본문 바로가기
KERD
논문KCI 등재

Ceftriaxone-sulbactam의 주요 호기성 및 혐기성 임상 분리균주에 대한 시험관내 항균력

In Vitro Activities of Ceftriaxone-Sulbactam against Major Aerobic and Anaerobic Bacteria from Clinical Samples

0

조회

0

다운로드

1

인용

0

참고문헌

키워드

초록

Background: β-lactam antibiotics are one of the most common antimicrobial agents. However, the increasing of β-lactamase-producing bacteria makes these agents less useful. Therefore, agents stable for β-lactamase have been developed. This study was conducted to determine the activities of the combination agent ceftriaxone-sulbactam and to compare its activities with other agents. Methods: A total of 437 clinical isolates of aerobic and anaerobic bacteria were collected in Severance Hospital from 2007 to 2011. Using 23 antimicrobial agents, antimicrobial susceptibility tests were performed using the Clinical and Laboratory Standards Institute (CLSI) agar dilution method. Results: The minimal inhibitory concentrations (MICs) of ceftriaxone and ceftriaxone-sulbactam were similar to or lower than those of other β-lactam antibiotics for methicillin-susceptible Staphylococcus aureus (MSSA), Streptococcus pneumoniae, S. pyogenes, and viridans group streptococci. For Moraxella catarrhalis, Neisseria gonorrhoeae, Haemophilus influenzae, and H. parainfluenzae, ceftriaxone and the ceftriaxone-sulbactam combination also show low MIC_(50) and MIC_(90). For extended-spectrum β-lactamase (ESBL)-producing E. coli, the MICs of ceftriaxone-sulbactam were lower than those of other cephalosporins. Among the anaerobes, ceftriaxone-sulbactam showed good activity compared to ceftriaxone alone for the Bacteroides fragilis group, B. thetaiotaomicron, other Bacteroides sp., Prevotella sp., and Porphyromonas sp. Conclusions: Ceftriaxone-sulbactam showed good antimicrobial activity and thus is useful for the treatment of infections by MSSA, S. pneumoniae,S. pyogenes, viridans group streptococci, M. catarrhalis, N. gonorrhoeae, H. influenzae, H. parainfluenzae, E. coli, and K. pneumoniae, B. fragilis group, B. thetaiotaomicron, other Bacteroides sp., Prevotella sp., and Porphyromonas sp.

Abstract

Background: β-lactam antibiotics are one of the most common antimicrobial agents. However, the increasing of β-lactamase-producing bacteria makes these agents less useful. Therefore, agents stable for β-lactamase have been developed. This study was conducted to determine the activities of the combination agent ceftriaxone-sulbactam and to compare its activities with other agents. Methods: A total of 437 clinical isolates of aerobic and anaerobic bacteria were collected in Severance Hospital from 2007 to 2011. Using 23 antimicrobial agents, antimicrobial susceptibility tests were performed using the Clinical and Laboratory Standards Institute (CLSI) agar dilution method. Results: The minimal inhibitory concentrations (MICs) of ceftriaxone and ceftriaxone-sulbactam were similar to or lower than those of other β-lactam antibiotics for methicillin-susceptible Staphylococcus aureus (MSSA), Streptococcus pneumoniae, S. pyogenes, and viridans group streptococci. For Moraxella catarrhalis, Neisseria gonorrhoeae, Haemophilus influenzae, and H. parainfluenzae, ceftriaxone and the ceftriaxone-sulbactam combination also show low MIC_(50) and MIC_(90). For extended-spectrum β-lactamase (ESBL)-producing E. coli, the MICs of ceftriaxone-sulbactam were lower than those of other cephalosporins. Among the anaerobes, ceftriaxone-sulbactam showed good activity compared to ceftriaxone alone for the Bacteroides fragilis group, B. thetaiotaomicron, other Bacteroides sp., Prevotella sp., and Porphyromonas sp. Conclusions: Ceftriaxone-sulbactam showed good antimicrobial activity and thus is useful for the treatment of infections by MSSA, S. pneumoniae,S. pyogenes, viridans group streptococci, M. catarrhalis, N. gonorrhoeae, H. influenzae, H. parainfluenzae, E. coli, and K. pneumoniae, B. fragilis group, B. thetaiotaomicron, other Bacteroides sp., Prevotella sp., and Porphyromonas sp.

