Clinical performance of Abbott ID NOW™ COVID-19 2.0 rapid molecular point-of-care test compared to three real-time RT-PCR assays

The Abbott ID NOW TM COVID-19 2.0 assay is a suitable rapid test for diagnosing COVID-19 in acute symptomatic subjects and can be used in point-of-care settings and low-resource settings. With results reported in 12 minutes or less, Abbott ID NOW TM COVID-19 2.0 facilitates timely diagnosis, enablin...

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Published inMicrobiology spectrum Vol. 13; no. 3; p. e0203324
Main Authors Iglesias-Ussel, Maria D., Bowie, Aleah, Anderson, Jack G., Li, Yin, Park, Lawrence P., Cardona, Jose F., Dennis, Patrick, Ebuh, Valentine, Geller, Steven A., Jain, Manish, McKenzie, Mark M., Merchant-Borna, Kian, Patel, Anand, Siegel, Amy, Strauss, Guy S., Thoppil, Joby J., Weinberg, Aaron S., Woods, Christopher W.
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 04.03.2025
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Summary:The Abbott ID NOW TM COVID-19 2.0 assay is a suitable rapid test for diagnosing COVID-19 in acute symptomatic subjects and can be used in point-of-care settings and low-resource settings. With results reported in 12 minutes or less, Abbott ID NOW TM COVID-19 2.0 facilitates timely diagnosis, enabling linkage to appropriate antiviral medication.
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Yin Li is a Senior Principal Biostatistician at Abbott Laboratories. Kian Merchant-Borna has served on scientific advisory boards for Abbott Diagnostics unrelated to the submitted work. Each author's institution received financial support for the performance of the study. Christopher W. Woods is employed and holds equity in Biomeme. He is on the advisory board for FHI Clinical and is a member of the Board of Directors for Global Health Innovation Alliance Accelerator.
ISSN:2165-0497
2165-0497
DOI:10.1128/spectrum.02033-24