Antimicrobial Activity of Ceftazidime-Avibactam (CAZ-AVI) among the Carbapenemase-Producing Gram-negative Rods Isolated from Clinical Samples

Publish Year: 1402
نوع سند: مقاله ژورنالی
زبان: English
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JR_JMMI-11-2_006

تاریخ نمایه سازی: 29 بهمن 1402

Abstract:

Introduction: Treating Gram-negative bacteria that produce extended-spectrum beta-lactamases (ESBLs), AmpC Beta lactamases, and carbapenemases is a significant clinical concern worldwide. To address this concern, Ceftazidime-Avibactam has been approved by the United States Food and Drug Administration (USFDA) as a practical option for combating multi-drug resistant (MDR) and extensively drug-resistant (XDR) organisms. Our study focused on determining the extent to which MDR Gram-negative organisms from various clinical samples exhibited resistance to CAZ-AVI. Methods: Conducted at a central India tertiary care teaching hospital, our prospective study analyzed ۲۵۸ Gram-negative bacteria specimens. These bacterial strains were identified using standard biochemical tests. ESBL production was detected using the combination disk method, while the AmpC enzyme was detected using the Epsilometer test (E-test). Furthermore, we assessed carbapenemase production using disk diffusion methods. Our study used the E-test to identify Metallo-beta-lactamases and Klebsiella pneumonia carbapenemase (KPC) activity. Additionally, we utilized the E-test to analyze the susceptibility patterns of CAZ-AVI. Results: Of the ۲۵۸ Gram-negative isolates studied, ۲۱۴ (۸۳%) were ESBL producers. Among these isolates, ۹۰ (۳۵%) showed evidence of AmpC beta-lactamase production, with ۱۷ (۱۹%) being pure AmpC producers and ۷۳ (۸۱%) being ESBL co-producers. ۵۵ (۲۱.۵۰%) were found to be carbapenemase producers. Among these isolates, ۳۴ (۶۲%) were MBL producers, while ۱۱ (۲۰%) were KPC producers. Of the carbapenemase-producing isolates, ۱۴ (۲۵.۵۰%) were resistant to CAZ-AVI. Among the MDR isolates, we found that CI ۱۰۹ (۹۰%), PB ۱۱۸ (۹۷.۵۰%), and FO ۱۱۳ (۹۳.۵۰%) were the most effective antimicrobial agents. Conclusions: Gram-negative organisms that produce ESBL, AmpC, Carbapenemase, MBL, and KPC are particularly challenging for clinicians and a significant threat worldwide. However, our study results suggest that CAZ-AVI could be an effective standard therapy for managing MDR Gram-negative organisms.

Authors

Ravi Kumar Sharma

Department of Microbiology, Motilal Nehru Medical College, Prayagraj, Uttar Pradesh, India

Monica Monica

Department of Microbiology, Motilal Nehru Medical College, Prayagraj, Uttar Pradesh, India

Arindam Chakraborty

Department of Microbiology, Motilal Nehru Medical College, Prayagraj, Uttar Pradesh, India

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  • Clinical and laboratory standards institute. ۲۰۲۱. Performance standards for antimicrobial ...
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  • Kamat US, Fereirra A, Amonkar D, Motghare DD, Kulkarni MS. ...
  • Singh N, Pattnaik D, Neogi DK, Jena J, Mallick B. ...
  • Gajamer VR, Bhattacharjee A, Paul D, Ingti B, Sarkar A, ...
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