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Clinical characteristics of children and young people admitted to hospital with covid-19 in United Kingdom: prospective multicentre observational cohort study
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Clinical characteristics of children and young people admitted to hospital with covid-19 in United Kingdom prospective multi.pdf | Published version | 544.48 kB | Adobe PDF | View/Open |
Title: | Clinical characteristics of children and young people admitted to hospital with covid-19 in United Kingdom: prospective multicentre observational cohort study |
Authors: | Swann, OV Holden, KA Turtle, L Pollock, L Fairfield, CJ Drake, TM Seth, S Egan, C Hardwick, HE Halpin, S Girvan, M Donohue, C Pritchard, M Patel, LB Ladhani, S Sigfrid, L Sinha, IP Olliaro, PL Nguyen-Van-Tam, JS Horby, PW Merson, L Carson, G Dunning, J Openshaw, PJM Baillie, JK Harrison, EM Docherty, AB Semple, MG |
Item Type: | Journal Article |
Abstract: | Objective To characterise the clinical features of children and young people admitted to hospital with laboratory confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in the UK and explore factors associated with admission to critical care, mortality, and development of multisystem inflammatory syndrome in children and adolescents temporarily related to coronavirus disease 2019 (covid-19) (MIS-C).Design Prospective observational cohort study with rapid data gathering and near real time analysis.Setting 260 hospitals in England, Wales, and Scotland between 17 January and 3 July 2020, with a minimum follow-up time of two weeks (to 17 July 2020).Participants 651 children and young people aged less than 19 years admitted to 138 hospitals and enrolled into the International Severe Acute Respiratory and emergency Infections Consortium (ISARIC) WHO Clinical Characterisation Protocol UK study with laboratory confirmed SARS-CoV-2.Main outcome measures Admission to critical care (high dependency or intensive care), in-hospital mortality, or meeting the WHO preliminary case definition for MIS-C.Results Median age was 4.6 (interquartile range 0.3-13.7) years, 35% (225/651) were under 12 months old, and 56% (367/650) were male. 57% (330/576) were white, 12% (67/576) South Asian, and 10% (56/576) black. 42% (276/651) had at least one recorded comorbidity. A systemic mucocutaneous-enteric cluster of symptoms was identified, which encompassed the symptoms for the WHO MIS-C criteria. 18% (116/632) of children were admitted to critical care. On multivariable analysis, this was associated with age under 1 month (odds ratio 3.21, 95% confidence interval 1.36 to 7.66; P=0.008), age 10-14 years (3.23, 1.55 to 6.99; P=0.002), and black ethnicity (2.82, 1.41 to 5.57; P=0.003). Six (1%) of 627 patients died in hospital, all of whom had profound comorbidity. 11% (52/456) met the WHO MIS-C criteria, with the first patient developing symptoms in mid-March. Children meeting MIS-C criteria were older (median age 10.7 (8.3-14.1) v 1.6 (0.2-12.9) years; P<0.001) and more likely to be of non-white ethnicity (64% (29/45) v 42% (148/355); P=0.004). Children with MIS-C were five times more likely to be admitted to critical care (73% (38/52) v 15% (62/404); P<0.001). In addition to the WHO criteria, children with MIS-C were more likely to present with fatigue (51% (24/47) v 28% (86/302); P=0.004), headache (34% (16/47) v 10% (26/263); P<0.001), myalgia (34% (15/44) v 8% (21/270); P<0.001), sore throat (30% (14/47) v (12% (34/284); P=0.003), and lymphadenopathy (20% (9/46) v 3% (10/318); P<0.001) and to have a platelet count of less than 150 × 109/L (32% (16/50) v 11% (38/348); P<0.001) than children who did not have MIS-C. No deaths occurred in the MIS-C group.Conclusions Children and young people have less severe acute covid-19 than adults. A systemic mucocutaneous-enteric symptom cluster was also identified in acute cases that shares features with MIS-C. This study provides additional evidence for refining the WHO MIS-C preliminary case definition. Children meeting the MIS-C criteria have different demographic and clinical features depending on whether they have acute SARS-CoV-2 infection (polymerase chain reaction positive) or are post-acute (antibody positive).Study registration ISRCTN66726260. |
