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[改良碳青霉烯灭活试验(mCIM)与乙二胺四乙酸协同碳青霉烯灭活试验(eCIM)联合检测产碳青霉烯酶肠杆菌科细菌的临床应用]

[Clinical application of mCIM and eCIM combined detection of carbapenemase-producing enterobacteriaceae].

作者信息

Hu Y M, Li J

机构信息

Department of Toxic Laboratory, Tianjin Medical University General Hospital, Tianjin 300052, China.

Department of Laboratory Medicine, Tianjin Medical University General Hospital, Tianjin 300052, China.

出版信息

Zhonghua Yu Fang Yi Xue Za Zhi. 2021 Apr 6;55(4):506-511. doi: 10.3760/cma.j.cn112150-20200821-01142.

Abstract

To explore the clinical application value of modified carbapenem inactivation test (mCIM) combined with EDTA-modified carbapenem inactivation test (eCIM) for detecting the carbapenemase of CRE isolated from infected patients in clinical diagnosis and infection control of CRE infection. Drug resistance of seventy eight non-repetitive enterobacteriaceae resistant to carbapenem antibiotics, which were isolated from clinically infected patients from January 2017 to December 2017 in the Tianjin Medical University General Hospital, was retrospectively analyzed. Meanwhile, Vitek2 Compact automatic bacterial identification instrument was used to identify the species and detect its minimum inhibitory concentration (MIC) for ertapenem and imipenem. Carbapenemase genes , , and were detected by PCR test, the genotype was determined by gene sequencing as the gold standard, and mCIM Combined eCIM test was used for carbapenemase detection of collected bacteria. Using PCR results as the standard, the sensitivity, specificity, positive predictive value, negative predictive value and Cohen' Kappa value of mCIM and eCIM were calculated, and the consistency of the combined detection results of mCIM and eCIM and PCR results was checked. Seventy eight carbapenem-resistant Enterobacteriaceae were detected by PCR, 74 carbapenemase gene positive and 4 negative, including 60 positive, 2 positive and positive Of the 7 strains, 3 strains were positive for , 1 strain was positive for , and 1 strain was both positive for and . The sensitivity of mCIM to detect carbapenemase is 100%, the specificity is 100%, and the Kappa value is 1.000; the combined detection of mCIM and eCIM for serine carbapenemase has a sensitivity of 100%, the specificity is 100%, and the Kappa value is 1.000; The sensitivity of combined detection of metallo-β-lactamase is 92.9%, the specificity is 100%, and the Kappa value is 0.955. The combined test of mCIM and eCIM which is used to detect carbapenemase in CRE costs low, doesn't require special reagents and equipment, has strong practicability, simple operation, and easy interpretation of results. According to the different genotypes of CRE bacteria, it provides important clinical diagnostic evidence for clinical CRE diagnosis, precise antimicrobial treatment and infection control.

摘要

探讨改良碳青霉烯灭活试验(mCIM)联合乙二胺四乙酸改良碳青霉烯灭活试验(eCIM)在临床诊断和控制耐碳青霉烯类肠杆菌科细菌(CRE)感染中检测感染患者分离出的CRE碳青霉烯酶的临床应用价值。回顾性分析2017年1月至2017年12月在天津医科大学总医院临床感染患者中分离出的78株对碳青霉烯类抗生素耐药的非重复肠杆菌科细菌的耐药情况。同时,使用Vitek2 Compact自动细菌鉴定仪鉴定菌种并检测其对厄他培南和美罗培南的最低抑菌浓度(MIC)。通过PCR检测碳青霉烯酶基因blaKPC、blaNDM、blaOXA-48和blaVIM,以基因测序作为金标准确定基因型,并使用mCIM联合eCIM试验对收集的细菌进行碳青霉烯酶检测。以PCR结果为标准,计算mCIM和eCIM的敏感性、特异性、阳性预测值、阴性预测值和Cohen's Kappa值,并检查mCIM和eCIM联合检测结果与PCR结果的一致性。通过PCR检测出78株耐碳青霉烯类肠杆菌科细菌,74株碳青霉烯酶基因阳性,4株阴性,其中blaKPC阳性60株,blaNDM阳性2株,blaOXA-48阳性7株,blaVIM阳性3株,blaNDM和blaVIM双阳性1株。mCIM检测碳青霉烯酶的敏感性为100%,特异性为100%,Kappa值为1.000;mCIM和eCIM联合检测丝氨酸碳青霉烯酶的敏感性为100%,特异性为100%,Kappa值为1.000;联合检测金属β-内酰胺酶的敏感性为92.9%,特异性为100%,Kappa值为0.955。mCIM和eCIM联合检测CRE中碳青霉烯酶成本低,无需特殊试剂和设备,实用性强,操作简单,结果易于判读。根据CRE细菌的不同基因型,为临床CRE诊断、精准抗菌治疗和感染控制提供重要的临床诊断依据。

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