Factors that Influence the Reported Sensitivity of Rapid Antigen Testing for SARS-CoV-2
Tests that detect the presence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) antigen in clinical specimens from the upper respiratory tract can provide a rapid means of coronavirus disease 2019 (COVID-19) diagnosis and help identify individuals who may be infectious and should isol...
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Published in | Frontiers in microbiology Vol. 12; p. 714242 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Frontiers Media S.A
05.10.2021
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Abstract | Tests that detect the presence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) antigen in clinical specimens from the upper respiratory tract can provide a rapid means of coronavirus disease 2019 (COVID-19) diagnosis and help identify individuals who may be infectious and should isolate to prevent SARS-CoV-2 transmission. This systematic review assesses the diagnostic accuracy of SARS-CoV-2 antigen detection in COVID-19 symptomatic and asymptomatic individuals compared to quantitative reverse transcription polymerase chain reaction (RT-qPCR) and summarizes antigen test sensitivity using meta-regression. In total, 83 studies were included that compared SARS-CoV-2 rapid antigen-based lateral flow testing (RALFT) to RT-qPCR for SARS-CoV-2. Generally, the quality of the evaluated studies was inconsistent; nevertheless, the overall sensitivity for RALFT was determined to be 75.0% (95% confidence interval: 71.0–78.0). Additionally, RALFT sensitivity was found to be higher for symptomatic vs. asymptomatic individuals and was higher for a symptomatic population within 7 days from symptom onset compared to a population with extended days of symptoms. Viral load was found to be the most important factor for determining SARS-CoV-2 antigen test sensitivity. Other design factors, such as specimen storage and anatomical collection type, also affect the performance of RALFT. RALFT and RT-qPCR testing both achieve high sensitivity when compared to SARS-CoV-2 viral culture. |
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AbstractList | Tests that detect the presence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) antigen in clinical specimens from the upper respiratory tract can provide a rapid means of coronavirus disease 2019 (COVID-19) diagnosis and help identify individuals who may be infectious and should isolate to prevent SARS-CoV-2 transmission. This systematic review assesses the diagnostic accuracy of SARS-CoV-2 antigen detection in COVID-19 symptomatic and asymptomatic individuals compared to quantitative reverse transcription polymerase chain reaction (RT-qPCR) and summarizes antigen test sensitivity using meta-regression. In total, 83 studies were included that compared SARS-CoV-2 rapid antigen-based lateral flow testing (RALFT) to RT-qPCR for SARS-CoV-2. Generally, the quality of the evaluated studies was inconsistent; nevertheless, the overall sensitivity for RALFT was determined to be 75.0% (95% confidence interval: 71.0–78.0). Additionally, RALFT sensitivity was found to be higher for symptomatic vs. asymptomatic individuals and was higher for a symptomatic population within 7 days from symptom onset compared to a population with extended days of symptoms. Viral load was found to be the most important factor for determining SARS-CoV-2 antigen test sensitivity. Other design factors, such as specimen storage and anatomical collection type, also affect the performance of RALFT. RALFT and RT-qPCR testing both achieve high sensitivity when compared to SARS-CoV-2 viral culture. Tests that detect the presence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) antigen in clinical specimens from the upper respiratory tract can provide a rapid means of coronavirus disease 2019 (COVID-19) diagnosis and help identify individuals who may be infectious and should isolate to prevent SARS-CoV-2 transmission. This systematic review assesses the diagnostic accuracy of SARS-CoV-2 antigen detection in COVID-19 symptomatic and asymptomatic individuals compared to quantitative reverse transcription polymerase chain reaction (RT-qPCR) and summarizes antigen test sensitivity using meta-regression. In total, 83 studies were included that compared SARS-CoV-2 rapid antigen-based lateral flow testing (RALFT) to RT-qPCR for SARS-CoV-2. Generally, the quality of the evaluated studies was inconsistent; nevertheless, the overall sensitivity for RALFT was determined to be 75.0% (95% confidence interval: 