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Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection

INTRODUCTION: Kawasaki disease (KD) can be associated with concomitant viral or bacterial infections. Children with persistent or recurrent fever 36 hours after the end of intravenous immunoglobulin (IVIG) are considered to be resistant to treatment and are at increased risk for coronary complicatio...

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Autores principales: Dionne, Audrey, Le, Cathie-Kim, Poupart, Steffany, Autmizguine, Julie, Meloche-Dumas, Léamarie, Turgeon, Jean, Fournier, Anne, Dahdah, Nagib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192641/
https://www.ncbi.nlm.nih.gov/pubmed/30332473
http://dx.doi.org/10.1371/journal.pone.0206001
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author Dionne, Audrey
Le, Cathie-Kim
Poupart, Steffany
Autmizguine, Julie
Meloche-Dumas, Léamarie
Turgeon, Jean
Fournier, Anne
Dahdah, Nagib
author_facet Dionne, Audrey
Le, Cathie-Kim
Poupart, Steffany
Autmizguine, Julie
Meloche-Dumas, Léamarie
Turgeon, Jean
Fournier, Anne
Dahdah, Nagib
author_sort Dionne, Audrey
collection PubMed
description INTRODUCTION: Kawasaki disease (KD) can be associated with concomitant viral or bacterial infections. Children with persistent or recurrent fever 36 hours after the end of intravenous immunoglobulin (IVIG) are considered to be resistant to treatment and are at increased risk for coronary complications. Although concomitant infection does not affect coronary outcome, it is unknown how it influences the response to IVIG treatment. METHODOLOGY: Retrospective cohort study between 2008 and 2016 in a tertiary pediatric university hospital, including 154 children, of which 59 (38%) had concomitant infection. RESULTS: Children with concomitant infection were more likely to have fever 48 hours after initial IVIG treatment (36% vs 20%, p = 0.05) and to be treated with a second dose (33% vs 18%, p = 0.04). Children with infection had higher C-reactive protein at the time of diagnosis (148 vs 112 mg/L, p = 0.04), and 48 hours after IVIG administration (111 vs 59 mg/L, p = 0.003). Nevertheless, there was no statistically significant difference in the prevalence of coronary complications (Z-score > 2.5) between children with and without concomitant infection (36% vs 39%, p = 0.68). CONCLUSION: Children with KD and concomitant infection are more likely to have persistent fever and elevated inflammatory markers after treatment. This association increases the likelihood of receiving a second dose of IVIG but not the risk of coronary complication. Accordingly, prospective studies to distinguish true IVIG resistance from infection induced persistent fever is warranted.
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spelling pubmed-61926412018-11-05 Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection Dionne, Audrey Le, Cathie-Kim Poupart, Steffany Autmizguine, Julie Meloche-Dumas, Léamarie Turgeon, Jean Fournier, Anne Dahdah, Nagib PLoS One Research Article INTRODUCTION: Kawasaki disease (KD) can be associated with concomitant viral or bacterial infections. Children with persistent or recurrent fever 36 hours after the end of intravenous immunoglobulin (IVIG) are considered to be resistant to treatment and are at increased risk for coronary complications. Although concomitant infection does not affect coronary outcome, it is unknown how it influences the response to IVIG treatment. METHODOLOGY: Retrospective cohort study between 2008 and 2016 in a tertiary pediatric university hospital, including 154 children, of which 59 (38%) had concomitant infection. RESULTS: Children with concomitant infection were more likely to have fever 48 hours after initial IVIG treatment (36% vs 20%, p = 0.05) and to be treated with a second dose (33% vs 18%, p = 0.04). Children with infection had higher C-reactive protein at the time of diagnosis (148 vs 112 mg/L, p = 0.04), and 48 hours after IVIG administration (111 vs 59 mg/L, p = 0.003). Nevertheless, there was no statistically significant difference in the prevalence of coronary complications (Z-score > 2.5) between children with and without concomitant infection (36% vs 39%, p = 0.68). CONCLUSION: Children with KD and concomitant infection are more likely to have persistent fever and elevated inflammatory markers after treatment. This association increases the likelihood of receiving a second dose of IVIG but not the risk of coronary complication. Accordingly, prospective studies to distinguish true IVIG resistance from infection induced persistent fever is warranted. Public Library of Science 2018-10-17 /pmc/articles/PMC6192641/ /pubmed/30332473 http://dx.doi.org/10.1371/journal.pone.0206001 Text en © 2018 Dionne et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dionne, Audrey
Le, Cathie-Kim
Poupart, Steffany
Autmizguine, Julie
Meloche-Dumas, Léamarie
Turgeon, Jean
Fournier, Anne
Dahdah, Nagib
Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection
title Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection
title_full Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection
title_fullStr Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection
title_full_unstemmed Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection
title_short Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection
title_sort profile of resistance to ivig treatment in patients with kawasaki disease and concomitant infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192641/
https://www.ncbi.nlm.nih.gov/pubmed/30332473
http://dx.doi.org/10.1371/journal.pone.0206001
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