TY - JOUR
T1 - Nationwide surveillance of bacterial respiratory pathogens conducted by the Surveillance Committee of Japanese Society of Chemotherapy, Japanese Association for Infectious Diseases, and Japanese Society for Clinical Microbiology in 2009
T2 - General view of the pathogens' antibacterial susceptibility
AU - Watanabe, Akira
AU - Yanagihara, Katsunori
AU - Matsumoto, Tetsuya
AU - Kohno, Shigeru
AU - Aoki, Nobuki
AU - Oguri, Toyoko
AU - Sato, Junko
AU - Muratani, Tetsuro
AU - Yagisawa, Morimasa
AU - Ogasawara, Kazuhiko
AU - Koashi, Naoto
AU - Kozuki, Tsuneo
AU - Komoto, Akira
AU - Takahashi, Yoshisaburo
AU - Tsuji, Toshikatsu
AU - Terada, Michinori
AU - Nakanishi, Kunio
AU - Hattori, Rikizo
AU - Hirako, Yukio
AU - Maruo, Akinori
AU - Minamitani, Shinichi
AU - Morita, Kohei
AU - Wakamura, Tomotaro
AU - Sunakawa, Keisuke
AU - Hanaki, Hideaki
AU - Ohsaki, Yoshinobu
AU - Honda, Yasuhito
AU - Sasaoka, Shoichi
AU - Takeda, Hiroaki
AU - Ikeda, Hideki
AU - Sugai, Atsuko
AU - Miki, Makoto
AU - Nakanowatari, Susumu
AU - Takahashi, Hiroshi
AU - Utagawa, Mutsuko
AU - Kobayashi, Nobuyuki
AU - Takasaki, Jin
AU - Konosaki, Hisami
AU - Aoki, Yasuko
AU - Shoji, Michi
AU - Goto, Hajime
AU - Saraya, Takeshi
AU - Kurai, Daisuke
AU - Okazaki, Mitsuhiro
AU - Kobayashi, Yoshio
AU - Katono, Yasuhiro
AU - Kawana, Akihiko
AU - Saionji, Katsu
AU - Miyazawa, Naoki
AU - Sato, Yoshimi
AU - Watanuki, Yuji
AU - Kudo, Makoto
AU - Ehara, Shigeru
AU - Tsukada, Hiroki
AU - Imai, Yumiko
AU - Watabe, Nobuei
AU - Aso, Sakura
AU - Honma, Yasuo
AU - Mikamo, Hiroshige
AU - Yamagishi, Yuka
AU - Takesue, Yoshio
AU - Wada, Yasunao
AU - Nakamura, Tadahiro
AU - Mitsuno, Noriko
AU - Mikasa, Keiichi
AU - Kasahara, Kei
AU - Uno, Kenji
AU - Sano, Reiko
AU - Miyashita, Naoyuki
AU - Kurokawa, Yukinori
AU - Takaya, Mariko
AU - Kuwabara, Masao
AU - Watanabe, Yaeko
AU - Doi, Masao
AU - Shimizu, Satomi
AU - Negayama, Kiyoshi
AU - Kadota, Junichi
AU - Hiramatsu, Kazufumi
AU - Morinaga, Yoshitomo
AU - Honda, Junichi
AU - Fujita, Masaki
AU - Iwata, Satoshi
AU - Iwamoto, Aikichi
AU - Ezaki, Takayuki
AU - Onodera, Shoichi
AU - Kusachi, Shinya
AU - Tateda, Kazuhiro
AU - Tanaka, Michio
AU - Totsuka, Kyoichi
AU - Niki, Yoshihito
AU - Matsumoto, Tetsuro
N1 - Funding Information:
Conflict of interest Akira Watanabe is a consultant to Daiichi-Sankyo, Mitsubishi Tanabe Pharma corporation, Toyama Chemical, and Otsuka Pharmaceutical. A.W. has received a speaker’s honorarium from MSD Japan, Glaxo SmithKline K.K., Shionogi & Co. Ltd., Daiichi-Sankyo, Taisho Toyama Pharmaceutical, Dainippon Sumitomo Pharma and Pfizer Japan Inc.; and grant support from Kyorin Pharmaceutical, Shionogi & Co. Ltd., Taisho Pharmaceutical, Toy-ama Chemical, Daiichi-Sankyo, Dainippon