Nationwide surveillance of antimicrobial susceptibility patterns of pathogens isolated from surgical site infections (SSI) in Japan
Abstract To investigate the trends of antimicrobial resistance in pathogens isolated from surgical site infections (SSI), a Japanese surveillance committee conducted the first nationwide survey. Seven main organisms were collected from SSI at 27 medical centers in 2010 and were shipped to a central...
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Veröffentlicht in: | Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 2012, Vol.18 (6), p.816-826 |
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creator | Takesue, Yoshio Watanabe, Akira Kusachi, Shinya Matsumoto, Tetsuro Iwamoto, Aikichi Totsuka, Kyoichi Sunakawa, Keisuke Yagisawa, Morimasa Sato, Junko Oguri, Toyoko Nakanishi, Kunio Hanaki, Hideaki Sumiyama, Yoshinobu Kitagawa, Yuko Wakabayashi, Go Koyama, Isamu Yanaga, Katsuhiko Konishi, Toshiro Fukushima, Ryoji Seki, Shiko Imai, Shun Shintani, Tsunehiro Tsukada, Hiroki Tsukada, Kazuhiro Omura, Kenji Mikamo, Hiroshige Takeyama, Hiromitsu Kusunoki, Masato Kubo, Shoji Shimizu, Junzo Hirai, Toshihiro Ohge, Hiroki Kadowaki, Akio Okamoto, Kohji Yanagihara, Katsunori |
description | Abstract To investigate the trends of antimicrobial resistance in pathogens isolated from surgical site infections (SSI), a Japanese surveillance committee conducted the first nationwide survey. Seven main organisms were collected from SSI at 27 medical centers in 2010 and were shipped to a central laboratory for antimicrobial susceptibility testing. A total of 702 isolates from 586 patients with SSI were included. Staphylococcus aureus (20.4 %) and Enterococcus faecalis (19.5 %) were the most common isolates, followed by Pseudomonas aeruginosa (15.4 %) and Bacteroides fragilis group (15.4 %). Methicillin-resistant S. aureus among S. aureus was 72.0 %. Vancomycin MIC 2 μg/ml strains accounted for 9.7 %. In Escherichia coli , 11 of 95 strains produced extended-spectrum β-lactamase ( Klebsiella pneumoniae , 0/53 strains). Of E. coli strains, 8.4 % were resistant to ceftazidime (CAZ) and 26.3 % to ciprofloxacin (CPFX). No P. aeruginosa strains produced metallo-β-lactamase. In P. aeruginosa , the resistance rates were 7.4 % to tazobactam/piperacillin (TAZ/PIPC), 10.2 % to imipenem (IPM), 2.8 % to meropenem, cefepime, and CPFX, and 0 % to gentamicin. In the B. fragilis group, the rates were 28.6 % to clindamycin, 5.7 % to cefmetazole, 2.9 % to TAZ/PIPC and IPM, and 0 % to metronidazole ( Bacteroides thetaiotaomicron ; 59.1, 36.4, 0, 0, 0 %). MIC90 of P. aeruginosa isolated 15 days or later after surgery rose in TAZ/PIPC, CAZ, IPM, and CPFX. In patients with American Society of Anesthesiologists (ASA) score ≥3, the resistance rates of P. aeruginosa to TAZ/PIPC and CAZ were higher than in patients with ASA ≤2. The data obtained in this study revealed the trend of the spread of resistance among common species that cause SSI. Timing of isolation from surgery and the patient’s physical status affected the selection of resistant organisms. |
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Seven main organisms were collected from SSI at 27 medical centers in 2010 and were shipped to a central laboratory for antimicrobial susceptibility testing. A total of 702 isolates from 586 patients with SSI were included. Staphylococcus aureus (20.4 %) and Enterococcus faecalis (19.5 %) were the most common isolates, followed by Pseudomonas aeruginosa (15.4 %) and Bacteroides fragilis group (15.4 %). Methicillin-resistant S. aureus among S. aureus was 72.0 %. Vancomycin MIC 2 μg/ml strains accounted for 9.7 %. In Escherichia coli , 