An Assessment of a Rapid SARS-CoV-2 Antigen Test in Bangladesh

Author:

Kawser Zannat1,Hossain Mohabbat1,Suliman Sara2,Lockman Shahin34,Gitaka Jesse56,Bandawe Gama7,Rahmat Redwan1,Hasan Imrul1,Siddik Abu Bakar1,Afrad Mokibul Hassan8,Rahman Mohammed Ziaur8,Miller Glenn9,Walt David R.91011,Ivers Louise C.1213,LaRocque Regina C.13,Harris Jason B.13,Qadri Firdausi8

Affiliation:

1. Institute for Developing Science and Health Initiatives (ideSHi), Dhaka, Bangladesh;

2. Division of Experimental Medicine, Zuckerberg San Francisco General Hospital, San Francisco, California;

3. Division of Infectious Diseases, Brigham and Women’s Hospital, Boston, Massachusetts;

4. Harvard T.H. Chan School of Public Health, Boston, Massachusetts;

5. Directorate of Research and Innovation, Mount Kenya University, Thika, Kenya;

6. Centre for Malaria Elimination, Mount Kenya University, Thika, Kenya;

7. Biological Sciences Department, Academy of Medical Sciences, Malawi University of Science and Technology, Thyolo, Malawi;

8. International Center for Diarrheal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh;

9. Mass General Brigham Center for COVID Innovation, Boston, Massachusetts;

10. Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, Massachusetts;

11. Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts;

12. Department of Global Health and Social Medicine, Harvard Medical School, Boston Massachusetts;

13. MGH Center for Global Health, Massachusetts General Hospital, Boston, Massachusetts

Abstract

ABSTRACT. Early detection of SARS-CoV-2 infection is crucial to prevent its spread. This study aimed to document test sensitivity/specificity, correlation with cycle threshold value from polymerase chain reaction (PCR), fitness-for-use in different populations and settings, and user perspectives that could inform large-scale implementation. In this study, we evaluated the performance of a rapid antigen detection test, BD Veritor, and compared this (and another rapid test, Standard Q) against reverse transcription PCR (RT-PCR) in terms of sensitivity and specificity in 130 symptomatic and 130 asymptomatic adults. In addition, we evaluated the suitability and ease of use of the BD Veritor test in a subsample of study participants (n = 42) and implementers (n = 5). At 95% confidence interval, the sensitivity of the BD Veritor and Standard Q test were 70% and 63% in symptomatic and 87% and 73% in asymptomatic individuals, respectively, regarding positive SARS-CoV-2 RT-PCR results. Overall, the BD Veritor test was 78% sensitive and 99.5% specific compared with RT-PCR irrespective of the cycle threshold. This warrants large field evaluation as well as use of the rapid antigen test for quick assessment of SARS-CoV-2 for containment of epidemics in the country.

Publisher

American Society of Tropical Medicine and Hygiene

Subject

Virology,Infectious Diseases,Parasitology

Reference18 articles.

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