Effect of rapid cefpodoxime disk screening for early detection of third-generation cephalosporin resistance in Escherichia coli and Klebsiella pneumoniae bacteremia.
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引用次数: 0
Abstract
Background: Several methods have been reported for detecting resistance genes or phenotypic testing on the day of positive blood culture in Escherichia coli or Klebsiella pneumoniae bacteremia. However, some facilities have not introduced these methods because of costs or other reasons. Toyota Kosei Hospital introduced cefpodoxime (CPDX) rapid screening on May 7, 2018, to enable early detection of third-generation cephalosporin resistance. In this study, we aimed to evaluate the effects of intervention with an Antimicrobial Stewardship Team using CPDX rapid screening.
Methods: Cefotaxime (CTX)-resistant E. coli or K. pneumoniae bacteremia cases were selected retrospectively and divided into two groups: the pre-CPDX screening (June 1, 2015, to May 6, 2018) and CPDX screening groups (July 7, 2018, to August 31, 2021). The primary outcome was the proportion of cases in which modifications were made to the administration of susceptible antimicrobial agents within 24 h of blood culture-positive reports.
Results: Overall, 63 patients in the pre-CPDX screening group and 84 patients in the CPDX screening group were eligible for analysis. The proportion of patients who modified to susceptible antimicrobial agents within 24 h of blood culture-positive reports was significantly increased in the CPDX screening group compared to that in the pre-CPDX screening group (6.3% vs. 22.6%, p = 0.010).
Conclusion: The results demonstrated that in CTX-resistant E. coli or K. pneumoniae bacteremia, CPDX rapid screening increased the proportion of early initiation of appropriate antimicrobial agents.
背景:在大肠埃希氏菌或肺炎克雷伯氏菌血症血培养阳性当天,已有几种检测耐药基因或表型的方法报道。然而,一些设施由于成本或其他原因而没有引入这些方法。丰田保生医院于2018年5月7日推出头孢多肟(CPDX)快速筛查,以早期发现第三代头孢菌素耐药。在这项研究中,我们旨在评估抗菌药物管理团队使用CPDX快速筛选的干预效果。方法:回顾性选择头孢噻肟(CTX)耐药大肠杆菌或肺炎克雷伯菌血症病例,分为CPDX前筛查组(2015年6月1日至2018年5月6日)和CPDX筛查组(2018年7月7日至2021年8月31日)。主要结果是在血培养阳性报告后24小时内修改敏感抗菌药物给药的病例比例。结果:总体而言,CPDX前筛查组有63例患者,CPDX筛查组有84例患者符合分析条件。CPDX筛查组在血培养阳性报告24 h内改用敏感抗菌药物的患者比例较CPDX前筛查组显著增加(6.3% vs. 22.6%, p = 0.010)。结论:结果表明,在耐ctx的大肠杆菌或肺炎克雷伯菌血症中,CPDX快速筛选可提高早期启动合适抗菌药物的比例。