[某综合医院耐头孢噻肟大肠杆菌检测趋势及广谱产β-内酰胺酶大肠杆菌血流感染临床特点]。

The Japanese journal of antibiotics Pub Date : 2014-12-01
Norihito Tarumoto, Masako Nobe, Masatsugu Uchida, Shigefumi Maesaki, Masahiko Tanaka
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摘要

近年来,头孢噻肟(CTX)-M型广谱β-内酰胺酶(ESBL)产生菌的社区大流行感染已成为公认的主要问题,该菌对CTX具有耐药性。当不能进行esbl确认试验时,可采用耐ctx大肠杆菌作为感染控制的替代方法。我们调查了我院无微生物科的第三代耐头孢菌素大肠杆菌的趋势及ESBL产大肠杆菌血流感染的临床特点。目的分析2009年1月- 2013年11月临床标本中耐ctx大肠杆菌的检测趋势、同期第三代头孢菌素的使用密度(AUD)及产esbl大肠杆菌BSI的临床特征。结果,2009年耐ctx大肠杆菌在住院和门诊大肠杆菌中所占比例分别为5.4%和3.9%,2013年分别为32.8%和17.8%。此外,澳元从2009年的20.6上升到2013年的28.9。在大肠杆菌引起的BSI中,产生esbl的大肠杆菌患者(n=8)与不产生esbl的大肠杆菌患者(n=32)相比,男性、卧床不起、使用导尿管、中心静脉导尿管、慢性肾功能衰竭的临床特征显著。
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[Trend of detection of cefotaxime-resistant Escherichia coli and clinical features of bloodstream infection due to extended-spectrum β-lactamase producing Escherichia coli in a general hospital].

Recently, the community pandemic infections of cefotaxime (CTX)-M type extended-spectrum β-lactamase (ESBL) producing bacteria, which is mostly resistant to CTX, has been well-known as major problems. When the ESBL-confirmation test cannot be done, CTX-resistant Escherichia coli might be used as the alternation method of infectious control. We investigated tendency of third-generation cephalosporin resistant E. coli and the clinical features of bloodstream infections (BSI) due to ESBL producing E. coli in our hospital, which has no department of microbial examination. We examined the trend of detection of CTX-resistant E. coli isolates from clinical samples from January 2009 to November 2013, and antimicrobial use density (AUD) of third-generation cephalosporins in the same period, and the clinical features of BSI of ESBL-producing E. coli. As a result, the percentages of CTX-resistant E. coli in all E. coli were 5.4% in inpatient and 3.9% in outpatient in 2009, but 32.8% and 17.8% in 2013, respectively. Additionally, AUD had increased from 20.6 in 2009 to 28.9 in 2013. In BSI due to E. coli, the clinical features which were male, bedridden patient and using urethral catheter, central venous catheter, chronic renal failure were significantly in the cases of ESBL-producing E. coli (n=8), compared to non-ESBL producing E. coli (n=32).

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