COMPARATIVE STUDIES ON ACTIVITIES OF ANTIMICROBIAL AGENTS AGAINST CAUSATIVE ORGANISMS ISOLATED FROM URINARY TRACT INFECTIONS (1988)
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- KOSAKAI NOZOMU
- Juntendo University Urayasu Hospital
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- KUMAMOTO YOSHIAKI
- Department of Urology, Sapporo Medical College
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- HIROSE TAKAOKI
- Department of Urology, Sapporo Medical College
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- TANAKA NORIAKI
- Department of Urology, Sapporo Medical College
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- HIKICHI YOSHINAO
- Katta Polyclinic Hospital
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- SHIGETA SHIRO
- Department of Bacteriology, Fukushima Medical College
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- SHIRAIWA YASUO
- Department of Urology, Fukushima Medical College
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- KAMEOKA HIROSHI
- Department of Urology, Fukushima Medical College
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- YOSHIDA HIROSHI
- Central Clinical Laboratories, Fukushima Medical College
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- OGATA MASAHIRO
- Central Clinical Laboratories, Fukushima Medical College
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- TAZAKI HIROSHI
- Department of Urology, School of Medicine, Keio University
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- IRI HISAMI
- Clinical Laboratories, School of Medicine, Keio University
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- UCHIDA HIROSHI
- Clinical Laboratories, School of Medicine, Keio University
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- KOBAYASHI YOSHIO
- Clinical Laboratories, School of Medicine, Keio University
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- MATSUDA SEIJI
- Department of Gynecology, Koto Hospital
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- KITAGAWA RYUICHI
- Department of Urology, Juntendo University School of Medicine
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- FUJITA KAZUHIKO
- Department of Urology, Juntendo University School of Medicine
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- HAYASHI YASUYUK
- Department of Clinical Pathology, Juntendo University School of Medicine
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- OGURI TOYOKO
- Clinical Laboratories, Juntendo University Hospital
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- FURUSAWA TARO
- Department of Urology, Kyoto Second Red Cross Hospital
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- TAKEUCHI YASUKO
- Clinical Laboratories, Kyoto Second Red Cross Hospital
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- MORIYAMA HIROMI
- Clinical Laboratories, Kyoto Second Red Cross Hospital
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- SHIBATA KIKUTARO
- Clinical Laboratories, Kyoto Second Red Cross Hospital
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- YONEZU SEIBUN
- The First Department of Internal Medicine, Kansai Medical University
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- TAKAHA MINATO
- Department of Urology, National Osaka Hospital
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- MATSUMIYA KIYOMI
- Department of Urology, National Osaka Hospital
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- TANAKA MICHIO
- Clinical Laboratories, National Osaka Hospital
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- YAMAGUCHI KEIZO
- Clinical Laboratories, School of Medicine, Nagasaki University
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- SUGAWARA KAZUYUKI
- Clinical Laboratories, School of Medicine, Nagasaki University
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- MOCHIDA CHIKAKO
- Clinical Laboratories, School of Medicine, Nagasaki University
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- HIRAKATA YOUICHI
- Clinical Laboratories, School of Medicine, Nagasaki University
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- IGARI JUN
- Department of Clinical Pathology, School of Health Science, Faculty of Medicine, University of Ryukyus
Bibliographic Information
- Other Title
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- 尿路感染症分離菌に対する経口並びに注射用抗菌・抗生剤の抗菌力比較 (第10報1988年)
- I. SUSCEPTIBILITY DISTRIBUTION
- その1.感受性について
Abstract
Isolation frequencies and sensitivities to antibacterial and antibiotic agents were investigated on 801 bacterial strains isolated from patients with urinary tract infections in 9 hospitals during the period of June to November 1988. Of the above total bacterial population, Gram-positive bacteria accounted for 29.3% and a majority of them were Enterococcus spp. Gram-negative bacteria accounted for 70.7% and most of them were Escherichia coli.<BR>1. Enterococcus faecalis<BR>Vancomycin was most active with its MIC90≤0.78μg/ml. Ampicillin, piperacillin, ofloxacin (OFLX), ciprofloxacin (CPFX) and imipenem (IPM) were also active.<BR>2. Staphylococcus aureus<BR>Arbekacin and minocycline were most active with their MIC90s 0.39μg/ml and 1.56μg/ml, respectively. Among penicillins, dicloxacillin was the most active. Activities of cephems were considerably lower.<BR>3. E. coli<BR>Most of the agents were tested active. Particularly the second and third generation cephems were active in a range of≤0.10-0.20μg/ml. Carumonam (CRMN), IPM, OFLX and CPFX were also active with MIC90s≤0.10μg/ml<BR>4. Klebsiella pneumoniae<BR>CRMN and IPM were highly active. Penicillins generally showed lower activities. Cephems and new quinolones had high activities with their MIC9os in a range of 0.39-0.78μg/ml.<BR>5. Proteus mirabilis<BR>The third generation cephems were active with their MIC90s in a range of≤0.10-0.20μg/ml. CRMN, OFLX and CPFX were also active with their MIC90s≤0.10μg/ml, 0.39μg/ml and 0.20g/ml, respectively.<BR>6. Pseudomonas aeruginosa<BR>IPM and tobramycin were active with their MIC90s 1.56μg/ml and 3.13μg/ml, respectively. CRMN and new quinolones showed MIC80s of 25-100μg/ml. Most of penicillins and cephems were not active.<BR>7. Other Gram-negative rods<BR>Against Citrobacter freundii, Enterobacter cloacae and Serratia marcescens, IPM, CPFX and OFLX were active. Penicillins and cephems were not so active. CRMN was active against S. marcescens with its MICK, at 6.25μg/ml.8
Journal
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- The Japanese Journal of Antibiotics
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The Japanese Journal of Antibiotics 45 (9), 1071-1102, 1992
Japan Antibiotics Research Association