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Abstract

Vol.61 No.6 November 2013

Susceptibilities of 4,080 bacterial strains of clinical isolates to tazobactam/piperacillin and other antimicrobial agents as of 2010

Keizo Yamaguchi1), Yoshikazu Ishii2), Kazuhiro Tateda2), Chikara Shimizu3), Akira Suwabe4), Mitsuo Kaku5), Akira Hishinuma6), Shigefumi Maesaki7), Yoshio Kobayashi8), Shigemi Kondo9), Tetsuya Matsumoto10), Morihiro Iwata11), Sayoko Kawakami12), Yoshihito Otsuka13), Masato Maekawa14), Tetsuya Yagi15), Yuka Yamagishi16), Shinichi Fujita17), Yukio Hida18), Kaname Nakatani19), Satoshi Ichiyama20), Ikuko Fujimoto21), Hisashi Kohno22), Hakuo Takahashi23), Nobuchika Kusano24), Yukinori Kurokawa25), Yaeko Watanabe26), Kiyoshi Negayama27), Hitoshi Miyamoto28), Makiko Kiyosuke29), Kouichi Mashiba30), Katsunori Yanagihara31), Yosuke Aoki32) and Kazufumi Hiramatsu33)

1)Department of Advanced and Integrated Analysis of Infectious Diseases, Toho University School of Medicine, 5-21-16 Omori-nishi, Ota-ku, Tokyo, Japan
2)Department of Microbiology and Infectious Diseases, Toho University School of Medicine
3)Division of Laboratory and Transfusion Medicine, Hokkaido University Hospital
4)Central Clinical Laboratory, Iwate Medical University Hospital
5)The Department of Clinical Laboratory, Tohoku University Graduate School of Medicine
6)Department of Infection Control and Clinical Laboratory Medicine, Dokkyo Medical University
7)Department of Infectious Disease and Infection Control, Saitama Medical University
8)Department of Laboratory Medicine, Keio University Hospital
9)Department of Laboratory Medicine, Juntendo University School of Medicine
10)Department of Microbiology, Tokyo Medical University
11)Department of Clinical Laboratory, Toho University Omori Medical Center
12)Department of Infection Control and Prevention, Teikyo University Hospital
13)Laboratory of Medicine, Kameda Medical Center
14)Department of Laboratory Medicine, Hamamatsu University School of Medicine
15)Center of National and Public University Hospital for Infection Control, Nagoya University Hospital
16)Department of Clinical Infectious Diseases, Aichi Medical University Hospital
17)Department of Infection Control and Prevention, Kanazawa University Hospital
18)Department of Clinical Laboratories, University of Fukui Hospital
19)Central Clinical Laboratories, Mie University Hospital
20)Department of Clinical Laboratory Medicine and Infectious Diseases, Kyoto University Graduate School of Medicine
21)Clinical Laboratory, Nara Medical University Hospital
22)Department of Clinical Laboratory, Tenri Hospital
23)Clinical Sciences and Laboratory Medicine, Kansai Medical University Hirakata Hospital
24)Department of Infectious Disease, Okayama University Hospital
25)Central Clinical Laboratory, Kawasaki Medical School Hospital
26)Department of Laboratory Medicine, Hiroshima Prefectural Hospital
27)Department of Clinical Laboratory, Kagawa University Hospital
28)Division of Medical Technology, Ehime University Hospital
29)Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Hospital
30)Department of General Medicine・Department of Clinical Laboratory, Kitakyushu Municipal Medical Center
31)Laboratory Medicine, Nagasaki University Hospital
32)Division of Infectious Disease and Hospital Epidemiology, Saga University Hospital
33)Clinical Laboratory Center, Oita University Hospital

Abstract

Surveillance of β-lactamase production and susceptibilities to antimicrobial agents including tazobactam/piperacillin(TAZ/PIPC) in 4,080 bacterial strains isolated in 2010 were conducted in Japan. β-Lactamase production was investigated over 90% of the strains of Moraxella catarrhalis, Escherichia coli, Citrobacter spp., Klebsiella pneumoniae, Enterobacter cloacae, Serratia marcescens, indole-positive Proteus spp., Pseudomonas aeruginosa, Acinetobacter spp. and Bacteroides fragilis group., about 60% of staphylococci and 11.1% of Haemophilus influenzae. An increase of the β-lactamase producers in H. influenzae strains was noted, when compared with previous investigations conducted between 2001 and 2006. Extended spectrum β-lactamase(ESBLs) producing strains in E. coli, K. pneumoniae and P. mirabilis were 17.8%, 3.9% and 12.8%, respectively. Increasing levels of ESBLs producers in E. coli, K. pneumoniae and P. mirabilis were investigated compared with previous investigations. Metallo β-lactamase producers in E. cloacae, P. aeruginosa and Acinetobacter spp. were 2.5%, 1.0% and 3.3%, respectively, and no strain of S. marcescens was detected. Susceptibility of 4,080 strains to TAZ/PIPC based on the criteria of the Clinical and Laboratory Standards Institute were distributed from 80.9% in P. aeruginosa to 100% in methicillin-susceptible S. aureus and coagulase-negative staphylococci, P. mirabilis, Proteus spp. (except for Proteus mirabilis) and H. influenzae including β-lactamase-negative ampicillin-resistant H. influenzae. When compared with those in previous investigations, susceptibility to TAZ/PIPC in this decade was not changed and some species of Enterobacteriaceae tend to be susceptible. From these results, TAZ/PIPC is considered as a useful initial therapeutic antimicrobial agent for the infectious diseases reported in various therapeutic guidelines.

Key word

tazobactam/piperacillin, β-lactamase, susceptibility

Received

August 22, 2013

Accepted

September 2, 2013

Jpn. J. Chemother. 61 (6): 514-525, 2013