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曲伐沙星治疗实验性金黄色葡萄球菌心内膜炎的疗效。

Efficacy of trovafloxacin against experimental Staphylococcus aureus endocarditis.

作者信息

Kaatz G W, Seo S M, Aeschlimann J R, Houlihan H H, Mercier R C, Rybak M J

机构信息

Department of Internal Medicine, Department of Veteran's Affairs Medical Center, Wayne State University, Detroit, Michigan 48201, USA.

出版信息

Antimicrob Agents Chemother. 1998 Feb;42(2):254-6. doi: 10.1128/AAC.42.2.254.

Abstract

Trovafloxacin is a new fluoronaphthyridone chemically and functionally related to members of the fluoroquinolone class of antimicrobial agents. The in vivo efficacy of the drug was compared with that of vancomycin by using the rabbit model of left-sided endocarditis. Rabbits infected with either a nafcillin-susceptible or -resistant test strain were treated with trovafloxacin (13.3 mg/kg of body weight every 12 h) or vancomycin (25 mg/kg of body weight every 8 h) for 4 days. In comparison with untreated controls, both antimicrobial agents effectively cleared bacteremia and significantly reduced bacterial counts in vegetations and tissues of animals infected with either test strain. No resistance to trovafloxacin emerged in test strains during therapy. We conclude that in this model trovafloxacin is as efficacious as vancomycin is and may serve as a viable alternative to vancomycin for use in humans with similar infections.

摘要

曲伐沙星是一种新型氟萘啶酮,在化学结构和功能上与氟喹诺酮类抗菌药物相关。通过使用左侧心内膜炎的兔模型,比较了该药物与万古霉素的体内疗效。用曲伐沙星(每12小时13.3mg/kg体重)或万古霉素(每8小时25mg/kg体重)治疗感染了对萘夫西林敏感或耐药测试菌株的兔子4天。与未治疗的对照组相比,两种抗菌药物均有效清除菌血症,并显著降低感染任一测试菌株动物的赘生物和组织中的细菌计数。治疗期间测试菌株未出现对曲伐沙星的耐药性。我们得出结论,在该模型中曲伐沙星与万古霉素疗效相当,对于患有类似感染的人类,可作为万古霉素的可行替代药物。

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The chemistry and biological profile of trovafloxacin.曲伐沙星的化学和生物学特性。
J Antimicrob Chemother. 1997 Jun;39 Suppl B:1-14. doi: 10.1093/jac/39.suppl_2.1.

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