112 results on '"Quilty, Billy J"'
Search Results
2. Natural and hybrid immunity following four COVID-19 waves: A prospective cohort study of mothers in South Africa
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Zar, Heather J., MacGinty, Rae, Workman, Lesley, Botha, Maresa, Johnson, Marina, Hunt, Adam, Burd, Tiffany, Nicol, Mark P., Flasche, Stefan, Quilty, Billy J., and Goldblatt, David
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- 2022
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3. Measuring the effects of COVID-19-related disruption on dengue transmission in southeast Asia and Latin America: a statistical modelling study
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Procter, Simon R, Wong, Kerry LM, Hellewell, Joel, Davies, Nicholas G, Jarvis, Christopher I, McCarthy, Ciara V, Medley, Graham, Meakin, Sophie R, Rosello, Alicia, Finch, Emilie, Lowe, Rachel, Pearson, Carl A B, Clifford, Samuel, Quilty, Billy J, Flasche, Stefan, Gibbs, Hamish P, Chapman, Lloyd A C, Atkins, Katherine E., Hodgson, David, Barnard, Rosanna C, Russell, Timothy W, Klepac, Petra, Jafari, Yalda, Eggo, Rosalind M, Mee, Paul, Quaife, Matthew, Endo, Akira, Funk, Sebastian, Hué, Stéphane, Kucharski, Adam J, Edmunds, W John, O'Reilly, Kathleen, Pung, Rachael, Villabona-Arenas, C Julian, Gimma, Amy, Abbas, Kaja, Prem, Kiesha, Knight, Gwenan M, Sun, Fiona Yueqian, Waites, William, Munday, James D, Koltai, Mihaly, Sandmann, Frank G, Tully, Damien C, Chen, Yuyang, Li, Naizhe, Lourenço, José, Wang, Lin, Cazelles, Bernard, Dong, Lu, Li, Bingying, Liu, Yang, Jit, Mark, Bosse, Nikos I, Abbott, Sam, Velayudhan, Raman, Wilder-Smith, Annelies, Tian, Huaiyu, and Brady, Oliver J
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- 2022
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4. Regional-based within-year seasonal variations in influenza-related health outcomes across mainland China: a systematic review and spatio-temporal analysis
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Diamond, Charlie, Gong, Hui, Sun, Fiona Yueqian, Liu, Yang, Quilty, Billy J., Jit, Mark, Yang, Juan, Yu, Hongjie, Edmunds, W. John, and Baguelin, Marc
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- 2022
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5. The potential health and economic value of SARS-CoV-2 vaccination alongside physical distancing in the UK: a transmission model-based future scenario analysis and economic evaluation
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Sun, Fiona Yueqian, Villabona-Arenas, C Julian, Nightingale, Emily S, Showering, Alicia, Knight, Gwenan M, Sherratt, Katharine, Liu, Yang, Abbas, Kaja, Funk, Sebastian, Endo, Akira, Hellewell, Joel, Rosello, Alicia, Lowe, Rachel, Quaife, Matthew, Gimma, Amy, Brady, Oliver, Williams, Jack, Procter, Simon R, Eggo, Rosalind M, Chan, Yung-Wai Desmond, Munday, James D, Barnard, Rosanna C, Gore-Langton, Georgia R, Bosse, Nikos I, Waterlow, Naomi R, Diamond, Charlie, Russell, Timothy W, Medley, Graham, Flasche, Stefan, Atkins, Katherine E, Prem, Kiesha, Simons, David, Auzenbergs, Megan, Tully, Damien C, Jarvis, Christopher I, van Zandvoort, Kevin, Abbott, Sam, Pearson, Carl A B, Jombart, Thibaut, Meakin, Sophie R, Foss, Anna M, Kucharski, Adam J, Quilty, Billy J, Gibbs, Hamish P, Clifford, Samuel, Klepac, Petra, Sandmann, Frank G, Davies, Nicholas G, Vassall, Anna, Edmunds, W John, and Jit, Mark
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- 2021
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6. Quarantine and testing strategies in contact tracing for SARS-CoV-2: a modelling study
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Atkins, Katherine E, Foss, Anna M, Waterlow, Naomi R, Abbas, Kaja, Lowe, Rachel, Pearson, Carl A B, Funk, Sebastian, Rosello, Alicia, Knight, Gwenan M, Bosse, Nikos I, Procter, Simon R, Gore-Langton, Georgia R, Showering, Alicia, Munday, James D, Sherratt, Katharine, Jombart, Thibaut, Nightingale, Emily S, Liu, Yang, Jarvis, Christopher I, Medley, Graham, Brady, Oliver, Gibbs, Hamish P, Simons, David, Williams, Jack, Tully, Damien C, Flasche, Stefan, Meakin, Sophie R, Zandvoort, Kevin, Sun, Fiona Y, Jit, Mark, Klepac, Petra, Quaife, Matthew, Eggo, Rosalind M, Sandmann, Frank G, Endo, Akira, Prem, Kiesha, Abbott, Sam, Barnard, Rosanna, Chan, Yung-Wai D, Auzenbergs, Megan, Gimma, Amy, Villabona-Arenas, C Julian, Davies, Nicholas G, Quilty, Billy J, Clifford, Samuel, Hellewell, Joel, Russell, Timothy W, Kucharski, Adam J, and Edmunds, W John
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- 2021
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7. Routine childhood immunisation during the COVID-19 pandemic in Africa: a benefit–risk analysis of health benefits versus excess risk of SARS-CoV-2 infection
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Houben, Rein M G J, Edmunds, W John, Villabona-Arenas, Christian Julian, Atkins, Katherine E, Knight, Gwenan M, Sun, Fiona Yueqian, Auzenbergs, Megan, Rosello, Alicia, Klepac, Petra, Hellewell, Joel, Russell, Timothy W, Tully, Damien C, Emery, Jon C, Gibbs, Hamish P, Munday, James D, Quilty, Billy J, Diamond, Charlie, Pearson, Carl A B, Leclerc, Quentin J, Nightingale, Emily S, Liu, Yang, Endo, Akira, Deol, Arminder K, Kucharski, Adam J, Abbott, Sam, Jarvis, Christopher I, O'Reilly, Kathleen, Jombart, Thibaut, Gimma, Amy, Bosse, Nikos I, Prem, Kiesha, Hué, Stéphane, Davies, Nicholas G, Eggo, Rosalind M, Clifford, Samuel, Medley, Graham, Abbas, Kaja, Procter, Simon R, van Zandvoort, Kevin, Clark, Andrew, Funk, Sebastian, Mengistu, Tewodaj, Hogan, Dan, Dansereau, Emily, Jit, Mark, and Flasche, Stefan
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- 2020
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8. Effectiveness of isolation, testing, contact tracing, and physical distancing on reducing transmission of SARS-CoV-2 in different settings: a mathematical modelling study
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Emery, Jon C, Medley, Graham, Munday, James D, Russell, Timothy W, Leclerc, Quentin J, Diamond, Charlie, Procter, Simon R, Gimma, Amy, Sun, Fiona Yueqian, Gibbs, Hamish P, Rosello, Alicia, van Zandvoort, Kevin, Hué, Stéphane, Meakin, Sophie R, Deol, Arminder K, Knight, Gwen, Jombart, Thibaut, Foss, Anna M, Bosse, Nikos I, Atkins, Katherine E, Quilty, Billy J, Lowe, Rachel, Prem, Kiesha, Flasche, Stefan, Pearson, Carl A B, Houben, Rein M G J, Nightingale, Emily S, Endo, Akira, Tully, Damien C, Liu, Yang, Villabona-Arenas, Julian, O'Reilly, Kathleen, Funk, Sebastian, Eggo, Rosalind M, Jit, Mark, Rees, Eleanor M, Hellewell, Joel, Clifford, Samuel, Jarvis, Christopher I, Abbott, Sam, Auzenbergs, Megan, Davies, Nicholas G, Simons, David, Kucharski, Adam J, Klepac, Petra, Conlan, Andrew J K, Kissler, Stephen M, Tang, Maria L, Fry, Hannah, Gog, Julia R, and Edmunds, W John
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- 2020
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9. Global, regional, and national estimates of the population at increased risk of severe COVID-19 due to underlying health conditions in 2020: a modelling study
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Nightingale, Emily S, O'Reilly, Kathleen, Jombart, Thibaut, Edmunds, W John, Rosello, Alicia, Sun, Fiona Yueqian, Atkins, Katherine E, Bosse, Nikos I, Clifford, Samuel, Russell, Timothy W, Deol, Arminder K, Liu, Yang, Procter, Simon R, Leclerc, Quentin J, Medley, Graham, Knight, Gwen, Munday, James D, Kucharski, Adam J, Pearson, Carl A B, Klepac, Petra, Prem, Kiesha, Houben, Rein M G J, Endo, Akira, Flasche, Stefan, Davies, Nicholas G, Diamond, Charlie, van Zandvoort, Kevin, Funk, Sebastian, Auzenbergs, Megan, Rees, Eleanor M, Tully, Damien C, Emery, Jon C, Quilty, Billy J, Abbott, Sam, Villabona-Arenas, Ch Julian, Hué, Stéphane, Hellewell, Joel, Gimma, Amy, Jarvis, Christopher I, Clark, Andrew, Jit, Mark, Warren-Gash, Charlotte, Guthrie, Bruce, Wang, Harry H X, Mercer, Stewart W, Sanderson, Colin, McKee, Martin, Troeger, Christopher, Ong, Kanyin L, Checchi, Francesco, Perel, Pablo, Joseph, Sarah, Gibbs, Hamish P, Banerjee, Amitava, and Eggo, Rosalind M
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- 2020
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10. Effects of non-pharmaceutical interventions on COVID-19 cases, deaths, and demand for hospital services in the UK: a modelling study
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Jombart, Thibaut, O'Reilly, Kathleen, Endo, Akira, Hellewell, Joel, Nightingale, Emily S, Quilty, Billy J, Jarvis, Christopher I, Russell, Timothy W, Klepac, Petra, Bosse, Nikos I, Funk, Sebastian, Abbott, Sam, Medley, Graham F, Gibbs, Hamish, Pearson, Carl A B, Flasche, Stefan, Jit, Mark, Clifford, Samuel, Prem, Kiesha, Diamond, Charlie, Emery, Jon, Deol, Arminder K, Procter, Simon R, van Zandvoort, Kevin, Sun, Yueqian Fiona, Munday, James D, Rosello, Alicia, Auzenbergs, Megan, Knight, Gwen, Houben, Rein M G J, Liu, Yang, Davies, Nicholas G, Kucharski, Adam J, Eggo, Rosalind M, Gimma, Amy, and Edmunds, W John
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- 2020
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11. The effect of control strategies to reduce social mixing on outcomes of the COVID-19 epidemic in Wuhan, China: a modelling study
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Flasche, Stefan, Clifford, Samuel, Pearson, Carl A B, Munday, James D, Abbott, Sam, Gibbs, Hamish, Rosello, Alicia, Quilty, Billy J, Jombart, Thibaut, Sun, Fiona, Diamond, Charlie, Gimma, Amy, van Zandvoort, Kevin, Funk, Sebastian, Jarvis, Christopher I, Edmunds, W John, Bosse, Nikos I, Hellewell, Joel, Prem, Kiesha, Liu, Yang, Russell, Timothy W, Kucharski, Adam J, Eggo, Rosalind M, Davies, Nicholas, Jit, Mark, and Klepac, Petra
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- 2020
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12. Early dynamics of transmission and control of COVID-19: a mathematical modelling study
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Sun, Fiona, Jit, Mark, Munday, James D, Davies, Nicholas, Gimma, Amy, van Zandvoort, Kevin, Gibbs, Hamish, Hellewell, Joel, Jarvis, Christopher I, Clifford, Sam, Quilty, Billy J, Bosse, Nikos I, Abbott, Sam, Klepac, Petra, Flasche, Stefan, Kucharski, Adam J, Russell, Timothy W, Diamond, Charlie, Liu, Yang, Edmunds, John, Funk, Sebastian, and Eggo, Rosalind M
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- 2020
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13. Feasibility of controlling COVID-19 outbreaks by isolation of cases and contacts
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Sun, Fiona, Flasche, Stefan, Quilty, Billy J, Davies, Nicholas, Liu, Yang, Clifford, Samuel, Klepac, Petra, Jit, Mark, Diamond, Charlie, Gibbs, Hamish, van Zandvoort, Kevin, Hellewell, Joel, Abbott, Sam, Gimma, Amy, Bosse, Nikos I, Jarvis, Christopher I, Russell, Timothy W, Munday, James D, Kucharski, Adam J, Edmunds, W John, Funk, Sebastian, and Eggo, Rosalind M
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- 2020
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14. Age-dependent effects in the transmission and control of COVID-19 epidemics
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Davies, Nicholas G., Klepac, Petra, Liu, Yang, Prem, Kiesha, Jit, Mark, Pearson, Carl A. B., and Quilty, Billy J.
