Research Evaluation Alongside Clinical Treatment in COVID-19 (REACT COVID-19): an observational and biobanking study

被引:15
作者
Burke, Hannah [1 ,2 ]
Freeman, Anna [1 ,2 ]
Dushianthan, Ahilanandan [1 ,2 ]
Celinski, Michael [1 ,2 ]
Batchelor, James [1 ,2 ,3 ,4 ]
Phan, Hang [1 ,4 ,5 ]
Borca, Florina [3 ,5 ]
Kipps, Christopher [1 ,2 ,3 ,5 ]
Thomas, Gareth J. [6 ]
Faust, Saul N. [1 ,2 ,3 ,5 ,7 ]
Sheard, Natasha [2 ]
Williams, Sarah [2 ]
Fitzpatrick, Paul [8 ]
Landers, Donal [8 ]
Wilkinson, Tom [1 ,2 ]
机构
[1] Univ Southampton, Fac Med, Southampton, Hants, England
[2] Univ Hosp Southampton NHS Fdn Trust, Southampton, Hants, England
[3] Univ Southampton, Inst Life Sci, Southampton, Hants, England
[4] Univ Southampton, Fac Med, Clin Informat Res Unit, Southampton, Hants, England
[5] Univ Hosp Southampton NHS Fdn Trust, NIHR Southampton Biomed Res Ctr, Southampton, Hants, England
[6] Univ Southampton, Fac Med, Canc Sci Unit, Southampton, Hants, England
[7] Univ Hosp Southampton NHS Fdn Trust, NIHR Southampton Clin Res Facil, Southampton, Hants, England
[8] Univ Manchester, Canc Biomarker Ctr, Canc Res UK, Manchester Inst, Manchester, Lancs, England
关键词
COVID-19; health informatics; protocols & guidelines; chronic airways disease; respiratory infections; respiratory medicine (see thoracic medicine);
D O I
10.1136/bmjopen-2020-043012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction The COVID-19 pandemic caused by SARS-CoV-2 places immense worldwide demand on healthcare services. Earlier identification of patients at risk of severe disease may allow intervention with experimental targeted treatments, mitigating the course of their disease and reducing critical care service demand. Methods and analysis This prospective observational study of patients tested or treated for SARS-CoV-2, who are under the care of the tertiary University Hospital Southampton NHS Foundation Trust (UHSFT), captured data from admission to discharge; data collection commenced on 7 March 2020. Core demographic and clinical information, as well as results of disease-defining characteristics, was captured and recorded electronically from hospital clinical record systems at the point of testing. Manual data were collected and recorded by the clinical research team for assessments which are not part of the structured electronic healthcare record, for example, symptom onset date. Thereafter, participant records were continuously updated during hospital stay and their follow-up period. Participants aged >16 years were given the opportunity to provide consent for excess clinical sample storage with optional further biological sampling. These anonymised samples were linked to the clinical data in the Real-time Analytics for Clinical Trials platform and were stored within a biorepository at UHSFT. Ethics and dissemination Ethical approval was obtained from the HRA Specific Review Board (REC 20/HRA/2986) for waiver of informed consent for the database-only cohort; the procedures conform with the Declaration of Helsinki. The study design, protocol and patient-facing documentation for the biobanking arm of the study have been approved by North West Research Ethics Committee (REC 17/NW/0632) as an amendment to the National Institute for Health Research Southampton Clinical Research Facility-managed Southampton Research Biorepository. This study will be published as peer-reviewed articles and presented at conferences, presentations and workshops.
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页数:10
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