Department of Microbiology, Cliniques universitaires Saint-Luc and Université Catholique de Louvain, Brussels, Belgium.
Department of Microbiology, Hôpital Erasme and Université Libre de Bruxelles (ULB), Brussels, Belgium.
J Antimicrob Chemother. 2019 Feb 1;74(2):357-359. doi: 10.1093/jac/dky429.
Rapid and effective screening of carbapenemase-producing Enterobacteriaceae (CPE) appears essential for adequate patient management and rapid implementation of infection control measures. Most of these screening techniques require a minimum of 24 h of culture. Molecular assays are an exception since these can be achieved within 1 h, but are expensive and usually require specialized facilities and trained personnel. In this context, lateral immunochromatography performed directly from rectal swab samples could represent a cost-effective alternative with a reduced turnaround time.
In this study, we assessed the performance of the OKN K-SeT test (Coris BioConcept, Gembloux, Belgium) for the rapid detection of OXA-48, KPC and NDM CPE directly from rectal swab samples.
A total of 149 residual rectal swabs, routinely screened for CPE through selective culture and confirmed by PCR, were tested with a defined protocol consisting of a 2.5 h incubation of the swab in an enrichment medium containing meropenem followed by OKN K-SeT testing after centrifugation.
This method displayed an overall sensitivity of 96% and a specificity of 100% with a limit of detection ranging between 104 and 105 cfu/mL.
Whereas this assay appears highly specific, it displays a reduced sensitivity compared with the standard procedure encompassing a culture step. Nonetheless, this rapid method allows an accelerated identification of most CPE carriers at a lower cost and, accordingly, the implementation of early appropriate management procedures.
快速有效地筛选碳青霉烯酶产生肠杆菌科(CPE)对于适当的患者管理和快速实施感染控制措施似乎至关重要。这些筛选技术大多需要至少 24 小时的培养。分子检测是一个例外,因为这些检测可以在 1 小时内完成,但成本高昂,通常需要专门的设施和经过培训的人员。在这种情况下,直接从直肠拭子样本进行侧向免疫层析检测可能是一种具有成本效益的替代方法,可缩短周转时间。
本研究评估了 OKN K-SeT 检测(比利时盖姆布罗克斯的 Coris BioConcept)直接从直肠拭子样本中快速检测 OXA-48、KPC 和 NDM CPE 的性能。
通过选择性培养对 149 份直肠拭子样本进行常规 CPE 筛查,并通过 PCR 进行确认。采用定义的方案对拭子进行测试,该方案包括将拭子在含有美罗培南的富集培养基中孵育 2.5 小时,然后离心后进行 OKN K-SeT 检测。
该方法的总体敏感性为 96%,特异性为 100%,检测限范围为 104 至 105 cfu/mL。
尽管该检测方法具有高度特异性,但与包含培养步骤的标准程序相比,其敏感性降低。然而,这种快速方法可以以较低的成本加速识别大多数 CPE 携带者,并相应地实施早期适当的管理程序。