11 of 95 strains produced extended-spectrum β-lactamase ( Klebsiella pneumoniae , 0/53 strains). Of E. coli strains, 8.4 % were resistant to ceftazidime (CAZ) and 26.3 % to ciprofloxacin (CPFX). No P. aeruginosa strains produced metallo-β-lactamase. In P. aeruginosa , the resistance rates were 7.4 % to tazobactam/piperacillin (TAZ/PIPC), 10.2 % to imipenem (IPM), 2.8 % to meropenem, cefepime, and CPFX, and 0 % to gentamicin. In the B. fragilis group, the rates were 28.6 % to clindamycin, 5.7 % to cefmetazole, 2.9 % to TAZ/PIPC and IPM, and 0 % to metronidazole ( Bacteroides thetaiotaomicron ; 59.1, 36.4, 0, 0, 0 %). MIC90 of P. aeruginosa isolated 15 days or later after surgery rose in TAZ/PIPC, CAZ, IPM, and CPFX. In patients with American Society of Anesthesiologists (ASA) score ≥3, the resistance rates of P. aeruginosa to TAZ/PIPC and CAZ were higher than in patients with ASA ≤2. The data obtained in this study revealed the trend of the spread of resistance among common species that cause SSI. Timing of isolation from surgery and the patient’s physical status affected the selection of resistant organisms.</description><identifier>ISSN: 1341-321X</identifier><identifier>EISSN: 1437-7780</identifier><identifier>DOI: 10.1007/s10156-012-0509-1</identifier><identifier>PMID: 23143280</identifier><language>eng</language><publisher>Japan: Elsevier Ltd</publisher><subject>Anti-Bacterial Agents - pharmacology ; Antibiotic susceptibility ; Bacteria - drug effects ; Bacteria - isolation & purification ; Bacteroides fragilis group ; Drug Resistance, Bacterial ; Hematology, Oncology and Palliative Medicine ; Humans ; Infectious Diseases ; Japan - epidemiology ; Medical Microbiology ; Medicine ; Medicine & Public Health ; Microbial Sensitivity Tests ; Surgical site infections ; Surgical Wound Infection - epidemiology ; Surgical Wound Infection - microbiology ; Surveillance ; Virology</subject><ispartof>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2012, Vol.18 (6), p.816-826</ispartof><rights>Japanese Society of Chemotherapy and the Japanese Association for Infectious Diseases</rights><rights>2012 Japanese Society of Chemotherapy and the Japanese Association for Infectious Diseases</rights><rights>Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c613t-bfcd8998e6078657ed57577397e51b00299aa640be9fb169493ed0e6f589a22a3</citedby><cites>FETCH-LOGICAL-c613t-bfcd8998e6078657ed57577397e51b00299aa640be9fb169493ed0e6f589a22a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10156-012-0509-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10156-012-0509-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23143280$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takesue, Yoshio</creatorcontrib><creatorcontrib>Watanabe, Akira</creatorcontrib><creatorcontrib>Kusachi, Shinya</creatorcontrib><creatorcontrib>Matsumoto, Tetsuro</creatorcontrib><creatorcontrib>Iwamoto, Aikichi</creatorcontrib><creatorcontrib>Totsuka, Kyoichi</creatorcontrib><creatorcontrib>Sunakawa, Keisuke</creatorcontrib><creatorcontrib>Yagisawa, Morimasa</creatorcontrib><creatorcontrib>Sato, Junko</creatorcontrib><creatorcontrib>Oguri, Toyoko</creatorcontrib><creatorcontrib>Nakanishi, Kunio</creatorcontrib><creatorcontrib>Hanaki, Hideaki</creatorcontrib><creatorcontrib>Sumiyama, Yoshinobu</creatorcontrib><creatorcontrib>Kitagawa, Yuko</creatorcontrib><creatorcontrib>Wakabayashi, Go</creatorcontrib><creatorcontrib>Koyama, Isamu</creatorcontrib><creatorcontrib>Yanaga, Katsuhiko</creatorcontrib><creatorcontrib>Konishi, Toshiro</creatorcontrib><creatorcontrib>Fukushima, Ryoji</creatorcontrib><creatorcontrib>Seki, Shiko</creatorcontrib><creatorcontrib>Imai, Shun</creatorcontrib><creatorcontrib>Shintani, Tsunehiro</creatorcontrib><creatorcontrib>Tsukada, Hiroki</creatorcontrib><creatorcontrib>Tsukada, Kazuhiro</creatorcontrib><creatorcontrib>Omura, Kenji</creatorcontrib><creatorcontrib>Mikamo, Hiroshige</creatorcontrib><creatorcontrib>Takeyama, Hiromitsu</creatorcontrib><creatorcontrib>Kusunoki, Masato</creatorcontrib><creatorcontrib>Kubo, Shoji</creatorcontrib><creatorcontrib>Shimizu, Junzo</creatorcontrib><creatorcontrib>Hirai, Toshihiro</creatorcontrib><creatorcontrib>Ohge, Hiroki</creatorcontrib><creatorcontrib>Kadowaki, Akio</creatorcontrib><creatorcontrib>Okamoto, Kohji</creatorcontrib><creatorcontrib>Yanagihara, Katsunori</creatorcontrib><title>Nationwide surveillance of antimicrobial susceptibility patterns of pathogens isolated from surgical site infections (SSI) in Japan</title><title>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</title><addtitle>J Infect Chemother</addtitle><addtitle>J Infect Chemother</addtitle><description>Abstract To investigate the trends of antimicrobial resistance in pathogens isolated from surgical site infections (SSI), a Japanese surveillance committee conducted the first nationwide survey. Seven main organisms were collected from SSI at 27 medical centers in 2010 and were shipped to a central laboratory for antimicrobial susceptibility testing. A total of 702 isolates from 586 patients with SSI were included. Staphylococcus aureus (20.4 %) and Enterococcus faecalis (19.5 %) were the most common isolates, followed by Pseudomonas aeruginosa (15.4 %) and Bacteroides fragilis group (15.4 %). Methicillin-resistant S. aureus among S. aureus was 72.0 %. Vancomycin MIC 2 μg/ml strains accounted for 9.7 %. In Escherichia coli , 11 of 95 strains produced extended-spectrum β-lactamase ( Klebsiella pneumoniae , 0/53 strains). Of E. coli strains, 8.4 % were resistant to ceftazidime (CAZ) and 26.3 % to ciprofloxacin (CPFX). No P. aeruginosa strains produced metallo-β-lactamase. In P. aeruginosa , the resistance rates were 7.4 % to tazobactam/piperacillin (TAZ/PIPC), 10.2 % to imipenem (IPM), 2.8 % to meropenem, cefepime, and CPFX, and 0 % to gentamicin. In the B. fragilis group, the rates were 28.6 % to clindamycin, 5.7 % to cefmetazole, 2.9 % to TAZ/PIPC and IPM, and 0 % to metronidazole ( Bacteroides thetaiotaomicron ; 59.1, 36.4, 0, 0, 0 %). MIC90 of P. aeruginosa isolated 15 days or later after surgery rose in TAZ/PIPC, CAZ, IPM, and CPFX. In patients with American Society of Anesthesiologists (ASA) score ≥3, the resistance rates of P. aeruginosa to TAZ/PIPC and CAZ were higher than in patients with ASA ≤2. The data obtained in this study revealed the trend of the spread of resistance among common species that cause SSI. Timing of isolation from surgery and the patient’s physical status affected the selection of resistant organisms.</description><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibiotic susceptibility</subject><subject>Bacteria - drug effects</subject><subject>Bacteria - isolation & purification</subject><subject>Bacteroides fragilis group</subject><subject>Drug Resistance, Bacterial</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Infectious Diseases</subject><subject>Japan - epidemiology</subject><subject>Medical Microbiology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Microbial Sensitivity Tests</subject><subject>Surgical site infections</subject><subject>Surgical Wound Infection - epidemiology</subject><subject>Surgical Wound Infection - microbiology</subject><subject>Surveillance</subject><subject>Virology</subject><issn>1341-321X</issn><issn>1437-7780</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uk1v1TAQjBCIfsAP4IJyLIfA2k7iWEhIqKJQVMHhgcTNcpLNY0sSp7ZT9M78cWylgMShJ6-9M7OaWWfZMwYvGYB85Rmwqi6A8QIqUAV7kB2zUshCygYexlqUrBCcfTvKTry_BmCyaprH2REXEcYbOM5-fTKB7PyTesz96m6RxtHMHeZ2yM0caKLO2ZbMGLu-wyVQSyOFQ76YENDNPgFj_d3uMV7I29EE7PPB2SkJ7qlLXAqY0zxgl4b5_Gy3u3wRH_KPZjHzk-zRYEaPT-_O0-zrxbsv5x-Kq8_vL8_fXhVdzUQo2qHrG6UarEE2dSWxr2QlpVASK9YCcKWMqUtoUQ0tq1WpBPaA9VA1ynBuxGl2tukuzt6s6IOeKHpKhtGuXjMuRVlXrIYIZRs0uvfe4aAXR5NxB81Ap-z1lr2O2euUvWaR8_xOfm0n7P8y_oQdAXwD-Nia9-j0tV3dHC3fq_p6I2FM5pYiyXeEcUM9uRin7i3dy37zH7sbaU47-YEH9P_max85epd-TPowMQrgUHHxG-CpuQQ</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Takesue, Yoshio</creator><creator>Watanabe, Akira</creator><creator>Kusachi, Shinya</creator><creator>Matsumoto, Tetsuro</creator><creator>Iwamoto, Aikichi</creator><creator>Totsuka, Kyoichi</creator><creator>Sunakawa, Keisuke</creator><creator>Yagisawa, Morimasa</creator><creator>Sato, Junko</creator><creator>Oguri, Toyoko</creator><creator>Nakanishi, Kunio</creator><creator>Hanaki, Hideaki</creator><creator>Sumiyama, Yoshinobu</creator><creator>Kitagawa, Yuko</creator><creator>Wakabayashi, Go</creator><creator>Koyama, Isamu</creator><creator>Yanaga, Katsuhiko</creator><creator>Konishi, Toshiro</creator><creator>Fukushima, Ryoji</creator><creator>Seki, Shiko</creator><creator>Imai, Shun</creator><creator>Shintani, Tsunehiro</creator><creator>Tsukada, Hiroki</creator><creator>Tsukada, Kazuhiro</creator><creator>Omura, Kenji</creator><creator>Mikamo, Hiroshige</creator><creator>Takeyama, Hiromitsu</creator><creator>Kusunoki, Masato</creator><creator>Kubo, Shoji</creator><creator>Shimizu, Junzo</creator><creator>Hirai, Toshihiro</creator><creator>Ohge, Hiroki</creator><creator>Kadowaki, Akio</creator><creator>Okamoto, Kohji</creator><creator>Yanagihara, Katsunori</creator><general>Elsevier Ltd</general><general>Springer Japan</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2012</creationdate><title>Nationwide surveillance of antimicrobial susceptibility patterns of pathogens isolated from surgical site infections (SSI) in Japan</title><author>Takesue, Yoshio ; Watanabe, Akira ; Kusachi, Shinya ; Matsumoto, Tetsuro ; Iwamoto, Aikichi ; Totsuka, Kyoichi ; Sunakawa, Keisuke ; Yagisawa, Morimasa ; Sato, Junko ; Oguri, Toyoko ; Nakanishi, Kunio ; Hanaki, Hideaki ; Sumiyama, Yoshinobu ; Kitagawa, Yuko ; Wakabayashi, Go ; Koyama, Isamu ; Yanaga, Katsuhiko ; Konishi, Toshiro ; Fukushima, Ryoji ; Seki, Shiko ; Imai, Shun ; Shintani, Tsunehiro ; Tsukada, Hiroki ; Tsukada, Kazuhiro ; Omura, Kenji ; Mikamo, Hiroshige ; Takeyama, Hiromitsu ; Kusunoki, Masato ; Kubo, Shoji ; Shimizu, Junzo ; Hirai, Toshihiro ; Ohge, Hiroki ; Kadowaki, Akio ; Okamoto, Kohji ; Yanagihara, Katsunori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c613t-bfcd8998e6078657ed57577397e51b00299aa640be9fb169493ed0e6f589a22a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Anti-Bacterial Agents - 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Academic</collection><jtitle>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takesue, Yoshio</au><au>Watanabe, Akira</au><au>Kusachi, Shinya</au><au>Matsumoto, Tetsuro</au><au>Iwamoto, Aikichi</au><au>Totsuka, Kyoichi</au><au>Sunakawa, Keisuke</au><au>Yagisawa, Morimasa</au><au>Sato, Junko</au><au>Oguri, Toyoko</au><au>Nakanishi, Kunio</au><au>Hanaki, Hideaki</au><au>Sumiyama, Yoshinobu</au><au>Kitagawa, Yuko</au><au>Wakabayashi, Go</au><au>Koyama, Isamu</au><au>Yanaga, Katsuhiko</au><au>Konishi, Toshiro</au><au>Fukushima, Ryoji</au><au>Seki, Shiko</au><au>Imai, Shun</au><au>Shintani, Tsunehiro</au><au>Tsukada, Hiroki</au><au>Tsukada, Kazuhiro</au><au>Omura, Kenji</au><au>Mikamo, Hiroshige</au><au>Takeyama, Hiromitsu</au><au>Kusunoki, Masato</au><au>Kubo, Shoji</au><au>Shimizu, Junzo</au><au>Hirai, Toshihiro</au><au>Ohge, Hiroki</au><au>Kadowaki, Akio</au><au>Okamoto, Kohji</au><au>Yanagihara, Katsunori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nationwide