Sumitomo Pharma, Taiho Pharma, and Meiji Seika Pharma. Shigeru Kohno has received a speaker’s honorarium from Glaxo SmithKline K.K., Shinogi & Co. Ltd., Astellas Pharma Inc., Daiichi-Sankyo, Taisho Toyama Pharmaceutical, Dainippon Sumitomo Pharma, Merck & Co., and Pfizer Japan Inc.; and grant support from Kyorin Pharmaceutical, Pfizer Japan Inc., Shinogi & Co. Ltd., Taisho Pharmaceutical, Toyama Chemical, Daiichi-Sankyo, Dainippon Sumitomo Pharma, Taiho Pharma, Meiji Seika Pharma, Astellas Pharma Inc., Merck & Co., Inc., Glaxo SmithKline K.K., and Chugai Pharmaceutical Co., Ltd. Tetsuya Matsumoto has received a speaker’s honorarium from Pfizer Japan Inc., Dainippon Sumitomo Pharma, and Meiji Seika Pharma. Naoto Koashi is an employee of Pfizer Japan Inc. Aikichi Iwamoto has received a speaker’s honorarium from Glaxo SmithKline K.K., Shinogi & Co. Ltd., Astellas Pharma Inc., Daiichi-Sankyo, Taisho Toyama Pharmaceutical, MSD Japan, Eiken Chemical Co. Ltd., Toyama Chemical, Janssen Pharmaceutical K.K., Abbott Japan Co. Ltd., ViiV Healthcare K.K., Bayer, Bristol-Myers Squibb, Torii Pharmaceutical Co. Ltd., Sysmex Corporation, and Pfizer Japan Inc.; and grant support from Toyama Chemical, Torii Pharmaceutical Co. Ltd., Astellas Pharma Inc., MSD Japan, Baxter, and Bristol-Myers Squibb. Keisuke Sunakawa has received a speaker’s honorarium from Meiji Seika Pharma, Taisho Toyama Pharmaceutical, and Shinogi & Co. Ltd. Hiroshige Mikamo has received a speaker’s honorarium from Astellas Pharma Inc., Daiichi-Sankyo, Taisho Toyama Pharmaceutical, Dainippon Sumitomo Pharma, and Pfizer Japan Inc. Satoshi Iwata has received a speaker’s honorarium from Meiji Seika Pharma, Pfizer Japan, Inc., Glaxo SmithKline K.K., Dainippon Sumitomo Pharma, MSD Japan, and Taisho Toyama Pharmaceutical Co., Ltd.; and grant support from Meiji Seika Pharma and Taisho Toyama Pharmaceutical. Yoshihito Niki has received a speaker’s honorarium from Astellas Pharma Inc., MSD Japan, Glaxo SmithKline K.K., Shionogi & Co. Ltd., Bayer, Daiichi-Sankyo, Taisho Toyama Pharmaceutical, Dai-nippon Sumitomo Pharma, and Pfizer Japan Inc.; and grant support from Astellas Pharma Inc., Kyorin Pharmaceutical, Shionogi & Co. Ltd., Taisho Pharmaceutical, Toyama Chemical, Daiichi-Sankyo, Dainippon Sumitomo Pharma, Taiho Pharma, Pfizer Japan Inc., Janssen Pharmaceutical K.K., and Meiji Seika Pharma.
Funding Information:
Acknowledgments This investigation was supported by grants from following pharmaceutical companies (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 Se-ika Kaisya, 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 in microbiological testing and Y. Suzuki, H. Endo, and Y. Yamaguchi for their technical assistance in this surveillance.
