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Clinical outcome of patients with refractory Kawasaki disease based on treatment modalities
PURPOSE: Although a significant number of reports on new therapeutic options for refractory Kawasaki disease (KD) such as steroid, infliximab, or repeated intravenous immunoglobulin (IVIG) are available, their effectiveness in reducing the prevalence of coronary artery lesions (CAL) remains controve...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Pediatric Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014912/ https://www.ncbi.nlm.nih.gov/pubmed/27610181 http://dx.doi.org/10.3345/kjp.2016.59.8.328 |
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author | Kim, Hyun Jung Lee, Hyo Eun Yu, Jae Won Kil, Hong Ryang |
author_facet | Kim, Hyun Jung Lee, Hyo Eun Yu, Jae Won Kil, Hong Ryang |
author_sort | Kim, Hyun Jung |
collection | PubMed |
description | PURPOSE: Although a significant number of reports on new therapeutic options for refractory Kawasaki disease (KD) such as steroid, infliximab, or repeated intravenous immunoglobulin (IVIG) are available, their effectiveness in reducing the prevalence of coronary artery lesions (CAL) remains controversial. This study aimed to define the clinical characteristics of patients with refractory KD and to assess the effects of adjuvant therapy on patient outcomes. METHODS: We performed a retrospective study of 38 refractory KD patients from January 2012 to March 2015. We divided these patients into 2 groups: group 1 received more than 3 IVIG administration+ steroid therapy, (n=7, 18.4%), and group 2 patients were unresponsive to initial IVIG and required steroid therapy or second IVIG (n=31, 81.6%). We compared the clinical manifestations, laboratory results, and echocardiographic findings between the groups and examined the clinical utility of additional therapies in both groups. RESULTS: A significant difference was found in the total duration of fever between the groups (13.0±4.04 days in group 1 vs. 8.87±2.30 days in group 2; P=0.035). At the end of the follow-up, all cases in group 1 showed suppressed CAL. In group 2, coronary artery aneurysm occurred in 2 patients (6.4 %). All the patients treated with intravenous corticosteroids without additional IVIG developed CALs including coronary artery aneurysms. CONCLUSION: No statistical difference was found in the development of CAL between the groups. Prospective, randomized, clinical studies are needed to elucidate the effects of adjunctive therapy in refractory KD patients. |
format | Online Article Text |
id | pubmed-5014912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Pediatric Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50149122016-09-08 Clinical outcome of patients with refractory Kawasaki disease based on treatment modalities Kim, Hyun Jung Lee, Hyo Eun Yu, Jae Won Kil, Hong Ryang Korean J Pediatr Original Article PURPOSE: Although a significant number of reports on new therapeutic options for refractory Kawasaki disease (KD) such as steroid, infliximab, or repeated intravenous immunoglobulin (IVIG) are available, their effectiveness in reducing the prevalence of coronary artery lesions (CAL) remains controversial. This study aimed to define the clinical characteristics of patients with refractory KD and to assess the effects of adjuvant therapy on patient outcomes. METHODS: We performed a retrospective study of 38 refractory KD patients from January 2012 to March 2015. We divided these patients into 2 groups: group 1 received more than 3 IVIG administration+ steroid therapy, (n=7, 18.4%), and group 2 patients were unresponsive to initial IVIG and required steroid therapy or second IVIG (n=31, 81.6%). We compared the clinical manifestations, laboratory results, and echocardiographic findings between the groups and examined the clinical utility of additional therapies in both groups. RESULTS: A significant difference was found in the total duration of fever between the groups (13.0±4.04 days in group 1 vs. 8.87±2.30 days in group 2; P=0.035). At the end of the follow-up, all cases in group 1 showed suppressed CAL. In group 2, coronary artery aneurysm occurred in 2 patients (6.4 %). All the patients treated with intravenous corticosteroids without additional IVIG developed CALs including coronary artery aneurysms. CONCLUSION: No statistical difference was found in the development of CAL between the groups. Prospective, randomized, clinical studies are needed to elucidate the effects of adjunctive therapy in refractory KD patients. The Korean Pediatric Society 2016-08 2016-08-24 /pmc/articles/PMC5014912/ /pubmed/27610181 http://dx.doi.org/10.3345/kjp.2016.59.8.328 Text en Copyright © 2016 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Hyun Jung Lee, Hyo Eun Yu, Jae Won Kil, Hong Ryang Clinical outcome of patients with refractory Kawasaki disease based on treatment modalities |
title | Clinical outcome of patients with refractory Kawasaki disease based on treatment modalities |
title_full | Clinical outcome of patients with refractory Kawasaki disease based on treatment modalities |
title_fullStr | Clinical outcome of patients with refractory Kawasaki disease based on treatment modalities |
title_full_unstemmed | Clinical outcome of patients with refractory Kawasaki disease based on treatment modalities |
title_short | Clinical outcome of patients with refractory Kawasaki disease based on treatment modalities |
title_sort | clinical outcome of patients with refractory kawasaki disease based on treatment modalities |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014912/ https://www.ncbi.nlm.nih.gov/pubmed/27610181 http://dx.doi.org/10.3345/kjp.2016.59.8.328 |
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