Title of article :
Evaluation of ceftriaxone-sulbactam-disodium edetate adjuvant combination against multi-drug resistant Gram-negative organisms
Author/Authors :
Gupta, Shilpi Department of Microbiology - Military Hospital - Bhopal, India , Kumar, Mahadevan Department of Microbiology - Bharati Vidyapeeth University Medical College - Pune, India , Shergill, Shelinder P.S. Department of Microbiology - Armed Forces Medical College - Pune, India , Tandel, Kundan Department of Microbiology - Command Hospital (Central Command) - Lucknow, India
Abstract :
Multi-drug resistant (MDR) Gram-negative bacteria are an emerging threat, both in hospital and community settings. As very few antibiotics are effective against such infections, the need of the hour is a new antibiotic or drug combination which can overcome the effect of extended-spectrum β-lactamases (ESBL) and metallo β-lactamases (MBL). A new antibiotic combination of ceftriaxone, sulbactam and disodium edetate (CSE) has recently been proposed to tackle the MDR organisms.
Objective
Our study was carried out to assess the susceptibility of ESBL- and MBL-producing Gram-negative organisms to CSE.
Methods
The study was conducted in a tertiary-care hospital in Delhi, India, from February 2017 to June 2017. A total of 179 MDR (85 ESBL + 94 MBL) Gram-negative isolates from various clinical samples, identified by an automated system (Vitek 2) were tested against CSE using the Kirby-Bauer disc diffusion method. Susceptibility to CSE was recorded based on interpretative zone sizes of ceftriaxone as per 2017 Clinical and Laboratory Standards Institute guidelines.
Results
The most common isolate was Escherichia coli (76/179; 42.4%) followed by Klebsiella pneumoniae (53/179; 29.6%) and Acinetobacter baumanii (27/179; 15.1%). The in vitro susceptibility of ESBL- and MBL-producing Gram-negative isolates to CSE was found to be 58/85 (68.2%) for ESBL and 37/94 (39.4%) for MBL.
Conclusion
The in vitro susceptibility results obtained for CSE against ESBL-producing organisms is promising. It has the potential to emerge as a carbapenem-sparing antibiotic, active against ESBL-producing strains. Further clinical studies are required to establish the clinical efficacy of CSE against MDR pathogens.
Keywords :
carbapenem-sparing , multi-drug resistance , disodium edetate , ceftriaxone sulbactam
Journal title :
African Journal of Laboratory Medicine