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Evaluation of late cardiac effects after multisystem inflammatory syndrome in children
Rik De Wolf1, Mahmoud Zaqout2,3, Kaoru Tanaka4
1Department of Pediatric Cardiology, University Hospital Brussels, Brussels, Belgium.
Insights
Most children recover fully from cardiac issues following Multisystem Inflammatory Syndrome in Children (MIS-C). However, some may experience persistent subclinical myocardial dysfunction, requiring ongoing monitoring.
Area of Science:
- Pediatric Cardiology
- Infectious Diseases
- Cardiovascular Medicine
Background:
- Multisystem Inflammatory Syndrome in Children (MIS-C) can cause significant cardiac problems during the acute phase.
- While most children recover, some may have lasting mid-term cardiac effects.
- Assessing late cardiac outcomes in MIS-C patients is crucial for understanding long-term health.
Purpose of the Study:
- To evaluate the late cardiac outcomes in children diagnosed with MIS-C.
- To identify any persistent cardiac sequelae after MIS-C.
- To assess the effectiveness of current treatment guidelines on long-term cardiac health.
Main Methods:
- A prospective observational multicenter study included 36 children with MIS-C and cardiac involvement.
- Follow-up assessments included NT-proBNP, echocardiography, 24-h Holter monitoring, and cardiac MRI (CMR) at least 6 months post-diagnosis.
- Cardiac function, coronary arteries, and myocardial scarring were evaluated.
Main Results:
- At diagnosis, 39% had reduced left ventricular ejection fraction (LVEF) and 36% had ECG abnormalities.
- At a mean follow-up of 12.1 months, most cardiac parameters normalized.
- However, 35% showed decreased LV global longitudinal strain (GLS), indicating subclinical myocardial dysfunction. One patient required heart transplantation due to severe fibrosis.
Conclusions:
- Late cardiac outcomes for MIS-C patients treated with current guidelines are generally excellent.
- Cardiac MRI revealed no myocardial scarring in children with normal systolic LV function.
- A subset of patients may experience persistent subclinical myocardial dysfunction (decreased GLS) requiring further investigation.
Introduction:
Multisystem inflammatory syndrome in children (MIS-C) is associated with important cardiovascular morbidity during the acute phase. Follow-up shows a swift recovery of cardiac abnormalities in most patients. However, a small portion of patients has persistent cardiac sequelae at mid-term. The goal of our study was to assess late cardiac outcomes of MIS-C.
Methods:
A prospective observational multicenter study was performed in children admitted with MIS-C and cardiac involvement between April 2020 and March 2022. A follow-up by NT-proBNP measurement, echocardiography, 24-h Holter monitoring, and cardiac MRI (CMR) was performed at least 6 months after MIS-C diagnosis.
Results:
We included 36 children with a median age of 10 (8.0-11.0) years, and among them, 21 (58%) were girls. At diagnosis, all patients had an elevated NT-proBNP, and 39% had a decreased left ventricular ejection fraction (LVEF) (<55%). ECG abnormalities were present in 13 (36%) patients, but none presented with arrhythmia. Almost two-thirds of patients (58%) had echocardiographic abnormalities such as coronary artery dilation (20%), pericardial effusion (17%), and mitral valve insufficiency (14%). A decreased echocardiographic systolic left ventricular (LV) function was detected in 14 (39%) patients. A follow-up visit was done at a mean time of 12.1 (±5.8) months (range 6-28 months). The ECG normalized in all except one, and no arrhythmias were detected on 24-h Holter monitoring. None had persistent coronary artery dilation or pericardial effusion. The NT-proBNP level and echocardiographic systolic LV function normalized in all patients, except for one, who had a severely reduced EF. The LV global longitudinal strain (GLS), as a marker of subclinical myocardial dysfunction, decreased (z < -2) in 35%. CMR identified one patient with severely reduced EF and extensive myocardial fibrosis requiring heart transplantation. None of the other patients had signs of myocardial scarring on CMR.
Conclusion:
Late cardiac outcomes after MIS-C, if treated according to the current guidelines, are excellent. CMR does not show any myocardial scarring in children with normal systolic LV function. However, a subgroup had a decreased GLS at follow-up, possibly as a reflection of persistent subclinical myocardial dysfunction.
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