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      Comparison of SARS-CoV-2 Reverse Transcriptase Polymerase Chain Reaction and BinaxNOW Rapid Antigen Tests at a Community Site During an Omicron Surge : A Cross-Sectional Study

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          Abstract

          This study compares the performance of the BinaxNOW rapid antigen test versus reverse transcriptase polymerase chain reaction for community-based detection of infection with the Omicron variant of SARS-CoV-2 in San Francisco, California, during January 2022.

          Abstract

          Visual Abstract. SARS-CoV-2 RT-PCR Versus BinaxNOW Rapid Antigen Test During Omicron Surge. This study compares the performance of the BinaxNOW rapid antigen test versus reverse transcriptase polymerase chain reaction for community-based detection of infection with the Omicron variant of SARS-CoV-2 in San Francisco, California, during January 2022.
          Visual Abstract.
          SARS-CoV-2 RT-PCR Versus BinaxNOW Rapid Antigen Test During Omicron Surge.

          This study compares the performance of the BinaxNOW rapid antigen test versus reverse transcriptase polymerase chain reaction for community-based detection of infection with the Omicron variant of SARS-CoV-2 in San Francisco, California, during January 2022.

          Abstract

          Background:

          SARS-CoV-2 rapid antigen tests are an important public health tool.

          Objective:

          To evaluate field performance of the BinaxNOW rapid antigen test (Abbott) compared with reverse transcriptase polymerase chain reaction (RT-PCR) for detecting infection with the Omicron variant of SARS-CoV-2.

          Design:

          Cross-sectional surveillance study.

          Setting:

          Free, walk-up, outdoor, urban community testing and vaccine site led by Unidos en Salud, serving a predominantly Latinx community highly impacted by COVID-19.

          Participants:

          Persons seeking COVID-19 testing in January 2022.

          Measurements:

          Simultaneous BinaxNOW and RT-PCR from nasal, cheek, and throat swabs, including cycle threshold (Ct) measures; a lower Ct value is a surrogate for higher amounts of virus.

          Results:

          Among 731 persons tested with nasal swabs, there were 296 (40.5%) positive results on RT-PCR; 98.9% were the Omicron variant. BinaxNOW detected 95.2% (95% CI, 91% to 98%) of persons who tested positive on RT-PCR with a Ct value below 30, 82.1% (CI, 77% to 87%) of those who tested positive on RT-PCR with a Ct value below 35, and 65.2% (CI, 60% to 71%) of all who were positive on RT-PCR. Among 75 persons with simultaneous nasal and cheek swabs, BinaxNOW using a cheek swab failed to detect 91% (20 of 22) of specimens that were positive on BinaxNOW with a nasal swab. Among persons with simultaneous nasal and throat swabs who were positive on RT-PCR with a Ct value below 30, 42 of 49 (85.7%) were detected by nasal BinaxNOW, 23 of 49 (46.9%) by throat BinaxNOW, and 44 of 49 (89.8%) by either.

          Limitation:

          Participants were a cross-sectional sample from a community-based sentinel surveillance site, precluding study of viral or symptom dynamics.

          Conclusion:

          BinaxNOW detected persons with high SARS-CoV-2 levels during the Omicron surge, enabling rapid responses to positive test results. Cheek or throat swabs should not replace nasal swabs. As currently recommended, high-risk persons with an initial negative BinaxNOW result should have repeated testing.

          Primary Funding Source:

          University of California, San Francisco.

