Coronary artery complications in patients with Kawasaki disease who successfully responded to the standard initial IVIG treatment.

IF 4.3 3区 医学 Q1 PEDIATRICS Archives of Disease in Childhood Pub Date : 2024-11-19 DOI:10.1136/archdischild-2024-327419
Sotaro Takaki, Tohru Kobayashi, Masanari Kuwabara, Naoto Kato, Koki Kosami, Ryusuke Ae
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Abstract

Objectives: To identify clinical characteristics of patients with non-refractory Kawasaki disease (KD), which were defined as those who successfully responded to the standard initial intravenous immunoglobulin (IVIG) treatment (2 g/kg/day, single infusion) without any secondary or later additional specific treatments, and to investigate the factors associated with the development of coronary artery (CA) complications in patients with non-refractory KD.

Design: Retrospective cohort study.

Setting: Hospitals specialising in paediatrics and hospitals with ≥100 beds and a paediatric department throughout Japan.

Patients: A total of 122 489 patients who developed KD across Japan during 2011-2018.

Main outcome measures: CA abnormalities identified after acute illness of KD (defined as CA sequelae).

Results: A total of 69 735 patients with non-refractory KD were identified, of which 672 (0.96%) experienced CA sequelae. Among patients with non-refractory KD, the presence of CA abnormalities identified at initial echocardiographic assessment was strongly associated with CA sequelae (adjusted OR (95% CI): 37.8 (31.9 to 44.7)). CA sequelae was also associated with male patients, infants (<12 months old), older patients (≥60 months old) and patients who received delayed initial IVIG treatment (>7 days from KD onset). Subgroup analyses demonstrated that delayed initial IVIG treatment was significantly associated with the development of CA sequelae in both patients with and without CA abnormalities identified at initial echocardiographic assessment.

Conclusions: Approximately 1% of patients with non-refractory KD may develop CA sequelae. Our findings highlight the importance of initial echocardiographic assessment and early initiation of IVIG treatments for patients with KD.

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对标准初始 IVIG 治疗成功应答的川崎病患者的冠状动脉并发症。
目的:确定非难治性川崎病(KD)患者的临床特征:确定非难治性川崎病(KD)患者的临床特征,非难治性川崎病是指对标准初始静脉注射免疫球蛋白(IVIG)治疗(2克/千克/天,单次输注)成功应答,且未接受任何二次或后期额外特定治疗的患者;研究非难治性川崎病患者发生冠状动脉(CA)并发症的相关因素:设计:回顾性队列研究:背景:日本全国的儿科专科医院和床位数≥100张且设有儿科的医院:主要结果测量指标:KD急性期后发现的CA异常(定义为CA后遗症):共发现69 735例非难治性KD患者,其中672例(0.96%)出现CA后遗症。在非难治性 KD 患者中,初次超声心动图评估发现的 CA 异常与 CA 后遗症密切相关(调整 OR (95% CI):37.8 (31.9 至 44.7))。CA后遗症还与男性患者和婴儿(距KD发病7天)有关。亚组分析表明,在初次超声心动图评估时发现CA异常和未发现CA异常的患者中,初次IVIG治疗延迟与CA后遗症的发生显著相关:大约1%的非难治性KD患者可能会出现CA后遗症。我们的研究结果强调了对 KD 患者进行初始超声心动图评估和尽早开始 IVIG 治疗的重要性。
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来源期刊
CiteScore
5.80
自引率
3.80%
发文量
291
审稿时长
3-6 weeks
期刊介绍: Archives of Disease in Childhood is an international peer review journal that aims to keep paediatricians and others up to date with advances in the diagnosis and treatment of childhood diseases as well as advocacy issues such as child protection. It focuses on all aspects of child health and disease from the perinatal period (in the Fetal and Neonatal edition) through to adolescence. ADC includes original research reports, commentaries, reviews of clinical and policy issues, and evidence reports. Areas covered include: community child health, public health, epidemiology, acute paediatrics, advocacy, and ethics.
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