Performance of Rapid Antigen Tests to Detect Symptomatic and Asymptomatic SARS-CoV-2 Infection : A Prospective Cohort Study.


Journal

Annals of internal medicine
ISSN: 1539-3704
Titre abrégé: Ann Intern Med
Pays: United States
ID NLM: 0372351

Informations de publication

Date de publication:
07 2023
Historique:
medline: 19 7 2023
pubmed: 3 7 2023
entrez: 3 7 2023
Statut: ppublish

Résumé

The performance of rapid antigen tests (Ag-RDTs) for screening asymptomatic and symptomatic persons for SARS-CoV-2 is not well established. To evaluate the performance of Ag-RDTs for detection of SARS-CoV-2 among symptomatic and asymptomatic participants. This prospective cohort study enrolled participants between October 2021 and January 2022. Participants completed Ag-RDTs and reverse transcriptase polymerase chain reaction (RT-PCR) testing for SARS-CoV-2 every 48 hours for 15 days. Participants were enrolled digitally throughout the mainland United States. They self-collected anterior nasal swabs for Ag-RDTs and RT-PCR testing. Nasal swabs for RT-PCR were shipped to a central laboratory, whereas Ag-RDTs were done at home. Of 7361 participants in the study, 5353 who were asymptomatic and negative for SARS-CoV-2 on study day 1 were eligible. In total, 154 participants had at least 1 positive RT-PCR result. The sensitivity of Ag-RDTs was measured on the basis of testing once (same-day), twice (after 48 hours), and thrice (after a total of 96 hours). The analysis was repeated for different days past index PCR positivity (DPIPPs) to approximate real-world scenarios where testing initiation may not always coincide with DPIPP 0. Results were stratified by symptom status. Among 154 participants who tested positive for SARS-CoV-2, 97 were asymptomatic and 57 had symptoms at infection onset. Serial testing with Ag-RDTs twice 48 hours apart resulted in an aggregated sensitivity of 93.4% (95% CI, 90.4% to 95.9%) among symptomatic participants on DPIPPs 0 to 6. When singleton positive results were excluded, the aggregated sensitivity on DPIPPs 0 to 6 for 2-time serial testing among asymptomatic participants was lower at 62.7% (CI, 57.0% to 70.5%), but it improved to 79.0% (CI, 70.1% to 87.4%) with testing 3 times at 48-hour intervals. Participants tested every 48 hours; therefore, these data cannot support conclusions about serial testing intervals shorter than 48 hours. The performance of Ag-RDTs was optimized when asymptomatic participants tested 3 times at 48-hour intervals and when symptomatic participants tested 2 times separated by 48 hours. National Institutes of Health RADx Tech program.

Sections du résumé

BACKGROUND
The performance of rapid antigen tests (Ag-RDTs) for screening asymptomatic and symptomatic persons for SARS-CoV-2 is not well established.
OBJECTIVE
To evaluate the performance of Ag-RDTs for detection of SARS-CoV-2 among symptomatic and asymptomatic participants.
DESIGN
This prospective cohort study enrolled participants between October 2021 and January 2022. Participants completed Ag-RDTs and reverse transcriptase polymerase chain reaction (RT-PCR) testing for SARS-CoV-2 every 48 hours for 15 days.
SETTING
Participants were enrolled digitally throughout the mainland United States. They self-collected anterior nasal swabs for Ag-RDTs and RT-PCR testing. Nasal swabs for RT-PCR were shipped to a central laboratory, whereas Ag-RDTs were done at home.
PARTICIPANTS
Of 7361 participants in the study, 5353 who were asymptomatic and negative for SARS-CoV-2 on study day 1 were eligible. In total, 154 participants had at least 1 positive RT-PCR result.
MEASUREMENTS
The sensitivity of Ag-RDTs was measured on the basis of testing once (same-day), twice (after 48 hours), and thrice (after a total of 96 hours). The analysis was repeated for different days past index PCR positivity (DPIPPs) to approximate real-world scenarios where testing initiation may not always coincide with DPIPP 0. Results were stratified by symptom status.
RESULTS
Among 154 participants who tested positive for SARS-CoV-2, 97 were asymptomatic and 57 had symptoms at infection onset. Serial testing with Ag-RDTs twice 48 hours apart resulted in an aggregated sensitivity of 93.4% (95% CI, 90.4% to 95.9%) among symptomatic participants on DPIPPs 0 to 6. When singleton positive results were excluded, the aggregated sensitivity on DPIPPs 0 to 6 for 2-time serial testing among asymptomatic participants was lower at 62.7% (CI, 57.0% to 70.5%), but it improved to 79.0% (CI, 70.1% to 87.4%) with testing 3 times at 48-hour intervals.
LIMITATION
Participants tested every 48 hours; therefore, these data cannot support conclusions about serial testing intervals shorter than 48 hours.
CONCLUSION
The performance of Ag-RDTs was optimized when asymptomatic participants tested 3 times at 48-hour intervals and when symptomatic participants tested 2 times separated by 48 hours.
PRIMARY FUNDING SOURCE
National Institutes of Health RADx Tech program.

