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      KCI등재 SCOPUS

      Impact of Revised Broad-Spectrum Cephalosporin Clinical and Laboratory Standards Institute Breakpoints on Susceptibility in Enterobacteriaceae Producing AmpC β-Lactamase

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      https://www.riss.kr/link?id=A103554090

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      We evaluated the impact of revised Clinical and Laboratory Standards Institute (CLSI) breakpoints for broad-spectrum cephalosporins(BSCs) on the susceptibilities of 1,742 isolates of Enterobacter species, Serratia marcescens, Citrobacter freundii, andMorganella morganii. The 2011 CLSI criteria for cefotaxime and ceftazidime reduced the rates of susceptibility by 2.9% and5.9%, respectively. The 2014 CLSI criteria for cefepime reduced the rate of susceptibility by 13.9%, and categorized 11.8%isolates as susceptible-dose dependent (SDD) for cefepime. Among 183 isolates with extended-spectrum ß-lactamase (ESBL)phenotype, implementation of the new criteria reduced the rates of susceptibility to cefotaxime, ceftazidime, and cefepime by2.8%, 14.8%, and 53.6%, respectively. The proportion of ESBL phenotype among BSC-susceptible isolates was low (0.9% forcefotaxime, 3.0% for ceftazidime, and 3.3% for cefepime). In summary, implementation of new CLSI criteria led to little changein susceptibility to cefotaxime and ceftazidime but a substantial change in susceptibility to cefepime. The recognition of revisedCLSI criteria for BSC and SDD will help clinicians to select the optimal antibiotic and dosing regimen.
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      We evaluated the impact of revised Clinical and Laboratory Standards Institute (CLSI) breakpoints for broad-spectrum cephalosporins(BSCs) on the susceptibilities of 1,742 isolates of Enterobacter species, Serratia marcescens, Citrobacter freundii, and...

      We evaluated the impact of revised Clinical and Laboratory Standards Institute (CLSI) breakpoints for broad-spectrum cephalosporins(BSCs) on the susceptibilities of 1,742 isolates of Enterobacter species, Serratia marcescens, Citrobacter freundii, andMorganella morganii. The 2011 CLSI criteria for cefotaxime and ceftazidime reduced the rates of susceptibility by 2.9% and5.9%, respectively. The 2014 CLSI criteria for cefepime reduced the rate of susceptibility by 13.9%, and categorized 11.8%isolates as susceptible-dose dependent (SDD) for cefepime. Among 183 isolates with extended-spectrum ß-lactamase (ESBL)phenotype, implementation of the new criteria reduced the rates of susceptibility to cefotaxime, ceftazidime, and cefepime by2.8%, 14.8%, and 53.6%, respectively. The proportion of ESBL phenotype among BSC-susceptible isolates was low (0.9% forcefotaxime, 3.0% for ceftazidime, and 3.3% for cefepime). In summary, implementation of new CLSI criteria led to little changein susceptibility to cefotaxime and ceftazidime but a substantial change in susceptibility to cefepime. The recognition of revisedCLSI criteria for BSC and SDD will help clinicians to select the optimal antibiotic and dosing regimen.

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      참고문헌 (Reference)

      1 Andes D, "Treatment of infections with ESBL- producing organisms: pharmacokinetic and pharmacodynamic considerations" 11 (11): 10-17, 2005

      2 Choi SH, "Prevalence, microbiology, and clinical characteristics of extended-spectrum beta-lactamase- producing Enterobacter spp., Serratia marcescens, Citrobacter freundii, and Morganella morganii in Korea" 26 : 557-561, 2007

      3 김선종, "Prevalence and impact of extended-spectrum β-lactamase production on clinical outcomes in cancer patients with Enterobacter species bacteremia" 대한내과학회 29 (29): 637-646, 2014

      4 Clinical and Laboratory Standards Institue (CLSI), "Performance standards for antimicrobial susceptibility resting: 24th infomational supplment CLSI document M100-S24" CLSI 2014

      5 Clinical and Laboratory Standards Institue (CLSI), "Performance standards for antimicrobial susceptibility resting: 21th infomational supplment CLSI document M100-S21" CLSI 2011

      6 Hamada Y, "Impact of revised cefepime CLSI breakpoints on Escherichia coli and Klebsiella pneumoniae susceptibility and potential impact if applied to Pseudomonas aeruginosa" 53 : 1712-1714, 2015

      7 Stürenburg E, "Evaluation of a new cefepime-clavulanate ESBL Etest to detect extended-spectrum beta-lactamases in an Enterobacteriaceae strain collection" 54 : 134-138, 2004

