期刊文献+

监测利奈唑胺对临床分离的耐甲氧西林金黄色葡萄球菌的体外抗菌活性 被引量:1

Monitoring the antimicrobial activity in vitro of linezolid on clinical separated methicillin-resistant staphylococcus aureus
下载PDF
导出
摘要 目的了解临床分离的耐甲氧西林金黄色葡萄球菌(MRSA)对利奈唑胺的敏感性及对其他抗菌药物的耐药情况,为临床合理选用抗菌药物提供依据。方法收集本院2008年6月至2011年6月期间住院患者各类临床送检标本,进行细菌学培养鉴定,按湖北地区监测网统一方案进行药物敏感性试验,依据CLSI2009年版标准判读结果,用WHONET 5.4软件进行统计数据分析。结果 2008年6月至2011年6月期间共分离出金黄色葡萄球菌297株,其中MRSA 116株。分离出MRSA的标本以痰标本为主,其次为分泌物和血液。MRSA对利奈唑胺、万古霉素、替考拉林敏感率为100%;对复方新诺明、氯霉素敏感率大于80%;对青霉素、苯唑西林100%耐药;对其他药物敏感性较低。结论 MRSA对大部分抗菌药物仍维持较高的耐药率,利奈唑胺与万古霉素、替考拉林一样是为数不多,仍然对MRSA表现较强抗菌活性的药物之一。 Objective To understand the sensitivity of separated methicillin-resistant staphylococcus aureus(MRSA) on linezolid and the drug resistance to other antibiotics,and provide the basis for choosing antimicrobial drugs for clinical use.Methods We collected all kinds of isolated clinical specimens of hospitalized patients from June 2008 to June 2011,which were cultured and identified by bacteriology.According to Hubei area unified monitoring network scheme,we did the drug sensitivity test based on the standard of CLSI2009 edition standard interpretation results,with WHONET 5.4 software for statistical data analysis.Results From June 2008 to June 2011,297 strains of staphylococcus aureus(SAU) were separated,including 116 strains of MRSA.Isolated specimens of MRSA were mostly in sputum samples,followed by secretion and blood.The sensitive rate of MRSA to linezolid,vancomycin,teicoplanin was 100%;and that to compound sulfamethoxazole and chloromycetin was more than 80%;The drug resistance rate of MRSA to penicillin and oxacillin was 100%,and that to other drugs was low.Conclusion The drug resistance of MRSA to most antimicrobial drugs is high,but the sensitive rate of MRSA to linezolid,vancomycin and teicoplanin is high.
作者 朱明 朱磊
出处 《检验医学与临床》 CAS 2012年第13期1559-1560,共2页 Laboratory Medicine and Clinic
关键词 利奈唑胺 耐甲氧西林金黄色葡萄球菌 耐药 linezolid; methicillin-resistant staphylococcus aureus; drug resistance
  • 相关文献

参考文献11

  • 1林东昉.恶唑烷酮类抗菌药:利奈唑胺[J].中国抗感染化疗杂志,2001,1(3):184-186. 被引量:12
  • 2欧阳育琪,林应标,黄红卫,黄强,熊劲芝.多重耐药大肠埃希菌产β-内酰胺酶及耐药表型分析[J].检验医学与临床,2010,7(13):1283-1285. 被引量:3
  • 3应春妹,陆丽,汪雅萍,张灏,于嘉屏.大肠埃希菌和肺炎克雷伯菌超广谱β-内酰胺酶检测及其耐药基因分析[J].检验医学,2007,22(3):272-275. 被引量:31
  • 4Katayama Y,ho T, Hiramatsu K. A new class of genetic element, Staphylococcus cassette chromosome mee, encodes methicillin resistance in staphylococcus aureus[J]. Antimicrob Agents Chemother, 2000,44(6) : 1549-1555.
  • 5Cercenado E, Garcia-Garrote F, Bouza E. In vitro activity of linezolid agaist multiply resistant Gram-positive clinical isolates[J]. J Antimierob Chernother, 2001,47 (1) : 77-81.
  • 6Gemmell CG. Susceptibility of a variety of clinical isolates to linezolid: a European inter-country comparison [J]. J Antimicrob Chemother, 2001,48 ( 1 ) : 47-52.
  • 7Linden P. Ues of linczolid for gram positive infections[J]. Infect Med,2002,19(1) :25-32.
  • 8Diekema DJ ,Jones RN. Oxazoiidinone antibiotics[J]. Lancet,2001,358(9297) : 1975-1982.
  • 9Sisson TL, Jungbluth GL, Hopkins NK. Age and sex effects on the pharmacokinetics of linezolid [J]. Eur J Clin Pharmacol, 2002,57 ( 11 ) : 793-797.
  • 10Cazzola M,Blasi F, Centanni S, et al. Advances in the research and development of chemotherapeutic agents for respiratory tract bacterial infections[J]. Pulm Pharmacol Ther, 2001,14(5) : 367-381.

二级参考文献32

  • 1朱德妹,汪复,张婴元.2003年上海地区细菌耐药性监测[J].中国抗感染化疗杂志,2005,5(1):4-12. 被引量:147
  • 2潘晓龙,周东升,吴祥林,富铮,孙芸,徐元宏.产超广谱β-内酰胺酶大肠埃希菌表型及基因型研究[J].检验医学,2005,20(5):462-466. 被引量:13
  • 3邵剑春,胡大春,杨绍敏,周玲,李超,刘德华.产ESBLs大肠埃希菌和肺炎克雷伯菌的检测及其基因分析[J].国外医学(临床生物化学与检验学分册),2005,26(12):872-876. 被引量:11
  • 4Hayden MK. Insights into the epidemiology and control of infection with vancom ycin resistant enterococci[J]. Clin Infect Dis,2001,31(4):1058-1065
  • 5Shinabarger DL, Marotti KR,Murray RW,et al.Mechanism of action of oxazolidinone s:effects of linezolid and eperezolid on translation reactions[J]. Antimicrob Agents Chemother,1997,41(10): 2132-2136
  • 6Kaatz GW,Seo SM. In vitro activities of oxazolidinone compounds U-100592 and U -100766 against Staphylococcus aureus and Staphylococcus epdermidis[J]. Antim icrob Agents Chemother, 1996,40(3):799-801
  • 7Zurenko GE,Yagi BH,Schaadt RD,et al.In vitro activities of U-100592 and U-1007 66,novel oxazolidinone antibacterial agents[J]. Antimicrob Agents Chemother,19 96,40(4):839-845
  • 8Jones RN,Johnson DM,Erwin ME.In vitro antimicrobial activities and spectra of U-100592 and U-100766,two novel fluorinated oxazolidinones[J]. Antimicrob Agents Chemother, 1996,40(3):720-726
  • 9Rybak MJ,Cappelletty DM,Moldovan T,et al.Comparative in vitro activities and p ostantibiotic effects of the oxazolidinone compounds eperezolid(PNU-100592) and linezolid(PNU-100766) versus vancomycin against Staphylococcus aureus,coagulas e-negative staphylococci, Enterococcus faecalis, and Enterococcus faecium[J ]. Antimicrob Agents Chemother,1998,42(3):721-724
  • 10Diekema DI,Jones RN. Oxazolidinones[J]. Drugs,2000,59(1):7-16

共引文献42

同被引文献7

引证文献1

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部