Evidence map›Paper›PMID 41864993›Full record

ArticleItalian journal of pediatrics2026

Retrospective study: clinical analysis of Kawasaki disease complicated with macrophage activation syndrome.

Wenhui Bie, Yuqiang Guan, Qingxia Du, Lei Li, Peiru Yu

Abstract read
In one paragraph

Article in Italian journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Wenhui BieDepartment of Cardiovascular Medicine, Jinan Children's Hospital, Jinan, 250022, China.ORCID http://orcid.org/0009-0003-4825-726X
Yuqiang GuanDepartment of Cardiovascular Medicine, Jinan Children's Hospital, Jinan, 250022, China.
Qingxia DuDepartment of Cardiovascular Medicine, Jinan Children's Hospital, Jinan, 250022, China.
Lei LiDepartment of Cardiovascular Medicine, Jinan Children's Hospital, Jinan, 250022, China.
Peiru YuDepartment of Cardiovascular Medicine, Jinan Children's Hospital, Jinan, 250022, China. 187262518@qq.com.

Funding

Science and Technology Development Program of Jinan Municipal Health Commission 2023-2-140
6 · The paper itself

Abstract

backgroundKawasaki disease complicated with macrophage activation syndrome (KD-MAS) has the characteristics of low incidence, high rate of sequelae, and high mortality. We aims to explore early warning indicators that can be used for the diagnosis of KD-MAS, providing a reference basis for early clinical intervention.

methodsThe clinical data of 15 children with KD-MAS and 140 children with Kawasaki disease (KD) admitted to Jinan Children’s Hospital from January 2020 to March 2025 were retrospectively collected, and statistical analysis was conducted on the above data of the KD-MAS group and the KD group.

resultsThere were no statistically significant differences between the two groups in terms of gender ratio, the proportion of incomplete Kawasaki disease, the incidence of coronary artery lesion, peripheral blood white blood cell(WBC) count, neutrophil ratio(N%), C-reactive protein(CRP), serum total bilirubin(STB) and serum potassium༈K+༉ level (P > 0.05). The age of onset in the KD-MAS group was significantly younger than that in the KD group, and the hospitalization time was longer (P < 0.05). Among the 9 KD-MAS children who completed bone marrow smear examination, 6 showed hemolysis phenomenon.The incidence of hepatosplenomegaly, organ damage, and insensitivity to intravenous immunoglobulin (IVIG) was higher in the KD-MAS group than in the KD group (P < 0.05).The levels of serum ferritin(SF), alanine aminotransferase(ALT), aspartate aminotransferase(AST), lactate dehydrogenase(LDH) and triglyceride(TG) in the KD-MAS group were higher than those in the KD group, while the levels of hemoglobin(HB), platelet(PLT) count, serum albumin(ALB), erythrocyte sedimentation rate(ESR), fibrinogen(FIB) and serum natrium(Na+) level were lower than those in the KD group (P < 0.05).The ROC curve analysis showed that the AUC values for indicators such as hepatomegaly, no response to IVIG treatment, SF, AST, FIB, PLT count, ALT, LDH, TG, and HB were all relatively high.

conclusionWhen children with KD show significant elevation of SF, hepatomegaly or no response to IVIG treatment, the possibility of concurrent MAS should be vigilant. Moreover, the simultaneous increase of AST, ALT, LDH and TG, along with the decrease of HB, PLT and FIB, has certain clinical significance in suggesting the occurrence of MAS.

Indexed as

Macrophage Activation SyndromeMucocutaneous Lymph Node SyndromeChild, PreschoolFemaleHumansImmunoglobulins, IntravenousInfantMaleRetrospective StudiesImmunoglobulins, IntravenousChildrenKawasaki diseaseMacrophage activation syndrome

Identifiers

PMID41864993
PMCPMC13130574

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