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자료유형
학술저널
저자정보
Jeong Seri (Department of Laboratory Medicine Kangnam Sacred Heart Hospital Hallym University College of Medici) Lee Nuri (Department of Laboratory Medicine Kangnam Sacred Heart Hospital Hallym University College of Medici) Park Min-Jeong (Department of Laboratory Medicine Kangnam Sacred Heart Hospital Hallym University College of Medici) Jeon Kibum (Department of Laboratory Medicine Hangang Sacred Heart Hospital Hallym University College of Medici) Kim Han-Sung (Department of Laboratory Medicine Hallym University Sacred Heart Hospital Hallym University College) Kim Hyun Soo (Department of Laboratory Medicine Dongtan Sacred Heart Hospital Hallym University College of Medici) Kim Jae-Seok (Department of Laboratory Medicine Kangdong Sacred Heart Hospital Seoul Korea) Song Wonkeun (Department of Laboratory Medicine Kangnam Sacred Heart Hospital Hallym University College of Medici)
저널정보
대한진단검사의학회 Annals of Laboratory Medicine Annals of Laboratory Medicine 제42권 제1호
발행연도
2022.1
수록면
36 - 46 (11page)
DOI
10.3343/alm.2022.42.1.36

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Background: The emergence of carbapenemase-producing Enterobacteriaceae (CPE) represents a major clinical problem. Recently, the occurrence of CPE has increased globally, but epidemiological patterns vary across region. We report the trends in the genotypic distribution and antimicrobial susceptibility of CPE isolated from rectal and clinical samples during a four-year period. Methods: Between January 2016 and December 2019, 1,254 nonduplicated CPE isolates were obtained from four university hospitals in Korea. Carbapenemase genotypes were determined by multiplex real-time PCR. Antimicrobial susceptibility was profiled using the Vitek 2 system (bioMerieux, Hazelwood, MO, USA) or MicroScan Walkaway-96 system (Siemens West Sacramento, CA, USA). The proportions of carbapenemase genotypes and nonsusceptibility were analyzed using Pearson’s chi-square test. Results: Among the 1,254 CPE isolates, 486 (38.8%), 371 (29.6%), 357 (28.5%), 8 (0.6%), 8 (0.6%), and 24 (1.9%) were Klebsiella pneumoniae carbapenemase (KPC), oxacillinase (OXA)-48-like, New Delhi metallo-β-lactamase (NDM), imipenemase (IMP), Verona integron-encoded metallo-β-lactamase (VIM), and multiple producers, respectively. The predominant species was K. pneumoniae (72.6%), followed by Escherichia coli (6.5%). More than 90% of the isolates harboring KPC, NDM, and OXA-48-like were nonsusceptible to cephalosporins, aztreonam, and carbapenems. Conclusions: The impact of CPE is primarily due to KPC-, NDM-, and OXA-48-like-producing K. pneumoniae isolates. Isolates carrying these carbapenemase are mostly multidrug-resistant. Control strategies based on these genotypic distributions and antimicrobial susceptibilities of CPE isolates are required.

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