Identifiants

pubmed: 37399548
doi: 10.7326/M23-0385
pmc: PMC10321467
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

975-982

Subventions

Organisme : NHLBI NIH HHS
ID : U54 HL143541
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001453
Pays : United States

Commentaires et corrections

Type : UpdateOf

Auteurs

Apurv Soni (A)

Program in Digital Medicine, Department of Medicine; Division of Health Systems Science, Department of Medicine; and Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts (A.S.).

Carly Herbert (C)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Honghuang Lin (H)

Program in Digital Medicine and Division of Health Systems Science, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (H.L., B.W.).

Yi Yan (Y)

Office of In Vitro Diagnostics, Office of Product Evaluation and Quality, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, Maryland (Y.Y., K.R., T.L.).

Caitlin Pretz (C)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Pamela Stamegna (P)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Biqi Wang (B)

Program in Digital Medicine and Division of Health Systems Science, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (H.L., B.W.).

Taylor Orwig (T)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Colton Wright (C)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Seanan Tarrant (S)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Stephanie Behar (S)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Thejas Suvarna (T)

CareEvolution, Ann Arbor, Michigan (T.S., S.S., E.H., C.N., V.K.).

Summer Schrader (S)

CareEvolution, Ann Arbor, Michigan (T.S., S.S., E.H., C.N., V.K.).

Emma Harman (E)

CareEvolution, Ann Arbor, Michigan (T.S., S.S., E.H., C.N., V.K.).

Chris Nowak (C)

CareEvolution, Ann Arbor, Michigan (T.S., S.S., E.H., C.N., V.K.).

Vik Kheterpal (V)

CareEvolution, Ann Arbor, Michigan (T.S., S.S., E.H., C.N., V.K.).

Lokinendi V Rao (LV)

Quest Diagnostics, Marlborough, Massachusetts (L.V.R., L.C.).

Lisa Cashman (L)

Quest Diagnostics, Marlborough, Massachusetts (L.V.R., L.C.).

Elizabeth Orvek (E)

Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts (E.O., D.A., A.Z., S.W., P.L., B.B., S.C.L.).

Didem Ayturk (D)

Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts (E.O., D.A., A.Z., S.W., P.L., B.B., S.C.L.).

Laura Gibson (L)

Division of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (L.G.).

Adrian Zai (A)

Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts (E.O., D.A., A.Z., S.W., P.L., B.B., S.C.L.).

Steven Wong (S)

Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts (E.O., D.A., A.Z., S.W., P.L., B.B., S.C.L.).

Peter Lazar (P)

Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts (E.O., D.A., A.Z., S.W., P.L., B.B., S.C.L.).

Ziyue Wang (Z)

Division of Cardiovascular Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (Z.W.).

Andreas Filippaios (A)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Bruce Barton (B)

Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts (E.O., D.A., A.Z., S.W., P.L., B.B., S.C.L.).

Chad J Achenbach (CJ)

Division of Infectious Diseases, Department of Medicine, Havey Institute for Global Health, Feinberg School of Medicine, Northwestern University, Chicago, Illinois (C.J.A., R.L.M.).

Robert L Murphy (RL)

Division of Infectious Diseases, Department of Medicine, Havey Institute for Global Health, Feinberg School of Medicine, Northwestern University, Chicago, Illinois (C.J.A., R.L.M.).

Matthew L Robinson (ML)

Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland (M.L.R., Y.C.M.).

Yukari C Manabe (YC)

Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland (M.L.R., Y.C.M.).

Shishir Pandey (S)

Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (C.H., C.P., P.S., T.O., C.W., S.T., S.B., A.F., S.P.).

Andres Colubri (A)

Department of Microbiology and Physiological Systems, University of Massachusetts Chan Medical School, Worcester, Massachusetts (A.C.).

Laurel O'Connor (L)

Department of Emergency Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (L.O., J.B.).

Stephenie C Lemon (SC)

Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts (E.O., D.A., A.Z., S.W., P.L., B.B., S.C.L.).

Nisha Fahey (N)

Program in Digital Medicine, Department of Medicine; Department of Population and Quantitative Health Sciences; and Department of Pediatrics, University of Massachusetts Chan Medical School, Worcester, Massachusetts (N.F.).

Katherine L Luzuriaga (KL)

University of Massachusetts Center for Clinical and Translational Science and Program in Molecular Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (K.L.L., N.H.).

Nathaniel Hafer (N)

University of Massachusetts Center for Clinical and Translational Science and Program in Molecular Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (K.L.L., N.H.).

Kristian Roth (K)

Office of In Vitro Diagnostics, Office of Product Evaluation and Quality, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, Maryland (Y.Y., K.R., T.L.).

Toby Lowe (T)

Office of In Vitro Diagnostics, Office of Product Evaluation and Quality, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, Maryland (Y.Y., K.R., T.L.).

Timothy Stenzel (T)

Division of Microbiology, Office of In Vitro Diagnostics, Office of Product Evaluation and Quality, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, Maryland (T.S.).

William Heetderks (W)

National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, Maryland (W.H.).

John Broach (J)

Department of Emergency Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (L.O., J.B.).

David D McManus (DD)

Program in Digital Medicine, Division of Health Systems Science, and Division of Cardiovascular Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts (D.D.M.).

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