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Epidemics -- Demographic aspects -- Risk factors -- Asia -- Canada -- Italy ,Age factors in disease -- Analysis ,Disease transmission -- Demographic aspects -- Risk factors ,Biological sciences ,Health - Abstract
The COVID-19 pandemic has shown a markedly low proportion of cases among children.sup.1-4. Age disparities in observed cases could be explained by children having lower susceptibility to infection, lower propensity to show clinical symptoms or both. We evaluate these possibilities by fitting an age-structured mathematical model to epidemic data from China, Italy, Japan, Singapore, Canada and South Korea. We estimate that susceptibility to infection in individuals under 20 years of age is approximately half that of adults aged over 20 years, and that clinical symptoms manifest in 21% (95% credible interval: 12-31%) of infections in 10- to 19-year-olds, rising to 69% (57-82%) of infections in people aged over 70 years. Accordingly, we find that interventions aimed at children might have a relatively small impact on reducing SARS-CoV-2 transmission, particularly if the transmissibility of subclinical infections is low. Our age-specific clinical fraction and susceptibility estimates have implications for the expected global burden of COVID-19, as a result of demographic differences across settings. In countries with younger population structures--such as many low-income countries--the expected per capita incidence of clinical cases would be lower than in countries with older population structures, although it is likely that comorbidities in low-income countries will also influence disease severity. Without effective control measures, regions with relatively older populations could see disproportionally more cases of COVID-19, particularly in the later stages of an unmitigated epidemic. A new epidemiological study shows reduced susceptibility to SARS-CoV-2 and decreased risk of developing severe symptoms in people aged younger than 20 years, suggesting that children have limited contribution to spread of COVID-19., Author(s): Nicholas G. Davies [sup.1] , Petra Klepac [sup.1] , Yang Liu [sup.1] , Kiesha Prem [sup.1] , Mark Jit [sup.1] , Carl A. B. Pearson [sup.1] , Billy J. [...]
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- 2020
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15. Importance of investing time and money in integrating large language model-based agents into outbreak analytics pipelines
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Epi Infectieziekten Team 1, Infection & Immunity, van Hoek, Albert Jan, Funk, Sebastian, Flasche, Stefan, Quilty, Billy J., van Kleef, Esther, Camacho, Anton, Kucharski, Adam J., Epi Infectieziekten Team 1, Infection & Immunity, van Hoek, Albert Jan, Funk, Sebastian, Flasche, Stefan, Quilty, Billy J., van Kleef, Esther, Camacho, Anton, and Kucharski, Adam J.
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- 2024
16. Combined analyses of within-host SARS-CoV-2 viral kinetics and information on past exposures to the virus in a human cohort identifies intrinsic differences of Omicron and Delta variants
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Russell, Timothy W., Townsley, Hermaleigh, Abbott, Sam, Hellewell, Joel, Carr, Edward J., Chapman, Lloyd A. C., Pung, Rachael, Quilty, Billy J., Hodgson, David, Fowler, Ashley S., Adams, Lorin, Bailey, Chris, Mears, Harriet V., Harvey, Ruth, Clayton, Bobbi, O’Reilly, Nicola, Ngai, Yenting, Nicod, Jerome, Gamblin, Steve, Williams, Bryan, Gandhi, Sonia, Swanton, Charles, Beale, Rupert, Bauer, David L. V., Wall, Emma C., Kucharski, Adam J., Russell, Timothy W., Townsley, Hermaleigh, Abbott, Sam, Hellewell, Joel, Carr, Edward J., Chapman, Lloyd A. C., Pung, Rachael, Quilty, Billy J., Hodgson, David, Fowler, Ashley S., Adams, Lorin, Bailey, Chris, Mears, Harriet V., Harvey, Ruth, Clayton, Bobbi, O’Reilly, Nicola, Ngai, Yenting, Nicod, Jerome, Gamblin, Steve, Williams, Bryan, Gandhi, Sonia, Swanton, Charles, Beale, Rupert, Bauer, David L. V., Wall, Emma C., and Kucharski, Adam J.
- Abstract
The emergence of successive Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) during 2020 to 2022, each exhibiting increased epidemic growth relative to earlier circulating variants, has created a need to understand the drivers of such growth. However, both pathogen biology and changing host characteristics—such as varying levels of immunity—can combine to influence replication and transmission of SARS-CoV-2 within and between hosts. Disentangling the role of variant and host in individual-level viral shedding of VOCs is essential to inform Coronavirus Disease 2019 (COVID-19) planning and response and interpret past epidemic trends. Using data from a prospective observational cohort study of healthy adult volunteers undergoing weekly occupational health PCR screening, we developed a Bayesian hierarchical model to reconstruct individual-level viral kinetics and estimate how different factors shaped viral dynamics, measured by PCR cycle threshold (Ct) values over time. Jointly accounting for both interindividual variation in Ct values and complex host characteristics—such as vaccination status, exposure history, and age—we found that age and number of prior exposures had a strong influence on peak viral replication. Older individuals and those who had at least 5 prior antigen exposures to vaccination and/or infection typically had much lower levels of shedding. Moreover, we found evidence of a correlation between the speed of early shedding and duration of incubation period when comparing different VOCs and age groups. Our findings illustrate the value of linking information on participant characteristics, symptom profile and infecting variant with prospective PCR sampling, and the importance of accounting for increasingly complex population exposure landscapes when analysing the viral kinetics of VOCs. Trial Registration: The Legacy study is a prospective observational cohort study of healthy adult volunteers undergoing weekly oc
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- 2024
17. Combined analyses of within-host SARS-CoV-2 viral kinetics and information on past exposures to the virus in a human cohort identifies intrinsic differences of Omicron and Delta variants
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Russell, Timothy W., primary, Townsley, Hermaleigh, additional, Abbott, Sam, additional, Hellewell, Joel, additional, Carr, Edward J., additional, Chapman, Lloyd A. C., additional, Pung, Rachael, additional, Quilty, Billy J., additional, Hodgson, David, additional, Fowler, Ashley S., additional, Adams, Lorin, additional, Bailey, Chris, additional, Mears, Harriet V., additional, Harvey, Ruth, additional, Clayton, Bobbi, additional, O’Reilly, Nicola, additional, Ngai, Yenting, additional, Nicod, Jerome, additional, Gamblin, Steve, additional, Williams, Bryan, additional, Gandhi, Sonia, additional, Swanton, Charles, additional, Beale, Rupert, additional, Bauer, David L. V., additional, Wall, Emma C., additional, and Kucharski, Adam J., additional
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- 2024
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18. Importance of investing time and money in integrating large language model-based agents into outbreak analytics pipelines
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van Hoek, Albert Jan, Funk, Sebastian, Flasche, Stefan, Quilty, Billy J, van Kleef, Esther, Camacho, Anton, and Kucharski, Adam J
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- 2024
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19. Within-host SARS-CoV-2 viral kinetics informed by complex life course exposures reveals different intrinsic properties of Omicron and Delta variants
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Russell, Timothy W, primary, Townsley, Hermaleigh, additional, Abbott, Sam, additional, Hellewell, Joel, additional, Carr, Edward J, additional, Chapman, Lloyd, additional, Pung, Rachael, additional, Quilty, Billy J, additional, Hodgson, David, additional, Fowler, Ashley, additional, Adams, Lorin, additional, Bailey, Christopher, additional, Mears, Harriet V, additional, Harvey, Ruth, additional, Clayton, Bobbi, additional, O'Reilly, Nicola, additional, Ngai, Yenting, additional, Nicod, Jerome, additional, Gamblin, Steve, additional, Williams, Bryan, additional, Gandhi, Sonia, additional, Swanton, Charles, additional, Beale, Rupert, additional, Bauer, David LV, additional, Wall, Emma C, additional, and Kucharski, Adam, additional
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- 2023
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20. Public perceptions and interactions with UK COVID-19 Test, Trace and Isolate policies, and implications for pandemic infectious disease modelling
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Marshall, Guy C., primary, Skeva, Rigina, additional, Jay, Caroline, additional, Silva, Miguel E. P., additional, Fyles, Martyn, additional, House, Thomas, additional, Davis, Emma L., additional, Pi, Li, additional, Medley, Graham F., additional, Quilty, Billy J., additional, Dyson, Louise, additional, Yardley, Lucy, additional, and Fearon, Elizabeth, additional
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- 2022
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21. Effect of pneumococcal conjugate vaccine on prevalence of otitis media with effusion among children in Vietnam
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Toizumi, Michiko, primary, Satoh, Chisei, additional, Quilty, Billy J., additional, Nguyen, Hien Anh Thi, additional, Madaniyazi, Lina, additional, Le, Lien Thuy, additional, Ng, Chris Fook Sheng, additional, Hara, Minoru, additional, Iwasaki, Chihiro, additional, Takegata, Mizuki, additional, Kitamura, Noriko, additional, Nation, Monica Larissa, additional, Satzke, Catherine, additional, Kumai, Yoshihiko, additional, Do, Hung Thai, additional, Bui, Minh Xuan, additional, Mulholland, Kim, additional, Flasche, Stefan, additional, Dang, Duc Anh, additional, Kaneko, Kenichi, additional, and Yoshida, Lay-Myint, additional
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- 2022
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22. The impact of COVID-19 vaccination in prisons in England and Wales: a metapopulation model
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McCarthy, Ciara V., O’Mara, Oscar, van Leeuwen, Edwin, Sherratt, Katharine, Abbas, Kaja, Wong, Kerry LM, Atkins, Katherine E., Lowe, Rachel, Meakin, Sophie R, Davies, Nicholas G., Russell, Timothy W, O’Reilly, Kathleen, Hué, Stéphane, Finch, Emilie, Villabona-Arenas, C Julian, Edmunds, W John, Jafari, Yalda, Tully, Damien C, Bosse, Nikos I, Pearson, Carl A B, Hodgson, David, Kucharski, Adam J, Medley, Graham, Liu, Yang, Procter, Simon R, Waites, William, Abbott, Sam, Barnard, Rosanna C, Sun, Fiona Yueqian, Gibbs, Hamish P, Eggo, Rosalind M, Chapman, Lloyd A C, Flasche, Stefan, Endo, Akira, Mee, Paul, Munday, James D, Koltai, Mihaly, Gimma, Amy, Jarvis, Christopher I, Quaife, Matthew, Clifford, Samuel, Funk, Sebastian, Prem, Kiesha, Knight, Gwenan M, Pung, Rachael, Brady, Oliver, Quilty, Billy J, Jit, Mark, and Sandmann, Frank
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Public health ,COVID-19 Vaccines ,Wales ,Mathematical model ,England ,SARS-CoV-2 ,Prisons ,Vaccination ,Public Health, Environmental and Occupational Health ,Humans ,COVID-19 ,Middle Aged - Abstract
Background High incidence of cases and deaths due to coronavirus disease 2019 (COVID-19) have been reported in prisons worldwide. This study aimed to evaluate the impact of different COVID-19 vaccination strategies in epidemiologically semi-enclosed settings such as prisons, where staff interact regularly with those incarcerated and the wider community. Methods We used a metapopulation transmission-dynamic model of a local prison in England and Wales. Two-dose vaccination strategies included no vaccination, vaccination of all individuals who are incarcerated and/or staff, and an age-based approach. Outcomes were quantified in terms of COVID-19-related symptomatic cases, losses in quality-adjusted life-years (QALYs), and deaths. Results Compared to no vaccination, vaccinating all people living and working in prison reduced cases, QALY loss and deaths over a one-year period by 41%, 32% and 36% respectively. However, if vaccine introduction was delayed until the start of an outbreak, the impact was negligible. Vaccinating individuals who are incarcerated and staff over 50 years old averted one death for every 104 vaccination courses administered. All-staff-only strategies reduced cases by up to 5%. Increasing coverage from 30 to 90% among those who are incarcerated reduced cases by around 30 percentage points. Conclusions The impact of vaccination in prison settings was highly dependent on early and rapid vaccine delivery. If administered to both those living and working in prison prior to an outbreak occurring, vaccines could substantially reduce COVID-19-related morbidity and mortality in prison settings.
