首页> 外文期刊>Annals of Clinical Microbiology and Antimicrobials >High fluoroquinolone MIC is associated with fluoroquinolone treatment failure in urinary tract infections caused by fluoroquinolone susceptible Escherichia coli
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High fluoroquinolone MIC is associated with fluoroquinolone treatment failure in urinary tract infections caused by fluoroquinolone susceptible Escherichia coli

机译:高氟喹诺酮类MIC与因氟喹诺酮易感性大肠杆菌引起的尿路感染中氟喹诺酮治疗失败有关

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Background Suboptimal clinical response to fluoroquinolone (FQ) therapy has been clearly documented in patients with Salmonella typhi infection with reduced FQ susceptibility. However, the clinical impact of reduced FQ susceptibility on other infections including E. coli urinary tract infections (UTIs) has never been evaluated. Methods We conducted a retrospective cohort study of female patients with fluoroquinolone susceptible E. coli (FQSEC) UTIs who received FQ therapy at outpatient services within University of Pennsylvania Health System, Philadelphia. Exposed patients were those with high MIC-FQSEC UTIs (the levofloxacin MIC?>?0.12 but?≤?2?mg/L) while unexposed patients were those with low MIC-FQSEC UTIs (the levofloxacin MIC?≤?0.12?mg/L). The primary treatment outcome was treatment failure within 10?weeks after initiation of FQ therapy. Results From May 2008 to April 2011, we enrolled 29 exposed patients and 246 unexposed patients. Two patients in each group experienced treatment failure; exposed vs. unexposed (6.9 vs. 0.8%; p =?0.06). Risk difference and risk ratio (RR) for treatment failure were 0.06 [95% CI ?0.03–0.15; exact -p =?0.06] and 8.48 [95% CI 1.24–57.97; exact -p =?0.06], respectively. After adjusting for underlying cerebrovascular disease, the RR was 7.12 (95% CI 1.20–42.10; MH- p =?0.04). Conclusion Our study demonstrated the negative impact of reduced FQ susceptibility on the treatment response to FQ therapy in FQSEC UTIs. This negative impact may be more intensified in other serious infections. Future studies in other clinical situations should be conducted to fill the gap of knowledge.
机译:背景技术在伤寒沙门氏菌感染的患者中,对氟喹诺酮(FQ)治疗的亚最佳临床反应已得到明确证明,且FQ敏感性降低。但是,从未评估过FQ敏感性降低对其他感染(包括大肠杆菌泌尿道感染(UTIs))的临床影响。方法我们对在费城宾夕法尼亚大学卫生系统门诊接受FQ治疗的氟喹诺酮敏感型大肠杆菌(FQSEC)UTI女性患者进行了回顾性队列研究。暴露患者为MIC-FQSEC UTI高的患者(左氧氟沙星MIC≥0.12,但≤≤2?mg / L),未暴露患者为MIC-FQSEC UTI低的患者(左氧氟沙星MIC <≤0.12?mg / L)。 L)。主要的治疗结果是开始FQ治疗后10周内的治疗失败。结果自2008年5月至2011年4月,我们招募了29名暴露患者和246名未暴露患者。每组两名患者出现治疗失败;暴露与未暴露(6.9 vs. 0.8%; p =?0.06)。治疗失败的风险差异和风险比(RR)为0.06 [95%CI?0.03–0.15;精确-p =?0.06]和8.48 [95%CI 1.24-57.97;精确-p =?0.06]。调整基础脑血管疾病后,RR为7.12(95%CI 1.20-42.10; MH-p =?0.04)。结论我们的研究表明FQ敏感性降低对FQSEC UTI对FQ治疗的治疗反应具有负面影响。在其他严重感染中,这种负面影响可能会更加严重。应该在其他临床情况下进行进一步的研究以填补知识空白。

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