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Kawasaki-like multisystem inflammatory syndrome in children during the covid-19 pandemic in Paris, France: prospective observational study.

Toubiana, J; Poirault, C; Corsia, A; Bajolle, F; Fourgeaud, J; Angoulvant, F; Debray, A; Basmaci, R; Salvador, E; Biscardi, S; et al. Toubiana, J; Poirault, C; Corsia, A; Bajolle, F; Fourgeaud, J; Angoulvant, F; Debray, A; Basmaci, R; Salvador, E; Biscardi, S; Frange, P; Chalumeau, M; Casanova, J-L; Cohen, JF; Allali, S (2020) Kawasaki-like multisystem inflammatory syndrome in children during the covid-19 pandemic in Paris, France: prospective observational study. BMJ, 369. m2094. ISSN 1756-1833 https://doi.org/10.1136/bmj.m2094
SGUL Authors: Basmaci, Romain

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Abstract

OBJECTIVES: To describe the characteristics of children and adolescents affected by an outbreak of Kawasaki-like multisystem inflammatory syndrome and to evaluate a potential temporal association with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. DESIGN: Prospective observational study. SETTING: General paediatric department of a university hospital in Paris, France. PARTICIPANTS: 21 children and adolescents (aged ≤18 years) with features of Kawasaki disease who were admitted to hospital between 27 April and 11 May 2020 and followed up until discharge by 15 May 2020. MAIN OUTCOME MEASURES: The primary outcomes were clinical and biological data, imaging and echocardiographic findings, treatment, and outcomes. Nasopharyngeal swabs were prospectively tested for SARS-CoV-2 using reverse transcription-polymerase chain reaction (RT-PCR) and blood samples were tested for IgG antibodies to the virus. RESULTS: 21 children and adolescents (median age 7.9 (range 3.7-16.6) years) were admitted with features of Kawasaki disease over a 15 day period, with 12 (57%) of African ancestry. 12 (57%) presented with Kawasaki disease shock syndrome and 16 (76%) with myocarditis. 17 (81%) required intensive care support. All 21 patients had noticeable gastrointestinal symptoms during the early stage of illness and high levels of inflammatory markers. 19 (90%) had evidence of recent SARS-CoV-2 infection (positive RT-PCR result in 8/21, positive IgG antibody detection in 19/21). All 21 patients received intravenous immunoglobulin and 10 (48%) also received corticosteroids. The clinical outcome was favourable in all patients. Moderate coronary artery dilations were detected in 5 (24%) of the patients during hospital stay. By 15 May 2020, after 8 (5-17) days of hospital stay, all patients were discharged home. CONCLUSIONS: The ongoing outbreak of Kawasaki-like multisystem inflammatory syndrome among children and adolescents in the Paris area might be related to SARS-CoV-2. In this study an unusually high proportion of the affected children and adolescents had gastrointestinal symptoms, Kawasaki disease shock syndrome, and were of African ancestry.

Item Type: Article
Additional Information: This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Keywords: Adolescent, Adrenal Cortex Hormones, Antibodies, Viral, Betacoronavirus, Child, Child, Preschool, Coronavirus Infections, Female, Humans, Immunoglobulins, Intravenous, Male, Nasopharynx, Pandemics, Paris, Pneumonia, Viral, Prospective Studies, RNA, Viral, Systemic Inflammatory Response Syndrome, Nasopharynx, Humans, Pneumonia, Viral, Coronavirus Infections, Adrenal Cortex Hormones, Immunoglobulins, Intravenous, RNA, Viral, Antibodies, Viral, Prospective Studies, Adolescent, Child, Child, Preschool, Paris, Female, Male, Systemic Inflammatory Response Syndrome, Pandemics, Betacoronavirus
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: BMJ
ISSN: 1756-1833
Language: eng
Dates:
DateEvent
3 June 2020Published
26 May 2020Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
PubMed ID: 32493739
Web of Science ID: WOS:000548578300002
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/112219
Publisher's version: https://doi.org/10.1136/bmj.m2094

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