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Risk stratification of patients admitted to hospital with covid-19 using the ISARIC WHO Clinical Characterisation Protocol: development and validation of the 4C Mortality Score.
Knight, Stephen R; Ho, Antonia; Pius, Riinu; Buchan, Iain; Carson, Gail; Drake, Thomas M; Dunning, Jake; Fairfield, Cameron J; Gamble, Carrol; Green, Christopher A; Gupta, Rishi; Halpin, Sophie; Hardwick, Hayley E; Holden, Karl A; Horby, Peter W; Jackson, Clare; Mclean, Kenneth A; Merson, Laura; Nguyen-Van-Tam, Jonathan S; Norman, Lisa; Noursadeghi, Mahdad; Olliaro, Piero L; Pritchard, Mark G; Russell, Clark D; Shaw, Catherine A; Sheikh, Aziz; Solomon, Tom; Sudlow, Cathie; Swann, Olivia V; Turtle, Lance Cw; Openshaw, Peter Jm; Baillie, J Kenneth; Semple, Malcolm G; Docherty, Annemarie B; Harrison, Ewen M.
  • Knight SR; Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Ho A; Medical Research Council, University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Pius R; Department of Infectious Diseases, Queen Elizabeth University Hospital, Glasgow, UK.
  • Buchan I; Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Carson G; Institute of Population Health Sciences, University of Liverpool, Liverpool, UK.
  • Drake TM; ISARIC Global Support Centre, Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Dunning J; Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Fairfield CJ; National Infection Service, Public Health England, London, UK.
  • Gamble C; National Heart and Lung Institute, Imperial College London, London, UK.
  • Green CA; Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Gupta R; Liverpool Clinical Trials Centre, University of Liverpool, Liverpool, UK.
  • Halpin S; Institute of Microbiology & Infection, University of Birmingham, Birmingham, UK.
  • Hardwick HE; Institute of Global Health, University College London, London, UK.
  • Holden KA; Liverpool Clinical Trials Centre, University of Liverpool, Liverpool, UK.
  • Horby PW; NIHR Health Protection Research Unit, Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK.
  • Jackson C; NIHR Health Protection Research Unit, Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK.
  • Mclean KA; ISARIC Global Support Centre, Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Merson L; Liverpool Clinical Trials Centre, University of Liverpool, Liverpool, UK.
  • Nguyen-Van-Tam JS; Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Norman L; ISARIC Global Support Centre, Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Noursadeghi M; Division of Epidemiology and Public Health, University of Nottingham School of Medicine, Nottingham, UK.
  • Olliaro PL; Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Pritchard MG; Division of Infection and Immunity, University College London, London, UK.
  • Russell CD; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Shaw CA; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Sheikh A; Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
  • Solomon T; Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Sudlow C; Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Swann OV; NIHR Health Protection Research Unit, Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK.
  • Turtle LC; Walton Centre NHS Foundation Trust, Liverpool, UK.
  • Openshaw PJ; Health Data Research UK, London, UK.
  • Baillie JK; Department of Child Life and Health, University of Edinburgh, Edinburgh, UK.
  • Semple MG; NIHR Health Protection Research Unit, Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK.
  • Docherty AB; Tropical & Infectious Disease Unit, Royal Liverpool University Hospital, Liverpool, UK.
  • Harrison EM; National Heart and Lung Institute, Imperial College London, London, UK.
BMJ ; 370: m3339, 2020 09 09.
Article in English | MEDLINE | ID: covidwho-751530
Preprint
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ABSTRACT

OBJECTIVE:

To develop and validate a pragmatic risk score to predict mortality in patients admitted to hospital with coronavirus disease 2019 (covid-19).

DESIGN:

Prospective observational cohort study.

SETTING:

International Severe Acute Respiratory and emerging Infections Consortium (ISARIC) World Health Organization (WHO) Clinical Characterisation Protocol UK (CCP-UK) study (performed by the ISARIC Coronavirus Clinical Characterisation Consortium-ISARIC-4C) in 260 hospitals across England, Scotland, and Wales. Model training was performed on a cohort of patients recruited between 6 February and 20 May 2020, with validation conducted on a second cohort of patients recruited after model development between 21 May and 29 June 2020.

PARTICIPANTS:

Adults (age ≥18 years) admitted to hospital with covid-19 at least four weeks before final data extraction. MAIN OUTCOME

MEASURE:

In-hospital mortality.

RESULTS:

35 463 patients were included in the derivation dataset (mortality rate 32.2%) and 22 361 in the validation dataset (mortality rate 30.1%). The final 4C Mortality Score included eight variables readily available at initial hospital assessment age, sex, number of comorbidities, respiratory rate, peripheral oxygen saturation, level of consciousness, urea level, and C reactive protein (score range 0-21 points). The 4C Score showed high discrimination for mortality (derivation cohort area under the receiver operating characteristic curve 0.79, 95% confidence interval 0.78 to 0.79; validation cohort 0.77, 0.76 to 0.77) with excellent calibration (validation calibration-in-the-large=0, slope=1.0). Patients with a score of at least 15 (n=4158, 19%) had a 62% mortality (positive predictive value 62%) compared with 1% mortality for those with a score of 3 or less (n=1650, 7%; negative predictive value 99%). Discriminatory performance was higher than 15 pre-existing risk stratification scores (area under the receiver operating characteristic curve range 0.61-0.76), with scores developed in other covid-19 cohorts often performing poorly (range 0.63-0.73).

CONCLUSIONS:

An easy-to-use risk stratification score has been developed and validated based on commonly available parameters at hospital presentation. The 4C Mortality Score outperformed existing scores, showed utility to directly inform clinical decision making, and can be used to stratify patients admitted to hospital with covid-19 into different management groups. The score should be further validated to determine its applicability in other populations. STUDY REGISTRATION ISRCTN66726260.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Coronavirus Infections / Betacoronavirus / Hospitalization Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials / Reviews Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: BMJ Journal subject: Medicine Year: 2020 Document Type: Article Affiliation country: Bmj.m3339

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Coronavirus Infections / Betacoronavirus / Hospitalization Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials / Reviews Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: BMJ Journal subject: Medicine Year: 2020 Document Type: Article Affiliation country: Bmj.m3339