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- 2022
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23. Waning rate of immunity and duration of protective immunity against diphtheria toxoid as a function of age and number of doses: Systematic review and quantitative data analysis
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Kitamura, Noriko, primary, Bahkali, Khawater, additional, Chem, Elvis D, additional, Quilty, Billy J, additional, Edwards, Tansy, additional, Toizumi, Michiko, additional, and Yoshida, Lay-Myint, additional
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- 2022
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24. Natural and hybrid immunity following four COVID-19 waves in a South African cohort
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Zar, Heather J, primary, MacGinty, Rae, additional, Workman, Lesley, additional, Botha, Maresa, additional, Johnson, Marina, additional, Hunt, Adam, additional, Bird, Tiffany, additional, Nicol, Mark P, additional, Flasche, Stefan, additional, Quilty, Billy J, additional, and Goldblatt, David, additional
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- 2022
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25. Measuring the effects of COVID-19-related disruption on dengue transmission in southeast Asia and Latin America: a statistical modelling study
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Chen, Yuyang, primary, Li, Naizhe, additional, Lourenço, José, additional, Wang, Lin, additional, Cazelles, Bernard, additional, Dong, Lu, additional, Li, Bingying, additional, Liu, Yang, additional, Jit, Mark, additional, Bosse, Nikos I, additional, Abbott, Sam, additional, Velayudhan, Raman, additional, Wilder-Smith, Annelies, additional, Tian, Huaiyu, additional, Brady, Oliver J, additional, Procter, Simon R, additional, Wong, Kerry LM, additional, Hellewell, Joel, additional, Davies, Nicholas G, additional, Jarvis, Christopher I, additional, McCarthy, Ciara V, additional, Medley, Graham, additional, Meakin, Sophie R, additional, Rosello, Alicia, additional, Finch, Emilie, additional, Lowe, Rachel, additional, Pearson, Carl A B, additional, Clifford, Samuel, additional, Quilty, Billy J, additional, Flasche, Stefan, additional, Gibbs, Hamish P, additional, Chapman, Lloyd A C, additional, Atkins, Katherine E., additional, Hodgson, David, additional, Barnard, Rosanna C, additional, Russell, Timothy W, additional, Klepac, Petra, additional, Jafari, Yalda, additional, Eggo, Rosalind M, additional, Mee, Paul, additional, Quaife, Matthew, additional, Endo, Akira, additional, Funk, Sebastian, additional, Hué, Stéphane, additional, Kucharski, Adam J, additional, Edmunds, W John, additional, O'Reilly, Kathleen, additional, Pung, Rachael, additional, Villabona-Arenas, C Julian, additional, Gimma, Amy, additional, Abbas, Kaja, additional, Prem, Kiesha, additional, Knight, Gwenan M, additional, Sun, Fiona Yueqian, additional, Waites, William, additional, Munday, James D, additional, Koltai, Mihaly, additional, Sandmann, Frank G, additional, and Tully, Damien C, additional
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- 2022
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26. The effect of travel restrictions on the geographical spread of COVID-19 between large cities in China: a modelling study
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Quilty, Billy J., Diamond, Charlie, Liu, Yang, Gibbs, Hamish, Russell, Timothy W., Jarvis, Christopher I., Prem, Kiesha, Pearson, Carl A. B., Clifford, Samuel, Flasche, Stefan, Emery, Jon C., Auzenbergs, Megan, Davies, Nicholas, Nightingale, Emily S., van Zandvoort, Kevin, Jombart, Thibaut, Deol, Arminder K., Edmunds, W. John, Hellewell, Joel, Funk, Sebastian, Abbott, Sam, Sun, Fiona, Endo, Akira, Rosello, Alicia, Gimma, Amy, Procter, Simon R., Bosse, Nikos I., O’Reilly, Kathleen, Medley, Graham, Munday, James D., Houben, Rein M. G. J., Kucharski, Adam J., Knight, Gwenan M., Klepac, Petra, Eggo, Rosalind M., and Jit, Mark
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Mainland China ,Wuhan ,China ,Coronavirus disease 2019 (COVID-19) ,Pneumonia, Viral ,lcsh:Medicine ,Travel restrictions ,Modelling ,law.invention ,03 medical and health sciences ,Betacoronavirus ,0302 clinical medicine ,Beijing ,law ,Prevalence ,Medicine ,Humans ,030212 general & internal medicine ,Cities ,Socioeconomics ,Pandemics ,Mobility ,Cordon sanitaire ,Travel ,Delay ,High prevalence ,business.industry ,SARS-CoV-2 ,Incidence (epidemiology) ,Health Policy ,Incidence ,lcsh:R ,Outbreaks ,Outbreak ,COVID-19 ,General Medicine ,Models, Theoretical ,3. Good health ,Transmission (mechanics) ,business ,Coronavirus Infections ,030217 neurology & neurosurgery ,Research Article - Abstract
Background To contain the spread of COVID-19, a cordon sanitaire was put in place in Wuhan prior to the Lunar New Year, on 23 January 2020. We assess the efficacy of the cordon sanitaire to delay the introduction and onset of local transmission of COVID-19 in other major cities in mainland China. Methods We estimated the number of infected travellers from Wuhan to other major cities in mainland China from November 2019 to February 2020 using previously estimated COVID-19 prevalence in Wuhan and publicly available mobility data. We focused on Beijing, Chongqing, Hangzhou, and Shenzhen as four representative major cities to identify the potential independent contribution of the cordon sanitaire and holiday travel. To do this, we simulated outbreaks generated by infected arrivals in these destination cities using stochastic branching processes. We also modelled the effect of the cordon sanitaire in combination with reduced transmissibility scenarios to simulate the effect of local non-pharmaceutical interventions. Results We find that in the four cities, given the potentially high prevalence of COVID-19 in Wuhan between December 2019 and early January 2020, local transmission may have been seeded as early as 1–8 January 2020. By the time the cordon sanitaire was imposed, infections were likely in the thousands. The cordon sanitaire alone did not substantially affect the epidemic progression in these cities, although it may have had some effect in smaller cities. Reduced transmissibility resulted in a notable decrease in the incidence of infection in the four studied cities. Conclusions Our results indicate that sustained transmission was likely occurring several weeks prior to the implementation of the cordon sanitaire in four major cities of mainland China and that the observed decrease in incidence was likely attributable to other non-pharmaceutical, transmission-reducing interventions.
