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Towards a sensitive and accurate interpretation of molecular testing for SARS-CoV-2: a rapid review of 264 studies
- Kamelia R. Stanoeva1,2 , Annemiek A. van der Eijk3 , Adam Meijer1 , Laetitia M. Kortbeek1 , Marion P.G. Koopmans3 , Chantal B.E.M. Reusken1,3,4
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View Affiliations Hide AffiliationsAffiliations: 1 Center for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands 2 European Public Health Microbiology Training Programme (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden 3 Department of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands 4 Global Outbreak Alert and Response Network (GOARN), Geneva, SwitzerlandChantal Reuskenchantal.reusken rivm.nl
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Citation style for this article: Stanoeva Kamelia R., van der Eijk Annemiek A., Meijer Adam, Kortbeek Laetitia M., Koopmans Marion P.G., Reusken Chantal B.E.M.. Towards a sensitive and accurate interpretation of molecular testing for SARS-CoV-2: a rapid review of 264 studies. Euro Surveill. 2021;26(10):pii=2001134. https://doi.org/10.2807/1560-7917.ES.2021.26.10.2001134 Received: 06 Jun 2020; Accepted: 20 Oct 2020
Abstract
Sensitive molecular diagnostics and correct test interpretation are crucial for accurate COVID-19 diagnosis and thereby essential for good clinical practice. Furthermore, they are a key factor in outbreak control where active case finding in combination with isolation and contact tracing are crucial.
With the objective to inform the public health and laboratory responses to the pandemic, we reviewed current published knowledge on the kinetics of SARS-CoV-2 infection as assessed by RNA molecular detection in a wide range of clinical samples.
We performed an extensive search on studies published between 1 December 2019 and 15 May 2020, reporting on molecular detection and/or isolation of SARS-CoV-2 in any human laboratory specimen.
We compiled a dataset of 264 studies including 32,515 COVID-19 cases, and additionally aggregated data points (n = 2,777) from sampling of 217 adults with known infection timeline. We summarised data on SARS-CoV-2 detection in the respiratory and gastrointestinal tract, blood, oral fluid, tears, cerebrospinal fluid, peritoneal fluid, semen, vaginal fluid; where provided, we also summarised specific observations on SARS-CoV-2 detection in pregnancy, infancy, children, adolescents and immunocompromised individuals.
Optimal SARS-CoV-2 molecular testing relies on choosing the most appropriate sample type, collected with adequate sampling technique, and with the infection timeline in mind. We outlined knowledge gaps and directions for future well-documented systematic studies.
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