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Performance evaluation of automated BD Phoenix NMIC-500 panel for carbapenemase detection in carbapenem-resistant and carbapenem-susceptible Enterobacterales.
Journal of Microbiological Methods ( IF 2.2 ) Pub Date : 2020-09-03 , DOI: 10.1016/j.mimet.2020.106042
Hanwool Cho 1 , Jung Ok Kim 1 , Ji Eun Choi 1 , Howon Lee 1 , Woong Heo 1 , Young Jong Cha 1 , In Young Yoo 1 , Yeon-Joon Park 1
Affiliation  

Rapid detection of carbapenemases and accurate reporting of carbapenem MICs is critical for appropriate treatment and infection control. We evaluated the BD Phoenix NMIC-500 panel for detection and classification of carbapenemases and antimicrobial susceptibility testing (AST) for carbapenems. A total of 235 isolates were tested; 47 carbapenemase-producing Enterobacterales, 52 non-carbapenemase-producing carbapenem-resistant Enterobacterales (non-CP-CRE), 136 carbapenem-susceptible Enterobacterales (CSE). The sensitivity of carbapenemase-producing organism (CPO) detection was 97.9%, the specificity was 100% for CSE but 32.7% for non-CP-CREs. All the 35 false-positive cases were non-CP-CREs; 23 out of the 35 were determined as untyped carbapenemase producer (CP), nine were mistyped as class B, and three were as class A. The detection rate/correct classification rate for class A, B, and D carbapenemase was 100%/78.6%, 100%/100%, and 80%/60%, respectively. To supplement the low specificity, it is suggested to report carbapenemase-producer (CP) positive results as “carbapenem-resistant, CP-suspicious” and perform the confirmatory test. The EA and CA for ertapenem, imipenem, and meropenem was 99.1%/99.6%, 89.4%/90.6%, and 95.3%/95.7%.

In conclusion, the BD Phoenix CPO detect panel provides advantage in that the carbapenemase test is automated and the results can be obtained within 6 h but the low specificity in CREs needs to be improved. In addition, accurate reporting of meropenem MICs will be helpful for clinicians to choose treatment options.



中文翻译:

BD Phoenix NMIC-500自动化面板在耐碳青霉烯和对碳青霉烯敏感的肠杆菌中检测碳青霉烯酶的性能评估。

快速检测碳青霉烯酶和准确报告碳青霉烯MICs对于适当的治疗和感染控制至关重要。我们评估了BD Phoenix NMIC-500面板对碳青霉烯酶的检测和分类以及对碳青霉烯类药物的药敏试验(AST)。总共测试了235个分离株。47个产生碳青霉烯酶的肠杆菌,52个非产生卡巴培南姆的耐碳青霉烯的肠杆菌(非CP-CRE),136个对碳青霉烯敏感的肠杆菌(CSE)。产碳青霉烯酶的生物(CPO)检测的灵敏度为97.9%,对CSE的特异性为100%,对非CP-CRE的特异性为32.7%。35例假阳性病例均为非CP-CRE。在35个样本中,有23个被确定为未分型的碳青霉烯酶生产商(CP),有9个被误分为B类,三个被分类为A类。A,B和D类碳青霉菌酶的检出率/正确分类率为100%/ 78.6 %,100%/ 100%和80%/ 60%。为了补充低特异性,建议报告碳青霉烯酶生产者(CP)阳性结果为“耐卡巴培南,可疑CP”并进行确认试验。厄他培南,亚胺培南和美洛培南的EA和CA为99.1%/ 99.6%,89.4%/ 90.6%和95.3%/ 95.7%。

总之,BD Phoenix CPO检测板具有的优势在于,碳青霉烯酶测试是自动化的,可以在6小时内获得结果,但CRE的低特异性需要改善。此外,准确报告美罗培南MIC有助于临床医生选择治疗方案。

更新日期:2020-09-03
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