Thromboembolism in children with multisystem inflammatory syndrome: a literature review

Neethu M Menon1, Lakshmi V Srivaths2

  • 1Division of Hematology, Department of Pediatrics, University of Texas Health Science Center at Houston, 7000 Fannin Street, Houston, TX, 77030, USA. Neethu.m.menon@uth.tmc.edu.

Pediatric Research
|January 15, 2022
PubMed

Insights

Thromboembolism (TE) is a serious complication of Multisystem Inflammatory Syndrome in Children (MIS-C) following SARS-CoV-2 infection. This review found TE in 33 children, primarily those aged 12+, highlighting the need for careful risk assessment.

Area of Science:

  • Pediatrics
  • Infectious Diseases
  • Cardiology

Background:

  • Multisystem Inflammatory Syndrome in Children (MIS-C) is a hyperinflammatory condition following SARS-CoV-2 infection.
  • Thromboembolism (TE) is an emerging complication of MIS-C, impacting pediatric patients.
  • Published data on TE in MIS-C patients is limited, necessitating a comprehensive review.

Purpose of the Study:

  • To compile and analyze all reported cases of TE in children diagnosed with MIS-C.
  • To determine the incidence, characteristics, and outcomes of TE in MIS-C.
  • To inform clinical practice regarding TE prevention and management in MIS-C.

Main Methods:

  • Systematic review of published literature on TE as a complication of MIS-C.
  • Inclusion of all reported cases of TE in MIS-C patients.
  • Analysis of patient demographics, TE types, and clinical outcomes.

Main Results:

  • 33 cases of TE were identified in MIS-C patients, with an overall incidence of 1.4-6.5%.
  • TE predominantly affected children aged 12 years and older.
  • Cerebral infarcts constituted one-third of cases; other TE included deep vein thrombosis and pulmonary embolism, with a 9% mortality rate.

Conclusions:

  • TE is a significant complication of MIS-C, associated with considerable morbidity and mortality.
  • Older children (≥12 years) are more frequently affected by TE.
  • Further prospective studies are required to optimize thromboprophylaxis strategies in high-risk MIS-C patients.

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