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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/16188
Title: Phenotypic expression and prevalence of multi drug resistant extended spectrum beta-lactamase producing Escherichia coli and Klebsiella pneumoniae in Karachi, Pakistan
Authors: Sakina Fatima
Muhammad, Iyad Naeem
Khan, Muhammad Naseem
Subia Jamil
Keywords: ESBL
Escherichia coli
Klebsiella pneumoniae
double disc synergy test
double disc synergy test
multidrug resistance.
Issue Date: 20-Jul-2018
Publisher: Karachi: Pakistan Botanical Society, University of Karachi
Citation: Fatima, S., Muhammad, I. N., Khan, M. N., & Jamil, S. (2018). Phenotypic expression and prevalence of multi drug resistant extended spectrum beta-lactamase producing Escherichia coli and Klebsiella pneumoniae in Karachi, Pakistan. Pak J Pharm Sci, 31(4), 1379-84.
Abstract: The aim of the present study was to evaluate the prevalence rate of ESBL producing Gram negative isolates of E. coli, K. pneumoniae and P. mirabilis, to determine the association of various factors with ESBL production and therapeutic options for the treatment. Total 352 isolates were subjected for identification of ESBL by double disc synergy test. Antimicrobial susceptibility was performed using CLSI guidelines and statistical association between ESBL/Non ESBL producers were determined by chi square at significant level of 0.05. A total of 96 isolates were ESBL positive (27%), females were 67% whereas males were 33%. E. coli was most prevalent pathogen (82%) followed by Klebsiella pneumoniae (17%). Furthermore 75% of ESBL associated infections were urinary tract infections. 95% of ESBL producing isolates were multidrug resistant and zobactam/piperacillin combination and imipenem are good choices with 100% and 97% susceptibility respectively. E coli (OR 2.83, 95% CI 1.585-5.072, RR 2.22, p 0.0004) and K. pneumoniae (OR 0.52, 95% CI 0.285-0.952, RR 0.609, p 0.032) were significantly associated with ESBL production. The spread of ESBL producing multidrug resistant E. coli and K. pneumoniae has increased and proper screening for ESBL identification is needed because of limited therapeutic antibiotic choices.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/16188
ISSN: 1011-601X
Appears in Collections:Issue 04

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