| Literature DB >> 34356552 |
Ravindra Pawar1, Vijay Gavade2, Nivedita Patil1, Vijay Mali1,3, Amol Girwalkar4,5, Vyankatesh Tarkasband5, Sanjog Loya2, Amit Chavan2, Narendra Nanivadekar6, Rahul Shinde7, Uday Patil2, Satyan Lakshminrusimha8.
Abstract
Multisystem inflammatory syndrome in children (MIS-C) is a post-infectious immune-mediated condition, seen 3-5 weeks after COVID-19. Maternal SARS-CoV-2 may potentially cause a similar hyperinflammatory syndrome in neonates due to transplacental transfer of antibodies. We reviewed the perinatal history, clinical features, and outcomes of 20 neonates with features consistent with MIS-C related to maternal SARS-CoV-2 in Kolhapur, India, from 1 September 2020 to 30 April 2021. Anti-SARS-CoV-2 IgG and IgM antibodies were tested in all neonates. Fifteen singletons and five twins born to eighteen mothers with a history of COVID-19 disease or exposure during pregnancy presented with features consistent with MIS-C during the first 5 days after birth. Nineteen were positive for anti-SARS-CoV-2 IgG and all were negative for IgM antibodies. All mothers were asymptomatic and therefore not tested by RTPCR-SARS-CoV-2 at delivery. Eighteen neonates (90%) had cardiac involvement with prolonged QTc, 2:1 AV block, cardiogenic shock, or coronary dilatation. Other findings included respiratory failure (40%), fever (10%), feeding intolerance (30%), melena (10%), and renal failure (5%). All infants had elevated inflammatory biomarkers and received steroids and IVIG. Two infants died. We speculate that maternal SARS-CoV-2 and transplacental antibodies cause multisystem inflammatory syndrome in neonates (MIS-N). Immunomodulation may be beneficial in some cases, but further studies are needed.Entities:
Keywords: COVID-19; anti SARS-CoV-2 antibodies; multisystem inflammatory syndrome in children (MIS-C); neonate
Year: 2021 PMID: 34356552 DOI: 10.3390/children8070572
Source DB: PubMed Journal: Children (Basel) ISSN: 2227-9067