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 in | Microbiology spectrum Vol. 13; no. 3; p. e0203324 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
04.03.2025
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Subjects | |
Online Access | Get full text |
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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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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 |