71.0-78.0). Additionally, RALFT sensitivity was found to be higher for symptomatic vs. asymptomatic individuals and was higher for a symptomatic population within 7 days from symptom onset compared to a population with extended days of symptoms. Viral load was found to be the most important factor for determining SARS-CoV-2 antigen test sensitivity. Other design factors, such as specimen storage and anatomical collection type, also affect the performance of RALFT. RALFT and RT-qPCR testing both achieve high sensitivity when compared to SARS-CoV-2 viral culture.Tests that detect the presence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) antigen in clinical specimens from the upper respiratory tract can provide a rapid means of coronavirus disease 2019 (COVID-19) diagnosis and help identify individuals who may be infectious and should isolate to prevent SARS-CoV-2 transmission. This systematic review assesses the diagnostic accuracy of SARS-CoV-2 antigen detection in COVID-19 symptomatic and asymptomatic individuals compared to quantitative reverse transcription polymerase chain reaction (RT-qPCR) and summarizes antigen test sensitivity using meta-regression. In total, 83 studies were included that compared SARS-CoV-2 rapid antigen-based lateral flow testing (RALFT) to RT-qPCR for SARS-CoV-2. Generally, the quality of the evaluated studies was inconsistent; nevertheless, the overall sensitivity for RALFT was determined to be 75.0% (95% confidence interval: 71.0-78.0). Additionally, RALFT sensitivity was found to be higher for symptomatic vs. asymptomatic individuals and was higher for a symptomatic population within 7 days from symptom onset compared to a population with extended days of symptoms. Viral load was found to be the most important factor for determining SARS-CoV-2 antigen test sensitivity. Other design factors, such as specimen storage and anatomical collection type, also affect the performance of RALFT. RALFT and RT-qPCR testing both achieve high sensitivity when compared to SARS-CoV-2 viral culture. |
Author | Manabe, Yukari C. Gary, Devin S. Cooper, Lauren Cooper, Charles K. Mann, Joseph Andrews, Jeffrey C. Pekosz, Andrew Mills, Dorsey Parvu, Valentin Lin, Yu-Chih |
AuthorAffiliation | 3 Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, MD , United States 4 Department of Emergency Medicine, Johns Hopkins University School of Medicine , Baltimore, MD , United States 1 Becton, Dickinson and Company, BD Life Sciences–Integrated Diagnostic Solutions , Sparks, MD , United States 2 W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health , Baltimore, MD , United States |
AuthorAffiliation_xml | – name: 1 Becton, Dickinson and Company, BD Life Sciences–Integrated Diagnostic Solutions , Sparks, MD , United States – name: 3 Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, MD , United States – name: 4 Department of Emergency Medicine, Johns Hopkins University School of Medicine , Baltimore, MD , United States – name: 2 W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health , Baltimore, MD , United States |
Author_xml | – sequence: 1 givenname: Valentin surname: Parvu fullname: Parvu, Valentin – sequence: 2 givenname: Devin S. surname: Gary fullname: Gary, Devin S. – sequence: 3 givenname: Joseph surname: Mann fullname: Mann, Joseph – sequence: 4 givenname: Yu-Chih surname: Lin fullname: Lin, Yu-Chih – sequence: 5 givenname: Dorsey surname: Mills fullname: Mills, Dorsey – sequence: 6 givenname: Lauren surname: Cooper fullname: Cooper, Lauren – sequence: 7 givenname: Jeffrey C. surname: Andrews fullname: Andrews, Jeffrey C. – sequence: 8 givenname: Yukari C. surname: Manabe fullname: Manabe, Yukari C. – sequence: 9 givenname: Andrew surname: Pekosz fullname: Pekosz, Andrew – sequence: 10 givenname: Charles K. surname: Cooper fullname: Cooper, Charles K. |
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ContentType | Journal Article |
Copyright | Copyright © 2021 Parvu, Gary, Mann, Lin, Mills, Cooper, Andrews, Manabe, Pekosz and Cooper. Copyright © 2021 Parvu, Gary, Mann, Lin, Mills, Cooper, Andrews, Manabe, Pekosz and Cooper. 2021 Parvu, Gary, Mann, Lin, Mills, Cooper, Andrews, Manabe, Pekosz and Cooper |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Maurizio Sanguinetti, Catholic University of the Sacred Heart, Italy This article was submitted to Infectious Diseases, a section of the journal Frontiers in Microbiology Reviewed by: Piyush Baindara, University of Missouri, United States; Yean Kong Yong, Xiamen University, Malaysia |
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