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Immunosuppressive Treatment for Myocarditis in the Pediatric Population: A Meta-Analysis

The use of immunosuppressants in the treatment of myocarditis in children remains controversial. The aim of this meta-analysis is to summarize the current empirical evidence for immunosuppressive treatment for myocarditis in the pediatric population. We searched PubMed, MEDLINE, and Embase for artic...

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Autores principales: He, Bing, Li, Xiaoou, Li, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873897/
https://www.ncbi.nlm.nih.gov/pubmed/31803693
http://dx.doi.org/10.3389/fped.2019.00430
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author He, Bing
Li, Xiaoou
Li, Dan
author_facet He, Bing
Li, Xiaoou
Li, Dan
author_sort He, Bing
collection PubMed
description The use of immunosuppressants in the treatment of myocarditis in children remains controversial. The aim of this meta-analysis is to summarize the current empirical evidence for immunosuppressive treatment for myocarditis in the pediatric population. We searched PubMed, MEDLINE, and Embase for articles to identify studies analyzing the efficiency of immunosuppressive treatment in the pediatric population. Pooled estimates were generated using fixed- or random-effect models. Heterogeneity within studies was assessed using Cochran's Q and I(2) statistics. Funnel plots and Begg's rank correlation method were constructed to evaluate publication bias. Sensitivity analyses were also conducted to evaluate the potential sources of heterogeneity. After a detailed screening of 159 studies, six separate studies were identified, with 181 patients in the immunosuppressive treatment group, and 199 in the conventional treatment group. The immunosuppressive treatment group showed a significant improvement in left ventricular ejection fraction (LVEF) [mean difference 1.10; 95% CI: 0.41, 1.79] and significantly decreased left ventricular end-diastolic dimension (LVEDD) [mean difference −0.77 mm, 95% CI: −1.35 to −0.20 mm] when compared to the conventional treatment group. Furthermore, the risk of death and heart transplant in conventional treatment was significantly higher than in the immunosuppressive treatment group [relative risk (RR): 4.74; 95% CI: 2.69, 8.35]. No significant heterogeneity across the studies was observed. There was no evidence of publication bias when assessed by Begg's test. Conclusions: There may be a possible benefit, in the short term, to the addition of immunosuppressive therapy in the management of myocarditis in the pediatric population. However, further prospective investigation is warranted to validate this finding.
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spelling pubmed-68738972019-12-04 Immunosuppressive Treatment for Myocarditis in the Pediatric Population: A Meta-Analysis He, Bing Li, Xiaoou Li, Dan Front Pediatr Pediatrics The use of immunosuppressants in the treatment of myocarditis in children remains controversial. The aim of this meta-analysis is to summarize the current empirical evidence for immunosuppressive treatment for myocarditis in the pediatric population. We searched PubMed, MEDLINE, and Embase for articles to identify studies analyzing the efficiency of immunosuppressive treatment in the pediatric population. Pooled estimates were generated using fixed- or random-effect models. Heterogeneity within studies was assessed using Cochran's Q and I(2) statistics. Funnel plots and Begg's rank correlation method were constructed to evaluate publication bias. Sensitivity analyses were also conducted to evaluate the potential sources of heterogeneity. After a detailed screening of 159 studies, six separate studies were identified, with 181 patients in the immunosuppressive treatment group, and 199 in the conventional treatment group. The immunosuppressive treatment group showed a significant improvement in left ventricular ejection fraction (LVEF) [mean difference 1.10; 95% CI: 0.41, 1.79] and significantly decreased left ventricular end-diastolic dimension (LVEDD) [mean difference −0.77 mm, 95% CI: −1.35 to −0.20 mm] when compared to the conventional treatment group. Furthermore, the risk of death and heart transplant in conventional treatment was significantly higher than in the immunosuppressive treatment group [relative risk (RR): 4.74; 95% CI: 2.69, 8.35]. No significant heterogeneity across the studies was observed. There was no evidence of publication bias when assessed by Begg's test. Conclusions: There may be a possible benefit, in the short term, to the addition of immunosuppressive therapy in the management of myocarditis in the pediatric population. However, further prospective investigation is warranted to validate this finding. Frontiers Media S.A. 2019-11-15 /pmc/articles/PMC6873897/ /pubmed/31803693 http://dx.doi.org/10.3389/fped.2019.00430 Text en Copyright © 2019 He, Li and Li. 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
He, Bing
Li, Xiaoou
Li, Dan
Immunosuppressive Treatment for Myocarditis in the Pediatric Population: A Meta-Analysis
title Immunosuppressive Treatment for Myocarditis in the Pediatric Population: A Meta-Analysis
title_full Immunosuppressive Treatment for Myocarditis in the Pediatric Population: A Meta-Analysis
title_fullStr Immunosuppressive Treatment for Myocarditis in the Pediatric Population: A Meta-Analysis
title_full_unstemmed Immunosuppressive Treatment for Myocarditis in the Pediatric Population: A Meta-Analysis
title_short Immunosuppressive Treatment for Myocarditis in the Pediatric Population: A Meta-Analysis
title_sort immunosuppressive treatment for myocarditis in the pediatric population: a meta-analysis
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873897/
https://www.ncbi.nlm.nih.gov/pubmed/31803693
http://dx.doi.org/10.3389/fped.2019.00430
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