The Oxford Royal College of General Practitioners Clinical Informatics Digital Hub: Protocol to Develop Extended COVID-19 Surveillance and Trial Platforms

Routinely recorded primary care data have been used for many years by sentinel networks for surveillance. More recently, real world data have been used for a wider range of research projects to support rapid, inexpensive clinical trials. Because the partial national lockdown in the United Kingdom du...

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Veröffentlicht in:JMIR public health and surveillance 2020-07, Vol.6 (3), p.e19773-e19773
Hauptverfasser: de Lusignan, Simon, Jones, Nicholas, Dorward, Jienchi, Byford, Rachel, Liyanage, Harshana, Briggs, John, Ferreira, Filipa, Akinyemi, Oluwafunmi, Amirthalingam, Gayatri, Bates, Chris, Lopez Bernal, Jamie, Dabrera, Gavin, Eavis, Alex, Elliot, Alex J, Feher, Michael, Krajenbrink, Else, Hoang, Uy, Howsam, Gary, Leach, Jonathan, Okusi, Cecilia, Nicholson, Brian, Nieri, Philip, Sherlock, Julian, Smith, Gillian, Thomas, Mark, Thomas, Nicholas, Tripathy, Manasa, Victor, William, Williams, John, Wood, Ian, Zambon, Maria, Parry, John, O'Hanlon, Shaun, Joy, Mark, Butler, Chris, Marshall, Martin, Hobbs, F D Richard
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Sprache:eng
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Zusammenfassung:Routinely recorded primary care data have been used for many years by sentinel networks for surveillance. More recently, real world data have been used for a wider range of research projects to support rapid, inexpensive clinical trials. Because the partial national lockdown in the United Kingdom due to the coronavirus disease (COVID-19) pandemic has resulted in decreasing community disease incidence, much larger numbers of general practices are needed to deliver effective COVID-19 surveillance and contribute to in-pandemic clinical trials. The aim of this protocol is to describe the rapid design and development of the Oxford Royal College of General Practitioners Clinical Informatics Digital Hub (ORCHID) and its first two platforms. The Surveillance Platform will provide extended primary care surveillance, while the Trials Platform is a streamlined clinical trials platform that will be integrated into routine primary care practice. We will apply the FAIR (Findable, Accessible, Interoperable, and Reusable) metadata principles to a new, integrated digital health hub that will extract routinely collected general practice electronic health data for use in clinical trials and provide enhanced communicable disease surveillance. The hub will be findable through membership in Health Data Research UK and European metadata repositories. Accessibility through an online application system will provide access to study-ready data sets or developed custom data sets. Interoperability will be facilitated by fixed linkage to other key sources such as Hospital Episodes Statistics and the Office of National Statistics using pseudonymized data. All semantic descriptors (ie, ontologies) and code used for analysis will be made available to accelerate analyses. We will also make data available using common data models, starting with the US Food and Drug Administration Sentinel and Observational Medical Outcomes Partnership approaches, to facilitate international studies. The Surveillance Platform will provide access to data for health protection and promotion work as authorized through agreements between Oxford, the Royal College of General Practitioners, and Public Health England. All studies using the Trials Platform will go through appropriate ethical and other regulatory approval processes. The hub will be a bottom-up, professionally led network that will provide benefits for member practices, our health service, and the population served. Data will only be used for SQUIRE (
ISSN:2369-2960
2369-2960
DOI:10.2196/19773