摘要
目的分析抗菌药物对肝硬化患者感染产超广谱β-内酰胺酶(ESBLs)大肠埃希菌的疗效。方法选择2006-2013年收治的3 600例肝硬化患者临床资料,对其抗感染治疗疗效进行回顾性分析。结果 3 600例患者发生感染803例,感染率为22.30%,其中产ESBLs大肠埃希菌感染100例,感染率为12.45%;首用喹诺酮类抗菌药物和肝硬化分级ChildpughA在死亡组和生存组感染患者之间差异有统计学意义(P<0.05);在抗感染中,有效与无效的单因素分析显示肝硬化分级Child-pugh C与菌血症差异有统计学意义(P<0.05);而上消化道出血和肝性脑病在生存和死亡组间差异无统计学意义。结论肝硬化患者产ESBLs大肠埃希菌感染使用抗菌药物的疗效较低,其中喹诺酮类药物比三代头孢更适合作为一线用药,抗感染并积极进行保肝治疗,同时及时提供细菌鉴定以及药敏报告,为临床靶向治疗提供重要依据。
OBJECTIVE To investigate the effect of antibiotic treatment in infections caused by extended-spectrum 6- lactamase(ESBL) producing Escherichia coli in patients with cirrhosis. METHODS From 2006 to 2013 the clinical data of cirrhosis patients with infections caused by extended-spectrum β-1actamase(ESBL) producing E. coli were collected, and the effect of antibiotic treatment was analyzed retrospectively. RESULTS Among 3 600 cases, there were 803 cases of infections, with the infection rate of 22. 30%, including 100 cases of infections caused by ESBLs-producing E. coli(12.45%) . There were significantly differences in the first use of quinolone and grading ChildpughA between death group and survival group (P〈0.05) ; in anti-infection, single factor analysis showed that there were significantly differences in Child-pugh C and bacteremia (P 〈 0. 05); while there were no significant differences in the upper gastrointestinal bleeding and hepatic eneephalopathy between death group and survival group. CONCLUSION The treatment with antibiotic in infections caused by ESBLs-producing E. coli in cirrhotic patients was less effective. Quinolones are more suitable than the third generation cephalosporins as first- line therapy. Anti-infection and hepatoproteetion treatment should be performed, and bacterial identification and susceptibility test results should be provided in time to provide an important basis for clinical targeted therapy.
出处
《中华医院感染学杂志》
CAS
CSCD
北大核心
2014年第3期617-619,共3页
Chinese Journal of Nosocomiology
基金
国家自然科学基金资助项目(81074354)
关键词
抗菌药物
肝硬化
大肠埃希菌
超广谱Β-内酰胺酶
耐药性
Antimicrobial agents
Cirrhosis
Escherichia coli
Extended-spectrum β-laetamase
Drug resistance