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Evaluation of late cardiac effects after multisystem inflammatory syndrome in children

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-te...

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Autores principales: De Wolf, Rik, Zaqout, Mahmoud, Tanaka, Kaoru, Muiño-Mosquera, Laura, van Berlaer, Gerlant, Vandekerckhove, Kristof, Dewals, Wendy, De Wolf, Daniël
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484557/
https://www.ncbi.nlm.nih.gov/pubmed/37691776
http://dx.doi.org/10.3389/fped.2023.1253608
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author De Wolf, Rik
Zaqout, Mahmoud
Tanaka, Kaoru
Muiño-Mosquera, Laura
van Berlaer, Gerlant
Vandekerckhove, Kristof
Dewals, Wendy
De Wolf, Daniël
author_facet De Wolf, Rik
Zaqout, Mahmoud
Tanaka, Kaoru
Muiño-Mosquera, Laura
van Berlaer, Gerlant
Vandekerckhove, Kristof
Dewals, Wendy
De Wolf, Daniël
author_sort De Wolf, Rik
collection PubMed
description 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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spelling pubmed-104845572023-09-08 Evaluation of late cardiac effects after multisystem inflammatory syndrome in children De Wolf, Rik Zaqout, Mahmoud Tanaka, Kaoru Muiño-Mosquera, Laura van Berlaer, Gerlant Vandekerckhove, Kristof Dewals, Wendy De Wolf, Daniël Front Pediatr Pediatrics 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. Frontiers Media S.A. 2023-08-24 /pmc/articles/PMC10484557/ /pubmed/37691776 http://dx.doi.org/10.3389/fped.2023.1253608 Text en © 2023 De Wolf, Zaqout, Tanaka, Muiño-Mosquera, van Berlaer, Vandekerckhove, Dewals and De Wolf. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
De Wolf, Rik
Zaqout, Mahmoud
Tanaka, Kaoru
Muiño-Mosquera, Laura
van Berlaer, Gerlant
Vandekerckhove, Kristof
Dewals, Wendy
De Wolf, Daniël
Evaluation of late cardiac effects after multisystem inflammatory syndrome in children
title Evaluation of late cardiac effects after multisystem inflammatory syndrome in children
title_full Evaluation of late cardiac effects after multisystem inflammatory syndrome in children
title_fullStr Evaluation of late cardiac effects after multisystem inflammatory syndrome in children
title_full_unstemmed Evaluation of late cardiac effects after multisystem inflammatory syndrome in children
title_short Evaluation of late cardiac effects after multisystem inflammatory syndrome in children
title_sort evaluation of late cardiac effects after multisystem inflammatory syndrome in children
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484557/
https://www.ncbi.nlm.nih.gov/pubmed/37691776
http://dx.doi.org/10.3389/fped.2023.1253608
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