PY - 2012/10
Y1 - 2012/10
N2 - For the purpose of nationwide surveillance of antimicrobial susceptibility of bacterial respiratory pathogens from patients in Japan, the Japanese Society of Chemotherapy (JSC) started a survey in 2006. From 2009, JSC continued the survey in collaboration with the Japanese Association for Infectious Diseases and the Japanese Society for Clinical Microbiology. The fourth-year survey was conducted during the period from January and April 2009 by the three societies. A total of 684 strains were collected from clinical specimens obtained from well-diagnosed adult patients with respiratory tract infections. Susceptibility testing was evaluable with 635 strains (130 Staphylococcus aureus, 127 Streptococcus pneumoniae, 4 Streptococcus pyogenes, 123 Haemophilus influenzae, 70 Moraxella catarrhalis, 78 Klebsiella pneumoniae, and 103 Pseudomonas aeruginosa). A maximum of 45 antibacterial agents including 26 b-lactams (four penicillins, three penicillins in combination with b-lactamase inhibitors, four oral cephems, eight parenteral cephems, one monobactam, five carbapenems, and one penem), four aminoglycosides, four macrolides (including 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). Incidence of methicillin-resistant S. aureus (MRSA) was as high as 58.5 %, and that of penicillin-intermediate and penicillin-resistant S. pneumoniae (PISP and PRSP) was 6.3 % and 0.0 %, respectively. Among H. influenzae, 21.1 % of them were found to be b-lactamase-non-producing ampicillin (ABPC)-intermediately resistant (BLNAI), 18.7 % to be b-lactamasenon- producing ABPC-resistant (BLNAR), and 5.7 % to be b-lactamase-producing ABPC-resistant (BLPAR) strains. A high frequency (76.5 %) of b-lactamase-producing strains has been suspected in Moraxella catarrhalis isolates. Four (3.2 %) extended-spectrum b-lactamase-producing K. pneumoniae were found among 126 strains. Four isolates (2.5 %) of P. aeruginosa were found to be metallob- lactamase-producing strains, including three (1.9 %) suspected multi-drug resistant strains showing resistance against imipenem, amikacin, and ciprofloxacin. Continuous national surveillance of the antimicrobial susceptibility of respiratory pathogens is crucial to monitor changing patterns of susceptibility and to be able to update treatment recommendations on a regular basis.
AB - For the purpose of nationwide surveillance of antimicrobial susceptibility of bacterial respiratory pathogens from patients in Japan, the Japanese Society of Chemotherapy (JSC) started a survey in 2006. From 2009, JSC continued the survey in collaboration with the Japanese Association for Infectious Diseases and the Japanese Society for Clinical Microbiology. The fourth-year survey was conducted during the period from January and April 2009 by the three societies. A total of 684 strains were collected from clinical specimens obtained from well-diagnosed adult patients with respiratory tract infections. Susceptibility testing was evaluable with 635 strains (130 Staphylococcus aureus, 127 Streptococcus pneumoniae, 4 Streptococcus pyogenes, 123 Haemophilus influenzae, 70 Moraxella catarrhalis, 78 Klebsiella pneumoniae, and 103 Pseudomonas aeruginosa). A maximum of 45 antibacterial agents including 26 b-lactams (four penicillins, three penicillins in combination with b-lactamase inhibitors, four oral cephems, eight parenteral cephems, one monobactam, five carbapenems, and one penem), four aminoglycosides, four macrolides (including 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). Incidence of methicillin-resistant S. aureus (MRSA) was as high as 58.5 %, and that of penicillin-intermediate and penicillin-resistant S. pneumoniae (PISP and PRSP) was 6.3 % and 0.0 %, respectively. Among H. influenzae, 21.1 % of them were found to be b-lactamase-non-producing ampicillin (ABPC)-intermediately resistant (BLNAI), 18.7 % to be b-lactamasenon- producing ABPC-resistant (BLNAR), and 5.7 % to be b-lactamase-producing ABPC-resistant (BLPAR) strains. A high frequency (76.5 %) of b-lactamase-producing strains has been suspected in Moraxella catarrhalis isolates. Four (3.2 %) extended-spectrum b-lactamase-producing K. pneumoniae were found among 126 strains. Four isolates (2.5 %) of P. aeruginosa were found to be metallob- lactamase-producing strains, including three (1.9 %) suspected multi-drug resistant strains showing resistance against imipenem, amikacin, and ciprofloxacin. Continuous national surveillance of the antimicrobial susceptibility of respiratory pathogens is crucial to monitor changing patterns of susceptibility and to be able to update treatment recommendations on a regular basis.
KW - Resistance
KW - Respiratory tract infection
KW - Surveillance
KW - Susceptibility
UR - http://www.scopus.com/inward/record.url?scp=84871400356&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84871400356&partnerID=8YFLogxK
U2 - 10.1007/s10156-012-0434-3
DO - 10.1007/s10156-012-0434-3
M3 - Article
C2 - 22766652
AN - SCOPUS:84871400356
SN - 1341-321X
VL - 18
SP - 609
EP - 620
JO - Journal of Infection and Chemotherapy
JF - Journal of Infection and Chemotherapy
IS - 5
ER -