首页 | 本学科首页   官方微博 | 高级检索  
检索        

危重病者中心静脉导管性脓毒症病原学分析
引用本文:魏丹宏,李伟.危重病者中心静脉导管性脓毒症病原学分析[J].浙江预防医学,2004,16(4):6-8.
作者姓名:魏丹宏  李伟
作者单位:浙江大学医学院附属第二医院,浙江,杭州310009
摘    要:目的了解危重病患者中心静脉导管相关性脓毒症(CRS)的临床特点、菌群分布及药敏情况.方法对2001~2003年发生的40例中心静脉导管相关性脓毒症患者进行回顾性调查分析.结果40例CRS中,共分离出74株细菌,其中革兰氏阴性杆菌20株,革兰氏阳性球菌42株,真菌12株.CRS最常见的病原是表皮葡萄球菌和金黄色葡萄球菌.革兰氏阴性杆菌最常见的是绿脓假单胞菌.大多数细菌均有较高程度的耐药性.革兰氏阳性球菌对万古霉素的敏感率达100%,革兰氏阴性杆菌对亚胺培南及阿米卡星的敏感率分别为80%和65%.结论CRS的有效处理方法是及时拔除感染的导管.万古霉索和(或)阿米卡星可作为治疗CRS的首选用药.

关 键 词:中心静脉导管  脓毒症综合征  医院感染
文章编号:1007-0931(2004)04-0006-03
修稿时间:2003年3月25日

A Clinical and Etiologic Analysis on Central Venous Catheter-related Sepsis in Critical Patients
WEI Dan-hong,LI Wei..A Clinical and Etiologic Analysis on Central Venous Catheter-related Sepsis in Critical Patients[J].Zhejiang Journal of Preventive Medicine,2004,16(4):6-8.
Authors:WEI Dan-hong  LI Wei
Abstract:Objective To investigate the clinical characteristics, bacteria spectrum and drug-sensitivity in critical patients with central venous catheter-related sepsis (CRS). Methods A retrospective study was carried out among 40 critical patients with central venous catheter-related sepsis between Jan. 2001 and Feb.2003.Results 74 strains were isolated from these patients including 20 Gram-negative bacteria strains, 42 Gram-positive bacteria strains and 12 fungi strains. Staphylococcus epidermis and Staphylococcus aureus were the most frequent pathogens, and in Gram-negative bacteria, aeruginosus bacillus were the most frequent strains. The pathogens mostly had a relative higher drug-resistance. Gram-positive bacteria was sensitive to vancomycin with a 100% sensitivity, and Gram-negative bacteria was partial sensitive to imipenem with a 80% sensitivity and amikacin with a 65% sensitivity. Conclusions The effective treatment to patients with central venous catheter-related sepsis is prompt removal of infective catheters, and Vancomycin and amikacin may be the first chosen drugs.
Keywords:Central venous catheter  Sepsis  Hospital onset of infection
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号