Key result
Prenatal maternal COVID-19 linked to neonatal multisystem inflammatory syndrome presenting as subclinical myocarditis.
Why the study?
The characteristics and early outcomes of multisystem inflammatory syndrome in neonates following prenatal maternal COVID-19 infection were not well described.
Case Report (n=3)
Neonates with multisystem inflammatory syndrome following maternal COVID-19 infection may develop subclinical myocarditis characterized by elevated myocardial biomarkers despite normal echocardiographic function.
May warrant biomarker screening in neonates after maternal COVID-19; case report leaves open causal link and need for prospective validation.
BACKGROUND: The aim of this case series report is to evaluate the characteristics of multisystem inflammatory syndrome (MIS) in neonates following prenatal maternal COVID-19 infection. METHODS: We present a case series of three newborns (≤28 days of age) diagnosed with MIS due to the vertical transmission of SARS-CoV2 infection and admitted from 1 January 2021 to 1 June 2023. The inclusion criteria were negative RT-PCR-SARS-CoV-2 test in infants, initial negative IgM-SARS-CoV-2 in infants followed by the emergence of positive IgG-SARS-CoV-2 antibodies in infants and maternal COVID-19 infection in the third trimester of pregnancy. Patients enrolled in this case series were admitted due to acute febrile illnesses. RESULTS: All three cases occurred in patients born at a mean gestational age of 39 weeks and who were appropriate for gestational age. The mean age at admission was 18.3 days. Fibrinogen (>400 mg/dL) and ferritin (>120 mg/dL) were elevated above the upper normal limit. Elevated levels of myocardial biomarkers (D-dimers, N-terminal pro b-type natriuretic peptide troponin T and creatine phosphokinase myocardial band) were recorded, with normal heart function evaluated using echocardiography. All three patients were treated with antibiotics; one received intravenous immunoglobulin. A 4-week follow-up was completed in two patients when their myocardial biomarkers and ferritin were still elevated but lower compared with previous examinations. D-dimers levels were normalized in 2/3 patients. CONCLUSIONS: Subclinical myocarditis was diagnosed as an early outcome in infants with MIS diagnosed postnatally due to the vertical transmission of SARS-CoV2 infection and may represent a new challenge for pediatricians in the pandemic era.
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Terciu et al. (2023) conducted a case report in Multisystem inflammatory syndrome (MIS) (n=3). Prenatal maternal COVID-19 infection was evaluated on Subclinical myocarditis and elevated myocardial biomarkers. In a series of three neonates, prenatal maternal COVID-19 infection was associated with multisystem inflammatory syndrome presenting as subclinical myocarditis with elevated myocardial biomarkers.
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