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- 2020
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27. Travel measures in the SARS-CoV-2 variant era need clear objectives
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Kucharski, Adam J, Jit, Mark, Logan, James G, Cotten, Matthew, Clifford, Samuel, Quilty, Billy J, Russell, Timothy W, Peeling, Rosanna W, Antonio, Martin, and Heymann, David L
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- 2022
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28. Using trained dogs and organic semi-conducting sensors to identify asymptomatic and mild SARS-CoV-2 infections: an observational study
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Guest, Claire, Dewhirst, Sarah Y, Lindsay, Steve W, Allen, David J, Aziz, Sophie, Baerenbold, Oliver, Bradley, John, Chabildas, Unnati, Chen-Hussey, Vanessa, Clifford, Samuel, Cottis, Luke, Dennehy, Jessica, Foley, Erin, Gezan, Salvador A, Gibson, Tim, Greaves, Courtenay K, Kleinschmidt, Immo, Lambert, Sébastien, Last, Anna, Morant, Steve, Parker, Josephine E A, Pickett, John, Quilty, Billy J, Rooney, Ann, Shah, Manil, Somerville, Mark, Squires, Chelci, Walker, Martin, Logan, James G, Jones, Robert, Assis, Ana, Borthwick, Ewan, Caton, Laura, Edwards, Rachel, Heal, Janette, Hill, David, Jahan, Nazifa, Johnson, Cecelia, Kaye, Angela, Kirkpatrick, Emily, Kisha, Sarah, Ledeatte Williams, Zaena, Moar, Robert, Owonibi, Tolulope, Purcell, Benjamin, Rixson, Christopher, Spencer, Freya, Stefanidis, Anastasios, Stewart, Sophie, Tytheridge, Scott, Wakley, Sian, Wildman, Shanice, Aziz, Catherine, Care, Helen, Curtis, Emily, Dowse, Claire, Makepeace, Alan, Oultram, Sally-Anne, Smith, Jayde, Shenton, Fiona, Hutchins, Harry, Mart, Robert, Cartwright, Jo-anne, Forsey, Miranda, Goodsell, Kerry, Kittridge, Lauren, Nicholson, Anne, Ramos, Angelo, Ritches, Joanne, Setty, Niranjan, Vertue, Mark, Bergstrom, Malin, Chaudhary, Zain, De Wilton, Angus, Gaskell, Kate, Houlihan, Catherine, Jones, Imogen, Margaritis, Marios, Miralhes, Patricia, Owens, Leah, Rampling, Tommy, Rickman, Hannah, Boffito, Marta, Fernandez, Candida, Cotterell, Bryony, Guerdette, Anne-Marie, Tsaknis, George, Turns, Margaret, Walsh, Joanne, Frankland, Lisa, West, Raha, Holland, Maureen, Keenan, Natalie, Wassall, Helen, Young, Megan, Rangeley, Jade, Saalmink, Gwendolyn, Adlakha, Sanjay, Buckley, Philip, Allsop, Lynne, Smith, Susan, Sowter, Donna, Campbell, Alison, Jones, Julie, Laird, Steve, O’Toole, Sarah, Ryan, Courteney, Evans, Jessica, Rand, James, Schumacher, Natasha, Hazelton, Tracey, Dodgson, Andrew, Glasgow, Susannah, Kadiu, Denise, Lopuszansky, Orianne, Oommen, Anu, Prabhu, Joshi, Pursell, Molly, Turner, Jane, Walton, Hollie, Andrews, Robert, Cruickshank, Irena, Thompson, Catherine, Wainwright, Tania, Roebuck, Alun, Lawrence, Tara, Netherton, Kimberley, Hewitt, Claire, Shephardson, Sarah, Crasto, Winston Andrew, Lake, Judith, Musanhu, Rosemary, Walker, Rebecca, Burns, Karen, Higham, Andrew, Le Bas, Julie, Mackenzie, Nicola, Thatcher, Hilary, Beadle, Shannen, Buckley, Sarah, Castle, Gail, Fletcher, Aimee, Holbrook, Sara, Kane, Patricia, Lindley, Kate, Lowry, Tracey, Lupton, Stephanie, Oddy, Sharon, Slater, Lynda, Sylvester, Martin, Agwuh, Kenneth, Maxwell, Veronica, Ryder, Stephen, Topham, Kirsty, Egbuniwe, Obi, Matthews, Rebecca, Arenas-Pinto, Alejandro, Prymas, Paulina, Severn, Abigail, Shaw, Amber, Begum, Safia, Lenton, Daniel, Scriven, James, Leeman, Lucy, Rudge, Karen, Storr, Emma, Alvarez, Ana, Forster, Kate, Hind, Daniel, Cook, Natalie, Peeling, Rosanna, Carey, Peter, Wilson, Anne, and Davis, Jane
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Volatile Organic Compounds ,Dogs ,SARS-CoV-2 ,fungi ,Animals ,COVID-19 ,Humans ,Mass Screening ,General Medicine ,Asymptomatic Infections ,Sensitivity and Specificity - Abstract
Background A rapid, accurate, non-invasive diagnostic screen is needed to identify people with SARS-CoV-2 infection. We investigated whether organic semi-conducting (OSC) sensors and trained dogs could distinguish between people infected with asymptomatic or mild symptoms, and uninfected individuals, and the impact of screening at ports-of-entry. Methods Odour samples were collected from adults, and SARS-CoV-2 infection status confirmed using RT-PCR. OSC sensors captured the volatile organic compound (VOC) profile of odour samples. Trained dogs were tested in a double-blind trial to determine their ability to detect differences in VOCs between infected and uninfected individuals, with sensitivity and specificity as the primary outcome. Mathematical modelling was used to investigate the impact of bio-detection dogs for screening. Results About, 3921 adults were enrolled in the study and odour samples collected from 1097 SARS-CoV-2 infected and 2031 uninfected individuals. OSC sensors were able to distinguish between SARS-CoV-2 infected individuals and uninfected, with sensitivity from 98% (95% CI 95–100) to 100% and specificity from 99% (95% CI 97–100) to 100%. Six dogs were able to distinguish between samples with sensitivity ranging from 82% (95% CI 76–87) to 94% (95% CI 89–98) and specificity ranging from 76% (95% CI 70–82) to 92% (95% CI 88–96). Mathematical modelling suggests that dog screening plus a confirmatory PCR test could detect up to 89% of SARS-CoV-2 infections, averting up to 2.2 times as much transmission compared to isolation of symptomatic individuals only. Conclusions People infected with SARS-CoV-2, with asymptomatic or mild symptoms, have a distinct odour that can be identified by sensors and trained dogs with a high degree of accuracy. Odour-based diagnostics using sensors and/or dogs may prove a rapid and effective tool for screening large numbers of people. Trial Registration NCT04509713 (clinicaltrials.gov).
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- 2022
29. SARS-CoV-2 antibodies protect against reinfection for at least 6 months in a multicentre seroepidemiological workplace cohort
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Finch, Emilie, Lowe, Rachel, Fischinger, Stephanie, de St Aubin, Michael, Siddiqui, Sameed M., Dayal, Diana, Loesche, Michael A., Rhee, Justin, Beger, Samuel, Hu, Yiyuan, Gluck, Matthew J., Mormann, Benjamin, Hasdianda, Mohammad A., Musk, Elon R., Alter, Galit, Menon, Anil S., Nilles, Eric J., Kucharski, Adam J., Lei, Jiayao, Funk, Sebastian, Sun, Fiona Yueqian, Gimma, Amy, Nightingale, Emily S., Medley, Graham, Abbott, Sam, Krauer, Fabienne, Davies, Nicholas G., Jit, Mark, Endo, Akira, Brady, Oliver, Foss, Anna M., Chan, Yung-Wai Desmond, Jombart, Thibaut, van Zandvoort, Kevin, Eggo, Rosalind M., Liu, Yang, Knight, Gwenan M., Pearson, Carl A.B., Abbas, Kaja, Atkins, Katherine E., Clifford, Samuel, Koltai, Mihaly, Jafari, Yalda, Tully, Damien C., Jarvis, Christopher I., O'Reilly, Kathleen, Bosse, Nikos I., Prem, Kiesha, Quilty, Billy J., Procter, Simon R., Barnard, Rosanna C., Waites, William, McCarthy, Ciara, Munday, James D., Hodgson, David, Edmunds, W. John, Rosello, Alicia, Villabona-Arenas, C. Julian, Gibbs, Hamish P., Flasche, Stefan, Russell, Timothy W., Meakin, Sophie R., Hellewell, Joel, Waterlow, Naomi R., Quaife, Matthew, Sandmann, Frank G., and Barcelona Supercomputing Center
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Adult ,Time Factors ,Adolescent ,Long-term epidemic dynamics ,Medizin ,Antibodies, Viral ,Polymerase Chain Reaction ,COVID-19 (Malaltia) ,General Biochemistry, Genetics and Molecular Biology ,COVID-19 Serological Testing ,Young Adult ,COVID-19 (Disease) ,Seroepidemiologic Studies ,Humans ,Prospective Studies ,Workplace ,Aged ,General Immunology and Microbiology ,PCR (Biochemistry) ,SARS-CoV-2 ,General Neuroscience ,Immunity ,COVID-19 ,Odds ratio ,Middle Aged ,United States ,Serology ,Logistic Models ,COVID-19 Nucleic Acid Testing ,Reinfection ,Ciències de la salut::Medicina::Medicina comunitària i salut pública [Àrees temàtiques de la UPC] ,General Agricultural and Biological Sciences - Abstract
dentifying the potential for SARS-CoV-2 reinfection is crucial for understanding possible long-term epidemic dynamics. We analysed longitudinal PCR and serological testing data from a prospective cohort of 4,411 United States employees in 4 states between April 2020 and February 2021. We conducted a multivariable logistic regression investigating the association between baseline serological status and subsequent PCR test result in order to calculate an odds ratio for reinfection. We estimated an odds ratio for reinfection ranging from 0.14 (95% CI: 0.019 to 0.63) to 0.28 (95% CI: 0.05 to 1.1), implying that the presence of SARS-CoV-2 antibodies at baseline is associated with around 72% to 86% reduced odds of a subsequent PCR positive test based on our point estimates. This suggests that primary infection with SARS-CoV-2 provides protection against reinfection in the majority of individuals, at least over a 6-month time period. We also highlight 2 major sources of bias and uncertainty to be considered when estimating the relative risk of reinfection, confounders and the choice of baseline time point, and show how to account for both in reinfection analysis. The authors received funding from the following sources: EF was funded by the Medical Research Council (MR/N013638/1); AJK was supported by Wellcome Trust (206250/Z/17/Z) and National Institute for Health Research (NIHR200908); RL was funded by a Royal Society Dorothy Hodgkin Fellowship (https://royalsociety.org). EN was supported by the US Centers for Disease Control and Prevention (U01 U01GH002238). AM was supported by the Translational Research Institute for Space Health through NASA Cooperative Agreement (https://www.nasa.gov/hrp/tri; NNX16AO69A). GA was supported by the Massachusetts Consortium on Pathogen Readiness (https://masscpr.hms.harvard.edu/; MassCPR), the National Institutes of Health (3R37AI080289-11S1, R01AI146785, U19AI42790-01, U19AI135995-02, 1U01CA260476-01) and the Musk Foundation (http://www.muskfoundation.org/). The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. "Article signat per 18 autors/es: Emilie Finch ,Rachel Lowe,Stephanie Fischinger,Michael de St Aubin,Sameed M. Siddiqui,Diana Dayal,Michael A. Loesche,Justin Rhee,Samuel Beger,Yiyuan Hu,Matthew J. Gluck,Benjamin Mormann,Mohammad A. Hasdianda,Elon R. Musk,Galit Alter,Anil S. Menon ,Eric J. Nilles ,Adam J. Kucharski ,on behalf of the CMMID COVID-19 working group and the SpaceX COVID-19 Cohort Collaborative"
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- 2022
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30. Comparing human and model-based forecasts of COVID-19 in Germany and Poland
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Centre for the Mathematical Modelling of Infectious Diseases COVID-19 Working Group, Bosse, Nikos I., Abbott, Sam, Bracher, Johannes, Hain, Habakuk, Quilty, Billy J., Jit, Mark, van Leeuwen, Edwin, Cori, Anne, Funk, Sebastian, and McCaw, James M.
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Economics ,ddc:330 - Abstract
Forecasts based on epidemiological modelling have played an important role in shaping public policy throughout the COVID-19 pandemic. This modelling combines knowledge about infectious disease dynamics with the subjective opinion of the researcher who develops and refines the model and often also adjusts model outputs. Developing a forecast model is difficult, resource- and time-consuming. It is therefore worth asking what modelling is able to add beyond the subjective opinion of the researcher alone. To investigate this, we analysed different real-time forecasts of cases of and deaths from COVID-19 in Germany and Poland over a 1-4 week horizon submitted to the German and Polish Forecast Hub. We compared crowd forecasts elicited from researchers and volunteers, against a) forecasts from two semi-mechanistic models based on common epidemiological assumptions and b) the ensemble of all other models submitted to the Forecast Hub. We found crowd forecasts, despite being overconfident, to outperform all other methods across all forecast horizons when forecasting cases (weighted interval score relative to the Hub ensemble 2 weeks ahead: 0.89). Forecasts based on computational models performed comparably better when predicting deaths (rel. WIS 1.26), suggesting that epidemiological modelling and human judgement can complement each other in important ways.