      8 Sanders WE Jr, "Enterobacter spp.: pathogens poised to flourish at the turn of the century" 10 : 220-241, 1997

      9 Choi SH, "Emergence of antibiotic resistance during therapy for infections caused by Enterobacteriaceae producing AmpC beta-lactamase: implications for antibiotic use" 52 : 995-1000, 2008

      10 Jacoby GA, "Detection of extended-spectrum beta- lactamases in clinical isolates of Klebsiella pneumoniae and Escherichia coli" 34 : 908-911, 1996

      1 Andes D, "Treatment of infections with ESBL- producing organisms: pharmacokinetic and pharmacodynamic considerations" 11 (11): 10-17, 2005

      2 Choi SH, "Prevalence, microbiology, and clinical characteristics of extended-spectrum beta-lactamase- producing Enterobacter spp., Serratia marcescens, Citrobacter freundii, and Morganella morganii in Korea" 26 : 557-561, 2007

      3 김선종, "Prevalence and impact of extended-spectrum β-lactamase production on clinical outcomes in cancer patients with Enterobacter species bacteremia" 대한내과학회 29 (29): 637-646, 2014

      4 Clinical and Laboratory Standards Institue (CLSI), "Performance standards for antimicrobial susceptibility resting: 24th infomational supplment CLSI document M100-S24" CLSI 2014

      5 Clinical and Laboratory Standards Institue (CLSI), "Performance standards for antimicrobial susceptibility resting: 21th infomational supplment CLSI document M100-S21" CLSI 2011

      6 Hamada Y, "Impact of revised cefepime CLSI breakpoints on Escherichia coli and Klebsiella pneumoniae susceptibility and potential impact if applied to Pseudomonas aeruginosa" 53 : 1712-1714, 2015

      7 Stürenburg E, "Evaluation of a new cefepime-clavulanate ESBL Etest to detect extended-spectrum beta-lactamases in an Enterobacteriaceae strain collection" 54 : 134-138, 2004

      8 Sanders WE Jr, "Enterobacter spp.: pathogens poised to flourish at the turn of the century" 10 : 220-241, 1997

      9 Choi SH, "Emergence of antibiotic resistance during therapy for infections caused by Enterobacteriaceae producing AmpC beta-lactamase: implications for antibiotic use" 52 : 995-1000, 2008

      10 Jacoby GA, "Detection of extended-spectrum beta- lactamases in clinical isolates of Klebsiella pneumoniae and Escherichia coli" 34 : 908-911, 1996

      11 Towne TG, "Detection of SHV-type extended-spectrum beta-lactamase in Enterobacter isolates" 48 : 298-299, 210

      12 Cheong HS, "Clinical significance of infections caused by extended- spectrum beta-lactamase-producing Enterobacteriaceae blood isolates with inducible AmpC beta-lactamase" 18 : 446-452, 2012

      13 Kohner PC, "Cephalosporin MIC distribution of extended-spectrum-β-lactamase- and pAmpC-producing Escherichia coli and Klebsiella species" 47 : 2419-2425, 2009

      14 Lee NY, "Cefepime therapy for monomicrobial bacteremia caused by cefepime-susceptible extended-spectrum beta-lactamase- producing Enterobacteriaceae: MIC matters" 56 : 488-495, 2013

      15 Lee NY, "Cefepime therapy for monomicrobial Enterobacter cloacae bacteremia: Unfavorable outcomes in patients infected by cefepime-susceptible dose-dependent isolates" 59 : 7558-7563, 2015

      16 Dudley MN, "Antimicrobial Susceptibility Testing Subcommittee of the Clinical and Laboratory Standards Institute. Background and rationale for revised clinical and laboratory standards institute interpretive criteria (breakpoints) for Enterobacteriaceae and Pseudomonas aeruginosa: I. cephalosporins and aztreonam" 56 : 1301-1309, 2013

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 등재 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 등재 등재학술지 선정 (등재후보2차) KCI등재
      2010-02-25 학술지명변경 한글명 : 감염과화학요법 -> Infection and Chemotherapy
      외국어명 : Infection and Chemotherapy -> 미등록
      KCI등재후보
      2010-01-01 등재 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2009-08-25 학술지명변경 외국어명 : 미등록 -> Infection and Chemotherapy KCI등재후보
      2008-01-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
      2008-01-01 등재 등재후보 탈락 (등재후보1차)
      2006-01-01 등재 등재후보 1차 FAIL (등재후보2차) KCI등재후보
      2005-05-27 학술지등록 한글명 : 감염과화학요법
      외국어명 : 미등록
      KCI등재후보
      2005-01-01 등재 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2004-01-01 등재 등재후보 1차 FAIL (등재후보1차) KCI등재후보
      2002-01-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.24 0.24 0.24
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.2 0.2 0.46 0.29
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