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2022-09-01Zeitschriftenartikel
SARS-CoV-2 variants and the risk of pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 among children in Germany
dc.contributor.authorSorg, Anna Lisa
dc.contributor.authorSchönefeld, Viktoria
dc.contributor.authorSiedler, Anette
dc.contributor.authorHufnagel, Markus
dc.contributor.authorDoenhardt, Maren
dc.contributor.authorDiffloth, Natalie
dc.contributor.authorBerner, Reinhard
dc.contributor.authorvon Kries, Rüdiger
dc.contributor.authorArmann, Jakob Peter
dc.date.accessioned2024-09-02T15:46:16Z
dc.date.available2024-09-02T15:46:16Z
dc.date.issued2022-09-01none
dc.identifier.other10.1007/s15010-022-01908-6
dc.identifier.urihttp://edoc.rki.de/176904/12070
dc.description.abstractPurpose To investigate the relationship between the risk of pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) in children and the predominance of different SARS-CoV-2 variants of concern (VOC) over time. Methods In relation to the Alpha, Delta, and Omicron VOC phases of the pandemic, the risk of developing PIMS-TS was calculated by analyzing data for rtPCR-confirmed SARS-CoV-2 infections reported to the German statutory notification system, along with data captured by a separate, national PIMS-TS registry. Both overall infection rates and age group-specific ratios of PIMS-TS during the different pandemic phases were calculated using the Alpha period as the baseline. Results The PIMS-TS rate changed significantly over time. When the Alpha VOC was dominant [calendar week (CW) 11 in March–CW 31 in August 2021], the PIMS-TS rate was 6.19 [95% confidence intervals (95% CI) 5.17, 7.20]. When Delta prevailed (CW 32 in August 2021–CW 4 in January 2022), the rate decreased to 1.68 (95% CI 1.49, 1.87). During the Omicron phase (CW 5 in January–CW 16 in April 2022), the rate fell further to 0.89 (95% CI 0.79, 1.00). These changes correspond to a decreased PIMS-TS rate of 73% (rate ratio 0.271, 95% CI 0.222; 0.332) and 86% (rate ratio 0.048, 95% CI 0.037; 0.062), respectively, in comparison to the Alpha period. Rate ratios were nearly identical for all age groups. Conclusion The data strongly suggest an association between the risk for PIMS-TS and the prevailing VOC, with highest risk related to Alpha and the lowest to Omicron. Given the uniformity of the decreased risk across age groups, vaccination against SARS-CoV-2 does not appear to have a significant impact on the risk of children developing PIMS-TS.eng
dc.language.isoengnone
dc.publisherRobert Koch-Institut
dc.rights(CC BY 3.0 DE) Namensnennung 3.0 Deutschlandger
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/de/
dc.subjectPIMS-TSeng
dc.subjectMIS-Ceng
dc.subjectSARS-CoV-2eng
dc.subjectVariantseng
dc.subjectCOVID-19eng
dc.subjectriskeng
dc.subject.ddc610 Medizin und Gesundheitnone
dc.titleSARS-CoV-2 variants and the risk of pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 among children in Germanynone
dc.typearticle
dc.identifier.urnurn:nbn:de:0257-176904/12070-6
dc.type.versionpublishedVersionnone
local.edoc.container-titleInfectionnone
local.edoc.container-issn1439-0973none
local.edoc.pages7none
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-urlhttps://link.springer.com/journal/15010none
local.edoc.container-publisher-nameSpringer Naturenone
local.edoc.container-volume51none
local.edoc.container-reportyear2022none
local.edoc.container-firstpage729none
local.edoc.container-lastpage735none
dc.description.versionPeer Reviewednone

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