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          Most cited references19

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          Molnupiravir for Oral Treatment of Covid-19 in Nonhospitalized Patients

          Abstract Background New treatments are needed to reduce the risk of progression of coronavirus disease 2019 (Covid-19). Molnupiravir is an oral, small-molecule antiviral prodrug that is active against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Methods We conducted a phase 3, double-blind, randomized, placebo-controlled trial to evaluate the efficacy and safety of treatment with molnupiravir started within 5 days after the onset of signs or symptoms in nonhospitalized, unvaccinated adults with mild-to-moderate, laboratory-confirmed Covid-19 and at least one risk factor for severe Covid-19 illness. Participants in the trial were randomly assigned to receive 800 mg of molnupiravir or placebo twice daily for 5 days. The primary efficacy end point was the incidence hospitalization or death at day 29; the incidence of adverse events was the primary safety end point. A planned interim analysis was performed when 50% of 1550 participants (target enrollment) had been followed through day 29. Results A total of 1433 participants underwent randomization; 716 were assigned to receive molnupiravir and 717 to receive placebo. With the exception of an imbalance in sex, baseline characteristics were similar in the two groups. The superiority of molnupiravir was demonstrated at the interim analysis; the risk of hospitalization for any cause or death through day 29 was lower with molnupiravir (28 of 385 participants [7.3%]) than with placebo (53 of 377 [14.1%]) (difference, −6.8 percentage points; 95% confidence interval, −11.3 to −2.4; P=0.001). In the analysis of all participants who had undergone randomization, the percentage of participants who were hospitalized or died through day 29 was lower in the molnupiravir group than in the placebo group (6.8% [48 of 709] vs. 9.7% [68 of 699]; difference, −3.0 percentage points; 95% confidence interval, −5.9 to −0.1). Results of subgroup analyses were largely consistent with these overall results; in some subgroups, such as patients with evidence of previous SARS-CoV-2 infection, those with low baseline viral load, and those with diabetes, the point estimate for the difference favored placebo. One death was reported in the molnupiravir group and 9 were reported in the placebo group through day 29. Adverse events were reported in 216 of 710 participants (30.4%) in the molnupiravir group and 231 of 701 (33.0%) in the placebo group. Conclusions Early treatment with molnupiravir reduced the risk of hospitalization or death in at-risk, unvaccinated adults with Covid-19. (Funded by Merck Sharp and Dohme; MOVe-OUT ClinicalTrials.gov number, NCT04575597.)
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            Is Open Access

            Duration of infectiousness and correlation with RT-PCR cycle threshold values in cases of COVID-19, England, January to May 2020

            Severe acute respiratory syndrome coronavirus 2 viral load in the upper respiratory tract peaks around symptom onset and infectious virus persists for 10 days in mild-to-moderate coronavirus disease (n = 324 samples analysed). RT-PCR cycle threshold (Ct) values correlate strongly with cultivable virus. Probability of culturing virus declines to 8% in samples with Ct > 35 and to 6% 10 days after onset; it is similar in asymptomatic and symptomatic persons. Asymptomatic persons represent a source of transmissible virus.
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              Is Open Access

              Test sensitivity is secondary to frequency and turnaround time for COVID-19 screening

              Test sensitivity is secondary to frequency and turnaround time for COVID-19 screening.
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                Author and article information

