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Nationwide surveillance of bacterial respiratory pathogens conducted by the Japanese Society of Chemotherapy in 2008: general view of the pathogens’ antibacterial susceptibility

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Journal of Infection and Chemotherapy

Abstract

For the purpose of nationwide surveillance of the antimicrobial susceptibility of bacterial respiratory pathogens collected from patients in Japan, the Japanese Society of Chemotherapy conducted a third year of nationwide surveillance during the period from January to April 2008. A total of 1,097 strains were collected from clinical specimens obtained from well-diagnosed adult patients with respiratory tract infections. Susceptibility testing was evaluable with 987 strains (189 Staphylococcus aureus, 211 Streptococcus pneumoniae, 6 Streptococcus pyogenes, 187 Haemophilus influenzae, 106 Moraxella catarrhalis, 126 Klebsiella pneumoniae, and 162 Pseudomonas aeruginosa). A total of 44 antibacterial agents, including 26 β-lactams (four penicillins, three penicillins in combination with β-lactamase inhibitors, four oral cephems, eight parenteral cephems, one monobactam, five carbapenems, and one penem), three aminoglycosides, four macrolides (including a ketolide), one lincosamide, one tetracycline, two glycopeptides, six fluoroquinolones, and one oxazolidinone were used for the study. Analysis was conducted at the central reference laboratory according to the method recommended by the Clinical and Laboratory Standard Institute (CLSI). The incidence of methicillin-resistant S. aureus (MRSA) was as high as 59.8%, and those of penicillin-intermediate and penicillin-resistant S. pneumoniae (PISP and PRSP) were 35.5 and 11.8%, respectively. Among H. influenzae, 13.9% of them were found to be β-lactamase-non-producing ampicillin (ABPC)-intermediately resistant (BLNAI), 26.7% to be β-lactamase-non-producing ABPC-resistant (BLNAR), and 5.3% to be β-lactamase-producing ABPC-resistant (BLPAR) strains. A high frequency (76.5%) of β-lactamase-producing strains was suspected in Moraxella catarrhalis isolates. Four (3.2%) extended-spectrum β-lactamase-producing K. pneumoniae were found among 126 strains. Four isolates (2.5%) of P. aeruginosa were found to be metallo β-lactamase-producing strains, including three (1.9%) suspected multidrug-resistant strains showing resistance to imipenem, amikacin, and ciprofloxacin. Continual national surveillance of the antimicrobial susceptibility of respiratory pathogens is crucial in order to monitor changing patterns of susceptibility and to be able to update treatment recommendations on a regular basis.

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Acknowledgments

This investigation was supported by grants from the following pharmaceutical companies (in alphabetical order): Abbott Japan Co., Ltd.; Astellas Pharma Inc.; Banyu Pharmaceutical Co., Ltd.; Bayer Yakuhin, Ltd.; Chugai Pharmaceutical Co., Ltd.; Daiichi Sankyo Company Limited; Dainippon Sumitomo Pharma Co., Ltd.; Glaxo SmithKline K. K.; Kyorin Pharmaceutical Co., Ltd.; Meiji Seika Kaisha, Ltd.; Pfizer Japan Inc.; Sanofi-Aventis K.K., Shionogi & Co., Ltd.; Taiho Pharmaceutical Co., Ltd.; Taisho Pharmaceutical Co., Ltd.; Takeda Pharmaceutical Company Limited; and Toyama Chemical Co., Ltd. We are grateful to T. Nakae and C. Yanagisawa at the Kitasato Institute (Tokyo, Japan) for their encouragement with the microbiological testing and Y. Suzuki, H. Endo, and Y. Yamaguchi for their technical assistance in this surveillance.

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Correspondence to Yoshihito Niki.

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The members of The Japanese Society of Chemotherapy (JSC) Surveillance Committee are listed in the Appendix.

Appendix

Appendix

The Japanese Society of Chemotherapy Surveillance Committee

Y. Niki, T. Matsumoto, S. Kohno, N. Aoki, A. Watanabe, J. Sato, R. Hattori, N. Koashi, M. Terada, T. Kozuki, A. Maruo, K. Morita, K. Ogasawara, Y. Takahashi, K. Matsuda, K. Nakanishi, and K. Totsuka

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Niki, Y., Hanaki, H., Matsumoto, T. et al. Nationwide surveillance of bacterial respiratory pathogens conducted by the Japanese Society of Chemotherapy in 2008: general view of the pathogens’ antibacterial susceptibility. J Infect Chemother 17, 510–523 (2011). https://doi.org/10.1007/s10156-011-0214-5

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  • DOI: https://doi.org/10.1007/s10156-011-0214-5

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