全自动分子系统Alinity m上HCV和HIV-1检测的临床性能评估

IF 1.6 Q4 INFECTIOUS DISEASES Journal of clinical virology plus Pub Date : 2023-10-15 DOI:10.1016/j.jcvp.2023.100169
Tung Phan , Zachary Cravener , Janet Olean , Melissa McCullough , Jamie Gribschaw , Alan Wells
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引用次数: 0

摘要

全球临床实验室对分子病毒学检测的需求持续增长。Alinity m系统是一种全自动、连续、随机访问的分子诊断分析仪,旨在简化实验室工作流程。在本研究中,我们评估了Alinity m HCV和HIV-1检测的临床性能特征,以检测和量化71份血清和血浆标本中的这两种血源性病原体。Alinity m和Abbott m2000之间的总体定性一致性对HCV为100%,对HIV-1为94.4%。我们的数据表明,在Abbott m2000和Alinity m HCV和HIV-1检测的定量范围内存在微弱的偏差,表明它们之间的病毒载量有很强的相关性。总之,Alinity m HCV和HIV-1检测的结果与目前的前辈Abbott RealTime HCV和HIV1检测的结果相当。
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Clinical performance evaluation of HCV and HIV-1 assays on the fully automated molecular system Alinity m

The demand for molecular virology testing continues to grow in clinical laboratories worldwide. The Alinity m system is a fully automated, continuous, random-access molecular diagnostic analyzer that was designed to streamline the laboratory workflow. In this study, we assessed the clinical performance characteristics of the Alinity m HCV and HIV-1 assays to detect and quantify these two bloodborne pathogens in 71 serum and plasma specimens. The overall qualitative agreement between the Alinity m and Abbott m2000 was 100 % for HCV and 94.4 % for HIV-1. Our data demonstrated a weak bias across the quantitative range of the Abbott m2000 and Alinity m HCV and HIV-1 assays, indicating a strong correlation on viral loads between them. Taken together, the Alinity m HCV and HIV-1 assays had comparable results to their current predecessors, the Abbott RealTime HCV and HIV-1 assays.

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来源期刊
Journal of clinical virology plus
Journal of clinical virology plus Infectious Diseases
CiteScore
2.20
自引率
0.00%
发文量
0
审稿时长
66 days
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