Introduction:
Antimicrobial resistance is growing threat worldwide. Various resistance
mechanisms have been found. ? -Lactamase antibiotics have been the mainstay of
treatment for serious infections, and most active of these are carbapenems.
Predominant mechanism for resistance to ?-lactam antibiotics in gram negative
bacilli (GNB) is production of extended spectrum ?-lactamases (ESBLs), AmpC and
Metallobetalactamases (MBLs). Aims and objectives: To detect various
?-lactamases in gram negative organisms with special reference to Metallo
?-lactamases (MBLs) from a tertiary care centre. Materials and methods: Study
was carried out from December 2014 to June 2015. Total number of 569 gram
negative bacilli were isolated and identified according to standard guidelines.
ESBL detection was done by a screening test using Ceftazidime disc which was
further confirmed by a double-disc synergy test using Piperacillin-Tazobactum/
Cefipime. AmpC were screened by a cefoxitin disc, confirmed by
Cefoxitin-cefotaxime disk antagonism. Carbapenemase detection was done with
Imipenem screening test which were further subjected to MBL production testing.
Result: Amongst 569 isolates, 177(31.1%) were ESBL producers, 51 (9%) were AmpC
producers, 31(5.5%) were ESBL and AmpC co-producers and 116(20.4%) were
carbapenemase producers. Out of total 116 carbapenemase producing strains 110
(94.8%) were positive for carbapenemase production by Modified Hodge Test. In
phenotypic methods for MBL production, Meropenem-EDTA disc method detected 85
(73.3%) isolates followed by Imipenem-EDTA 68 (58.6 %) and Ceftazidime-EDTA 52
(44.8%). Conclusion: It is need of the hour to standardise various cost
effective and time saving methods to detect these resistance mechanisms with
routine AST in Clinical Microbiology laboratory.see more
No comments:
Post a Comment