{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,21]],"date-time":"2026-04-21T00:23:45Z","timestamp":1776731025477,"version":"3.51.2"},"reference-count":33,"publisher":"American Medical Association (AMA)","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi221009-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Characterizing the clinical symptoms and evolution of community-based SARS-CoV-2 infections may inform health practitioners and public health officials in a rapidly changing landscape of population immunity and viral variants.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi221009-5\">\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>To compare COVID-19 symptoms among people testing positive with a rapid antigen test (RAT) during the Omicron BA.1 variant period (December 1, 2021, to January 30, 2022) with the pre-Delta (January 10 to May 31, 2021) and Delta (June 1 to November 30, 2021) variant periods and to assess the duration of RAT positivity during the Omicron BA.1 surge.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi221009-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>This cross-sectional study was conducted from January 10, 2021, to January 31, 2022, at a walk-up community COVID-19 testing site in San Francisco, California. Participants included children and adults seeking COVID-19 testing with an RAT, regardless of age, vaccine status, or symptoms.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi221009-7\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>\n                      Fisher exact tests or \u03c7\n                      <jats:sup>2<\/jats:sup>\n                      tests were used to compare COVID-19 symptoms during the Omicron BA.1 period with the pre-Delta and Delta periods for vaccination status and age group. Among people returning for repeated testing during the Omicron period, the proportion with a positive RAT between 4 and 14 days from symptom onset or since first positive test if asymptomatic was estimated.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi221009-8\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Among 63\u202f277 persons tested (median [IQR] age, 32 [21-44] years, with 12.0% younger than 12 years; 52.0% women; and 68.5% Latinx), a total of 18\u202f301 people (28.9%) reported symptoms, of whom 4565 (24.9%) tested positive for COVID-19. During the Omicron BA.1 period, 3032 of 7283 symptomatic participants (41.6%) tested positive, and the numbers of these reporting cough and sore throat were higher than during pre-Delta and Delta periods (cough: 2044 [67.4%] vs 546 [51.3%] of 1065 participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001 for pre-Delta, and 281 [60.0%] of 468 participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.002, for Delta; sore throat: 1316 [43.4%] vs 315 [29.6%] of 1065 participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001 for pre-Delta, and 136 [29.1%] of 468 participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001, for Delta). Compared with the 1065 patients with positive test results in the pre-Delta period, congestion among the 3032 with positive results during the Omicron BA.1 period was more common (1177 [38.8%] vs 294 [27.6%] participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001), and loss of taste or smell (160 [5.3%] vs 183 [17.2%] participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) and fever (921 [30.4%] vs 369 [34.7%] participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.01) were less common. In addition, during the Omicron BA.1 period, fever was less common among the people with positive test results who had received a vaccine booster compared with those with positive test results who were unvaccinated (97 [22.5%] of 432 vs 42 [36.2%] of 116 participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.003), and fever and myalgia were less common among participants who had received a booster compared with those with positive results who had received only a primary series (fever: 97 [22.5%] of 432 vs 559 [32.8%] of 1705 participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001; myalgia: 115 [26.6%] of 432 vs 580 [34.0%] of 1705 participants,\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.003). During the Omicron BA.1 period, 5 days after symptom onset, 507 of 1613 people (31.1%) with COVID-19 stated that their symptoms were similar, and 95 people (5.9%) reported worsening symptoms. Among people testing positive, 80.2% of participants who were symptomatic and retested remained positive 5 days after symptom onset.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi221009-9\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this cross-sectional study, COVID-19 upper respiratory tract symptoms were more commonly reported during the Omicron BA.1 period than during the pre-Delta and Delta periods, with differences by vaccination status. Rapid antigen test positivity remained high 5 days after symptom onset, supporting guidelines requiring a negative test to inform the length of the isolation period.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2022.35844","type":"journal-article","created":{"date-parts":[[2022,10,10]],"date-time":"2022-10-10T11:23:39Z","timestamp":1665401019000},"page":"e2235844","source":"Crossref","is-referenced-by-count":38,"title":["COVID-19 Symptoms and Duration of Rapid Antigen Test Positivity at a Community Testing and Surveillance Site During Pre-Delta, Delta, and Omicron BA.1 Periods"],"prefix":"10.1001","volume":"5","author":[{"given":"Carina","family":"Marquez","sequence":"first","affiliation":[{"name":"Division of HIV, Infectious Diseases and Global Medicine, Zuckerberg San Francisco General Hospital, University of California, San Francisco, San Francisco"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrew 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California, San Francisco, San Francisco"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anthea","family":"Mitchell","sequence":"additional","affiliation":[{"name":"Chan-Zuckerberg Biohub, San Francisco, California"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chung-Yu","family":"Wang","sequence":"additional","affiliation":[{"name":"Chan-Zuckerberg Biohub, San Francisco, California"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Genay","family":"Pilarowski","sequence":"additional","affiliation":[{"name":"Unidos en Salud, San Francisco, California"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Salustiano","family":"Ribeiro","sequence":"additional","affiliation":[{"name":"Bay Area Phlebotomy and Laboratory Services, San Francisco, California"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Diane","family":"Jones","sequence":"additional","affiliation":[{"name":"Unidos en Salud, San Francisco, 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