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利奈唑胺对巴西分离出的革兰氏阳性球菌的抗菌活性。

Antimicrobial activity of linezolid against Gram-positive cocci isolated in Brazil.

作者信息

Sader H S, Gales A C, Jones R N

机构信息

Division of Infectious Diseases, Federal University of São Paulo, São Paulo, SP, Brazil.

出版信息

Braz J Infect Dis. 2001 Aug;5(4):171-6. doi: 10.1590/s1413-86702001000400002. Epub 2003 Mar 7.

Abstract

The new oxazolidinone linezolid and other antimicrobial agents used to treat Gram-positive infections were tested against 1,585 Gram-positive cocci; 1,260 staphylococci and enterococci isolates from patients hospitalized in Brazilian hospitals, and 325 S. pneumoniae isolates for patients with community acquired infections. Susceptibility testing was performed using broth microdilution according to NCCLS procedures. Linezolid was the most active compound and the only drug that inhibited 100% of the isolates at the susceptible breakpoint (< or = 4 microg/mL). Resistance to vancomycin was very rare (99.9% susceptibility), and both quinupristin/dalfopristin and gatifloxacin were active against approximately 90% of the strains evaluated. All other compounds inhibited less than 65% of the isolates. The excellent in vitro Gram-positive activity by linezolid, in this study, indicate that this compound may represent an important therapeutic option for the treatment of infections caused by these pathogens in Brazil.

摘要

新型恶唑烷酮类药物利奈唑胺及其他用于治疗革兰氏阳性菌感染的抗菌药物,对1585株革兰氏阳性球菌进行了测试;其中包括从巴西医院住院患者中分离出的1260株葡萄球菌和肠球菌,以及从社区获得性感染患者中分离出的325株肺炎链球菌。根据美国国家临床实验室标准委员会(NCCLS)的程序,采用肉汤微量稀释法进行药敏试验。利奈唑胺是活性最强的化合物,也是唯一一种在敏感折点(≤4μg/mL)时能抑制100%分离株的药物。对万古霉素的耐药性非常罕见(敏感性为99.9%),奎奴普丁/达福普汀和加替沙星对约90%的评估菌株有活性。所有其他化合物抑制的分离株不到65%。在本研究中,利奈唑胺出色的体外抗革兰氏阳性菌活性表明,该化合物可能是巴西治疗这些病原体引起的感染的重要治疗选择。

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