Critical care course of pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 and response to immunomodulation.
dc.contributor.author | Richens, Nicholas | |
dc.contributor.author | Kanthimathinathan, Hari Krishnan | |
dc.contributor.author | Sontakke, Sanket | |
dc.contributor.author | Chikermane, Ashish | |
dc.contributor.author | Jyothish, Deepthi | |
dc.contributor.author | Hackett, Scott | |
dc.contributor.author | Welch, Steven B | |
dc.contributor.author | Al-Abadi, Eslam | |
dc.contributor.author | Duncan, Heather P | |
dc.contributor.author | Richter, Alex G | |
dc.contributor.author | Scholefield, Barnaby R | |
dc.date.accessioned | 2024-07-15T15:28:38Z | |
dc.date.available | 2024-07-15T15:28:38Z | |
dc.date.issued | 2020-12-04 | |
dc.identifier.citation | Richens 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-0040-1721456 | en_US |
dc.identifier.issn | 2146-4618 | |
dc.identifier.doi | 10.1055/s-0040-1721456 | |
dc.identifier.pmid | 35734206 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14200/5146 | |
dc.description.abstract | We 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.iso | en | en_US |
dc.publisher | Thieme | en_US |
dc.relation.url | https://www.thieme-connect.com/products/ejournals/journal/10.1055/s-00029029 | en_US |
dc.rights | Thieme. All rights reserved. | |
dc.subject | Intensive care | en_US |
dc.subject | Cardiology | en_US |
dc.subject | Rheumatology | en_US |
dc.subject | Microbiology. Immunology | en_US |
dc.title | Critical care course of pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 and response to immunomodulation. | en_US |
dc.type | Article | en_US |
dc.source.journaltitle | Journal of Pediatric Intensive Care | en_US |
dc.source.volume | 11 | |
dc.source.issue | 2 | |
dc.source.beginpage | 124 | |
dc.source.endpage | 129 | |
dc.source.country | Germany | |
rioxxterms.version | NA | en_US |
dc.contributor.trustauthor | Hackett, Scott | |
dc.contributor.trustauthor | Welch, Steven B | |
dc.contributor.department | Pediatrics | en_US |
dc.contributor.role | Medical and Dental | en_US |
oa.grant.openaccess | na | en_US |