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      Extending the susceptible‐exposed‐infected‐removed (SEIR) model to handle the false negative rate and symptom‐based administration of COVID‐19 diagnostic tests: SEIR‐fansy

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          Abstract

          False negative rates of severe acute respiratory coronavirus 2 diagnostic tests, together with selection bias due to prioritized testing can result in inaccurate modeling of COVID‐19 transmission dynamics based on reported “case” counts. We propose an extension of the widely used Susceptible‐Exposed‐Infected‐Removed (SEIR) model that accounts for misclassification error and selection bias, and derive an analytic expression for the basic reproduction number R 0 as a function of false negative rates of the diagnostic tests and selection probabilities for getting tested. Analyzing data from the first two waves of the pandemic in India, we show that correcting for misclassification and selection leads to more accurate prediction in a test sample. We provide estimates of undetected infections and deaths between April 1, 2020 and August 31, 2021. At the end of the first wave in India, the estimated under‐reporting factor for cases was at 11.1 (95% CI: 10.7,11.5) and for deaths at 3.58 (95% CI: 3.5,3.66) as of February 1, 2021, while they change to 19.2 (95% CI: 17.9, 19.9) and 4.55 (95% CI: 4.32, 4.68) as of July 1, 2021. Equivalently, 9.0% (95% CI: 8.7%, 9.3%) and 5.2% (95% CI: 5.0%, 5.6%) of total estimated infections were reported on these two dates, while 27.9% (95% CI: 27.3%, 28.6%) and 22% (95% CI: 21.4%, 23.1%) of estimated total deaths were reported. Extensive simulation studies demonstrate the effect of misclassification and selection on estimation of R 0 and prediction of future infections. A R‐package SEIRfansy is developed for broader dissemination.

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          Most cited references34

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          Inference from Iterative Simulation Using Multiple Sequences

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            Correlation of Chest CT and RT-PCR Testing in Coronavirus Disease 2019 (COVID-19) in China: A Report of 1014 Cases

            Background Chest CT is used for diagnosis of 2019 novel coronavirus disease (COVID-19), as an important complement to the reverse-transcription polymerase chain reaction (RT-PCR) tests. Purpose To investigate the diagnostic value and consistency of chest CT as compared with comparison to RT-PCR assay in COVID-19. Methods From January 6 to February 6, 2020, 1014 patients in Wuhan, China who underwent both chest CT and RT-PCR tests were included. With RT-PCR as reference standard, the performance of chest CT in diagnosing COVID-19 was assessed. Besides, for patients with multiple RT-PCR assays, the dynamic conversion of RT-PCR results (negative to positive, positive to negative, respectively) was analyzed as compared with serial chest CT scans for those with time-interval of 4 days or more. Results Of 1014 patients, 59% (601/1014) had positive RT-PCR results, and 88% (888/1014) had positive chest CT scans. The sensitivity of chest CT in suggesting COVID-19 was 97% (95%CI, 95-98%, 580/601 patients) based on positive RT-PCR results. In patients with negative RT-PCR results, 75% (308/413) had positive chest CT findings; of 308, 48% were considered as highly likely cases, with 33% as probable cases. By analysis of serial RT-PCR assays and CT scans, the mean interval time between the initial negative to positive RT-PCR results was 5.1 ± 1.5 days; the initial positive to subsequent negative RT-PCR result was 6.9 ± 2.3 days). 60% to 93% of cases had initial positive CT consistent with COVID-19 prior (or parallel) to the initial positive RT-PCR results. 42% (24/57) cases showed improvement in follow-up chest CT scans before the RT-PCR results turning negative. Conclusion Chest CT has a high sensitivity for diagnosis of COVID-19. Chest CT may be considered as a primary tool for the current COVID-19 detection in epidemic areas. A translation of this abstract in Farsi is available in the supplement. - ترجمه چکیده این مقاله به فارسی، در ضمیمه موجود است.
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              Presumed Asymptomatic Carrier Transmission of COVID-19

              This study describes possible transmission of novel coronavirus disease 2019 (COVID-19) from an asymptomatic Wuhan resident to 5 family members in Anyang, a Chinese city in the neighboring province of Hubei.
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                Author and article information

                Contributors
                bhramar@umich.edu
                Journal
                Stat Med
                Stat Med
                10.1002/(ISSN)1097-0258
                SIM
                Statistics in Medicine
                John Wiley and Sons Inc. (Hoboken )
                0277-6715
                1097-0258
                27 February 2022
                15 June 2022
                27 February 2022
                : 41
                : 13 ( doiID: 10.1002/sim.v41.13 )
                : 2317-2337
                Affiliations
                [ 1 ] Department of Statistics Harvard University Cambridge Massachusetts USA
                [ 2 ] Department of Biostatistics University of Michigan Ann Arbor Michigan United States
                [ 3 ] Department of Epidemiology University of Michigan Ann Arbor Michigan USA
                [ 4 ] Department of Statistics Virginia Polytechnic Institute and State University Blacksburg Virginia USA
                Author notes
                [*] [* ] Correspondence Bhramar Mukherjee, Department of Biostatistics, University of Michigan, 1415 Washington Heights, SPH I, Ann Arbor, MI 48109, USA.

                Email: bhramar@ 123456umich.edu

                Author information
                https://orcid.org/0000-0002-3788-5944
                https://orcid.org/0000-0003-0118-4561
                https://orcid.org/0000-0001-5991-5182
                Article
                SIM9357
                10.1002/sim.9357
                9035093
                35224743
                400a221e-93b8-453f-a0d0-bea6ffb62bb4
                © 2022 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 05 February 2022
                : 24 September 2021
                : 08 February 2022
                Page count
                Figures: 8, Tables: 2, Pages: 21, Words: 10219
                Funding
                Funded by: Division of Cancer Prevention, National Cancer Institute , doi 10.13039/100007316;
                Award ID: 5P30CA046592‐27
                Funded by: Michigan Institute of Data Science (MIDAS), Precision Health Initiative and Rogel Scholar Fund at the University of Michigan , doi 10.13039/100015711;
                Funded by: Division of Mathematical Sciences , doi 10.13039/100000121;
                Award ID: 1712933
                Funded by: National Human Genome Research Institute , doi 10.13039/100000051;
                Award ID: 5R01HG008773‐05
                Award ID: P30 CA046592
                Funded by: National Science Foundation , doi 10.13039/501100008982;
                Award ID: 2015460
                Award ID: 1712933
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                15 June 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.6 mode:remove_FC converted:17.05.2022

                Biostatistics
                compartmental models,infection fatality rate,r package seirfansy ,reproduction number,selection bias,sensitivity,undetected infections

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