The effect of medium and inoculum on the activity of vancomycin and teicoplanin against coagulase-negative staphylococci.

Suppr

超能文献

作者信息

Felmingham D, Solomonides K, O'Hare M D, Wilson A P, Grüneberg R N

出版信息

J Antimicrob Chemother. 1987 Oct;20(4):609-10. doi: 10.1093/jac/20.4.609.

DOI:10.1093/jac/20.4.609

PMID:2960645

Abstract

摘要

相似文献

The effect of medium and inoculum on the activity of vancomycin and teicoplanin against coagulase-negative staphylococci.

J Antimicrob Chemother. 1987 Oct;20(4):609-10. doi: 10.1093/jac/20.4.609.

In-vitro induction of resistance in coagulase-negative staphylococci to vancomycin and teicoplanin.凝固酶阴性葡萄球菌对万古霉素和替考拉宁的体外耐药诱导

J Antimicrob Chemother. 1988 Sep;22(3):321-4. doi: 10.1093/jac/22.3.321.

Prevalence of Staphylococcus aureus and coagulase-negative staphylococci with decreased sensitivity to glycopeptides as assessed by determination of MICs.通过测定最低抑菌浓度评估对糖肽类敏感性降低的金黄色葡萄球菌和凝固酶阴性葡萄球菌的流行情况。

Eur J Clin Microbiol Infect Dis. 1990 Nov;9(11):820-2. doi: 10.1007/BF01967381.

[The invitro activity of teicoplanin and vancomycin against gram positive microorganisms (corrected)].替考拉宁和万古霉素对革兰氏阳性微生物的体外活性（校正后）

Mikrobiyol Bul. 1991 Oct;25(4):321-5.

Teicoplanin-resistant coagulase-negative staphylococci.

Lancet. 1987 Jan 3;1(8523):39. doi: 10.1016/s0140-6736(87)90724-0.

A comparison of the responses of staphylococci and streptococci to teicoplanin and vancomycin.葡萄球菌和链球菌对替考拉宁和万古霉素反应的比较。

J Antimicrob Chemother. 1987 Aug;20(2):155-64. doi: 10.1093/jac/20.2.155.

Percentages and distributions of teicoplanin- and vancomycin-resistant strains among coagulase-negative staphylococci.凝固酶阴性葡萄球菌中替考拉宁和万古霉素耐药菌株的百分比及分布情况。

Antimicrob Agents Chemother. 1990 May;34(5):899-900. doi: 10.1128/AAC.34.5.899.

Comparative evaluation of in vitro activity of teicoplanin and vancomycin against coagulase negative methicillin resistant staphylococci isolated from high-risk patients.

Biomed Pharmacother. 1991;45(1):43. doi: 10.1016/0753-3322(91)90153-k.

Synergy study of vancomycin or teicoplanin plus gentamicin against enterococci, Staphylococcus aureus and coagulase-negative staphylococci by time-kill method.采用时间杀菌法对万古霉素或替考拉宁联合庆大霉素针对肠球菌、金黄色葡萄球菌及凝固酶阴性葡萄球菌进行协同研究。

J Med Assoc Thai. 1991 Dec;74(12):669-74.

Influence of inoculum, medium and serum on the in-vitro susceptibility of coagulase-negative staphylococci to teicoplanin and vancomycin.接种物、培养基和血清对凝固酶阴性葡萄球菌体外对替考拉宁和万古霉素敏感性的影响。

J Antimicrob Chemother. 1996 Jun;37(6):1103-9. doi: 10.1093/jac/37.6.1103.

引用本文的文献

Molecular detection of antimicrobial resistance.抗菌药物耐药性的分子检测

Clin Microbiol Rev. 2001 Oct;14(4):836-71, table of contents. doi: 10.1128/CMR.14.4.836-871.2001.

Consequences of VanE-type resistance on efficacy of glycopeptides in vitro and in experimental endocarditis due to Enterococcus faecalis.粪肠球菌VanE型耐药对糖肽类药物体外及实验性心内膜炎疗效的影响。

Antimicrob Agents Chemother. 2001 Oct;45(10):2826-30. doi: 10.1128/AAC.45.10.2826-2830.2001.

Multidrug-resistant gram-positive pathogens. An update on current microbiological patterns.多重耐药革兰氏阳性病原体。当前微生物学模式的最新情况。

Drugs. 1997;54 Suppl 6:11-20. doi: 10.2165/00003495-199700546-00005.

Current perspectives on glycopeptide resistance.糖肽类耐药性的当前观点

Clin Microbiol Rev. 1995 Oct;8(4):585-615. doi: 10.1128/CMR.8.4.585.

Teicoplanin. A review of its antibacterial activity, pharmacokinetic properties and therapeutic potential.替考拉宁：抗菌活性、药代动力学特性及治疗潜力综述

Drugs. 1990 Sep;40(3):449-86. doi: 10.2165/00003495-199040030-00007.

In vitro activities of vancomycin and teicoplanin against coagulase-negative staphylococci isolated from neutropenic patients.万古霉素和替考拉宁对从中性粒细胞减少患者中分离出的凝固酶阴性葡萄球菌的体外活性。

Antimicrob Agents Chemother. 1990 May;34(5):901-3. doi: 10.1128/AAC.34.5.901.

Antimicrob Agents Chemother. 1990 May;34(5):899-900. doi: 10.1128/AAC.34.5.899.

Pharmacokinetic and pharmacodynamic requirements for antibiotic therapy of experimental endocarditis.实验性心内膜炎抗生素治疗的药代动力学和药效学要求。

Antimicrob Agents Chemother. 1992 Oct;36(10):2069-74. doi: 10.1128/AAC.36.10.2069.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验