                Journal
                Ann Intern Med
                Ann Intern Med
                aim
                Annals of Internal Medicine
                American College of Physicians
                0003-4819
                1539-3704
                15 March 2022
                15 March 2022
                : M22-0202
                Affiliations
                [01]University of California, San Francisco, San Francisco, California (J.S., C.M., D.B., G.C., V.J., D.H.)
                [02]Unidos en Salud, San Francisco, California (G.P., S.R., J.M., J.P., D.J., D.M.)
                [03]Chan Zuckerberg Biohub, San Francisco, California (C.W., A.M., J.D.)
                [04]University of California, Berkeley, Berkeley, California (R.P., M.P.)
                [05]Unidos en Salud and San Francisco Latino Task Force for COVID-19, San Francisco, California (S.R., V.T., S.R.)
                [06]California Department of Public Health, Richmond, California (R.N.)
                Author notes
                Disclaimer: The findings and conclusions in this article are those of the authors and do not necessarily represent the views or opinions of the California Department of Public Health or the California Health and Human Services Agency.
                Acknowledgment: The authors thank Priscilla Chan, MD, for her thoughtful discussion, suggestions, support, and close reading of the manuscript.
                Financial Support: Funding for this study was provided by UCSF, the Chan Zuckerberg Biohub, the San Francisco Department of Public Health, the Patrick J. McGovern Foundation, the McKinnon Family Foundation, Carl Kawaja and Wendy Holcombe, Martin and Leesa Romo, Mark and Carrie Casey, and Greg and Lisa Wendt. The BinaxNOW cards were provided by the California Department of Public Health.
                Reproducible Research Statement: Study protocol: Not applicable. Statistical code and data set: Not available.
                Corresponding Author: Diane Havlir, MD, University of California, San Francisco, 995 Potrero Avenue, San Francisco, CA 94110; e-mail, Diane.havlir@ 123456ucsf.edu .
                Author Contributions: Conception and design: J. DeRisi, D. Havlir, D. Jones, C. Marquez, M. Petersen, G. Pilarowski, V. Tulier-Laiwa.
                Analysis and interpretation of the data: J. DeRisi, D. Havlir, V. Jain, C. Marquez, A. Mitchell, M. Petersen, G. Pilarowski, R. Puccinelli, J. Schrom, C. Wang.
                Drafting of the article: J. DeRisi, D. Havlir, M. Petersen, J. Schrom.
                Critical revision for important intellectual content: G. Chamie, J. DeRisi, D. Havlir, V. Jain, C. Marquez, M. Petersen, G. Pilarowski, S. Ribeiro.
                Final approval of the article: D. Black, G. Chamie, J. DeRisi, D. Havlir, V. Jain, D. Jones, C. Marquez, J. Martinez, D. Martinez, A. Mitchell, R. Nakamura, J. Payan, M. Petersen, G. Pilarowski, R. Puccinelli, S. Ribeiro, Susana Rojas, Susy Rojas, J. Schrom, V. Tulier-Laiwa, C. Wang.
                Provision of study materials or patients: D. Black, D. Havlir, R. Nakamura, S. Ribeiro.
                Statistical expertise: M. Petersen.
                Obtaining of funding: J. DeRisi, D. Havlir.
                Administrative, technical, or logistic support: D. Black, J. DeRisi, D. Havlir, J. Martinez, D. Martinez, R. Nakamura, J. Payan, G. Pilarowski, S. Ribeiro, Susy Rojas.
                Collection and assembly of data: D. Black, J. DeRisi, D. Havlir, D. Martinez, J. Martinez, A. Mitchell, J. Payan, G. Pilarowski, R. Puccinelli, S. Ribeiro, Susy Rojas, C. Wang.
                Previous Posting: This manuscript was posted as a preprint on medRxiv on 12 January 2022. doi:10.1101/2022.01.08.22268954
                Author information
                https://orcid.org/0000-0002-3871-4311
                https://orcid.org/0000-0001-8270-8771
                https://orcid.org/0000-0002-8614-8326
                https://orcid.org/0000-0002-7482-2336
                https://orcid.org/0000-0002-0375-5500
                https://orcid.org/0000-0002-5860-8081
                https://orcid.org/0000-0002-4611-9205
                https://orcid.org/0000-0003-0761-3136
                Article
                aim-olf-M220202
                10.7326/M22-0202
                8943844
                35286144
                15f0c7e8-1d19-4b6d-875b-ba0a3f792195
                Copyright @ 2022

                This article is made available via the PMC Open Access Subset for unrestricted re-use for research, analyses, and text and data mining through PubMed Central. Acknowledgement of the original source shall include a notice similar to the following: "© 2020 American College of Physicians. Some rights reserved. This work permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited." These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                Categories
                Original Research
                8434, Antigens
                3122457, COVID-19
                3006, Prevention, policy, and public health
                3123756, Reverse transcriptase polymerase chain reaction
                early, Currently Online First
                coronavirus, Coronavirus Disease 2019 (COVID-19)
                poc-eligible, POC Eligible

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