STUDIES ON SULBACTAM/CEFOPERAZONE
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- KUNII OTOHIKO
- Department of Internal Medicine, Institute of Medical Science, University of Tokyo
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- KOMATSU TAKASHI
- Department of Internal Medicine, Institute of Medical Science, University of Tokyo
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- NISHIYA HAJIME
- Department of Internal Medicine, Institute of Medical Science, University of Tokyo
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- HIRAYAMA MASAKIYO
- Department of Internal Medicine, Institute of Medical Science, University of Tokyo
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- ONO YASUO
- Department of Internal Medicine, Institute of Medical Science, University of Tokyo
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- MIWA SHIRO
- Department of Internal Medicine, Institute of Medical Science, University of Tokyo
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- ERIGUCHI MASAZUMI
- Department of Surgery, Institute of Medical Science, University of Tokyo
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- HONDA HIRAKU
- Department of Surgery, Institute of Medical Science, University of Tokyo
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- TOMORI GENICHI
- Department of Internal Medicine, Tokyo Metropolitan Fuchu Hospital
Bibliographic Information
- Other Title
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- Sulbactam/Cefoperazoneに関する研究
Abstract
Bacteriological and clinical effects of a new β-lactamase inhibitor, sulbactam (SBT), in combination with cefoperazone (CPZ) at a ratio of 1: I were investigated.<BR>The sensitivities of 101 strains of clinically isolated Gram-negative rods were measured against SBT/CPZ combination in comparison with CPZ, CMZ and CEZ.<BR>MIC's of SBT/CPZ against E. coli (41 strains) ranged between 0.1-100μg/ml with the peak MIC of 0.2-0.4μg/ml, which were superior to those of CEZ and CMZ, but equal to or 1 tube higher than those of CPZ most strains. Against Klebsiella (20 strains), MIC's of SBT/CPZ were distributed between < 0.1-25μg/ml with thepeak at 0.4μg/ml, which were superior to those of CEZ and CMZ, but equal to those of CPZ. Against P. aeruginosa (20 strains), MIC's of SBT/CPZ were distributed between 0.4-100μg/ml with the peak at 6.4 μg/ml, and mostly equal to or 1 tube higher than those of CPZ.<BR>Clinically, the SBT/CPZ was administered at a dose of 1-2g twice a day for 14-31 days by either dripinfusion or i.v. bolus to 7 patients; 5 cases of pneumonia and 1 case each of cholangitis and gingivitis. The overall efficacy was: excellent, 1; good, 5; poor, 1. No side effect was observed, but some laboratory abnormalities were detected in 4 cases, two of which had no clear causal relationship with the drug administration. Among the others, the increase of GOT and eosinophils was observed in one case, and the increase of GOT and GPT was observed in another. However, the increases in both cases were transient and mild.
Journal
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- CHEMOTHERAPY
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CHEMOTHERAPY 32 (Supplement4), 236-243, 1984
Japanese Society of Chemotherapy
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Details 詳細情報について
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- CRID
- 1390001206282565248
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- NII Article ID
- 130004194447
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- ISSN
- 18845894
- 00093165
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed