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[The expert consensus on diagnosis and acute-phase treatment of Kawasaki disease].[川崎病诊断与急性期治疗专家共识]
Zhonghua Er Ke Za Zhi. 2022 Jan 2;60(1):6-13. doi: 10.3760/cma.j.cn112140-20211018-00879.
2
[Challenges in the diagnosis and treatment of Kawasaki disease].[川崎病诊断与治疗中的挑战]
Zhonghua Er Ke Za Zhi. 2022 Jan 2;60(1):3-5. doi: 10.3760/cma.j.cn112140-20211104-00927.
3
JCS/JSCS 2020 Guideline on Diagnosis and Management of Cardiovascular Sequelae in Kawasaki Disease.《日本循环学会/日本小儿循环学会2020年川崎病心血管后遗症诊断与管理指南》
Circ J. 2020 Jul 22;84(8):1348-1407. doi: 10.1253/circj.CJ-19-1094. Epub 2020 Jul 8.
4
Procalcitonin as a Biomarker of Unresponsiveness to Intravenous Immunoglobulin for Kawasaki Disease.降钙素原作为川崎病静脉注射免疫球蛋白无反应的生物标志物。
Pediatr Infect Dis J. 2020 Sep;39(9):857-861. doi: 10.1097/INF.0000000000002716.
5
Risk Factors of Intravenous Immunoglobulin Resistance in Children With Kawasaki Disease: A Meta-Analysis of Case-Control Studies.川崎病患儿静脉注射免疫球蛋白抵抗的危险因素:病例对照研究的Meta分析
Front Pediatr. 2020 Apr 21;8:187. doi: 10.3389/fped.2020.00187. eCollection 2020.
6
Platelet Count Variation and Risk for Coronary Artery Abnormalities in Kawasaki Disease.血小板计数变化与川崎病冠状动脉异常风险的关系。
Pediatr Infect Dis J. 2020 Mar;39(3):197-203. doi: 10.1097/INF.0000000000002563.
7
Predictors of intravenous immunoglobulin-resistant Kawasaki disease in children: a meta-analysis of 4442 cases.预测儿童静脉注射免疫球蛋白抵抗川崎病的因素:4442 例病例的荟萃分析。
Eur J Pediatr. 2018 Aug;177(8):1279-1292. doi: 10.1007/s00431-018-3182-2. Epub 2018 Jun 8.
8
Predictors of Intravenous Immunoglobulin Nonresponse and Racial Disparities in Kawasaki Disease.川崎病静脉注射免疫球蛋白无反应的预测因素及种族差异。
Pediatr Infect Dis J. 2018 Dec;37(12):1227-1234. doi: 10.1097/INF.0000000000002019.
9
Factors Predicting Resistance to Intravenous Immunoglobulin Treatment and Coronary Artery Lesion in Patients with Kawasaki Disease: Analysis of the Korean Nationwide Multicenter Survey from 2012 to 2014.川崎病患者静脉注射免疫球蛋白治疗抵抗及冠状动脉病变的预测因素:2012年至2014年韩国全国多中心调查分析
Korean Circ J. 2018 Jan;48(1):71-79. doi: 10.4070/kcj.2017.0136. Epub 2017 Nov 9.
10
Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association.川崎病的诊断、治疗和长期管理:美国心脏协会发布的一份面向医疗保健专业人员的科学声明。
Circulation. 2017 Apr 25;135(17):e927-e999. doi: 10.1161/CIR.0000000000000484. Epub 2017 Mar 29.

[川崎病急性期肝损伤与冠状动脉病变及静脉注射免疫球蛋白无反应的相关性]

[Association of liver damage with coronary artery lesion and no response to intravenous immunoglobulin in the acute stage of Kawasaki disease].

作者信息

Hu Hui-Min, Chen Xiao-Zheng, Zhang Yong-Lan, DU Zhong-Dong

机构信息

Department of Cardiology, Beijing Children's Hospital, Capital Medical University/National Center for Children's Health, Beijing 100045, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2022 Jun 15;24(6):681-686. doi: 10.7499/j.issn.1008-8830.2112094.

DOI:10.7499/j.issn.1008-8830.2112094
PMID:35762436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9250406/
Abstract

OBJECTIVES

To summarize the clinical features of liver damage in children in the acute stage of Kawasaki disease (KD), and to investigate the clinical value of liver damage in predicting coronary artery lesion and no response to intravenous immunoglobulin (IVIG) in children with KD.

METHODS

The medical data were collected from 925 children who were diagnosed with KD for the first time in Beijing Children's Hospital from January 1, 2016 to December 31, 2017. According to the presence or absence of abnormal alanine aminotransferase (ALT) level on admission, the children were divided into a liver damage group (=284) and a non-liver damage group (=641). A logistic regression analysis was used to investigate the clinical value of the indicators including liver damage in predicting coronary artery lesion and no response to IVIG in children with KD.

RESULTS

Compared with the non-liver damage group, the liver damage group had a significantly earlier admission time and significantly higher serum levels of inflammatory indicators (<0.05). The liver damage group had a significantly higher incidence rate of coronary artery lesion on admission than the non-liver damage group (=0.034). After initial IVIG therapy, the liver damage group had a significantly higher proportion of children with no response to IVIG than the non-liver damage group (<0.001). In children with KD, coronary artery lesion was associated with the reduction in the hemoglobin level and the increases in platelet count, C-reactive protein, and ALT (<0.05), and no response to IVIG was associated with limb changes, the reduction in the hemoglobin level, the increases in platelet count, C-reactive protein, and ALT, and coronary artery lesion (<0.05).

CONCLUSIONS

Compared with those without liver damage, the children in the early stage of KD with liver damage tend to develop clinical symptoms early and have higher levels of inflammatory indicators, and they are more likely to have coronary artery lesion and show no response to IVIG treatment.

摘要

目的

总结川崎病(KD)急性期儿童肝损伤的临床特征,并探讨肝损伤对预测KD患儿冠状动脉病变及静脉注射免疫球蛋白(IVIG)无反应的临床价值。

方法

收集2016年1月1日至2017年12月31日在北京儿童医院首次诊断为KD的925例患儿的病历资料。根据入院时丙氨酸氨基转移酶(ALT)水平是否异常,将患儿分为肝损伤组(n = 284)和非肝损伤组(n = 641)。采用logistic回归分析探讨包括肝损伤在内的各项指标对预测KD患儿冠状动脉病变及IVIG无反应的临床价值。

结果

与非肝损伤组相比,肝损伤组入院时间明显更早,炎症指标血清水平明显更高(P<0.05)。肝损伤组入院时冠状动脉病变发生率明显高于非肝损伤组(P = 0.034)。初始IVIG治疗后,肝损伤组IVIG无反应患儿的比例明显高于非肝损伤组(P<0.001)。在KD患儿中,冠状动脉病变与血红蛋白水平降低、血小板计数、C反应蛋白和ALT升高有关(P<0.05),IVIG无反应与肢体变化、血红蛋白水平降低、血小板计数、C反应蛋白和ALT升高以及冠状动脉病变有关(P<0.05)。

结论

与无肝损伤的患儿相比,KD早期有肝损伤的患儿临床症状出现较早,炎症指标水平较高,更易发生冠状动脉病变且对IVIG治疗无反应。