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

被引:742
作者
Knight, Stephen R. [1 ]
Ho, Antonia [2 ,3 ]
Pius, Riinu [1 ]
Buchan, Iain [4 ]
Carson, Gail [5 ]
Drake, Thomas M. [1 ]
Dunning, Jake [6 ,7 ]
Fairfield, Cameron J. [1 ]
Gamble, Carrol [8 ]
Green, Christopher A. [9 ]
Gupta, Rishi [10 ]
Halpin, Sophie [8 ]
Hardwick, Hayley E. [11 ]
Holden, Karl A. [11 ]
Horby, Peter W.
Jackson, Clare [8 ]
Mclean, Kenneth A. [1 ]
Merson, Laura
Nguyen-Van-Tam, Jonathan S. [12 ]
Norman, Lisa [1 ]
Noursadeghi, Mahdad [13 ]
Olliaro, Piero L. [14 ]
Pritchard, Mark G. [14 ]
Russell, Clark D. [15 ]
Shaw, Catherine A. [1 ]
Sheikh, Aziz [1 ]
Solomon, Tom [11 ,16 ]
Sudlow, Cathie [11 ,17 ]
Swann, Olivia, V [18 ]
Turtle, Lance C. W. [11 ,19 ]
Openshaw, Peter J. M.
Baillie, J. Kenneth [20 ,21 ]
Semple, Malcolm G. [11 ,22 ]
Docherty, Annemarie B. [21 ]
Harrison, Ewen M. [23 ]
机构
[1] Univ Edinburgh, Usher Inst, Med Informat Ctr, Edinburgh, Midlothian, Scotland
[2] Univ Glasgow Ctr Virus Res, Med Res Council, Glasgow, Lanark, Scotland
[3] Queen Elizabeth Univ Hosp, Dept Infect Dis, Glasgow, Lanark, Scotland
[4] Univ Liverpool, Inst Populat Hlth Sci, Liverpool, Merseyside, England
[5] Univ Oxford, Nuffield Dept Med, ISARIC Global Support Ctr, Ctr Trop Med & Global Hlth, Oxford, England
[6] Publ Hlth England, Natl Infect Serv, London, England
[7] Imperial Coll London, Natl Heart & Lung Inst, London, England
[8] Univ Liverpool, Liverpool Clin Trials Ctr, Liverpool, Merseyside, England
[9] Univ Birmingham, Inst Microbiol Infect, Birmingham, W Midlands, England
[10] UCL, Inst Global Hlth, London, England
[11] Univ Liverpool, Inst Infect, Fac Hlth & Life Sci, NIHR Hlth Protect Res Unit, Liverpool, Merseyside, England
[12] Univ Nottingham, Div Epidemiol & Publ Hlth, Sch Med, Nottingham, England
[13] UCL, Div Infect & Immun, London, England
[14] Univ Oxford, Nuffield Dept Med, Ctr Trop Med & Global Hlth, Oxford, England
[15] Univ Edinburgh, Med Res Inst, Edinburgh, Midlothian, Scotland
[16] Walton Ctr NHS Fdn Trust, Liverpool, Merseyside, England
[17] Hlth Data Res UK, London, England
[18] Univ Edinburgh, Dept Child Life & Hlth, Edinburgh, Midlothian, Scotland
[19] Royal Liverpool Univ Hosp, Infect Dis Unit, Liverpool, Merseyside, England
[20] Univ Edinburgh, Roslin Inst, Edinburgh, Midlothian, Scotland
[21] Royal Infirm Edinburgh NHS Trust, Intens Care Unit, Edinburgh, Midlothian, Scotland
[22] Univ Liverpool, Inst Pk, Alder Hey Childrens Hosp, Liverpool L12 2AP, Merseyside, England
[23] Univ Edinburgh, Dept Clin Surg, Edinburgh, Midlothian, Scotland
来源
BMJ-BRITISH MEDICAL JOURNAL | 2020年 / 370卷
基金
英国惠康基金; 英国医学研究理事会;
关键词
COMMUNITY-ACQUIRED PNEUMONIA; SEVERITY; PERFORMANCE; CURB-65; SEPSIS; ADULTS; CURVE;
D O I
10.1136/bmj.m3339
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 ConsortiumISARIC-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 a18 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: calibrationin-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
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