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dc.contributor.authorRichens, Nicholas
dc.contributor.authorKanthimathinathan, Hari Krishnan
dc.contributor.authorSontakke, Sanket
dc.contributor.authorChikermane, Ashish
dc.contributor.authorJyothish, Deepthi
dc.contributor.authorHackett, Scott
dc.contributor.authorWelch, Steven B
dc.contributor.authorAl-Abadi, Eslam
dc.contributor.authorDuncan, Heather P
dc.contributor.authorRichter, Alex G
dc.contributor.authorScholefield, Barnaby R
dc.date.accessioned2024-07-15T15:28:38Z
dc.date.available2024-07-15T15:28:38Z
dc.date.issued2020-12-04
dc.identifier.citationRichens N, Kanthimathinathan HK, Sontakke S, Chikermane A, Jyothish D, Hackett S, Welch SB, Al-Abadi E, Duncan HP, Richter AG, Scholefield BR. Critical Care Course of Pediatric Inflammatory Multisystem Syndrome Temporally Associated with SARS-CoV-2 and Response to Immunomodulation. J Pediatr Intensive Care. 2020 Dec 4;11(2):124-129. doi: 10.1055/s-0040-1721456en_US
dc.identifier.issn2146-4618
dc.identifier.doi10.1055/s-0040-1721456
dc.identifier.pmid35734206
dc.identifier.urihttp://hdl.handle.net/20.500.14200/5146
dc.description.abstractWe describe the critical care course of children with a novel hyperinflammatory syndrome associated with coronavirus disease 2019 (COVID-19) pediatric inflammatory multisystem syndrome temporally associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), with focus on trajectory before and after immunomodulation. Overall, 10 patients who met the U.K. Royal College of Pediatrics and Child Health case definition during a 2-month study period were analyzed. All tested positive for SARS-CoV-2 IgG antibody. Although only 20% were ventilated, 100% required inotropic or vasopressor support. All children had significantly raised inflammatory markers with a median C-reactive protein of 248 (175-263) mg/L, ferritin of 1,561 (726-2,255) µg/L, and troponin-I of 723 (351-2,235) ng/L. Six patients had moderately impaired myocardial function and two had severe impairment. None needed extracorporeal membrane oxygenation. Despite severe illness only a brief period of critical care support of 3 to 5 days was required. Eight received at least one dose of intravenous immunoglobulin. Six received high-dose steroids. Clinical improvement including cardiovascular stability and reduction in inflammatory markers may have occurred with and without immunomodulation.en_US
dc.language.isoenen_US
dc.publisherThiemeen_US
dc.relation.urlhttps://www.thieme-connect.com/products/ejournals/journal/10.1055/s-00029029en_US
dc.rightsThieme. All rights reserved.
dc.subjectIntensive careen_US
dc.subjectCardiologyen_US
dc.subjectRheumatologyen_US
dc.subjectMicrobiology. Immunologyen_US
dc.titleCritical care course of pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 and response to immunomodulation.en_US
dc.typeArticleen_US
dc.source.journaltitleJournal of Pediatric Intensive Careen_US
dc.source.volume11
dc.source.issue2
dc.source.beginpage124
dc.source.endpage129
dc.source.countryGermany
rioxxterms.versionNAen_US
dc.contributor.trustauthorHackett, Scott
dc.contributor.trustauthorWelch, Steven B
dc.contributor.departmentPediatricsen_US
dc.contributor.roleMedical and Dentalen_US
oa.grant.openaccessnaen_US


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