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Corticosteroids and Intravenous Immunoglobulin in Pediatric Myocarditis: A Meta-Analysis

Background: The efficacy of corticosteroids and intravenous immunoglobulin (IVIG) in pediatric myocarditis remains controversial. Objectives: The authors performed a meta-analysis to assess the therapeutic efficacy of corticosteroids and IVIG in children with myocarditis. Methods: We retrieved the t...

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Autores principales: Li, Yining, Yu, Yuqing, Chen, Selena, Liao, Ying, Du, Junbao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706783/
https://www.ncbi.nlm.nih.gov/pubmed/31475124
http://dx.doi.org/10.3389/fped.2019.00342
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author Li, Yining
Yu, Yuqing
Chen, Selena
Liao, Ying
Du, Junbao
author_facet Li, Yining
Yu, Yuqing
Chen, Selena
Liao, Ying
Du, Junbao
author_sort Li, Yining
collection PubMed
description Background: The efficacy of corticosteroids and intravenous immunoglobulin (IVIG) in pediatric myocarditis remains controversial. Objectives: The authors performed a meta-analysis to assess the therapeutic efficacy of corticosteroids and IVIG in children with myocarditis. Methods: We retrieved the trials on corticosteroids and IVIG therapy, respectively, in pediatric myocarditis from nine databases up to December 2018. Statistical analysis was performed using Review Manager 5.3. Results: Our analysis included 8 studies and 334 pediatric patients. The data demonstrated that children receiving corticosteroids showed no significant improvement on left ventricular ejection fraction (LVEF) from 1 to 8 month-follow-up (MD = 5.17%, 95% CI = −0.26% to 10.60%, P = 0.06), and no significant improvement in death or heart transplantation incidence at the end of follow-up (OR = 1.33, 95% CI = 0.27–6.70, P = 0.73). However, children receiving IVIG revealed a statistically remarkable increase in LVEF at a follow-up over the course of 6 months to 1 year (MD = 18.91%, 95% CI = 11.74–26.08%, P < 0.00001), and a decrease in death or heart transplantation at the end of follow-up (OR = 0.31, 95% CI = 0.12–0.75, P = 0.01). Further comparisons showed that the mortality and heart transplantation rate of children with myocarditis treated with IVIG were significantly lower than those with corticosteroid therapy (t' = 11.336, P < 0.001). Conclusions: IVIG might be beneficial to improve LVEF and survival for myocarditis in children. However, the present evidence does not support corticosteroids as superior to conventional therapy in children with myocarditis. Further randomized controlled trials with a larger sample size are required.
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spelling pubmed-67067832019-08-30 Corticosteroids and Intravenous Immunoglobulin in Pediatric Myocarditis: A Meta-Analysis Li, Yining Yu, Yuqing Chen, Selena Liao, Ying Du, Junbao Front Pediatr Pediatrics Background: The efficacy of corticosteroids and intravenous immunoglobulin (IVIG) in pediatric myocarditis remains controversial. Objectives: The authors performed a meta-analysis to assess the therapeutic efficacy of corticosteroids and IVIG in children with myocarditis. Methods: We retrieved the trials on corticosteroids and IVIG therapy, respectively, in pediatric myocarditis from nine databases up to December 2018. Statistical analysis was performed using Review Manager 5.3. Results: Our analysis included 8 studies and 334 pediatric patients. The data demonstrated that children receiving corticosteroids showed no significant improvement on left ventricular ejection fraction (LVEF) from 1 to 8 month-follow-up (MD = 5.17%, 95% CI = −0.26% to 10.60%, P = 0.06), and no significant improvement in death or heart transplantation incidence at the end of follow-up (OR = 1.33, 95% CI = 0.27–6.70, P = 0.73). However, children receiving IVIG revealed a statistically remarkable increase in LVEF at a follow-up over the course of 6 months to 1 year (MD = 18.91%, 95% CI = 11.74–26.08%, P < 0.00001), and a decrease in death or heart transplantation at the end of follow-up (OR = 0.31, 95% CI = 0.12–0.75, P = 0.01). Further comparisons showed that the mortality and heart transplantation rate of children with myocarditis treated with IVIG were significantly lower than those with corticosteroid therapy (t' = 11.336, P < 0.001). Conclusions: IVIG might be beneficial to improve LVEF and survival for myocarditis in children. However, the present evidence does not support corticosteroids as superior to conventional therapy in children with myocarditis. Further randomized controlled trials with a larger sample size are required. Frontiers Media S.A. 2019-08-16 /pmc/articles/PMC6706783/ /pubmed/31475124 http://dx.doi.org/10.3389/fped.2019.00342 Text en Copyright © 2019 Li, Yu, Chen, Liao and Du. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). 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
Li, Yining
Yu, Yuqing
Chen, Selena
Liao, Ying
Du, Junbao
Corticosteroids and Intravenous Immunoglobulin in Pediatric Myocarditis: A Meta-Analysis
title Corticosteroids and Intravenous Immunoglobulin in Pediatric Myocarditis: A Meta-Analysis
title_full Corticosteroids and Intravenous Immunoglobulin in Pediatric Myocarditis: A Meta-Analysis
title_fullStr Corticosteroids and Intravenous Immunoglobulin in Pediatric Myocarditis: A Meta-Analysis
title_full_unstemmed Corticosteroids and Intravenous Immunoglobulin in Pediatric Myocarditis: A Meta-Analysis
title_short Corticosteroids and Intravenous Immunoglobulin in Pediatric Myocarditis: A Meta-Analysis
title_sort corticosteroids and intravenous immunoglobulin in pediatric myocarditis: a meta-analysis
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706783/
https://www.ncbi.nlm.nih.gov/pubmed/31475124
http://dx.doi.org/10.3389/fped.2019.00342
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