Becton, Dickinson and Company, BD Life Sciences-Integrated Diagnostic Solutions, Sparks, Maryland, USA.
Becton, Dickinson and Company, BD Life Sciences, San Diego, California, USA.
Microbiol Spectr. 2022 Apr 27;10(2):e0180721. doi: 10.1128/spectrum.01807-21. Epub 2022 Apr 12.
Differential diagnosis of COVID-19 and/or influenza (flu) at point of care is critical for efficient patient management and treatment of both these diseases. The study presented here characterizes the BD Veritor System for Rapid Detection of SARS-CoV-2 and Flu A+B ("Veritor SARS-CoV-2/Flu") triplex assay. The performance for SARS-CoV-2 detection was determined using 298 specimens from patients reporting COVID-19 symptoms within 7 days from symptom onset (DSO) in comparison with the Lyra SARS-CoV-2 RT-PCR (reverse transcriptase PCR) assay ("Lyra SARS-CoV-2") as the reference. The performance for flu A and flu B detection was determined using 75 influenza-positive and 40 influenza-negative retrospective specimens in comparison with the previously FDA-cleared BD Veritor System for Rapid Detection of Flu A+B assay ("Veritor Flu") as the reference. The Veritor SARS-CoV-2/Flu assay met the FDA EUA acceptance criteria (86.7%; 95% confidence interval [95% CI]: 75.8 to 93.1) for SARS-CoV-2 testing compared to Lyra SARS-CoV-2. The Veritor SARS-CoV-2/Flu assay also demonstrated 100% agreement with the Veritor Flu for Flu A+B assay. For flu A detection, the lower bound of the 95% CI was 91.2%; for flu B detection, the lower bound was 90.0%. The dual detection capability of Veritor SARS-CoV-2/Flu for the etiologic agents causing COVID-19 and flu will allow efficient differentiation between the two illnesses, inform disease management, and facilitate optimal treatment. COVID-19 and flu are two respiratory illnesses which share similar clinical symptoms. The BD Veritor SARS-CoV-2/Flu assay has high sensitivity and specificity for detecting the SARS-CoV-2 and influenza A/B, the two etiologic agents causing COVID-19 and flu, respectively. This dual detection capability is critical when overlap occurs between the COVID-19 pandemic and the flu season. This triplex assay will allow efficient differentiation between the two respiratory illnesses and support a point-of-care physician diagnosis to facilitate the proper treatment and disease management for patients exhibiting overlapping symptoms.
在护理点对 COVID-19 和/或流感(流感)进行鉴别诊断对于有效管理患者和治疗这两种疾病至关重要。本研究介绍了 BD Veritor 系统对 SARS-CoV-2 和 Flu A+B 的快速检测(“Veritor SARS-CoV-2/Flu”)三重检测的特点。使用 298 份来自于症状出现后 7 天内报告 COVID-19 症状的患者的标本,与 Lyra SARS-CoV-2 RT-PCR(逆转录酶 PCR)检测(“Lyra SARS-CoV-2”)作为参考,对 SARS-CoV-2 的检测性能进行了测定。使用 75 份流感阳性和 40 份流感阴性的回顾性标本,与之前获得 FDA 批准的 BD Veritor 系统对 Flu A+B 的快速检测(“Veritor Flu”)进行比较,对流感 A 和流感 B 的检测性能进行了测定。与 Lyra SARS-CoV-2 相比,Veritor SARS-CoV-2/Flu 检测符合 FDA EUA 接受标准(86.7%;95%置信区间[95%CI]:75.8 至 93.1)。Veritor SARS-CoV-2/Flu 检测还与 Veritor Flu 对 Flu A+B 检测完全一致。对于流感 A 的检测,95%CI 的下限为 91.2%;对于流感 B 的检测,下限为 90.0%。Veritor SARS-CoV-2/Flu 对导致 COVID-19 和流感的病原体的双重检测能力将允许有效地区分这两种疾病,告知疾病管理,并促进最佳治疗。COVID-19 和流感是两种具有相似临床症状的呼吸道疾病。BD Veritor SARS-CoV-2/Flu 检测对 SARS-CoV-2 和流感 A/B(分别导致 COVID-19 和流感的两种病原体)具有高灵敏度和特异性。当 COVID-19 大流行与流感季节重叠时,这种双重检测能力至关重要。该三联检测将允许有效地区分这两种呼吸道疾病,并支持在护理点进行医生诊断,以促进对出现重叠症状的患者进行适当的治疗和疾病管理。