Background: World Health Organization identified some as superbugs because of their high production and spread of extended-spectrum beta-lactamases (ESBL) and carbapenemases. Moreover, their resistance against commonly prescribed antibiotics left few choices of drugs to treat infection. This study is aimed at determining the magnitude of ESBL and carbapenemase-producing pathogens and their antimicrobial resistance pattern.
Materials And Methods: A hospital-based cross-sectional study was carried out from February to April 2019 in the Northwestern Ethiopia region. A total of 384 patients presumptive for bacterial infections were conveniently enrolled in the study. Specimens were collected and processed following standard bacteriological procedures. Drug susceptibility tests were performed using disk diffusion technique. ESBL and carbapenemase enzymes were tested by double disk diffusion and modified carbapenem inhibition methods, respectively. The data obtained were analyzed using SPSS version 22 software, and descriptive statistics were summarized in tables and graphs.
Results: Out of 384 clinical specimens processed 100 (26%) were culture positive for . The proportion of infection was relatively higher among in-patients 86 (32.6%) than out-patients 14 (11.7%). Overall, 35 (9.1%) was the leading isolate followed by 31 (8.1%). 15 (15.6%) was the most frequent isolate from bloodstream infection and is the leading isolate from intensive care unit patients 15 (38.3%). Overall, 44 (44%) of were extended-spectrum beta-lactamase producers. Among them, spp. was the leading one 4 (80%) followed by 6 (60%) and . 18 (58.1%). Furthermore, 6 (6%) of were carbapenemase-producers, in which 5 (50%) of . and 3 (9.7%) of . had highest percentage. ESBL and carbapenemase-producing isolates of are alarmingly spreading in the study area. Thus, improving the infection prevention strategy and further screening at the national level is recommended to develop the optimal use of antibiotics.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837423 | PMC |
http://dx.doi.org/10.1155/2022/5727638 | DOI Listing |
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