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铜绿假单胞菌对新旧β-内酰胺类抗生素及氨基糖苷类抗生素的体外敏感性

In-vitro susceptibility of Pseudomonas aeruginosa to old and new beta-lactam antibiotics and aminoglycosides.

作者信息

Van der Auwera P, Schuyteneer F

出版信息

J Antimicrob Chemother. 1983 Jun;11(6):511-5. doi: 10.1093/jac/11.6.511.

DOI:10.1093/jac/11.6.511
PMID:6411673
Abstract

In-vitro, activities of gentamicin, tobramycin, netilmicin, amikacin, cefsulodin, latamoxef (moxalactam), carbenicillin, ticarcillin and piperacillin were compared against 147 randomly selected strains of Pseudomonas aeruginosa. Tobramycin was the most active aminoglycoside (MIC 90:4 mg/l), complete cross resistance with gentamicin (MIC 90:8 mg/l) was observed. Amikacin was the best alternative aminoglycoside (MIC 90:12 mg/l) Netilmicin showed only moderate activity (MIC 90:16 mg/l). Cefsulodin was the most active beta-lactam antibiotic (MIC 90:8 mg/l) but significant cross-resistance was observed with ticarcillin (MIC 90:32 mg/l) and piperacillin (MIC 90:12 micrograms/ml). Carbenicillin was two dilutions less active than ticarcillin, latamoxef showed a good activity (MIC 90:64 mg/l). Having the highest ratio between serum achievable concentration and MIC 90, piperacillin could be the best alternative drug to the aminoglycosides, of the tested antibiotics.

摘要

在体外实验中,比较了庆大霉素、妥布霉素、奈替米星、阿米卡星、头孢磺啶、拉氧头孢(羟羧氧酰胺菌素)、羧苄西林、替卡西林和哌拉西林对147株随机选择的铜绿假单胞菌的活性。妥布霉素是活性最强的氨基糖苷类药物(MIC90:4毫克/升),观察到与庆大霉素完全交叉耐药(MIC90:8毫克/升)。阿米卡星是最佳的替代氨基糖苷类药物(MIC90:12毫克/升),奈替米星仅表现出中等活性(MIC90:16毫克/升)。头孢磺啶是活性最强的β-内酰胺类抗生素(MIC90:8毫克/升),但观察到与替卡西林(MIC90:32毫克/升)和哌拉西林(MIC90:12微克/毫升)有显著交叉耐药。羧苄西林的活性比替卡西林低两个稀释度,拉氧头孢表现出良好的活性(MIC90:64毫克/升)。在受试抗生素中,哌拉西林的血清可达到浓度与MIC90之比最高,可能是氨基糖苷类药物的最佳替代药物。

相似文献

1
In-vitro susceptibility of Pseudomonas aeruginosa to old and new beta-lactam antibiotics and aminoglycosides.铜绿假单胞菌对新旧β-内酰胺类抗生素及氨基糖苷类抗生素的体外敏感性
J Antimicrob Chemother. 1983 Jun;11(6):511-5. doi: 10.1093/jac/11.6.511.
2
Comparative antibacterial activities of new beta-lactam antibiotics against Pseudomonas aeruginosa.新型β-内酰胺类抗生素对铜绿假单胞菌的抗菌活性比较
Chemotherapy. 1985;31(4):292-6. doi: 10.1159/000238350.
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Latamoxef in combination with aminoglycosides against Pseudomonas aeruginosa: similarity with ticarcillin.拉氧头孢联合氨基糖苷类药物治疗铜绿假单胞菌:与替卡西林的相似性
Chemotherapy. 1985;31(2):102-11. doi: 10.1159/000238321.
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Pathol Biol (Paris). 1987 May;35(5):558-62.
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Infection. 1982;10 Suppl 3:S257-61. doi: 10.1007/BF01640684.
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[Value of bactericidal curves in the optimal selection of a beta-lactam-aminoglycoside combination on Pseudomonas aeruginosa. In vitro study of 40 strains of Pseudomonas aeruginosa isolated in pediatric intensive care units].[杀菌曲线在优化选择β-内酰胺类抗生素与氨基糖苷类抗生素联合治疗铜绿假单胞菌中的价值。对儿科重症监护病房分离出的40株铜绿假单胞菌进行的体外研究]
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Susceptibility of Pseudomonas aeruginosa strains isolated from hospitalized children.从住院儿童中分离出的铜绿假单胞菌菌株的易感性。
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Activity of cefsulodin, other beta-lactams, and aminoglycosides against Pseudomonas aeruginosa.头孢磺啶、其他β-内酰胺类抗生素及氨基糖苷类抗生素对铜绿假单胞菌的活性。
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In vitro activity of piperacillin, ticarcillin, and mezlocillin alone and in combination with aminoglycosides against Pseudomonas aeruginosa.哌拉西林、替卡西林和美洛西林单独及与氨基糖苷类联合应用对铜绿假单胞菌的体外活性。
Antimicrob Agents Chemother. 1986 Jul;30(1):25-30. doi: 10.1128/AAC.30.1.25.

引用本文的文献

1
Clinical pharmacokinetics of the third generation cephalosporins.第三代头孢菌素的临床药代动力学
Clin Pharmacokinet. 1985 Mar-Apr;10(2):101-43. doi: 10.2165/00003088-198510020-00001.
2
In vitro activity of carumonam (RO 17-2301) and twelve other antimicrobials against clinical isolates of Pseudomonas aeruginosa.卡芦莫南(RO 17-2301)及其他12种抗菌药物对铜绿假单胞菌临床分离株的体外活性
Eur J Clin Microbiol. 1986 Jun;5(3):292-6. doi: 10.1007/BF02017784.
3
Netilmicin. A review of its antibacterial activity, pharmacokinetic properties and therapeutic use.
奈替米星。对其抗菌活性、药代动力学特性及治疗用途的综述。
Drugs. 1989 Nov;38(5):703-56. doi: 10.2165/00003495-198938050-00003.