Multisystem inflammatory syndrome in pediatric COVID-19 patients: a meta-analysis

World J Pediatr. 2021 Apr;17(2):141-151. doi: 10.1007/s12519-021-00419-y. Epub 2021 Feb 20.

Abstract

Background: We aimed to systematically review the clinical and laboratory features of patients with the multisystem inflammatory syndrome in pediatrics diagnosed during the COVID-19 pandemic.

Data sources: A literature search in Web of Science, PubMed, Scopus, and Science Direct was made up to June 29, 2020.

Results: Analysis of 15 articles (318 COVID-19 patients) revealed that although many patients presented with the typical multisystem inflammatory syndrome in pediatrics, Kawasaki-like features as fever (82.4%), polymorphous maculopapular exanthema (63.7%), oral mucosal changes (58.1%), conjunctival injections (56.0%), edematous extremities (40.7%), and cervical lymphadenopathy (28.5%), atypical gastrointestinal (79.4%) and neurocognitive symptoms (31.8%) were also common. They had elevated serum lactic acid dehydrogenase, D-dimer, C-reactive protein, procalcitonin, interleukin-6, troponin I levels, and lymphopenia. Nearly 77.0% developed hypotension, and 68.1% went into shock, while 41.1% had acute kidney injury. Intensive care was needed in 73.7% of cases; 13.2% were intubated, and 37.9% required mechanical ventilation. Intravenous immunoglobulins and steroids were given in 87.7% and 56.9% of the patients, respectively, and anticoagulants were utilized in 67.0%. Pediatric patients were discharged after a hospital stay of 6.77 days on average (95% CI 4.93-8.6).

Conclusions: Recognizing the typical and atypical presentation of the multisystem inflammatory syndrome in pediatric COVID-19 patients has important implications in identifying children at risk. Monitoring cardiac and renal decompensation and early interventions in patients with multisystem inflammatory syndrome is critical to prevent further morbidity.

Keywords: COVID-19; Kawasaki-like syndrome; Multisystem inflammatory syndrome in pediatrics; SARS-CoV-2.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Biomarkers / blood
  • COVID-19 / diagnosis*
  • COVID-19 / therapy*
  • Child
  • Critical Care
  • Diagnosis, Differential
  • Humans
  • Pandemics
  • SARS-CoV-2
  • Systemic Inflammatory Response Syndrome / diagnosis*
  • Systemic Inflammatory Response Syndrome / therapy*

Substances

  • Biomarkers

Supplementary concepts

  • pediatric multisystem inflammatory disease, COVID-19 related