AI Article Synopsis

  • The study explores the rising issue of bloodstream infections (BSIs) in Rwanda, focusing on the types of bacteria involved and their susceptibility to antibiotics from 2020 to 2022.
  • A total of 1,532 blood culture tests were analyzed, revealing that Gram-negative and Gram-positive bacteria accounted for 48.2% and 51.8% of cases, respectively, with notable species being Staphylococcus aureus and Klebsiella.
  • The findings highlight the effectiveness of various antibiotics, including Amikacin and Meropenem, in treating these infections, and suggest a need for improved strategies in managing antimicrobial resistance (AMR) in Rwanda.

Article Abstract

: The burden of bacterial bloodstream infections (BSIs) is rapidly increasing in Africa including Rwanda. : This is a retrospective study that investigates the diversity, distribution, and antimicrobial susceptibility profiles of BSI bacteria in three tertiary referral hospitals in Rwanda between 2020 and 2022. : A total of 1532 blood culture tests were performed for visiting patients. Overall, the proportions of Gram-negative and Gram-positive bacteria were 48.2% and 51.8, respectively. was the predominant species accounting for 25% of all Gram-positive BSI species, and Klebsiella species represented 41% of all Gram-negative BSI species. Antimicrobial susceptibility testing revealed that Amikacin exhibited the highest activity against spp., spp., and in >92% of cases and spp. in 75.7%. Meropenem and Imipenem were highly efficacious to spp. (100% susceptibility), spp. (96.2% and 91.7%, respectively), and (94.7% and 95.5%, respectively). The susceptibility of spp., , and spp. to Vancomycin was 100%, 99.5%, and 97.1%, respectively. spp. was highly sensitive to Colistin (98.7%), Polymyxin B (85.6%), Imipenem (84.9%), and Meropenem (78.5%). : We recommend strengthening the implementation of integrated transdisciplinary and multisectoral One Health including AMR stewardship for the surveillance, prevention, and control of AMR in Rwanda.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11591390PMC
http://dx.doi.org/10.3390/antibiotics13111084DOI Listing

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