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. 2021 Oct 1;4(10):e2132776. doi: 10.1001/jamanetworkopen.2021.32776

Error in Results, Discussion, and Table

PMCID: PMC8486979  PMID: 34596676

In the Research Letter titled “Validation of an At-Home Direct Antigen Rapid Test for COVID-19,”1 published August 27, 2021, the combined sensitivity of the direct antigen rapid test should have been 96.2% (95% CI, 88.8%-100.0%), not 96.3% (95% CI, 89.5%-100.0%). These numbers appeared in the Results, Discussion, and Table. This article has been corrected.1

Reference

  • 1.Harmon A, Chang C, Salcedo N, et al. Validation of an at-home direct antigen rapid test for COVID-19. JAMA Netw Open. 2021;4(8):e2126931. doi: 10.1001/jamanetworkopen.2021.26931 [DOI] [PMC free article] [PubMed] [Google Scholar]

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