2020
DOI: 10.2147/idr.s245397
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<p>Epidemic Characteristics of Carbapenem-Resistant <em>Klebsiella pneumoniae</em> in the Pediatric Intensive Care Unit of Yanbian University Hospital, China</p>

Abstract: Introduction: Carbapenem-resistant Enterobacteriaceae (CRE) pose a serious threat to clinical patient management and public health, as they are generally resistant to most antibiotics and cause infections with high mortality rates. Klebsiella pneumoniae ranks second among Enterobacteriaceae species that cause nosocomial infections. In this study, we investigated the epidemic characteristics of carbapenem-resistant K. pneumoniae (CRKP) in the pediatric intensive care unit (PICU) of Yanbian University Hospital. … Show more

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Cited by 8 publications
(5 citation statements)
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“…19 The DNA of the strains was extracted by boiling method as PCR template. 20 Polymerase chain reaction (PCR) was used to detect carbapenem resistance genes (bla KPC , bla NDM , bla OXA-48 , bla VIM , bla IMP ), ESBL genes (bla CTX-M-1G , bla CTX-M-2G , bla CTX-M-8G , bla CTX-M-9G , bla SHV , bla TEM , bla OXA-1 ), plasmid-mediated quinolone resistance (PMQR) genes (qnrA, qnrB, qnrS, aac(6ʹ)-Ibcr), 16S rRNA methylase genes (armA, rmtB) and colistin resistance gene (mcr-1). [21][22][23][24][25] The positive amplified products were sequenced, and the sequences were compared with the database in the National Center for Biotechnology Information (NCBI) (https://www.ncbi.nlm.nih.gov/) by BLAST searches.…”
Section: Phenotypic Screening and Detection Of Resistant Determinantsmentioning
confidence: 99%
“…19 The DNA of the strains was extracted by boiling method as PCR template. 20 Polymerase chain reaction (PCR) was used to detect carbapenem resistance genes (bla KPC , bla NDM , bla OXA-48 , bla VIM , bla IMP ), ESBL genes (bla CTX-M-1G , bla CTX-M-2G , bla CTX-M-8G , bla CTX-M-9G , bla SHV , bla TEM , bla OXA-1 ), plasmid-mediated quinolone resistance (PMQR) genes (qnrA, qnrB, qnrS, aac(6ʹ)-Ibcr), 16S rRNA methylase genes (armA, rmtB) and colistin resistance gene (mcr-1). [21][22][23][24][25] The positive amplified products were sequenced, and the sequences were compared with the database in the National Center for Biotechnology Information (NCBI) (https://www.ncbi.nlm.nih.gov/) by BLAST searches.…”
Section: Phenotypic Screening and Detection Of Resistant Determinantsmentioning
confidence: 99%
“…Recommended by the CLSI2020, in this study, phenotypic screening for preliminarily determining whether the strain produced metallo-carbapenemase was performed in accordance with the modified Carbapenem Inactivation Method (mCIM) and EDTA-Modified Carbapenem Inactivation Method (eCIM). 25 To be brief, a single colony of isolates was inoculated into a tube containing 2 mL trypticase soy broth (TSB) and a tube containing 2 mL TSB with 5mM EDTA, respectively, and then stir the colony immediately to dissolve enough to be invisible. A disk containing 10 μg meropenem was placed in each tube and incubated at 37°C for 4 h. After that, these disks were taken out and placed on MH agar plates that were inoculated with a lawn of the meropenem-susceptible Escherichia coli ATCC25922 (0.5 McFarland standard).…”
Section: Methodsmentioning
confidence: 99%
“…The most commonly contaminated samples were collected from humidifiers, refrigerators, incubators, medication trolleys, trays and boxes and intensive care equipment. In a pediatric ICU, endemic multidrug-resistant Klebsiella pneumoniae was frequently isolated [ 68 , 69 ].…”
Section: Surfaces As a Potential Source Of Infectionmentioning
confidence: 99%