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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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          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 × 10 9/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.

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          Most cited references21

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          Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention

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            Epidemiological Characteristics of 2143 Pediatric Patients With 2019 Coronavirus Disease in China

            To identify the epidemiological characteristics and transmission patterns of pediatric patients with the 2019 novel coronavirus disease (COVID-19) in China.
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              Features of 20 133 UK patients in hospital with covid-19 using the ISARIC WHO Clinical Characterisation Protocol: prospective observational cohort study

              Abstract Objective To characterise the clinical features of patients admitted to hospital with coronavirus disease 2019 (covid-19) in the United Kingdom during the growth phase of the first wave of this outbreak who were enrolled in the International Severe Acute Respiratory and emerging Infections Consortium (ISARIC) World Health Organization (WHO) Clinical Characterisation Protocol UK (CCP-UK) study, and to explore risk factors associated with mortality in hospital. Design Prospective observational cohort study with rapid data gathering and near real time analysis. Setting 208 acute care hospitals in England, Wales, and Scotland between 6 February and 19 April 2020. A case report form developed by ISARIC and WHO was used to collect clinical data. A minimal follow-up time of two weeks (to 3 May 2020) allowed most patients to complete their hospital admission. Participants 20 133 hospital inpatients with covid-19. Main outcome measures Admission to critical care (high dependency unit or intensive care unit) and mortality in hospital. Results The median age of patients admitted to hospital with covid-19, or with a diagnosis of covid-19 made in hospital, was 73 years (interquartile range 58-82, range 0-104). More men were admitted than women (men 60%, n=12 068; women 40%, n=8065). The median duration of symptoms before admission was 4 days (interquartile range 1-8). The commonest comorbidities were chronic cardiac disease (31%, 5469/17 702), uncomplicated diabetes (21%, 3650/17 599), non-asthmatic chronic pulmonary disease (18%, 3128/17 634), and chronic kidney disease (16%, 2830/17 506); 23% (4161/18 525) had no reported major comorbidity. Overall, 41% (8199/20 133) of patients were discharged alive, 26% (5165/20 133) died, and 34% (6769/20 133) continued to receive care at the reporting date. 17% (3001/18 183) required admission to high dependency or intensive care units; of these, 28% (826/3001) were discharged alive, 32% (958/3001) died, and 41% (1217/3001) continued to receive care at the reporting date. Of those receiving mechanical ventilation, 17% (276/1658) were discharged alive, 37% (618/1658) died, and 46% (764/1658) remained in hospital. Increasing age, male sex, and comorbidities including chronic cardiac disease, non-asthmatic chronic pulmonary disease, chronic kidney disease, liver disease and obesity were associated with higher mortality in hospital. Conclusions ISARIC WHO CCP-UK is a large prospective cohort study of patients in hospital with covid-19. The study continues to enrol at the time of this report. In study participants, mortality was high, independent risk factors were increasing age, male sex, and chronic comorbidity, including obesity. This study has shown the importance of pandemic preparedness and the need to maintain readiness to launch research studies in response to outbreaks. Study registration ISRCTN66726260.
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                Author and article information

                Contributors
                Role: clinical lecturer in paediatric infectious diseases
                Role: NIHR academic clinical fellow in paediatrics
                Role: consultant in adult infectious diseases
                Role: consultant in paediatric infectious diseases
                Role: clinical research fellow
                Role: clinical research fellow
                Role: senior data scientist
                Role: masters student
                Role: project manager
                Role: supervising data manager
                Role: data manager
                Role: clinical trials coordinator
                Role: specialty registrar in public health medicine
                Role: specialist registrar in paediatric respiratory medicine
                Role: reader in paediatric infectious disease
                Role: clinical research fellow
                Role: consultant physician in paediatric respiratory medicine and honorary senior clinical lecturer in child health
                Role: professor of poverty related infectious diseases
                Role: professor of health protection
                Role: professor of emerging infectious diseases
                Role: head of data and associate director
                Role: head of ISARIC global support centre
                Role: head of emerging infections and zoonoses
                Role: professor of experimental medicine
                Role: academic consultant in critical care medicine
                Role: professor of surgery and data science
                Role: senior clinical lecturer and honorary consultant in critical care
                Role: professor of outbreak medicine and child health and consultant physician in paediatric respiratory medicine
                Journal
                BMJ
                BMJ
                BMJ-UK
                bmj
                The BMJ
                BMJ Publishing Group Ltd.
                0959-8138
                1756-1833
                2020
                27 August 2020
                : 370
                : m3249
                Affiliations
                [1 ]Department of Child Life and Health, University of Edinburgh, Edinburgh, UK
                [2 ]Royal Hospital for Sick Children, Paediatric Infectious Diseases, Edinburgh, UK
                [3 ]Women’s and Children’s Health, Institute of Translational Medicine, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK
                [4 ]Respiratory Medicine, Alder Hey Children’s NHS Foundation Trust, Liverpool L12 2AP, UK
                [5 ]Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK
                [6 ]Infectious diseases Unit, Royal Liverpool University Hospital, Liverpool, UK
                [7 ]Paediatric Infectious Diseases, Royal Hospital for Children, Glasgow, UK
                [8 ]Centre for Medical Informatics, Usher Institute, University of Edinburgh, Edinburgh, UK
                [9 ]Institute for Adaptive and Neural Computation, School of Informatics, University of Edinburgh, UK
                [10 ]Liverpool Clinical Trials Centre, University of Liverpool, Liverpool, UK
                [11 ]Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK
                [12 ]Respiratory Medicine, Alder Hey Children’s Hospital, Liverpool, UK
                [13 ]Immunisation and Countermeasures Division, Public Health England, Colindale, UK
                [14 ]Paediatric Infectious Disease, St George’s Hospital, London, UK
                [15 ]ISARIC Global Support Centre, Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK
                [16 ]Division of Epidemiology and Public Health, University of Nottingham School of Medicine, Nottingham, UK
                [17 ]United Kingdom Department of Health and Social Care, London, UK
                [18 ]National Infection Service, Public Health England, [A: Where?]
                [19 ]National Heart and Lung Institute, Imperial College London, London, UK
                [20 ]Roslin Institute, University of Edinburgh, Edinburgh, UK
                [21 ]Intensive Care Unit, Royal Infirmary Edinburgh, Edinburgh, UK
                Author notes
                Correspondence to: M G Semple m.g.semple@ 123456liverpool.ac.uk (or @ProfCalumSemple on Twitter)
                Author information
                https://orcid.org/0000-0001-9700-0418
                Article
                swao060426
                10.1136/bmj.m3249
                7488201
                32960186
                9f4aeb7c-c0f8-445c-8102-d48f8d97ba70
                © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. No commercial re-use. See rights and permissions. Published by BMJ.

                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/.

                History
                : 17 August 2020
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