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        <datestamp>2026-09-15T05:35:13Z</datestamp>
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          <dc:title>Table 1_Temporal association between influenza A and B positivity and fever-clinic visit burden in Shanghai, China, 2022–2025: a retrospective time-series study.docx</dc:title>
          <dc:creator>Shan Yu (219591)</dc:creator>
          <dc:creator>Tongtong Xu (4959505)</dc:creator>
          <dc:creator>Cunzheng Song (24912562)</dc:creator>
          <dc:creator>Xiaosong Chen (621316)</dc:creator>
          <dc:creator>Yueqiu Gao (8610597)</dc:creator>
          <dc:subject>Public Health and Health Services not elsewhere classified</dc:subject>
          <dc:subject>fever clinic</dc:subject>
          <dc:subject>healthcare utilization</dc:subject>
          <dc:subject>hospital preparedness</dc:subject>
          <dc:subject>influenza A</dc:subject>
          <dc:subject>influenza B</dc:subject>
          <dc:subject>respiratory virus surveillance</dc:subject>
          <dc:description>Background&lt;p&gt;Temporal changes in respiratory virus circulation after the COVID-19 pandemic have created new challenges for fever-clinic preparedness. Outpatient influenza laboratory activity may provide useful operational information, but its type-specific temporal relationship with subsequent fever-clinic burden has not been well characterized.&lt;/p&gt;Methods&lt;p&gt;We conducted a retrospective time-series study using aggregated fever-clinic visit records and outpatient influenza testing data from Renji Hospital, Shanghai, China, from 2022 to 2025. Lead–lag correlations were evaluated over a primary −28 to +28-day window using 7-day centered moving averages, with trailing moving averages and an extended −56 to +56-day window as sensitivity analyses. High-burden days were defined as days with visits at or above the 90th percentile. Adjusted quasi-Poisson models accounted for day of week, calendar month, calendar year, and testing volume. Additional analyses excluded 2022, evaluated adjacent 0–21-day influenza A leads, and used Newey–West autocorrelation-robust inference.&lt;/p&gt;Results&lt;p&gt;We included 254,346 fever-clinic visits and 303,597 outpatient influenza testing episodes. Overall influenza positivity was 33.96%, with 84,819 influenza A-positive and 18,504 influenza B-positive episodes. Influenza A was the main contributor to increased overall activity, particularly in 2023 and 2025. Peak correlations occurred at −12 days for overall influenza positivity and −15 days for influenza A positivity, whereas influenza B peaked at the positive boundary of the primary window. In the extended analysis, the influenza B peak shifted to +50 days, indicating no stable leading relationship. High-burden days were preceded by higher overall influenza and influenza A positivity than reference days. In the conventional testing-volume-adjusted model, influenza A positivity at a 15-day lead was associated with daily fever-clinic visits, but this association was attenuated after exclusion of 2022 and was no longer statistically significant with Newey–West inference. Adjacent-lag analyses did not identify a robust positive day-specific association after false discovery rate correction.&lt;/p&gt;Conclusion&lt;p&gt;Outpatient influenza A positivity showed clearer temporal alignment with subsequent fever-clinic burden than influenza B. Although the fixed 15-day estimate was sensitive to period restriction and residual serial correlation, influenza A positivity may still serve as a complementary hospital-level surveillance indicator rather than a stand-alone forecasting tool.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T05:35:13Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fpubh.2026.1912599.s003</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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