期刊文献+

ICU重症患者多重耐药性嗜麦芽窄食单胞菌暴发感染分子流行病学研究 被引量:4

MOLECULAR EPIDEMIOLOGY STUDY ON STENOTROPHOMONAS MALTOPHILIA INFECTION IN PATIENTS IN ICU
下载PDF
导出
摘要 [目的]研究ICU重症患者连续发生嗜麦芽窄食单胞菌感染,并追踪其感染源。[方法]收集2006年3~4月间ICU9例重症患者行纤支镜检查后痰标本中分离出的9株pma菌株,工作人员手分离的pma菌株2株,纤支镜冲洗液分离的pma菌株2株,进行抗生素型分析、PFGE全DNA指纹图技术分子分型,确定菌株的亲缘关系。[结果]9例患者感染的9株pma,有8株PFGE基因型相同,并与2株分离自ICU工作人员手的pma和2株分离自纤支镜的pma基因型一致。[结论]8例机械通气患者感染的pma来自于同一克隆,ICU内存在pma暴发感染。消毒不彻底的纤支镜和医护人员的手污染可能是引起本次暴发感染的感染源。 [Objective] To investigate a potential outbreak of Stenotrophomonas maltophilia (pma) infection occurred in patients in ICU and to track the source of infection. [ Methods] 13 pma strains were isolated from 9 patients in ICU ( 9 strains), hands of medical staffs in ICU (2 strains) and fiberscopes used for intubations and aspiration (2 strains) from March to April in 2006. Antibiotic susceptibility data of all strains were collected. Homology of the strains was analyzed by the methods of anfibiotype and PFGE genotype. [Results] Of the 9 pma isolated from patients in ICU, eight had identical PFGE genotype. The isolates from two ICU staffs and two fiberscopes displayed the same genotype with the eight patients above. [Conclusions] 8 pma strains of patients in ICU come from the same clone. This result proves that clone transmission had occured in patients in ICU. Contaminated fiberscopes and hands of staffs may be the source of infection.
出处 《现代预防医学》 CAS 北大核心 2007年第3期506-508,共3页 Modern Preventive Medicine
关键词 嗜麦芽窄食单胞菌 分子流行病学 重症监护病房 Stenotrophomonas maltophilia Molecular Epidemiology ICU
  • 相关文献

参考文献4

二级参考文献19

  • 1李耘,李家泰,王进,中国细菌耐药监测研究组.中国重症监护病房细菌耐药性监测研究[J].中华检验医学杂志,2004,27(11):733-738. 被引量:122
  • 2段广才,高守一,祁国明,刘延清.霍乱弧菌O139与O1及非O1菌关系的研究[J].中华微生物学和免疫学杂志,1995,15(4):230-233. 被引量:13
  • 3Dentton M,Kerr KG.Microbiological and clinical aspects of infection associated with Stenotropomonas maltophilia[J].Clin Microbiol Rev,1998; 11 (1):57-80.
  • 4Versalovic J,Koeuth T,Lupski JK,et al.Distribution of repetitive DNA sequences in enterbacteria and application to fingerprinting of genomes[J].Nucl Acids R es,1991; 19(24):6823-6831.
  • 5Barbier FN,Boutiba BI,Nouvello M,et al.Molecular investigation of Stenotrophomonas maltophilia isolates exhibiting rapid emergence of ticarcillin-clavulanate resistance[J].J Hosp Infect,2000; 45(1):35-41.
  • 6Sillber S,Pfaller MA,Hollis R J,et al.Evalution of three molecular typing techniques for nonfermentative Gram-negative bacilli.Infect Control Hosp Epidemiol[J].2004;25(l 0):847-851.
  • 7Avison MB,Higgins CS,von Heldrich C J,et al.Plasmid location and molecular heterogenity of the L1 and L2 betalactamase genes of Stenotrophomonas maltophilia[J].Antimicrob Agents Chemother,2001; 45(2):413-419.
  • 8Denton M, Todd N J, Kerr KG, et al. Molecular epidemialogy of Stenotrophomonas maltophilia isolated from clinical specimens from patients with cystic fibrosis and associated environmental samples. J Clin Microbiol, 1998,36 : 1953-1958.
  • 9Tenover FC, Arbeit RD, Goering RV, et al. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis:criteria for bacterial strain typing. J Clin Micrebiol, 1995,33:2233-2239.
  • 10Valdezate S, Vindel A, Loza E, et al. Antimicrobial susceptibilities of unique Stenotrophomonas maltophilia clinical strains. Antimicrob Agents Chemother,2001,45 : 1581-1584.

共引文献20

同被引文献52

引证文献4

二级引证文献78

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