Back

Multisystem inflammatory syndrome in European White children - study of 274 cases

Ludwikowska, K. M.; Okarska-Napierala, M.; Dudek, N.; Tracewski, P.; Kusa, J.; Piwonski, K.; Afelt, A.; Cysewski, D.; Biela, M.; Werner, B.; Jackowska, T.; Suski, C.; Kursa, M. B.; Kuchar, E.; Szenborn, L.

2021-03-31 pediatrics
10.1101/2021.03.30.21254584 medRxiv
Show abstract

BackgroundDespite the growing literature on multisystem inflammatory syndrome in children (MIS-C), the data in European White population is limited. Our aim was to capture MIS-C emergence in Poland (central Europe) and to describe its characteristics with a focus on severity determinants. MethodsPatients who met the MIS-C definition (fever, multiorgan failure, inflammation, and proven SARS-CoV-2 infection or contact) were reported retrospectively and prospectively in an online survey. Study definitions fulfilment was automatically evaluated by a dedicated software. For the assessment of univariate relationships, either directed or divided by sex, age, or disease severity, we used the test for two categorical variables and the Kruskal-Wallis test for categorical-continuous variable pairs. FindingsThe analysis involved 274 children, 62.8% boys, median age 8.8 years. Besides one Asian, all were European White. Merely 23 (8.4%) required paediatric intensive care treatment (PICU). They were older (11.2 vs. 8.4 years), and at hospital admission had higher respiratory rate (30 v. 20/minute), lower systolic blood pressure (89 vs. 100 mmHg), prolonged capillary refill time (40% vs. 11%), and decreased consciousness (22% vs. 5%). Teenage boys had more common cardiac involvement (fraction 25.9% vs. 14.7%) and macrophage activation syndrome (31.0% vs. 15.2%) than others. Boys were also more often hospitalised in PICU with age (from median 11.2 years to 9.1). InterpretationThe severity of MIS-C is not as uniform as it seemed, ethnicity and sex may affect MIS-C phenotype. Management might not be universally applicable and should rather be adjusted to the specific population. FundingPSP: 501-D402-20-0006100

Matching journals

The top 2 journals account for 50% of the predicted probability mass.

1
Pediatric Infectious Disease Journal
16 papers in training set
Top 0.1%
33.2%
2
Frontiers in Pediatrics
29 papers in training set
Top 0.1%
18.8%
50% of probability mass above
3
BMJ Paediatrics Open
21 papers in training set
Top 0.1%
6.4%
4
Pediatric Pulmonology
14 papers in training set
Top 0.1%
4.9%
5
The Journal of Pediatrics
15 papers in training set
Top 0.2%
3.6%
6
Pediatrics
10 papers in training set
Top 0.1%
3.6%
7
Archives of Disease in Childhood
15 papers in training set
Top 0.2%
3.1%
8
BMJ Open
554 papers in training set
Top 6%
3.1%
9
PLOS ONE
4510 papers in training set
Top 48%
2.1%
10
Journal of the Pediatric Infectious Diseases Society
10 papers in training set
Top 0.1%
1.9%
11
Medicine
30 papers in training set
Top 1%
1.7%
12
European Respiratory Journal
54 papers in training set
Top 1%
1.5%
13
Pediatric Research
18 papers in training set
Top 0.3%
1.2%
14
Eurosurveillance
80 papers in training set
Top 1.0%
1.2%
15
Annals of Translational Medicine
17 papers in training set
Top 1%
0.9%
16
BMJ
49 papers in training set
Top 1.0%
0.9%
17
Swiss Medical Weekly
12 papers in training set
Top 0.2%
0.9%
18
Scientific Reports
3102 papers in training set
Top 71%
0.9%
19
Frontiers in Immunology
586 papers in training set
Top 8%
0.7%
20
Archives of Clinical and Biomedical Research
28 papers in training set
Top 4%
0.5%
21
Vaccines
196 papers in training set
Top 3%
0.5%
22
Critical Care
14 papers in training set
Top 0.8%
0.5%