surveillance of antimicrobial susceptibility patterns of pathogens isolated from surgical site infections (SSI) in Japan</atitle><jtitle>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</jtitle><stitle>J Infect Chemother</stitle><addtitle>J Infect Chemother</addtitle><date>2012</date><risdate>2012</risdate><volume>18</volume><issue>6</issue><spage>816</spage><epage>826</epage><pages>816-826</pages><issn>1341-321X</issn><eissn>1437-7780</eissn><abstract>Abstract To investigate the trends of antimicrobial resistance in pathogens isolated from surgical site infections (SSI), a Japanese surveillance committee conducted the first nationwide survey. Seven main organisms were collected from SSI at 27 medical centers in 2010 and were shipped to a central laboratory for antimicrobial susceptibility testing. A total of 702 isolates from 586 patients with SSI were included. Staphylococcus aureus (20.4 %) and Enterococcus faecalis (19.5 %) were the most common isolates, followed by Pseudomonas aeruginosa (15.4 %) and Bacteroides fragilis group (15.4 %). Methicillin-resistant S. aureus among S. aureus was 72.0 %. Vancomycin MIC 2 μg/ml strains accounted for 9.7 %. In Escherichia coli , 11 of 95 strains produced extended-spectrum β-lactamase ( Klebsiella pneumoniae , 0/53 strains). Of E. coli strains, 8.4 % were resistant to ceftazidime (CAZ) and 26.3 % to ciprofloxacin (CPFX). No P. aeruginosa strains produced metallo-β-lactamase. In P. aeruginosa , the resistance rates were 7.4 % to tazobactam/piperacillin (TAZ/PIPC), 10.2 % to imipenem (IPM), 2.8 % to meropenem, cefepime, and CPFX, and 0 % to gentamicin. In the B. fragilis group, the rates were 28.6 % to clindamycin, 5.7 % to cefmetazole, 2.9 % to TAZ/PIPC and IPM, and 0 % to metronidazole ( Bacteroides thetaiotaomicron ; 59.1, 36.4, 0, 0, 0 %). MIC90 of P. aeruginosa isolated 15 days or later after surgery rose in TAZ/PIPC, CAZ, IPM, and CPFX. In patients with American Society of Anesthesiologists (ASA) score ≥3, the resistance rates of P. aeruginosa to TAZ/PIPC and CAZ were higher than in patients with ASA ≤2. The data obtained in this study revealed the trend of the spread of resistance among common species that cause SSI. Timing of isolation from surgery and the patient’s physical status affected the selection of resistant organisms.</abstract><cop>Japan</cop><pub>Elsevier Ltd</pub><pmid>23143280</pmid><doi>10.1007/s10156-012-0509-1</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1341-321X |
ispartof | Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2012, Vol.18 (6), p.816-826 |
issn | 1341-321X 1437-7780 |
language | eng |
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source | MEDLINE; Springer Nature - Complete Springer Journals; Alma/SFX Local Collection |
subjects | Anti-Bacterial Agents - pharmacology Antibiotic susceptibility Bacteria - drug effects Bacteria - isolation & purification Bacteroides fragilis group Drug Resistance, Bacterial Hematology, Oncology and Palliative Medicine Humans Infectious Diseases Japan - epidemiology Medical Microbiology Medicine Medicine & Public Health Microbial Sensitivity Tests Surgical site infections Surgical Wound Infection - epidemiology Surgical Wound Infection - microbiology Surveillance Virology |
title | Nationwide surveillance of antimicrobial susceptibility patterns of pathogens isolated from surgical site infections (SSI) in Japan |
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