참고문헌 (14)

  1. Livermore DM, "ß-Lactamases in laboratory and clinical resistance", Clin Microbiol Rev, 8, pp.557~584 (1995)
  2. Nordmann P, "Trends in ß-lactam resistance among Enterobacteriaceae", Clin Infect Dis, 27, pp.100~106 (1998)
  3. Moellering RC Jr, "Meeting the challenges of ß -lactamases", J Antimicrob Chemother, 31, pp.1~8 (1993)
  4. Sutherland R, "ß-lactam", ß-lactamase inhibitor combinations: development, antibacterial activity and clinical applications, 1995, pp.23, 191~200
  5. Bhattacharjee A, "Role of ß-lactamase inhibitors in enterobacterial isolates producing extended-spectrum ßlactamases", J Antimicrob Chemother, 61, pp.309~314 (2008)
  6. Fantin B, "Activity of sulbactam in combination with ceftriaxone in vitro and in experimental endocarditis caused by Escherichia coli producing SHV-2-like ß-lactamase", Antimicrob Agents Chemother, 34, pp.581~586 (1990)
  7. Caron F, "Ceftriaxone-sulbactam combination in rabbit endocarditis caused by a strain of Klebsiella pneumoniae producing extended-broad-spectrum TEM-3 ß-lactamase", Antimicrob Agents Chemother, 34, pp.2070~2074 (1990)
  8. Ferreira L, "Direct identification of urinary tract pathogens from urine samples by matrix-assisted laser desorption ionization-time of flight mass spectrometry", J Clin Microbiol, 48, pp.2110~2115 (2010)
  9. Moretti M, "CLSI EP17-A protocol: a useful tool for better understanding the low end performance of total prostate-specific antigen assays", Clin Chim Acta, 412, pp.1143~1145 (2011)
  10. Rice LB, "Resistance to cefoperazone-sulbactam in Klebsiella pneumoniae: evidence for enhanced resistance resulting from the coexistence of two different resistance mechanisms", Antimicrob Agents Chemother, 37, pp.1061~1064 (1993)
  11. Kaczmarek FS, "Genetic and molecular characterization of ß-lactamase-negative ampicillin-resistant Haemophilus influenzae with unusually high resistance to ampicillin", Antimicrob Agents Chemother, 48, pp.1630~1639 (2004)
  12. Kyungwon Lee, "Metallo-β-Lactamase-Producing Pseudomonas spp. in Korea: High Prevalence of Isolates with VIM-2 Type and Emergence of Isolates with IMP-1 Type", Yonsei Medical Journal, 50(3), pp.335~339 (2009), 연세대학교의과대학
  13. Nordmann P, "Emerging carbapenemases in Gram-negative aerobes", Clin Microbiol Infect, 8, pp.321~331 (2002)
  14. Michalopoulos A, "Treatment of Acinetobacter infections", Expert Opin Pharmacother, 11, pp.779~788 (2010)

관련 논문AI추천

Multicenter Study of Antimicrobial Susceptibility of Anaerobic Bacteria in Korea in 2012어영, 김명숙, 김미나, 박연준, 이경원, 이양순대한진단검사의학회 · Annals of Laboratory Medicine2015 · 제35권 제5호Comparison of Clinical and Laboratory Standards Institute and European Committee on Antimicrobial Susceptibility Testing Breakpoints for β-Lactams in Enterobacteriaceae Producing Extended-Spectrumβ-Lactamases and/or Plasmid-Mediated AmpCβ-Lactamases김재석, 김한성, 김현수, 박민정, 송원근, 이규만대한임상미생물학회 · Annals of Clinical Microbiology2011 · 제14권 제1호In vitro Antibacterial Activity of Doripenem against Gram-Negative Blood Isolates in a Korean Tertiary Care Center안미영, 이미경, 정진원, 최성호대한감염학회 · Infection and Chemotherapy2015 · 제47권 제3호알부민이 첨가된 시험관내 약역학 감염모델을 이용한 폐렴알균 치료에서 Ceftriaxone 일일 1회 요법김시현, 박선희, 신완식, 유진홍, 이동건, 전혜선, 최수미, 최정현, 허지안대한감염학회 · Infection and Chemotherapy2006 · 제38권 제6호임상 검체에서 분리된 세균에 대한 Cefcapene의 시험관내 항균력곽이경, 김남중, 김양수, 류지소, 우준희, 이미숙, 정진용, 최상호, 추은주대한감염학회 · Infection and Chemotherapy2005 · 제37권 제3호경구용 세팔로스포린계 항생제 Cefditoren pivoxil의 주요 임상분리세균에 대한 시험관내 항균력김의종, 이재규, 이종윤대한감염학회 · Infection and Chemotherapy2003 · 제35권 제4호

이 간행물의 다른 논문 (9건)