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- 2022
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31. Comparing human and model-based forecasts of COVID-19 in Germany and Poland
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Bosse, Nikos I., Abbott, Sam, Bracher, Johannes, Hain, Habakuk, Quilty, Billy J., Jit, Mark, van Leeuwen, Edwin, Cori, Anne, Funk, Sebastian, and Centre for the Mathematical Modelling of Infectious Diseases COVID-19 Working Group
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Cellular and Molecular Neuroscience ,Computational Theory and Mathematics ,Ecology ,Modeling and Simulation ,Genetics ,COVID-19 ,Humans ,Poland ,Molecular Biology ,Communicable Diseases ,Pandemics ,Ecology, Evolution, Behavior and Systematics ,Forecasting - Abstract
1AbstractForecasts based on epidemiological modelling have played an important role in shaping public policy throughout the COVID-19 pandemic. This modelling combines knowledge about infectious disease dynamics with the subjective opinion of the researcher who develops and refines the model and often also adjusts model outputs. Developing a forecast model is difficult, resource- and time-consuming. It is therefore worth asking what modelling is able to add beyond the subjective opinion of the researcher alone. To investigate this, we analysed different real-time forecasts of cases of and deaths from COVID-19 in Germany and Poland over a 1-4 week horizon submitted to the German and Polish Forecast Hub. We compared crowd forecasts elicited from researchers and volunteers, against a) forecasts from two semi-mechanistic models based on common epidemiological assumptions and b) the ensemble of all other models submitted to the Forecast Hub. We found crowd forecasts, despite being overconfident, to outperform all other methods across all forecast horizons when forecasting cases (weighted interval score relative to the Hub ensemble 2 weeks ahead: 0.89). Forecasts based on computational models performed comparably better when predicting deaths (rel. WIS 1.26), suggesting that epidemiological modelling and human judgement can complement each other in important ways.
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- 2021
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32. Test to release from isolation after testing positive for SARS-CoV-2
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Quilty, Billy J., primary, Pulliam, Juliet R. C., additional, and Pearson, Carl A. B., additional
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- 2022
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33. Strategies to reduce the risk of SARS-CoV-2 importation from international travellers: modelling estimations for the United Kingdom, July 2020
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Clifford, Samuel, Quilty, Billy J, Russell, Timothy W, Liu, Yang, Chan, Yung-Wai D, Pearson, Carl AB, Eggo, Rosalind M, Endo, Akira, CMMID COVID-19 Working Group, Flasche, Stefan, Edmunds, W John, and Centre for Mathematical Modelling of Infectious Diseases (CMMID)
- Abstract
BackgroundTo mitigate SARS-CoV-2 transmission risks from international air travellers, many countries implemented a combination of up to 14 days of self-quarantine upon arrival plus PCR testing in the early stages of the COVID-19 pandemic in 2020.AimTo assess the effectiveness of quarantine and testing of international travellers to reduce risk of onward SARS-CoV-2 transmission into a destination country in the pre-COVID-19 vaccination era.MethodsWe used a simulation model of air travellers arriving in the United Kingdom from the European Union or the United States, incorporating timing of infection stages while varying quarantine duration and timing and number of PCR tests.ResultsQuarantine upon arrival with a PCR test on day 7 plus a 1-day delay for results can reduce the number of infectious arriving travellers released into the community by a median 94% (95% uncertainty interval (UI): 89-98) compared with a no quarantine/no test scenario. This reduction is similar to that achieved by a 14-day quarantine period (median > 99%; 95% UI: 98-100). Even shorter quarantine periods can prevent a substantial amount of transmission; all strategies in which travellers spend at least 5 days (mean incubation period) in quarantine and have at least one negative test before release are highly effective (median reduction 89%; 95% UI: 83-95)).ConclusionThe effect of different screening strategies impacts asymptomatic and symptomatic individuals differently. The choice of an optimal quarantine and testing strategy for unvaccinated air travellers may vary based on the number of possible imported infections relative to domestic incidence.
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- 2021
34. Contact tracing is an imperfect tool for controlling COVID-19 transmission and relies on population adherence
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Davis, Emma L., Lucas, Tim C. D., Borlase, Anna, Pollington, Timothy M., Abbott, Sam, Ayabina, Diepreye, Crellen, Thomas, Hellewell, Joel, Pi, Li, Medley, Graham F., Hollingsworth, T. Déirdre, Klepac, Petra, Lowe, Rachel, Endo, Akira, Davies, Nicholas, Gore-Langton, Georgia R., Russell, Timothy W., Bosse, Nikos I., Quaife, Matthew, Kucharski, Adam J., Nightingale, Emily S., Pearson, Carl A. B., Gibbs, Hamish, O’Reilly, Kathleen, Jombart, Thibaut, Rees, Eleanor M., Deol, Arminder K., Hué, Stéphane, Auzenbergs, Megan, Houben, Rein M. G. J., Funk, Sebastian, Li, Yang, Sun, Fiona, Prem, Kiesha, Quilty, Billy J., Villabona-Arenas, Julian, Barnard, Rosanna C., Hodgson, David, Foss, Anna, Jarvis, Christopher I., Meakin, Sophie R., Eggo, Rosalind M., Abbas, Kaja, Zandvoort, Kevin Van, Emery, Jon C., Tully, Damien C., Sandmann, Frank G., Edmunds, W. John, Gimma, Amy, Knight, Gwen, Munday, James D., Diamond, Charlie, Jit, Mark, Leclerc, Quentin, Rosello, Alicia, Chan, Yung-Wai Desmond, Simons, David, Clifford, Sam, Flasche, Stefan, Procter, Simon R., Atkins, Katherine E., Davis, Emma L. [0000-0001-6261-775X], Lucas, Tim C. D. [0000-0003-4694-8107], Borlase, Anna [0000-0002-3189-7047], Pollington, Timothy M. [0000-0002-9688-5960], Crellen, Thomas [0000-0003-2934-1063], Medley, Graham F. [0000-0002-0030-7278], Hollingsworth, T. Déirdre [0000-0001-5962-4238], Klepac, Petra [0000-0003-4132-3933], and Apollo - University of Cambridge Repository
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631/114/2397 ,692/699/255/2514 ,article ,692/700/478/174 ,631/326/596/4130 - Abstract
Emerging evidence suggests that contact tracing has had limited success in the UK in reducing the R number across the COVID-19 pandemic. We investigate potential pitfalls and areas for improvement by extending an existing branching process contact tracing model, adding diagnostic testing and refining parameter estimates. Our results demonstrate that reporting and adherence are the most important predictors of programme impact but tracing coverage and speed plus diagnostic sensitivity also play an important role. We conclude that well-implemented contact tracing could bring small but potentially important benefits to controlling and preventing outbreaks, providing up to a 15% reduction in R. We reaffirm that contact tracing is not currently appropriate as the sole control measure.
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- 2021
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35. SARS-CoV-2 antigen testing: weighing the false positives against the costs of failing to control transmission
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Fearon, Elizabeth, Buchan, Iain E, Das, Rajenki, Davis, Emma L, Fyles, Martyn, Hall, Ian, Hollingsworth, T Deirdre, House, Thomas, Jay, Caroline, Medley, Graham F, Pellis, Lorenzo, Quilty, Billy J, Silva, Miguel E P, Stage, Helena B, and Wingfield, Tom
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- 2021
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36. Simulating respiratory disease transmission within and between classrooms to assess pandemic management strategies at schools
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Endo (遠藤彰), Akira, Uchida (内田満夫), Mitsuo, Liu (刘扬), Yang, Atkins, Katherine E., Kucharski, Adam J., Funk, Sebastian, Abbas, Kaja, van Zandvoort, Kevin, Bosse, Nikos I, Waterlow, Naomi R, Tully, Damien C, Meakin, Sophie R, Quaife, Matthew, Russell, Timothy W, Jit, Mark, Foss, Anna M, Rosello, Alicia, Quilty, Billy J, Prem, Kiesha, Knight, Gwenan M, Abbott, Sam, Klepac, Petra, Brady, Oliver, Pearson, Carl A B, Medley, Graham, Clifford, Samuel, Jarvis, Christopher I, Munday, James D, Sandmann, Frank G, Sun, Fiona Yueqian, Jombart, Thibaut, Hellewell, Joel, Gibbs, Hamish P, Barnard, Rosanna C, Eggo, Rosalind M, Gimma, Amy, Williams, Jack, Davies, Nicholas G., Nightingale, Emily S, Procter, Simon R, Edmunds, W John, Showering, Alicia, Lowe, Rachel, Sherratt, Katharine, Villabona-Arenas, C Julian, Simons, David, Chan, Yung-Wai Desmond, and Flasche, Stefan
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Multidisciplinary ,Schools ,school ,class size ,COVID-19 ,Disease Outbreaks ,Influenza, Human/epidemiology ,Influenza, Human ,Humans ,Computer Simulation ,social network ,Pandemics/prevention & control ,Child ,influenza ,Pandemics ,Respiratory Tract Infections ,mathematical model ,COVID-19/epidemiology ,Disease Outbreaks/prevention & control - Abstract
The global spread of coronavirus disease 2019 (COVID-19) has emphasized the need for evidence-based strategies for the safe operation of schools during pandemics that balance infection risk with the society's responsibility of allowing children to attend school. Due to limited empirical data, existing analyses assessing school-based interventions in pandemic situations often impose strong assumptions, for example, on the relationship between class size and transmission risk, which could bias the estimated effect of interventions, such as split classes and staggered attendance. To fill this gap in school outbreak studies, we parameterized an individual-based model that accounts for heterogeneous contact rates within and between classes and grades to a multischool outbreak data of influenza. We then simulated school outbreaks of respiratory infectious diseases of ongoing threat (i.e., COVID-19) and potential threat (i.e., pandemic influenza) under a variety of interventions (changing class structures, symptom screening, regular testing, cohorting, and responsive class closures). Our results suggest that interventions changing class structures (e.g., reduced class sizes) may not be effective in reducing the risk of major school outbreaks upon introduction of a case and that other precautionary measures (e.g., screening and isolation) need to be employed. Class-level closures in response to detection of a case were also suggested to be effective in reducing the size of an outbreak., Proceedings of the National Academy of Sciences, 119(37), art. no. e2203019119; 2022
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- 2022
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37. The potential for vaccination-induced herd immunity against the SARS-CoV-2 B.1.1.7 variant
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Hodgson, David, Flasche, Stefan, Jit, Mark, Kucharski, Adam J, Abbott, Sam, Edmunds, W John, Davies, Nicholas G., Eggo, Rosalind M, Medley, Graham, Lei, Jiayao, Liu, Yang, Tully, Damien C, McCarthy, Ciara V, Mee, Paul, Endo, Akira, Hellewell, Joel, Funk, Sebastian, Jombart, Thibaut, Jafari, Yalda, Brady, Oliver, Prem, Kiesha, Krauer, Fabienne, Koltai, Mihaly, Waterlow, Naomi R, Russell, Timothy W, Meakin, Sophie R, O'Reilly, Kathleen, Bosse, Nikos I, Waites, William, Nightingale, Emily S, Lowe, Rachel, Chan, Yung-Wai Desmond, Atkins, Katherine E., Quilty, Billy J, Sandmann, Frank G, van Zandvoort, Kevin, Villabona-Arenas, C Julian, Gibbs, Hamish P, Munday, James D, Foss, Anna M, Gimma, Amy, Pearson, Carl A B, Barnard, Rosanna C, Quaife, Matthew, Sun, Fiona Yueqian, Rosello, Alicia, Pung, Rachael, Jarvis, Christopher I, Finch, Emilie, Abbas, Kaja, Clifford, Samuel, Knight, Gwenan M, and Procter, Simon R
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0301 basic medicine ,Immunity, Herd ,2019-20 coronavirus outbreak ,Age structure ,Epidemiology ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Biology ,Virus ,Herd immunity ,03 medical and health sciences ,Herd Immunity ,0302 clinical medicine ,Immunity ,Virology ,Seroprevalence ,Humans ,030212 general & internal medicine ,Child ,seroprevalence ,SARS-CoV-2 ,Vaccination ,Public Health, Environmental and Occupational Health ,COVID-19 ,biochemical phenomena, metabolism, and nutrition ,030104 developmental biology ,Immunology ,Rapid Communication - Abstract
We assess the feasibility of reaching the herd immunity threshold against SARS-CoV-2 through vaccination, considering vaccine effectiveness (VE), transmissibility of the virus and the level of pre-existing immunity in populations, as well as their age structure. If highly transmissible variants of concern become dominant in areas with low levels of naturally-acquired immunity and/or in populations with large proportions of < 15 year-olds, control of infection without non-pharmaceutical interventions may only be possible with a VE ≥ 80%, and coverage extended to children. Initial reports of vaccine effectiveness against severe acute respiratory syndrome coronavirus 2 (SARSCoV-2), the virus responsible for coronavirus disease (COVID-19), have suggested a substantial reduction of the risk of infection [1]. Nevertheless, with the emergence of more transmissible variants such as B.1.1.7 [2], how large-scale immunisation programmes against SARS-CoV-2 will perform is currently unclear. This study assesses the potential of COVID-19 vaccination to generate herd immunity and takes into account vaccine effectiveness, naturally-acquired immunity and achievable vaccination coverage (depending on the population age structure), as well as two transmissibility scenarios ((i) with pre-B.1.1.7, and (ii) with exclusively B.1.1.7 variants).
