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How to detect and reduce potential sources of biases in studies of SARS-CoV-2 and COVID-19.
Accorsi, Emma K; Qiu, Xueting; Rumpler, Eva; Kennedy-Shaffer, Lee; Kahn, Rebecca; Joshi, Keya; Goldstein, Edward; Stensrud, Mats J; Niehus, Rene; Cevik, Muge; Lipsitch, Marc.
Affiliation
  • Accorsi EK; Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA. eaccorsi@g.harvard.edu.
  • Qiu X; Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
  • Rumpler E; Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
  • Kennedy-Shaffer L; Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
  • Kahn R; Department of Mathematics and Statistics, Vassar College, Poughkeepsie, NY, 12604, USA.
  • Joshi K; Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
  • Goldstein E; Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
  • Stensrud MJ; Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
  • Niehus R; Department of Mathematics, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
  • Cevik M; Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
  • Lipsitch M; Division of Infection and Global Health Research, School of Medicine, University of St Andrews, St Andrews, UK.
Eur J Epidemiol ; 36(2): 179-196, 2021 Feb.
Article in En | MEDLINE | ID: mdl-33634345
ABSTRACT
In response to the coronavirus disease (COVID-19) pandemic, public health scientists have produced a large and rapidly expanding body of literature that aims to answer critical questions, such as the proportion of the population in a geographic area that has been infected; the transmissibility of the virus and factors associated with high infectiousness or susceptibility to infection; which groups are the most at risk of infection, morbidity and mortality; and the degree to which antibodies confer protection to re-infection. Observational studies are subject to a number of different biases, including confounding, selection bias, and measurement error, that may threaten their validity or influence the interpretation of their results. To assist in the critical evaluation of a vast body of literature and contribute to future study design, we outline and propose solutions to biases that can occur across different categories of observational studies of COVID-19. We consider potential biases that could occur in five categories of studies (1) cross-sectional seroprevalence, (2) longitudinal seroprotection, (3) risk factor studies to inform interventions, (4) studies to estimate the secondary attack rate, and (5) studies that use secondary attack rates to make inferences about infectiousness and susceptibility.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Research Design / COVID-19 Type of study: Observational_studies / Risk_factors_studies Limits: Humans Language: En Journal: Eur J Epidemiol Journal subject: EPIDEMIOLOGIA Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Research Design / COVID-19 Type of study: Observational_studies / Risk_factors_studies Limits: Humans Language: En Journal: Eur J Epidemiol Journal subject: EPIDEMIOLOGIA Year: 2021 Type: Article Affiliation country: United States