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Treatment of immunoglobulin-resistant kawasaki disease: a Bayesian network meta-analysis of different regimens
BACKGROUND: This study aimed to gather evidence from clinical trials on the efficacy and safety of the available treatments for intravenous immunoglobulin (IVIG)-resistant Kawasaki disease (KD) in children. METHODS: This work adopted the Newcastle–Ottawa scale to analyse the quality of the enrolled...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373588/ https://www.ncbi.nlm.nih.gov/pubmed/37520059 http://dx.doi.org/10.3389/fped.2023.1149519 |
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author | Pan, Yan Fan, Qihong Hu, Luoyi |
author_facet | Pan, Yan Fan, Qihong Hu, Luoyi |
author_sort | Pan, Yan |
collection | PubMed |
description | BACKGROUND: This study aimed to gather evidence from clinical trials on the efficacy and safety of the available treatments for intravenous immunoglobulin (IVIG)-resistant Kawasaki disease (KD) in children. METHODS: This work adopted the Newcastle–Ottawa scale to analyse the quality of the enrolled articles. A network meta-analysis was performed using clinical trials that compared drugs used to treat IVIG-resistant KD. Aggregate Data Drug Information System software v.1.16.5 was employed to analyse whether infliximab, second IVIG infusions, and intravenous pulse methylprednisolone (IVMP) were safe and effective. RESULTS: Ten studies, involving 704 patients with IVIG-resistant KD, were identified and analysed. Overall, infliximab exhibited remarkable antipyretic activity compared with the second IVIG infusions (2.46, 1.00–6.94). According to the drug rank, infliximab was the best option against IVIG-resistant KD. Regarding adverse effects, the infliximab group was more prone to hepatomegaly. A second IVIG infusion was more likely to result in haemolytic anaemia. IVMP treatment was more susceptible to bradycardia, hyperglycaemia, hypertension, and hypothermia. In addition, infliximab, IVMP, and the second IVIG infusions showed no significant differences in the risk of developing a coronary artery aneurysm (CAA). CONCLUSION: Infliximab was the best option against IVIG-resistant KD, and IVMP, infliximab, and second IVIG infusions have not significant differences of prevent CAA in patients with IVIG-resistant KD. SYSTEMATIC REVIEW REGISTRATION: Identifier: https://osf.io/3894y. |
format | Online Article Text |
id | pubmed-10373588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103735882023-07-28 Treatment of immunoglobulin-resistant kawasaki disease: a Bayesian network meta-analysis of different regimens Pan, Yan Fan, Qihong Hu, Luoyi Front Pediatr Pediatrics BACKGROUND: This study aimed to gather evidence from clinical trials on the efficacy and safety of the available treatments for intravenous immunoglobulin (IVIG)-resistant Kawasaki disease (KD) in children. METHODS: This work adopted the Newcastle–Ottawa scale to analyse the quality of the enrolled articles. A network meta-analysis was performed using clinical trials that compared drugs used to treat IVIG-resistant KD. Aggregate Data Drug Information System software v.1.16.5 was employed to analyse whether infliximab, second IVIG infusions, and intravenous pulse methylprednisolone (IVMP) were safe and effective. RESULTS: Ten studies, involving 704 patients with IVIG-resistant KD, were identified and analysed. Overall, infliximab exhibited remarkable antipyretic activity compared with the second IVIG infusions (2.46, 1.00–6.94). According to the drug rank, infliximab was the best option against IVIG-resistant KD. Regarding adverse effects, the infliximab group was more prone to hepatomegaly. A second IVIG infusion was more likely to result in haemolytic anaemia. IVMP treatment was more susceptible to bradycardia, hyperglycaemia, hypertension, and hypothermia. In addition, infliximab, IVMP, and the second IVIG infusions showed no significant differences in the risk of developing a coronary artery aneurysm (CAA). CONCLUSION: Infliximab was the best option against IVIG-resistant KD, and IVMP, infliximab, and second IVIG infusions have not significant differences of prevent CAA in patients with IVIG-resistant KD. SYSTEMATIC REVIEW REGISTRATION: Identifier: https://osf.io/3894y. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10373588/ /pubmed/37520059 http://dx.doi.org/10.3389/fped.2023.1149519 Text en © 2023 Pan, Fan and Hu. 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 Pan, Yan Fan, Qihong Hu, Luoyi Treatment of immunoglobulin-resistant kawasaki disease: a Bayesian network meta-analysis of different regimens |
title | Treatment of immunoglobulin-resistant kawasaki disease: a Bayesian network meta-analysis of different regimens |
title_full | Treatment of immunoglobulin-resistant kawasaki disease: a Bayesian network meta-analysis of different regimens |
title_fullStr | Treatment of immunoglobulin-resistant kawasaki disease: a Bayesian network meta-analysis of different regimens |
title_full_unstemmed | Treatment of immunoglobulin-resistant kawasaki disease: a Bayesian network meta-analysis of different regimens |
title_short | Treatment of immunoglobulin-resistant kawasaki disease: a Bayesian network meta-analysis of different regimens |
title_sort | treatment of immunoglobulin-resistant kawasaki disease: a bayesian network meta-analysis of different regimens |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373588/ https://www.ncbi.nlm.nih.gov/pubmed/37520059 http://dx.doi.org/10.3389/fped.2023.1149519 |
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