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- 2021
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38. Quarantine and testing strategies in contact tracing for SARS-CoV-2: a modelling study
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Quilty, Billy J, Clifford, Samuel, Hellewell, Joel, Russell, Timothy W, Kucharski, Adam J, Flasche, Stefan, Edmunds, W John, and Centre for the Mathematical Modelling of Infectious Diseases COV
- Abstract
BACKGROUND: In most countries, contacts of confirmed COVID-19 cases are asked to quarantine for 14 days after exposure to limit asymptomatic onward transmission. While theoretically effective, this policy places a substantial social and economic burden on both the individual and wider society, which might result in low adherence and reduced policy effectiveness. We aimed to assess the merit of testing contacts to avert onward transmission and to replace or reduce the length of quarantine for uninfected contacts. METHODS: We used an agent-based model to simulate the viral load dynamics of exposed contacts, and their potential for onward transmission in different quarantine and testing strategies. We compared the performance of quarantines of differing durations, testing with either PCR or lateral flow antigen (LFA) tests at the end of quarantine, and daily LFA testing without quarantine, against the current 14-day quarantine strategy. We also investigated the effect of contact tracing delays and adherence to both quarantine and self-isolation on the effectiveness of each strategy. FINDINGS: Assuming moderate levels of adherence to quarantine and self-isolation, self-isolation on symptom onset alone can prevent 37% (95% uncertainty interval [UI] 12-56) of onward transmission potential from secondary cases. 14 days of post-exposure quarantine reduces transmission by 59% (95% UI 28-79). Quarantine with release after a negative PCR test 7 days after exposure might avert a similar proportion (54%, 95% UI 31-81; risk ratio [RR] 0·94, 95% UI 0·62-1·24) to that of the 14-day quarantine period, as would quarantine with a negative LFA test 7 days after exposure (50%, 95% UI 28-77; RR 0·88, 0·66-1·11) or daily testing without quarantine for 5 days after tracing (50%, 95% UI 23-81; RR 0·88, 0·60-1·43) if all tests are returned negative. A stronger effect might be possible if individuals isolate more strictly after a positive test and if contacts can be notified faster. INTERPRETATION: Testing might allow for a substantial reduction in the length of, or replacement of, quarantine with a small excess in transmission risk. Decreasing test and trace delays and increasing adherence will further increase the effectiveness of these strategies. Further research is required to empirically evaluate the potential costs (increased transmission risk, false reassurance) and benefits (reduction in the burden of quarantine, increased adherence) of such strategies before adoption as policy. FUNDING: National Institute for Health Research, UK Research and Innovation, Wellcome Trust, EU Horizon 2021, and the Bill & Melinda Gates Foundation.
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- 2021
39. Implications of the school-household network structure on SARS-CoV-2 transmission under school reopening strategies in England
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Munday, James D., Sherratt, Katharine, Meakin, Sophie, Endo, Akira, Pearson, Carl A. B., Hellewell, Joel, Abbott, Sam, Bosse, Nikos I., Eggo, Rosalind M., Simons, David, O’Reilly, Kathleen, Russell, Timothy W., Lowe, Rachel, Leclerc, Quentin J., Emery, Jon C., Klepac, Petra, Nightingale, Emily S., Quaife, Matthew, van Zandvoort, Kevin, Knight, Gwenan M., Jombart, Thibaut, Villabona-Arenas, C. Julian, Rees, Eleanor M., Diamond, Charlie, Auzenbergs, Megan, Medley, Graham, Foss, Anna M., Gore-Langton, Georgia R., Deol, Arminder K., Jit, Mark, Gibbs, Hamish P., Procter, Simon R., Rosello, Alicia, Jarvis, Christopher I., Liu, Yang, Houben, Rein M. G. J., Hué, Stéphane, Clifford, Samuel, Quilty, Billy J., Gimma, Amy, Tully, Damien C., Sun, Fiona Yueqian, Prem, Kiesha, Atkins, Katherine E., Wallinga, Jacco, Edmunds, W. John, van Hoek, Albert Jan, and Funk, Sebastian
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0301 basic medicine ,Economic growth ,2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,Adolescent ,genetic structures ,Epidemiology ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Science ,education ,General Physics and Astronomy ,Network structure ,Risk Assessment ,General Biochemistry, Genetics and Molecular Biology ,Article ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,law ,Risk Factors ,Pandemic ,Disease Transmission, Infectious ,Humans ,Computational models ,030212 general & internal medicine ,Disease Transmission, Infectious/prevention & control ,England/epidemiology ,Child ,Pandemics ,COVID-19/epidemiology ,Family Characteristics ,Multidisciplinary ,Schools ,SARS-CoV-2 ,SARS-CoV-2/isolation & purification ,COVID-19 ,General Chemistry ,Schools/organization & administration ,030104 developmental biology ,Transmission (mechanics) ,England ,Viral infection ,Child, Preschool ,Business ,Risk assessment ,Disease transmission - Abstract
In early 2020 many countries closed schools to mitigate the spread of SARS-CoV-2. Since then, governments have sought to relax the closures, engendering a need to understand associated risks. Using address records, we construct a network of schools in England connected through pupils who share households. We evaluate the risk of transmission between schools under different reopening scenarios. We show that whilst reopening select year-groups causes low risk of large-scale transmission, reopening secondary schools could result in outbreaks affecting up to 2.5 million households if unmitigated, highlighting the importance of careful monitoring and within-school infection control to avoid further school closures or other restrictions., Many countries have closed schools as part of their COVID-19 response. Here, the authors model SARS-CoV-2 transmission on a network of schools and households in England, and find that risk of transmission between schools is lower if primary schools are open than if secondary schools are open.
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- 2021
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40. The potential health and economic value of SARS-CoV-2 vaccination alongside physical distancing in the UK: a transmission model-based future scenario analysis and economic evaluation
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Sandmann, Frank G, primary, Davies, Nicholas G, additional, Vassall, Anna, additional, Edmunds, W John, additional, Jit, Mark, additional, Sun, Fiona Yueqian, additional, Villabona-Arenas, C Julian, additional, Nightingale, Emily S, additional, Showering, Alicia, additional, Knight, Gwenan M, additional, Sherratt, Katharine, additional, Liu, Yang, additional, Abbas, Kaja, additional, Funk, Sebastian, additional, Endo, Akira, additional, Hellewell, Joel, additional, Rosello, Alicia, additional, Lowe, Rachel, additional, Quaife, Matthew, additional, Gimma, Amy, additional, Brady, Oliver, additional, Williams, Jack, additional, Procter, Simon R, additional, Eggo, Rosalind M, additional, Chan, Yung-Wai Desmond, additional, Munday, James D, additional, Barnard, Rosanna C, additional, Gore-Langton, Georgia R, additional, Bosse, Nikos I, additional, Waterlow, Naomi R, additional, Diamond, Charlie, additional, Russell, Timothy W, additional, Medley, Graham, additional, Flasche, Stefan, additional, Atkins, Katherine E, additional, Prem, Kiesha, additional, Simons, David, additional, Auzenbergs, Megan, additional, Tully, Damien C, additional, Jarvis, Christopher I, additional, van Zandvoort, Kevin, additional, Abbott, Sam, additional, Pearson, Carl A B, additional, Jombart, Thibaut, additional, Meakin, Sophie R, additional, Foss, Anna M, additional, Kucharski, Adam J, additional, Quilty, Billy J, additional, Gibbs, Hamish P, additional, Clifford, Samuel, additional, and Klepac, Petra, additional
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- 2021
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41. Comparing human and model-based forecasts of COVID-19 in Germany and Poland.
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Bosse, Nikos I., Abbott, Sam, Bracher, Johannes, Hain, Habakuk, Quilty, Billy J., Jit, Mark, van Leeuwen, Edwin, Cori, Anne, and Funk, Sebastian
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FORECASTING ,COVID-19 ,COVID-19 pandemic ,DEATH forecasting ,EPIDEMIOLOGICAL models ,ECONOMIC indicators - Abstract
Forecasts based on epidemiological modelling have played an important role in shaping public policy throughout the COVID-19 pandemic. This modelling combines knowledge about infectious disease dynamics with the subjective opinion of the researcher who develops and refines the model and often also adjusts model outputs. Developing a forecast model is difficult, resource- and time-consuming. It is therefore worth asking what modelling is able to add beyond the subjective opinion of the researcher alone. To investigate this, we analysed different real-time forecasts of cases of and deaths from COVID-19 in Germany and Poland over a 1-4 week horizon submitted to the German and Polish Forecast Hub. We compared crowd forecasts elicited from researchers and volunteers, against a) forecasts from two semi-mechanistic models based on common epidemiological assumptions and b) the ensemble of all other models submitted to the Forecast Hub. We found crowd forecasts, despite being overconfident, to outperform all other methods across all forecast horizons when forecasting cases (weighted interval score relative to the Hub ensemble 2 weeks ahead: 0.89). Forecasts based on computational models performed comparably better when predicting deaths (rel. WIS 1.26), suggesting that epidemiological modelling and human judgement can complement each other in important ways. Author Summary: Mathematical models of COVID-19 have played a key role in informing governments across the world. While mathematical models are informed by our knowledge of infectious disease dynamics, they are ultimately developed and iteratively adjusted by the researchers and shaped by their subjective opinions. To investigate what modelling is able to add beyond the subjective opinion of the researcher alone, we compared human forecasts with model-based predictions of COVID-19 cases and deaths submitted to the so-called German/Polish Forecast Hub (which collates a variety of models from a range of teams). | We found that our human forecasts consistently outperformed an aggregate of all available model-based forecasts when predicting cases, but not when predicting deaths. Our findings suggest that human insight may be most valuable when forecasting highly uncertain quantities, which depend on many factors that are hard to model using equations, while mathematical models may be most useful in settings like predicting deaths, where leading indicators with a clear connection to the target variable are available. This potentially has very relevant policy implications, as agencies informing policy-makers could benefit from routinely eliciting human forecasts in addition to model-based predictions to inform policies. [ABSTRACT FROM AUTHOR]
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- 2022
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42. Changing travel patterns in China during the early stages of the COVID-19 pandemic
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Gibbs, Hamish, Liu, Yang, Pearson, Carl A. B., Jarvis, Christopher I., Grundy, Chris, Quilty, Billy J., Diamond, Charlie, Simons, David, Gimma, Amy, Leclerc, Quentin J., Auzenbergs, Megan, Lowe, Rachel, O’Reilly, Kathleen, Quaife, Matthew, Hellewell, Joel, Knight, Gwenan M., Jombart, Thibaut, Klepac, Petra, Procter, Simon R., Deol, Arminder K., Rees, Eleanor M., Flasche, Stefan, Kucharski, Adam J., Abbott, Sam, Sun, Fiona Yueqian, Endo, Akira, Medley, Graham, Munday, James D., Meakin, Sophie R., Bosse, Nikos I., Edmunds, W. John, Davies, Nicholas G., Prem, Kiesha, Hué, Stéphane, Villabona-Arenas, C. Julian, Nightingale, Emily S., Houben, Rein M. G. J., Foss, Anna M., Tully, Damien C., Emery, Jon C., van Zandvoort, Kevin, Atkins, Katherine E., Rosello, Alicia, Funk, Sebastian, Jit, Mark, Clifford, Samuel, Russell, Timothy W., and Eggo, Rosalind M.
