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Published on: January 14, 2014
Correlation of Clinical and Laboratory Features of Multisystem Inflammatory Syndrome in Children with
Nenad Barišić1,2, Gordana Vijatov-Đurić1,2, Borko Milanović1,2
1Faculty of Medicine, University of Novi Sad, Hajduk Veljkova 3, 21000 Novi Sad, Serbia.
Insights
In children with Multisystem Inflammatory Syndrome, high fever and blood urea nitrogen levels predict abnormal echocardiograms. High-sensitivity troponin I did not show significant predictive value for cardiac findings in MIS-C patients.
Area of Science:
- Pediatric Cardiology
- Pediatric Infectious Diseases
- Pediatric Critical Care Medicine
Background:
- Multisystem Inflammatory Syndrome (MIS-C) is a serious condition affecting children.
- Echocardiography is crucial for assessing cardiac involvement in MIS-C.
- Identifying predictors of echocardiographic abnormalities is vital for timely intervention.
Purpose of the Study:
- To determine clinical and laboratory markers predicting abnormal echocardiographic findings in pediatric MIS-C.
- To evaluate the correlation of high-sensitivity troponin I with echocardiographic outcomes.
- To assess the predictive value of blood urea nitrogen and fever severity.
Main Methods:
- Retrospective analysis of 61 children (0-18 years) diagnosed with MIS-C.
- Comparison of clinical and laboratory data between normal and abnormal echocardiography groups.
- Statistical analysis including point-biserial correlation and logistic regression.
Main Results:
- Elevated high-sensitivity troponin I was found in 65.57% of MIS-C patients, but did not significantly correlate with echocardiographic findings.
- Blood urea nitrogen levels and high fever showed a statistically significant positive correlation with abnormal echocardiographic findings.
- Logistic regression identified blood urea nitrogen and fever as significant predictors (p=0.002 and p=0.013, respectively).
Conclusions:
- Blood urea nitrogen levels and high fever are significant predictors of abnormal echocardiographic findings in pediatric MIS-C.
- High-sensitivity troponin I levels are not reliable predictors of cardiac abnormalities in MIS-C.
- These findings aid in risk stratification and management of children with MIS-C.
Abstract:
Background and Objectives: The aim of this study was to identify clinical features and laboratory findings that correlate with and predict pathological echocardiographic findings in children diagnosed with Multisystem Inflammatory Syndrome. Materials and Methods: Retrospective study included all patients aged 0-18 diagnosed with Multisystem Inflammatory Syndrome and hospitalized at our clinic from July 2020 to December 2022. The clinical and laboratory data of 61 patients were studied and compared between two subgroups (normal/abnormal echocardiography). Results: Elevated values of high-sensitivity troponin I were observed in 65.57% patients with MIS-C. The mean high-sensitivity troponin I value in the whole sample was 400.89 ± 1989.31 pg/mL. In patients with pathological echocardiographic findings, the mean value was 1240.24 ± 3609 pg/mL, while in patients with normal echocardiographic findings, it was 52.87 ± 71.86 pg/mL. Even though mean value was higher in the group of patients with abnormal echocardiography, no statistically significant difference was observed between high-sensitivity troponin I values in patients with and without pathological echocardiographic findings. Troponin levels were not in good correlation with pathological echocardiographic findings (point-biserial correlation; rpb = 0.25, p = 0.054) and were not good predictors of pathological echocardiographic findings (logistic regression; Chi2 = 3.77, p = 0.052). Logistic regression showed significant positive correlation of blood urea nitrogen levels and the degree of fever with abnormal echocardiographic findings (Chi2 = 10.04, p 0.002/Chi2 = 6.10, p = 0.013, respectively). Conclusions: Only blood urea nitrogen levels and high fever showed statistically significant correlation and predictive value for abnormal echocardiographic findings in children with Multisystem Inflammatory Syndrome. High sensitive troponin I had no significant power to discriminate between normal and abnormal echocardiographic findings.
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