Abstract

BackgroundThe aim of RApid community Point-of-care Testing fOR COVID-19 (RAPTOR-C19) is to assess the diagnostic accuracy of multiple current and emerging point-of-care tests (POCTs) for active and past SARS-CoV2 infection in the community setting. RAPTOR-C19 will provide the community testbed to the COVID-19 National DiagnOstic Research and Evaluation Platform (CONDOR).MethodsRAPTOR-C19 incorporates a series of prospective observational parallel diagnostic accuracy studies of SARS-CoV2 POCTs against laboratory and composite reference standards in patients with suspected current or past SARS-CoV2 infection attending community settings. Adults and children with suspected current SARS-CoV2 infection who are having an oropharyngeal/nasopharyngeal (OP/NP) swab for laboratory SARS-CoV2 reverse transcriptase Digital/Real-Time Polymerase Chain Reaction (d/rRT-PCR) as part of clinical care or community-based testing will be invited to participate. Adults (≥ 16 years) with suspected past symptomatic infection will also be recruited. Asymptomatic individuals will not be eligible. At the baseline visit, all participants will be asked to submit samples for at least one candidate point-of-care test (POCT) being evaluated (index test/s) as well as an OP/NP swab for laboratory SARS-CoV2 RT-PCR performed by Public Health England (PHE) (reference standard for current infection). Adults will also be asked for a blood sample for laboratory SARS-CoV-2 antibody testing by PHE (reference standard for past infection), where feasible adults will be invited to attend a second visit at 28 days for repeat antibody testing. Additional study data (e.g. demographics, symptoms, observations, household contacts) will be captured electronically. Sensitivity, specificity, positive, and negative predictive values for each POCT will be calculated with exact 95% confidence intervals when compared to the reference standard. POCTs will also be compared to composite reference standards constructed using paired antibody test results, patient reported outcomes, linked electronic health records for outcomes related to COVID-19 such as hospitalisation or death, and other test results.DiscussionHigh-performing POCTs for community use could be transformational. Real-time results could lead to personal and public health impacts such as reducing onward household transmission of SARS-CoV2 infection, improving surveillance of health and social care staff, contributing to accurate prevalence estimates, and understanding of SARS-CoV2 transmission dynamics in the population. In contrast, poorly performing POCTs could have negative effects, so it is necessary to undertake community-based diagnostic accuracy evaluations before rolling these out.Trial registrationISRCTN, ISRCTN14226970

Highlights

  • The aim of RApid community Point-of-care Testing fOR COVID-19 (RAPTOR-C19) is to assess the diagnostic accuracy of multiple current and emerging point-of-care tests (POCTs) for active and past SARS-CoV2 infection in the community setting

  • RApid community Point-of-care Testing fOR COVID-19 (RAPTOR-C19) is the community testbed to the COVID-19 National DiagnOstic Research and Evaluation Platform (CONDOR) [24]

  • Assess the standard diagnostic accuracy of POCTs for active SARS-CoV-2 infection compared to the Public Health England (PHE) reference laboratory standard or equivalent

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Summary

Methods

Aim To assess the diagnostic accuracy of multiple current and emerging POCTs for active or past SARS-CoV-2 infection in the community setting. Assess the diagnostic accuracy of POCTs for active SARS-CoV-2 infection against an enhanced composite reference standard using multiple tests data, linked electronic health records (EHR) data, and patient reported outcomes data. Assess the diagnostic accuracy of POCTs for past SARS-CoV-2 infection against an enhanced composite reference standard using multiple tests data, linked EHRs, and patient reported outcomes data. Adults (> 16 years) (a) Male or female (b) With suspected current or past COVID-19 (symptomatic SARSCoV2 infection) (c) Having OP/NP swab for laboratory SARS-CoV2 RT-PCR as part of clinical care/testing (d) Willing and able to give informed consent for participation in the study 2. Study design RAPTOR-C19 will incorporate a series of prospective observational parallel diagnostic accuracy studies of SARS-CoV-2 POCTs against laboratory and composite reference standards in patients with suspected current or past COVID-19 attending community settings such as general practice. Hospital admission or death (within 28 days) citing SARS-CoV- Hospital admission or death (within 28 days) citing SARS-CoV-

Discussion
Background
1.1.35. COVID IgG Negative
Strengths and limitations
Conclusion
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