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A multicentre study to determine the efficacy of flomoxef against extended-spectrum beta-lactamase producing in Malaysia. | LitMetric

AI Article Synopsis

Article Abstract

Background: The high burden of extended-spectrum beta-lactamase-producing (ESBL)-producing Enterobacterales worldwide, especially in the densely populated South East Asia poses a significant threat to the global transmission of antibiotic resistance. Molecular surveillance of ESBL-producing pathogens in this region is vital for understanding the local epidemiology, informing treatment choices, and addressing the regional and global implications of antibiotic resistance.

Methods: Therefore, an inventory surveillance of the ESBL- (ESBL-EC) isolates responsible for infections in Malaysian hospitals was conducted. Additionally, the efficacy of flomoxef and other established antibiotics against ESBL-EC was evaluated.

Results: A total of 127 non-repetitive ESBL-EC strains isolated from clinical samples were collected during a multicentre study performed in five representative Malaysian hospitals. Of all the isolates, 33.9% were isolated from surgical site infections and 85.8% were hospital-acquired infections. High rates of resistance to cefotaxime (100%), cefepime (100%), aztreonam (100%) and trimethoprim-sulfamethoxazole (100%) were observed based on the broth microdilution test. Carbapenems remained the most effective antibiotics against the ESBL-EC, followed by flomoxef. Antibiotic resistance genes were identified by PCR. The was the most prevalent ESBL gene, with 28 isolates (22%) harbouring only, 27 isolates (21.3%) co-harbouring and , and ten isolates (7.9%) co-harbouring and . A generalised linear model showed significant antibacterial activity of imipenem against different types of infection. Besides carbapenems, this study also demonstrated a satisfactory antibacterial activity of flomoxef (81.9%) on ESBL-EC, regardless of the types of ESBL genes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10691355PMC
http://dx.doi.org/10.7717/peerj.16393DOI Listing

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