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0301 basic medicine ,Time Factors ,Epidemiology ,General Physics and Astronomy ,Transportation ,0302 clinical medicine ,Health care ,Pandemic ,Computational models ,030212 general & internal medicine ,lcsh:Science ,Holidays ,Travel ,0303 health sciences ,Multidisciplinary ,Geography ,Public Health ,Coronavirus Infections ,Mainland China ,China ,2019-20 coronavirus outbreak ,medicine.medical_specialty ,Coronavirus disease 2019 (COVID-19) ,Science ,Pneumonia, Viral ,Policy and public health in microbiology ,Article ,General Biochemistry, Genetics and Molecular Biology ,Betacoronavirus ,03 medical and health sciences ,Development economics ,medicine ,Humans ,Pandemics ,030304 developmental biology ,Population Density ,SARS-CoV-2 ,business.industry ,Public health ,COVID-19 ,General Chemistry ,030104 developmental biology ,13. Climate action ,lcsh:Q ,Demographic economics ,business ,Delivery of Health Care ,human activities - Abstract
Understanding changes in human mobility in the early stages of the COVID-19 pandemic is crucial for assessing the impacts of travel restrictions designed to reduce disease spread. Here, relying on data from mainland China, we investigate the spatio-temporal characteristics of human mobility between 1st January and 1st March 2020, and discuss their public health implications. An outbound travel surge from Wuhan before travel restrictions were implemented was also observed across China due to the Lunar New Year, indicating that holiday travel may have played a larger role in mobility changes compared to impending travel restrictions. Holiday travel also shifted healthcare pressure related to COVID-19 towards locations with lower healthcare capacity. Network analyses showed no sign of major changes in the transportation network after Lunar New Year. Changes observed were temporary and did not lead to structural reorganisation of the transportation network during the study period., COVID-19-related travel restrictions were imposed in China around the same time as major annual holiday migrations, with unknown combined impacts on mobility patterns. Here, the authors show that restructuring of the travel network in response to restrictions was temporary, whilst holiday-related travel increased pressure on healthcare services with lower capacity.
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- 2020
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43. Using a real-world network to model localized COVID-19 control strategies
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Firth, Josh A., Hellewell, Joel, Klepac, Petra, Kissler, Stephen, Jit, Mark, Atkins, Katherine E., Clifford, Samuel, Villabona-Arenas, C. Julian, Meakin, Sophie R., Diamond, Charlie, Bosse, Nikos I., Munday, James D., Prem, Kiesha, Foss, Anna M., Nightingale, Emily S., Zandvoort, Kevin van, Davies, Nicholas G., Gibbs, Hamish P., Medley, Graham, Gimma, Amy, Flasche, Stefan, Simons, David, Auzenbergs, Megan, Russell, Timothy W., Quilty, Billy J., Rees, Eleanor M., Leclerc, Quentin J., Edmunds, W. John, Funk, Sebastian, Houben, Rein M. G. J., Knight, Gwenan M., Abbott, Sam, Sun, Fiona Yueqian, Lowe, Rachel, Tully, Damien C., Procter, Simon R., Jarvis, Christopher I., Endo, Akira, O’Reilly, Kathleen, Emery, Jon C., Jombart, Thibaut, Rosello, Alicia, Deol, Arminder K., Quaife, Matthew, Hué, Stéphane, Liu, Yang, Eggo, Rosalind M., Pearson, Carl A. B., Kucharski, Adam J., and Spurgin, Lewis G.
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0301 basic medicine ,Social network ,Coronavirus disease 2019 (COVID-19) ,business.industry ,Computer science ,Distancing ,Control (management) ,General Medicine ,Tracing ,Computer security ,computer.software_genre ,General Biochemistry, Genetics and Molecular Biology ,law.invention ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,Transmission (mechanics) ,law ,030220 oncology & carcinogenesis ,Isolation (database systems) ,business ,computer ,Contact tracing - Abstract
Case isolation and contact tracing can contribute to the control of COVID-19 outbreaks1,2. However, it remains unclear how real-world social networks could influence the effectiveness and efficiency of such approaches. To address this issue, we simulated control strategies for SARS-CoV-2 transmission in a real-world social network generated from high-resolution GPS data that were gathered in the course of a citizen-science experiment3,4. We found that tracing the contacts of contacts reduced the size of simulated outbreaks more than tracing of only contacts, but this strategy also resulted in almost half of the local population being quarantined at a single point in time. Testing and releasing non-infectious individuals from quarantine led to increases in outbreak size, suggesting that contact tracing and quarantine might be most effective as a 'local lockdown' strategy when contact rates are high. Finally, we estimated that combining physical distancing with contact tracing could enable epidemic control while reducing the number of quarantined individuals. Our findings suggest that targeted tracing and quarantine strategies would be most efficient when combined with other control measures such as physical distancing.
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- 2020
44. The importance of supplementary immunisation activities to prevent measles outbreaks during the COVID-19 pandemic in Kenya
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Mburu, C. N., Ojal, J., Chebet, R., Akech, D., Karia, B., Tuju, J., Sigilai, A., Abbas, K., Jit, M., Funk, S., Smits, G., van Gageldonk, P. G. M., van der Klis, F. R. M., Tabu, C., Nokes, D. J., Munday, James D., Pearson, Carl A. B., Procter, Simon R., Brady, Oliver, Simons, David, Lowe, Rachel, Edmunds, W. John, Sherratt, Katharine, Barnard, Rosanna C., Rosello, Alicia, Kucharski, Adam J., Sun, Fiona Yueqian, Bosse, Nikos I., Klepac, Petra, Liu, Yang, Prem, Kiesha, Knight, Gwenan M., Endo, Akira, Abbott, Sam, Nightingale, Emily S., Jombart, Thibaut, Emery, Jon C., Gore-Langton, Georgia R., Hellewell, Joel, Rudge, James W., Gibbs, Hamish P., O’Reilly, Kathleen, van Zandvoort, Kevin, Chan, Yung-Wai Desmond, Tully, Damien C., Foss, Anna M., Jarvis, Christopher I., Atkins, Katherine E., Clifford, Samuel, Quaife, Matthew, Quilty, Billy J., Houben, Rein M. G. J., Eggo, Rosalind M., Medley, Graham, Meakin, Sophie R., Russell, Timothy W., Davies, Nicholas G., Diamond, Charlie, Deol, Arminder K., Villabona-Arenas, C. Julian, Hué, Stéphane, Auzenbergs, Megan, Leclerc, Quentin J., Gimma, Amy, Scott, JAG, Flasche, S., Adetifa, IMO, LSHTM CMMID COVID-19 Working Group, and Group, LSHTM CMMID COVID-19 Working
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Male ,COVID-19 ,Supplementary immunisation activities ,Vaccination coverage ,Outbreak ,Measles ,medicine.medical_specialty ,Adolescent ,Coronavirus disease 2019 (COVID-19) ,RJ ,Measles Vaccine ,030231 tropical medicine ,lcsh:Medicine ,Measles outbreak ,Disease Outbreaks ,Herd immunity ,03 medical and health sciences ,0302 clinical medicine ,Environmental health ,Epidemiology ,Pandemic ,medicine ,Humans ,030212 general & internal medicine ,Child ,Immunization Programs ,SARS-CoV-2 ,business.industry ,lcsh:R ,Infant, Newborn ,Infant ,General Medicine ,medicine.disease ,Kenya ,Increased risk ,Child, Preschool ,Female ,business ,RA ,Research Article - Abstract
Background The COVID-19 pandemic has disrupted routine measles immunisation and supplementary immunisation activities (SIAs) in most countries including Kenya. We assessed the risk of measles outbreaks during the pandemic in Kenya as a case study for the African Region. Methods Combining measles serological data, local contact patterns, and vaccination coverage into a cohort model, we predicted the age-adjusted population immunity in Kenya and estimated the probability of outbreaks when contact-reducing COVID-19 interventions are lifted. We considered various scenarios for reduced measles vaccination coverage from April 2020. Results In February 2020, when a scheduled SIA was postponed, population immunity was close to the herd immunity threshold and the probability of a large outbreak was 34% (8–54). As the COVID-19 contact restrictions are nearly fully eased, from December 2020, the probability of a large measles outbreak will increase to 38% (19–54), 46% (30–59), and 54% (43–64) assuming a 15%, 50%, and 100% reduction in measles vaccination coverage. By December 2021, this risk increases further to 43% (25–56), 54% (43–63), and 67% (59–72) for the same coverage scenarios respectively. However, the increased risk of a measles outbreak following the lifting of all restrictions can be overcome by conducting a SIA with ≥ 95% coverage in under-fives. Conclusion While contact restrictions sufficient for SAR-CoV-2 control temporarily reduce measles transmissibility and the risk of an outbreak from a measles immunity gap, this risk rises rapidly once these restrictions are lifted. Implementing delayed SIAs will be critical for prevention of measles outbreaks given the roll-back of contact restrictions in Kenya.
