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427株细菌L型医院感染与耐药分析 被引量:17

Analysis on 427 strains of bacteria L-form in nosocomial infection and the drug resistance
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摘要 目的 为提高医院感染细菌培养阳性率及抗菌药物的有效使用。方法 对我院 1995年 1月~ 1997年 12月从 1870例住院患者采取血、尿、脑脊液、胸腹水、胆汁等标本进行了常规与高渗同步培养的结果进行了对照分析。结果 分离出 L型细菌 4 2 7株 ,而普通培养均为阴性 ,阳性率提高了 2 2 .8% ,分离菌种达 11种之多 ;以金黄色葡萄球菌在各类标本中感染率占首位 ,19.4 4% ;大肠埃希菌占第 2位 ,16.4 % ,凝固酶阴性葡萄球菌、D群肠球菌、酵母菌占第 3位 ,分别为 11%、10 .77%、10 .3 % ;其它各菌属均占有一定比例。对青霉素、头孢类抗生素高度耐药 ,对红霉素、氯霉素、庆大霉素、林可霉素呈低度耐药。结论 采取同步培养可提高阳性率 ,为临床感染性疾病诊断和抗生素的合理使用提供了重要依据。 OBJECTIVE To enhance the positive culture rate of bacteria in nosoconial infection and to guide the proper use of antibiotics.METHODS The routine and hyperosmotic culture results performed on the samples of blood ,urine,cerebrospinal fluid,pleural effusion,ascites and bile from 1870 inpatients during Jan 1995 to Dec 1997 were analyzed in tandem.RESULTS 427 strains of bacteria L form were separated out with the synchronous culture method from the negative specimens on routine culture, the positive rate was increased by 22.8%.The posifive strains were belonged to 11 kinds of bacteria, in which the first was S.aureus,the second was E.coil,and then coagulase negative Staphylococcus,Enterococcus D group and yeast. Their positive rates were 19.44%,16.4%,11%,10.77%and 10.3% respectively.The drug sensitivity results showed that they were highly resistant to penicillin and cephalosporins,lower to erythromycin,chloramphenical, gentamicin and lincomycin. CONCLUSIONS The method step by step culture may not only increase the positive culture rate,but also provide very important clew in the diagnosis of doubtful cases and enhance the rational administration of antibiotics.
出处 《中华医院感染学杂志》 CAS CSCD 2000年第1期13-14,共2页 Chinese Journal of Nosocomiology
关键词 细菌L型 耐药分析 医院内感染 Bacteria L form Nosocomial infection Analysis of drug resistance
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参考文献6

  • 1李中兴 郑家齐.诊断细菌学[M].香港:黄河文化出版社,1992.512-513.
  • 2叶庆妩 王毓三.全国临床检验操作规程[M].南京:东南大学出版社,1992.380-382.
  • 3林特夫.细菌L型的生物特性与致病作用[J].微生物学通报,1985,12:32-32.
  • 4叶应妩,全国临床检验操作规程,1992年,380页
  • 5李中兴,诊断细菌学,1992年,512页
  • 6林特夫,微生物学通报,1985年,12卷,32页

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