2019
DOI: 10.1089/mdr.2017.0404
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Molecular Epidemiology and Drug Resistance Pattern of Carbapenem-ResistantKlebsiella pneumoniaeIsolates from Iran

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Cited by 40 publications
(43 citation statements)
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“…Carbapenem resistance in these is often mediated by NDM-1 and OXA-48 production followed by KPC (KPC-2), VIM (VIM-1 and VIM-4), and IMP (Rastegar Lari et al, 2013; Azimi et al, 2014; Nobari et al, 2014; Fazeli et al, 2015; Rajabnia et al, 2015; Firoozeh et al, 2016, 2017; Sedighi et al, 2017; Shahcheraghi et al, 2017; Armin et al, 2018; Ghotaslou et al, 2018; Hosseinzadeh et al, 2018; Moghadampour et al, 2018a). The majority of the studies reported no clonal relatedness among isolated carbapenem resistant K. pneumoniae in each center (Shahcheraghi et al, 2013; Jafari et al, 2018; Kiaei et al, 2018). This is with the exception of three centers where an identical genotype was observed for VIM-1 producers (Nobari et al, 2014), for NDM-1 producers the strains were distributed into two major clonal complexes including ST13 and ST392 (Shoja et al, 2018) and among NDM-1 and/or OXA-48 positive ones the predominant cluster/pulsotype was associated to ST11 and ST893 (Solgi et al, 2018).…”
Section: Distribution Of Multi-drug Resistant Organisms In Humansmentioning
confidence: 99%
“…Carbapenem resistance in these is often mediated by NDM-1 and OXA-48 production followed by KPC (KPC-2), VIM (VIM-1 and VIM-4), and IMP (Rastegar Lari et al, 2013; Azimi et al, 2014; Nobari et al, 2014; Fazeli et al, 2015; Rajabnia et al, 2015; Firoozeh et al, 2016, 2017; Sedighi et al, 2017; Shahcheraghi et al, 2017; Armin et al, 2018; Ghotaslou et al, 2018; Hosseinzadeh et al, 2018; Moghadampour et al, 2018a). The majority of the studies reported no clonal relatedness among isolated carbapenem resistant K. pneumoniae in each center (Shahcheraghi et al, 2013; Jafari et al, 2018; Kiaei et al, 2018). This is with the exception of three centers where an identical genotype was observed for VIM-1 producers (Nobari et al, 2014), for NDM-1 producers the strains were distributed into two major clonal complexes including ST13 and ST392 (Shoja et al, 2018) and among NDM-1 and/or OXA-48 positive ones the predominant cluster/pulsotype was associated to ST11 and ST893 (Solgi et al, 2018).…”
Section: Distribution Of Multi-drug Resistant Organisms In Humansmentioning
confidence: 99%
“…The increasing prevalence of multidrug-resistant (MDR) Gram-negative bacteria has led to re-introduction of colistin, especially for infections sustained by K. pneumoniae 4. Nevertheless, in the last years, colistin resistance has also emerged in CR -Kp with rates as high as 36% 3,13,14. In this case, resistance is due to structural modifications of lipopolysaccharide (LPS) that is the target for colistin.…”
Section: Introductionmentioning
confidence: 99%
“…Management of CR- Kp infections is associated with long hospitalizations and poor outcomes1,14 and complicated by MDR emergence, which severely limits antimicrobial treatment options 14. Since K. pneumoniae is among the most frequent agents in nosocomial settings,8 identification of outbreaks due to MDR strains is crucial.…”
Section: Introductionmentioning
confidence: 99%
“…Shokri et al (25) found that the tigecycline and fosfomycin are the most effective antibiotics against K. pneumonia and P. aeruginosa, who had New Dehli Metallo-β-lactamase, respectively, in Iranian patients. Moreover, a study recently conducted in Iran reported the effectiveness of tigecycline against K. pneumonia (26). According to an evidence-based review, carbapenem-resistant Gram-negative pathogens were the most challenging issue and antibiotic regimen, including carbapenem plus tigecycline or colistin, were the most effective therapeutic option in low-level resistance cases (27).…”
Section: Discussionmentioning
confidence: 99%