hygiene, contact precautions, and employing targeted surveillance with molecular detection are crucial for early identification and management of CPE.

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