Predictive role of culture-based MIC testing vs. genotyping for carbapenem-resistant Enterobacterales in a non-universal screening, highly resourced setting

IF 1 Q3 MEDICINE, GENERAL & INTERNAL Electronic Journal of General Medicine Pub Date : 2023-07-01 DOI:10.29333/ejgm/13181
Amani M. Alnimr
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Abstract

A lack of evidence of accuracy for various testing modalities for carbapenem-resistant Enterobacterales (CRE) reduces the efficiency of screening and delays the isolation of carriers. This study examined the performance of phenotypic detection of CRE in comparison to molecular testing. A cross-sectional study was conducted in an academic medical institution in Saudi Arabia on CRE-screened patients during a 36-month period (April 1, 2019, through March 31, 2022). Cases were followed up for their susceptibility status by the phenotypic gradient method and genotypes. Of 3,116 samples tested, 359 carbapenemase genes were detected in 297 strains (9.5%) belonging to 292 patients. Oxacilliniase-48 (OXA-48) was the most frequently detected genotype (n=190, 64%), followed by a combined New Delhi metallo-B-lactamase (NDM)/OXA-48 genotype (n=77, 25.9%). Variable missed isolation days were encountered for various genotypes (0-18.5 days), with an excellent clinical utility index obtained for screening the OXA-48 genotype phenotypically. The data provided some insights into the predictive role and shortcomings of the e-test alone in CRE screening. While it provided a reasonable approach in a CRE population dominated by OXA-48 genotypes, it was more likely to miss the NDM-incurred carbapenemase. Thus, local epidemiology in an institution must be considered when designing a local screening protocol in addition to consideration of cost and turnaround time.
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基于培养的MIC检测与碳青霉烯类耐药肠杆菌基因分型在非通用筛查、高资源环境中的预测作用
缺乏碳青霉烯类耐药肠杆菌(CRE)各种检测模式准确性的证据,降低了筛查效率,并延迟了携带者的分离。本研究检测了CRE表型检测与分子检测的性能。在沙特阿拉伯的一家学术医疗机构对36个月(2019年4月1日至2022年3月31日)的CRE筛查患者进行了一项横断面研究。通过表型梯度法和基因型对病例的易感性状况进行随访。在3116份测试样本中,在292名患者的297株菌株(9.5%)中检测到359个碳青霉烯酶基因。Oxacilliniase-48(OXA-48)是最常检测到的基因型(n=190,64%),其次是新德里金属B-乳糖酶(NDM)/OXA-48联合基因型(n=77,25.9%)。不同基因型(0-18.5天)都会出现不同的漏诊天数,在筛选OXA四十八基因型表型方面获得了良好的临床实用性指数。这些数据为单独的电子测试在CRE筛查中的预测作用和缺点提供了一些见解。虽然它在以OXA-48基因型为主的CRE群体中提供了一种合理的方法,但它更有可能错过NDM引起的碳青霉烯酶。因此,在设计本地筛查方案时,除了考虑成本和周转时间外,还必须考虑机构的本地流行病学。
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来源期刊
Electronic Journal of General Medicine
Electronic Journal of General Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
3.60
自引率
4.80%
发文量
79
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