Objectives: The aim of this study was to determine the proportion and mechanism of resistance to ceftriaxone and ceftazidime among species and and examine the burden of methicillin-resistant from caesarean section surgical site infections in Uganda.

Methods: Wound swabs from 109 caesarean section surgical site infections were cultured for pathogenic bacteria following standard microbiological procedures. The Kirby-Bauer disc diffusion technique was used for antimicrobial susceptibility testing. Methicillin-resistant diagnosis was based on polymerase chain reaction testing for the gene. Data were analysed using SPSS-IBM Statistics v.20.

Results: A total of 118 pathogens were recovered from 93 (85%) of 109 surgical site infections swabs. Of the 118 pathogens, gram-negative bacteria were 69 (58.5%), including 44 (37.3%) species, 11 (9.3%) , 6 (5.1%) species, and 8 (6.8%) other gram-negative bacteria. In total, 49 of the 118 pathogens were gram-positive bacteria, including 34 (28.8%) and 15 (12.7%) species. Resistance to ceftriaxone was detected in all 11 (100%) of the and in 43 (97.7%) of the 44 species and to ceftazidime in all 11 (100%) of the and 40 (91%) of the 44 species. Extended-spectrum beta-lactamase explained resistance to ceftazidime in 10 (91%) of the 11 and 19 (48%) of the 40 species. Carbapenemase production explained 15 (38%) of the 40 ceftazidime-resistant species. Methicillin-resistant was detected in 91% of .

Conclusion: species, , and -majority methicillin-resistant dominated the pathogens in caesarean section surgical site infections. Almost all of the and species were resistant to ceftriaxone or ceftazidime. Extended-spectrum beta-lactamase was the underlying resistance mechanism among almost all of the ceftriaxone- or ceftazidime-resistant However, this mechanism accounted for less than half of ceftriaxone- or ceftazidime-resistant species, where carbapenemases accounted for 40% of the resistance, a finding previously unreported in Uganda.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826261PMC
http://dx.doi.org/10.1177/2050312120970719DOI Listing

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