Editors: | Baillie, JK Semple, MG Openshaw, PJM Alex, B Bach, B Barclay, WS Bogaert, D Chand, M Cooke, GS Docherty, AB Dunning, J Da Silva Filipe, A Fletcher, T Green, CA Harrison, EM Hiscox, JA Ying Wai Ho, A Horby, PW Ijaz, S Khoo, S Klenerman, P Law, A Lim, WS Mentzer, AJ Merson, L Meynert, AM Noursadeghi, M Moore, SC Palmarini, M Paxton, WA Pollakis, G Price, N Rambaut, A Robertson, DL Russell, CD Sancho-Shimizu, V Scott, JT Sigfrid, L Solomon, T Sriskandan, S Stuart, D Summers, C Tedder, RS Thomson, EC Thwaites, RS Turtle, LCW Zambon, M Hardwick, H Donohue, C Ewins, J Oosthuyzen, W Griffiths, F Norman, L Pius, R Drake, TM Fairfield, CJ Knight, S Mclean, KA Murphy, D Shaw, CA Dalton, J Girvan, M Saviciute, E Roberts, S Harrison, J Marsh, L Connor, M Halpin, S Jackson, C Gamble, C Leeming, G Law, A Hendry, R Greenhalf, W Shaw, V McDonald, S Ahmed, KA Armstrong, JA Ashworth, M Asiimwe, IG Bakshi, S Barlow, SL Booth, L Brennan, B Bullock, K Catterall, BWA Clark, JJ Clarke, EA Cole, S Cooper, L Cox, H Davis, C Dincarslan, O Dunn, C Dyer, P Elliott, A Evans, A Fisher, LWS Foster, T Garcia-Dorival, I Greenhalf, W Gunning, P Hartley, C Ho, A Jensen, RL Jones, CB Jones, TR Khandaker, S King, K Kiy, RT Koukorava, C Lake, A Lant, S Latawiec, D Lavelle-Langham, L Lefteri, D Lett, L Livoti, LA Mancini, M McDonald, S McEvoy, L McLauchlan, J Metelmann, S Miah, NS Middleton, J Mitchell, J Moore, SC Murphy, EG Penrice-Randal, R Pilgrim, J Prince, T Reynolds, W Ridley, PM Sales, D Shaw, VE Shears, RK Small, B Subramaniam, KS Szemiel, A Taggart, A Tanianis, J Thomas, J Trochu, E Van Tonder, L Wilcock, E Zhang, JE Adeniji, K Agranoff, D Agwuh, K Ail, D Alegria, A Angus, B Ashish, A Atkinson, D Bari, S Barlow, G Barnass, S Barrett, N Bassford, C Baxter, D Beadsworth, M Bernatoniene, J Berridge, J Best, N Bothma, P Brealey, D Brittain-Long, R Bulteel, N Burden, T Burtenshaw, A Caruth, V Chadwick, D Chambler, D Chee, N Child, J Chukkambotla, S Clark, T Collini, P Cosgrove, C Cupitt, J Cutino-Moguel, M-T Dark, P Dawson, C Dervisevic, S Donnison, P Douthwaite, S DuRand, I Dushianthan, A Dyer, T Evans, C Eziefula, C Fegan, C Finn, A Fullerton, D Garg, S Garg, S Garg, A Godden, J Goldsmith, A Graham, C Hardy, E Hartshorn, S Harvey, D Havalda, P Hawcutt, DB Hobrok, M Hodgson, L Holme, A Hormis, A Jacobs, M Jain, S Jennings, P Kaliappan, A Kasipandian, V Kegg, S Kelsey, M Kendall, J Kerrison, C Kerslake, I Koch, O Koduri, G Koshy, G Laha, S Larkin, S Leiner, T Lillie, P Limb, J Linnett, V Little, J MacMahon, M MacNaughton, E Mankregod, R Masson, H Matovu, E McCullough, K McEwen, R Meda, M Mills, G Minton, J Mirfenderesky, M Mohandas, K Mok, Q Moon, J Moore, E Morgan, P Morris, C Mortimore, K Moses, S Mpenge, M Mulla, R Murphy, M Nagel, M Nagarajan, T Nelson, M Otahal, I Pais, M Panchatsharam, S Paraiso, H Patel, B Pepperell, J Peters, M Phull, M Pintus, S Pooni, JS Post, F Price, D Prout, R Rae, N Reschreiter, H Reynolds, T Richardson, N Roberts, M Roberts, D Rose, A Rousseau, G Ryan, B Saluja, T Shah, A Shanmuga, P Sharma, A Shawcross, A Sizer, J Smith, R Snelson, C Spittle, N Staines, N Stambach, T Stewart, R Subudhi, P Szakmany, T Tatham, K Thomas, J Thompson, C Thompson, R Tridente, A Tupper-Carey, D Twagira, M Ustianowski, A Vallotton, N Vincent-Smith, L Visuvanathan, S Vuylsteke, A Waddy, S Wake, R Walden, A Welters, I Whitehouse, T Whittaker, P Whittington, A Wijesinghe, M Williams, M Wilson, L Wilson, S Winchester, S Wiselka, M Wolverson, A Wooton, DG Workman, A Yates, B Young, P |
Issue Date: | 27-Aug-2020 |
Date of Acceptance: | 17-Aug-2020 |
URI: | http://hdl.handle.net/10044/1/84440 |
DOI: | 10.1136/bmj.m3249 |
Publisher: | BMJ Publishing Group Ltd |
Start Page: | 1 |
End Page: | 15 |
Journal / Book Title: | BMJ |
Volume: | 370 |
Copyright Statement: | © 2020 The Author(s). This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/. |
Keywords: | Science & Technology Life Sciences & Biomedicine Medicine, General & Internal General & Internal Medicine AGE Adolescent Age Factors Betacoronavirus Child Child, Preschool Cohort Studies Coronavirus Infections Critical Care Female Hospital Mortality Hospitalization Humans Infant Infant, Newborn Male Pandemics Pneumonia, Viral Respiration, Artificial Systemic Inflammatory Response Syndrome United Kingdom Young Adult ISARIC4C Investigators Humans Pneumonia, Viral Coronavirus Infections Respiration, Artificial Critical Care Hospitalization Hospital Mortality Cohort Studies Age Factors Adolescent Child Child, Preschool Infant Infant, Newborn Female Male Systemic Inflammatory Response Syndrome Young Adult Pandemics United Kingdom Betacoronavirus 1103 Clinical Sciences 1117 Public Health and Health Services General & Internal Medicine |
Notes: | elocation-id: m3249 |
Publication Status: | Published |
Online Publication Date: | 2020-08-27 |
Appears in Collections: | National Heart and Lung Institute Imperial College London COVID-19 |
This item is licensed under a Creative Commons License