Le Bars Hervé, Madany Neil, Lamoureux Claudie, Beauruelle Clémence, Vallet Sophie, Payan Christopher, Pilorgé Léa
Unity of Bacteriology, Department of Bacteriology-Virology-Parasitology-Mycology-Hygiene, Pole of Biology-Pathology, University Hospital of Brest, F-29200 Brest, France.
Unity of Virology, Department of Bacteriology-Virology-Parasitology-Mycology-Hygiene, Pole of Biology-Pathology, University Hospital of Brest, F-29200 Brest, France.
Diagnostics (Basel). 2023 Mar 15;13(6):1110. doi: 10.3390/diagnostics13061110.
Point-of-care syndromic PCR (POC SPCR) assays are useful tools for the rapid detection of the most common causative agents of community-acquired infections responsible for meningitis and encephalitis infections. We evaluated the performance characteristics of the new QIAstat-Dx Meningitis/Encephalitis panel (QS) compared to the laboratory reference methods and the POC SPCR Biofire FilmArray Meningitis Encephalitis Panel (FA). Viral (Enterovirus, Parechovirus, HSV-1, HSV-2, HHV-6, VZV) and bacterial ( K1, , , encapsulated , , , , ) pathogens were suspended at low concentrations and tested with the POC SPCR systems. The reproducibility, analytical specificity, carryover contamination, interferences and clinical samples were evaluated. All samples tested positive with both QS and FA except for those containing the lowest concentrations of Enterovirus-D68-B3, Echovirus-30 and which were only detected by FA. In terms of analytical specificity, we observed 3 false positive results out of 48 QS tests versus 1 out of 37 FA tests. For the other studied criteria, both QS and FA performed as expected. Our results suggest that the performance characteristics of QS are close to those of FA. A prospective multicenter study would be useful to complete the performances evaluation of QS.
即时护理综合征聚合酶链反应(POC SPCR)检测是快速检测引起脑膜炎和脑炎感染的社区获得性感染最常见病原体的有用工具。我们将新型QIAstat-Dx脑膜炎/脑炎检测板(QS)与实验室参考方法以及POC SPCR Biofire FilmArray脑膜炎脑炎检测板(FA)的性能特征进行了评估比较。将病毒(肠道病毒、帕利病毒、单纯疱疹病毒1型、单纯疱疹病毒2型、人疱疹病毒6型、水痘带状疱疹病毒)和细菌(K1、 、 、有荚膜的、 、 、 )病原体以低浓度悬浮,并使用POC SPCR系统进行检测。对其重现性、分析特异性、携带污染、干扰情况及临床样本进行了评估。除了含有最低浓度肠道病毒D68-B3、埃可病毒30型和 的样本仅被FA检测到外,所有样本经QS和FA检测均呈阳性。在分析特异性方面,我们在48次QS检测中观察到3例假阳性结果,而在37次FA检测中观察到1例假阳性结果。对于其他研究标准,QS和FA均表现符合预期。我们的结果表明,QS的性能特征与FA接近。一项前瞻性多中心研究将有助于完成对QS性能的评估。