Abbott® ID NOW™ COVID-19 rapid molecular assay versus Hologic® Panther Aptima™ SARS-CoV-2 assay in nasopharyngeal specimens: results from 1-year retrospective study in an emergency department
- PMID: 35843113
- PMCID: PMC9188679
- DOI: 10.1016/j.diagmicrobio.2022.115742
Abbott® ID NOW™ COVID-19 rapid molecular assay versus Hologic® Panther Aptima™ SARS-CoV-2 assay in nasopharyngeal specimens: results from 1-year retrospective study in an emergency department
Abstract
We compared ID Now™ and Hologic® Panther Aptima™ for the detection of SARS-COV-2. ID Now™ showed a positive and negative percent agreement of 86.9% and 99.7% respectively. This facilitates faster clinical decision-making, along with the rapid implementation of infection control measures, and improvement of patient flow in the emergency department toward inpatient wards.
Keywords: COVID-19; Hologic Panther Point of care device; ID NOW; SARS-CoV-2.
Copyright © 2022 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interests All authors declared that there is no conflict of interest in conducting this study.
References
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- Hologic. Aptima SARS CoV 2 assay - instruction for use 2021.
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- Abbott. Abbott. ID NOW COVID-19 product insert. 2020.
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