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Intravenous immunoglobulin-resistant Kawasaki disease: Risk factors in children in a middle-income country

BACKGROUND: Identifying risk factors in patients with intravenous immunoglobulin (IVIG) resistance Kawasaki disease (KD) is vital in managing and preventing coronary artery aneurysms (CAAs). We aimed to study the risk factors for IVIG resistance KD in Malaysian children. METHODS: This retrospective...

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Autores principales: Zahari, Norazah, Bah, Mohd Nizam Mat, Sulieman, Muhamad Faiz, Choo, Hung Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522152/
https://www.ncbi.nlm.nih.gov/pubmed/37767168
http://dx.doi.org/10.4103/apc.apc_159_22
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author Zahari, Norazah
Bah, Mohd Nizam Mat
Sulieman, Muhamad Faiz
Choo, Hung Liang
author_facet Zahari, Norazah
Bah, Mohd Nizam Mat
Sulieman, Muhamad Faiz
Choo, Hung Liang
author_sort Zahari, Norazah
collection PubMed
description BACKGROUND: Identifying risk factors in patients with intravenous immunoglobulin (IVIG) resistance Kawasaki disease (KD) is vital in managing and preventing coronary artery aneurysms (CAAs). We aimed to study the risk factors for IVIG resistance KD in Malaysian children. METHODS: This retrospective observational study of children with KD was conducted at two tertiary hospitals in Malaysia from January 2014 to December 2019. Multivariable binary logistic regression was used to analyze the risk factors associated with IVIG resistance. RESULTS: A total of 174 patients, 118 males (67.8%) with a median age of 1.4-year-old (interquartile range: 0.1–12.1-year-old), were analyzed. Early (<5 days) and late (>10 days) IVIG treatments were observed in 14 (8.1%) and 19 (11.0%), respectively. Thirty-two patients (18.4%) had IVIG resistance. The independent factors associated with IVIG resistance were high white cell count, hypoalbuminemia, and extremities changes with an odd ratio of 4.7, 3.0, and 4.0, respectively. In addition, CAA was significantly higher in IVIG resistance compared to IVIG responder patients (57.5% [19/33] vs. 23.4% [33/141], P < 0.001). The sensitivity was high in Harada (93.8%) but low in Kobayashi and Egami (46.9% and 34.4%, respectively). The specificity was high with Egami (79.6%) but low in Harada and Kobayashi (22.5% and 64.1%, respectively). CONCLUSION: Leukocytosis, hypoalbuminemia, and extremities changes were independent risk factors for IVIG resistance. The variation in sensitivity and specificity of the Japanese scoring makes it unsuitable for predicting IVIG resistance in Malaysian children.
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spelling pubmed-105221522023-09-27 Intravenous immunoglobulin-resistant Kawasaki disease: Risk factors in children in a middle-income country Zahari, Norazah Bah, Mohd Nizam Mat Sulieman, Muhamad Faiz Choo, Hung Liang Ann Pediatr Cardiol Original Article BACKGROUND: Identifying risk factors in patients with intravenous immunoglobulin (IVIG) resistance Kawasaki disease (KD) is vital in managing and preventing coronary artery aneurysms (CAAs). We aimed to study the risk factors for IVIG resistance KD in Malaysian children. METHODS: This retrospective observational study of children with KD was conducted at two tertiary hospitals in Malaysia from January 2014 to December 2019. Multivariable binary logistic regression was used to analyze the risk factors associated with IVIG resistance. RESULTS: A total of 174 patients, 118 males (67.8%) with a median age of 1.4-year-old (interquartile range: 0.1–12.1-year-old), were analyzed. Early (<5 days) and late (>10 days) IVIG treatments were observed in 14 (8.1%) and 19 (11.0%), respectively. Thirty-two patients (18.4%) had IVIG resistance. The independent factors associated with IVIG resistance were high white cell count, hypoalbuminemia, and extremities changes with an odd ratio of 4.7, 3.0, and 4.0, respectively. In addition, CAA was significantly higher in IVIG resistance compared to IVIG responder patients (57.5% [19/33] vs. 23.4% [33/141], P < 0.001). The sensitivity was high in Harada (93.8%) but low in Kobayashi and Egami (46.9% and 34.4%, respectively). The specificity was high with Egami (79.6%) but low in Harada and Kobayashi (22.5% and 64.1%, respectively). CONCLUSION: Leukocytosis, hypoalbuminemia, and extremities changes were independent risk factors for IVIG resistance. The variation in sensitivity and specificity of the Japanese scoring makes it unsuitable for predicting IVIG resistance in Malaysian children. Wolters Kluwer - Medknow 2023 2023-08-16 /pmc/articles/PMC10522152/ /pubmed/37767168 http://dx.doi.org/10.4103/apc.apc_159_22 Text en Copyright: © 2023 Annals of Pediatric Cardiology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Zahari, Norazah
Bah, Mohd Nizam Mat
Sulieman, Muhamad Faiz
Choo, Hung Liang
Intravenous immunoglobulin-resistant Kawasaki disease: Risk factors in children in a middle-income country
title Intravenous immunoglobulin-resistant Kawasaki disease: Risk factors in children in a middle-income country
title_full Intravenous immunoglobulin-resistant Kawasaki disease: Risk factors in children in a middle-income country
title_fullStr Intravenous immunoglobulin-resistant Kawasaki disease: Risk factors in children in a middle-income country
title_full_unstemmed Intravenous immunoglobulin-resistant Kawasaki disease: Risk factors in children in a middle-income country
title_short Intravenous immunoglobulin-resistant Kawasaki disease: Risk factors in children in a middle-income country
title_sort intravenous immunoglobulin-resistant kawasaki disease: risk factors in children in a middle-income country
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522152/
https://www.ncbi.nlm.nih.gov/pubmed/37767168
http://dx.doi.org/10.4103/apc.apc_159_22
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