Critical Care Course of Pediatric Inflammatory Multisystem Syndrome Temporally Associated with SARS-CoV-2 and Response to Immunomodulation.
Nicholas RichensHari Krishnan KanthimathinathanSanket SontakkeAshish ChikermaneDeepthi JyothishScott HackettSteven B WelchEslam Al-AbadiHeather P DuncanAlex G RichterBarnaby Robert ScholefieldPublished in: Journal of pediatric intensive care (2020)
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.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- extracorporeal membrane oxygenation
- high dose
- acute respiratory distress syndrome
- end stage renal disease
- young adults
- case report
- low dose
- newly diagnosed
- ejection fraction
- intensive care unit
- chronic kidney disease
- peritoneal dialysis
- left ventricular
- heart failure
- stem cell transplantation
- drug induced