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使用纸片扩散法和Etest法对利奈唑胺的抗菌谱和活性进行多中心评估:拉丁美洲Zyvox抗菌效力研究(LA-ZAPS)报告

Multicenter assessment of the linezolid spectrum and activity using the disk diffusion and Etest methods: report of the Zyvox(R) antimicrobial potency study in Latin America (LA-ZAPS).

作者信息

Ballow Charles H, Biedenbach Douglas J, Rossi Flavia, Jones Ronald N

机构信息

The Buffalo Clinical Research Center, Buffalo, NY, USA.

出版信息

Braz J Infect Dis. 2002 Jun;6(3):100-9. doi: 10.1590/s1413-86702002000300001.

Abstract

Linezolid was the first clinically applied member of the new antimicrobial class called the oxazolidinones. These agents have a powerful spectrum of activity focussed against Gram-positive organisms including strains with documented resistances to other antimicrobial classes. We conducted a multicenter surveillance (Zyvox Antimicrobial Potency Study; ZAPS) trial of qualifying Gram-positive isolates from 24 medical centers in eight countries in Latin America. The activity and spectrum of linezolid was compared to numerous agents including glycopeptides, quinupristin/dalfopristin, beta-lactams and fluoroquinolones when testing 2,640 strains by the standardized disk diffusion method or Etest (AB BIODISK, Solna, Sweden). The linezolid spectrum was complete against staphylococci (median zone diameter, 29 - 32 mm), as was the spectrum of vancomycin and quinupristin/dalfopristin. Among the enterococci, no linezolid resistance was detected, and the susceptibility rate was 93.1 - 96.4%. Only the vancomycin-susceptible Enterococcus faecium strains remained susceptible (92.8%) to quinupristin/dalfopristin. Marked differences in the glycopeptide resistance patterns (van A versus van B) were noted for the 22 isolates of VRE, thus requiring local susceptibility testing to direct therapy. Streptococcus pneumoniae and other species were very susceptible (100.0%) to linezolid, MIC(90) at 0.75 microg/ml. Penicillin non-susceptible rate was 27.7% and erythromycin resistance was at 17.4%. Other streptococci were also completely susceptible to linezolid (MIC(90), 1 microg/ml). These results provide the initial benchmark of potency and spectrum for linezolid in Latin American medical centers. Future comparisons should recognize that the oxazolidinones possess essentially a complete spectrum coverage of the monitored staphylococci, enterococci and streptococcal isolates in 2000-2001. This positions linezolid as the widest spectrum empiric choice against multi-resistant Gram-positive cocci, a spectrum of activity greater than available glycopeptides and the streptogramin combination.

摘要

利奈唑胺是新型抗菌药物恶唑烷酮类中首个临床应用的成员。这些药物具有强大的抗菌谱,主要针对革兰氏阳性菌,包括对其他抗菌药物耐药的菌株。我们在拉丁美洲八个国家的24个医疗中心开展了一项针对合格革兰氏阳性分离株的多中心监测(利奈唑胺抗菌效能研究;ZAPS)试验。采用标准化纸片扩散法或Etest(AB BIODISK,瑞典索尔纳)检测2640株菌株时,将利奈唑胺的活性和抗菌谱与多种药物进行了比较,这些药物包括糖肽类、奎奴普丁/达福普汀、β-内酰胺类和氟喹诺酮类。利奈唑胺对葡萄球菌的抗菌谱是完整的(抑菌圈直径中位数为29 - 32毫米),万古霉素和奎奴普丁/达福普汀的抗菌谱也是如此。在肠球菌中,未检测到利奈唑胺耐药,药敏率为93.1% - 96.4%。只有对万古霉素敏感的粪肠球菌菌株对奎奴普丁/达福普汀仍敏感(92.8%)。对于22株耐万古霉素肠球菌分离株,观察到糖肽类耐药模式(vanA与vanB)存在显著差异,因此需要进行当地药敏试验以指导治疗。肺炎链球菌和其他菌种对利奈唑胺非常敏感(100.0%),MIC(90)为0.75微克/毫升。青霉素不敏感率为27.7%,红霉素耐药率为17.4%。其他链球菌对利奈唑胺也完全敏感(MIC(90)为1微克/毫升)。这些结果为拉丁美洲医疗中心的利奈唑胺效力和抗菌谱提供了初步基准。未来的比较应认识到,恶唑烷酮类药物对2000 - 2001年监测的葡萄球菌、肠球菌和链球菌分离株基本上具有完整的抗菌谱覆盖。这使利奈唑胺成为针对多重耐药革兰氏阳性球菌的最广抗菌谱经验性选择,其抗菌谱活性大于现有的糖肽类和链阳菌素组合。

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