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- 2020
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45. Feasibility of controlling COVID-19 outbreaks by isolation of cases and contacts
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Hellewell, Joel, Abbott, Sam, Gimma, Amy, Bosse, Nikos I., Jarvis, Christopher I., Russell, Timothy W., Munday, James D., Kucharski, Adam J., Edmunds, W. John, Sun, Fiona, Flasche, Stefan, Quilty, Billy J., Davies, Nicholas, Liu, Yang, Clifford, Samuel, Klepac, Petra, Jit, Mark, Diamond, Charlie, Gibbs, Hamish, van Zandvoort, Kevin, Funk, Sebastian, Eggo, Rosalind M., and Centre for the Mathematical Modelling of Infectious Diseases COVID-19 Working Group
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medicine.medical_specialty ,Coronavirus disease 2019 (COVID-19) ,Isolation (health care) ,business.industry ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,lcsh:Public aspects of medicine ,030231 tropical medicine ,Outbreak ,COVID-19 ,lcsh:RA1-1270 ,General Medicine ,Article ,3. Good health ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,Transmission (mechanics) ,law ,Emergency medicine ,Medicine ,030212 general & internal medicine ,business ,Basic reproduction number ,Contact tracing ,Subclinical infection - Abstract
Summary Background Isolation of cases and contact tracing is used to control outbreaks of infectious diseases, and has been used for coronavirus disease 2019 (COVID-19). Whether this strategy will achieve control depends on characteristics of both the pathogen and the response. Here we use a mathematical model to assess if isolation and contact tracing are able to control onwards transmission from imported cases of COVID-19. Methods We developed a stochastic transmission model, parameterised to the COVID-19 outbreak. We used the model to quantify the potential effectiveness of contact tracing and isolation of cases at controlling a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-like pathogen. We considered scenarios that varied in the number of initial cases, the basic reproduction number (R0), the delay from symptom onset to isolation, the probability that contacts were traced, the proportion of transmission that occurred before symptom onset, and the proportion of subclinical infections. We assumed isolation prevented all further transmission in the model. Outbreaks were deemed controlled if transmission ended within 12 weeks or before 5000 cases in total. We measured the success of controlling outbreaks using isolation and contact tracing, and quantified the weekly maximum number of cases traced to measure feasibility of public health effort. Findings Simulated outbreaks starting with five initial cases, an R0 of 1·5, and 0% transmission before symptom onset could be controlled even with low contact tracing probability; however, the probability of controlling an outbreak decreased with the number of initial cases, when R0 was 2·5 or 3·5 and with more transmission before symptom onset. Across different initial numbers of cases, the majority of scenarios with an R0 of 1·5 were controllable with less than 50% of contacts successfully traced. To control the majority of outbreaks, for R0 of 2·5 more than 70% of contacts had to be traced, and for an R0 of 3·5 more than 90% of contacts had to be traced. The delay between symptom onset and isolation had the largest role in determining whether an outbreak was controllable when R0 was 1·5. For R0 values of 2·5 or 3·5, if there were 40 initial cases, contact tracing and isolation were only potentially feasible when less than 1% of transmission occurred before symptom onset. Interpretation In most scenarios, highly effective contact tracing and case isolation is enough to control a new outbreak of COVID-19 within 3 months. The probability of control decreases with long delays from symptom onset to isolation, fewer cases ascertained by contact tracing, and increasing transmission before symptoms. This model can be modified to reflect updated transmission characteristics and more specific definitions of outbreak control to assess the potential success of local response efforts. Funding Wellcome Trust, Global Challenges Research Fund, and Health Data Research UK.
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- 2020
46. Interventions targeting air travellers early in the pandemic may delay local outbreaks of SARS-CoV-2
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Clifford, Samuel J, Pearson, Carl A B, Klepac, Petra, Van Zandvoort, Kevin, Quilty, Billy J, Eggo, Rosalind M, and Flasche, Stefan
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human activities - Abstract
Background: We evaluated if interventions aimed at air travellers can delay establishment of a SARS-CoV-2 outbreak in a previously unaffected country. Methods: For countries with no sustained SARS-CoV-2 transmission and with no shared border with affected regions we simulated arriving infected air travellers. We assessed the effectiveness of syndromic screening at departure and/or arrival & traveller sensitisation to the COVID-2019-like symptoms with the aim to trigger rapid self-isolation and reporting on symptom onset to enable contact tracing. We assumed that syndromic screening would reduce the number of infected arrivals and that traveller sensitisation reduce the average number of secondary cases. We report the minimal expected delay achievable in 50% (75% & 97.5%) of simulations. In the simulations we account for uncertainty in the number of secondary cases in the absence of air traveller targeted interventions and the arrival times of infected cases and also present sensitivity analyses on arrival rates of infected travellers and the effectiveness of traveller sensitisation. Results: Under baseline assumptions exit and entry screening combined with traveller sensitisation can delay a local SARS-CoV-2 outbreak by at least 83 (75% of simulations: at least 36, 97.5% 8) days while there is no more than 1 infected traveller per week. The benefit of entry screening is small if exit screening is effective: the combination of only exit screening and traveller sensitisation can delay an outbreak by at least 76 (75%: 33, 97.5%: 7) days. With increasing rates of infected travellers, less effective sensitisation or without screening these delays shrink rapidly to a week or less. Conclusion: Syndromic screening and traveller sensitisation in combination could delay outbreaks in yet unaffected countries and support local containment efforts, but only if infected traveller numbers are very low.
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- 2020
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47. Effectiveness of airport screening at detecting travellers infected with novel coronavirus (2019-nCoV)
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Quilty, Billy J, Clifford, Sam, CMMID nCoV working group2, Flasche, Stefan, and Eggo, Rosalind M
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human activities - Abstract
We evaluated effectiveness of thermal passenger screening for 2019-nCoV infection at airport exit and entry to inform public health decision-making. In our baseline scenario, we estimated that 46% (95% confidence interval: 36 to 58) of infected travellers would not be detected, depending on incubation period, sensitivity of exit and entry screening, and proportion of asymptomatic cases. Airport screening is unlikely to detect a sufficient proportion of 2019-nCoV infected travellers to avoid entry of infected travellers.
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- 2020
48. The local burden of disease during the first wave of the COVID-19 epidemic in England: estimation using different data sources from changing surveillance practices.
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Nightingale, Emily S., Abbott, Sam, Russell, Timothy W., CMMID Covid-19 Working Group, Rees, Eleanor M., Eggo, Rosalind M., Quaife, Matthew, Sun, Fiona Yueqian, Pearson, Carl A. B., Prem, Kiesha, Munday, James D., Meakin, Sophie R., Medley, Graham, van Zandvoort, Kevin, Edmunds, W. John, Rosello, Alicia, Funk, Sebastian, O'Reilly, Kathleen, Quilty, Billy J., and Procter, Simon R.
- Abstract
Background: The COVID-19 epidemic has differentially impacted communities across England, with regional variation in rates of confirmed cases, hospitalisations and deaths. Measurement of this burden changed substantially over the first months, as surveillance was expanded to accommodate the escalating epidemic. Laboratory confirmation was initially restricted to clinical need ("pillar 1") before expanding to community-wide symptomatics ("pillar 2"). This study aimed to ascertain whether inconsistent measurement of case data resulting from varying testing coverage could be reconciled by drawing inference from COVID-19-related deaths. Methods: We fit a Bayesian spatio-temporal model to weekly COVID-19-related deaths per local authority (LTLA) throughout the first wave (1 January 2020–30 June 2020), adjusting for the local epidemic timing and the age, deprivation and ethnic composition of its population. We combined predictions from this model with case data under community-wide, symptomatic testing and infection prevalence estimates from the ONS infection survey, to infer the likely trajectory of infections implied by the deaths in each LTLA. Results: A model including temporally- and spatially-correlated random effects was found to best accommodate the observed variation in COVID-19-related deaths, after accounting for local population characteristics. Predicted case counts under community-wide symptomatic testing suggest a total of 275,000–420,000 cases over the first wave - a median of over 100,000 additional to the total confirmed in practice under varying testing coverage. This translates to a peak incidence of around 200,000 total infections per week across England. The extent to which estimated total infections are reflected in confirmed case counts was found to vary substantially across LTLAs, ranging from 7% in Leicester to 96% in Gloucester with a median of 23%. Conclusions: Limitations in testing capacity biased the observed trajectory of COVID-19 infections throughout the first wave. Basing inference on COVID-19-related mortality and higher-coverage testing later in the time period, we could explore the extent of this bias more explicitly. Evidence points towards substantial under-representation of initial growth and peak magnitude of infections nationally, to which different parts of the country contribute unequally. [ABSTRACT FROM AUTHOR]
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- 2022
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49. Effectiveness of isolation, testing, contact tracing, and physical distancing on reducing transmission of SARS-CoV-2 in different settings: a mathematical modelling study
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Kucharski, Adam J, primary, Klepac, Petra, additional, Conlan, Andrew J K, additional, Kissler, Stephen M, additional, Tang, Maria L, additional, Fry, Hannah, additional, Gog, Julia R, additional, Edmunds, W John, additional, Emery, Jon C, additional, Medley, Graham, additional, Munday, James D, additional, Russell, Timothy W, additional, Leclerc, Quentin J, additional, Diamond, Charlie, additional, Procter, Simon R, additional, Gimma, Amy, additional, Sun, Fiona Yueqian, additional, Gibbs, Hamish P, additional, Rosello, Alicia, additional, van Zandvoort, Kevin, additional, Hué, Stéphane, additional, Meakin, Sophie R, additional, Deol, Arminder K, additional, Knight, Gwen, additional, Jombart, Thibaut, additional, Foss, Anna M, additional, Bosse, Nikos I, additional, Atkins, Katherine E, additional, Quilty, Billy J, additional, Lowe, Rachel, additional, Prem, Kiesha, additional, Flasche, Stefan, additional, Pearson, Carl A B, additional, Houben, Rein M G J, additional, Nightingale, Emily S, additional, Endo, Akira, additional, Tully, Damien C, additional, Liu, Yang, additional, Villabona-Arenas, Julian, additional, O'Reilly, Kathleen, additional, Funk, Sebastian, additional, Eggo, Rosalind M, additional, Jit, Mark, additional, Rees, Eleanor M, additional, Hellewell, Joel, additional, Clifford, Samuel, additional, Jarvis, Christopher I, additional, Abbott, Sam, additional, Auzenbergs, Megan, additional, Davies, Nicholas G, additional, and Simons, David, additional
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- 2020
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50. Routine childhood immunisation during the COVID-19 pandemic in Africa: a benefit–risk analysis of health benefits versus excess risk of SARS-CoV-2 infection
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Abbas, Kaja, primary, Procter, Simon R, additional, van Zandvoort, Kevin, additional, Clark, Andrew, additional, Funk, Sebastian, additional, Mengistu, Tewodaj, additional, Hogan, Dan, additional, Dansereau, Emily, additional, Jit, Mark, additional, Flasche, Stefan, additional, Houben, Rein M G J, additional, Edmunds, W John, additional, Villabona-Arenas, Christian Julian, additional, Atkins, Katherine E, additional, Knight, Gwenan M, additional, Sun, Fiona Yueqian, additional, Auzenbergs, Megan, additional, Rosello, Alicia, additional, Klepac, Petra, additional, Hellewell, Joel, additional, Russell, Timothy W, additional, Tully, Damien C, additional, Emery, Jon C, additional, Gibbs, Hamish P, additional, Munday, James D, additional, Quilty, Billy J, additional, Diamond, Charlie, additional, Pearson, Carl A B, additional, Leclerc, Quentin J, additional, Nightingale, Emily S, additional, Liu, Yang, additional, Endo, Akira, additional, Deol, Arminder K, additional, Kucharski, Adam J, additional, Abbott, Sam, additional, Jarvis, Christopher I, additional, O'Reilly, Kathleen, additional, Jombart, Thibaut, additional, Gimma, Amy, additional, Bosse, Nikos I, additional, Prem, Kiesha, additional, Hué, Stéphane, additional, Davies, Nicholas G, additional, Eggo, Rosalind M, additional, Clifford, Samuel, additional, and Medley, Graham, additional
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- 2020
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