6月龄以下婴儿川崎病的临床特征分析
收稿日期: 2025-10-17
录用日期: 2026-01-05
网络出版日期: 2026-03-06
Clinical characteristics of Kawasaki disease under 6 months infants
Received date: 2025-10-17
Accepted date: 2026-01-05
Online published: 2026-03-06
目的 本研究旨在分析6月龄以下川崎病(KD)患儿的临床表现、冠状动脉损害特征以及静脉注射免疫球蛋白(IVIg)无应答的独立危险因素与预测指标。方法 对2020年1月至2024年12月在医院住院治疗的435例KD患儿的资料进行回顾性分析。将所有患儿划分为0~5月龄组(6月龄以下)和6~12月龄组,0~5月龄组进一步分为不完全性KD(iKD)组与完全性KD(cKD)组。分析0~5月龄组与6~12月龄组患儿主要临床特征的差异,并比较iKD组和 cKD组的临床表型异同。运用多因素logistic回归分析0~5月龄组冠状动脉病变(CAL)和IVIg无应答的危险因素,通过受试者工作特征(ROC)曲线评估相关变量对IVIg无应答的预测价值。结果 0~5月龄组179例(41.1%),其卡疤红肿发生率、血小板计数等炎症相关指标显著高于6~12月龄组,而结膜充血等典型症状及白蛋白、血红蛋白水平显著更低,CAL发生率(47.5%)更高(均P<0.05)。0~5月龄组中iKD 73例(40.8%),典型症状更少,CAL 发生率(58.9%)和IVIg无应答率均高于cKD组(均P<0.05)。0~5月龄组多因素分析发现,卡疤红肿(OR=2.81,95%CI:1.44~5.48,P=0.002)与CAL发生呈正相关;结膜充血与IVIg抵抗呈显著负相关(OR=0.15,95%CI:0.03~0.89,P=0.036),而中性粒细胞/淋巴细胞比值(NLR)≥3.78(OR=3.17,95%CI:1.37~7.31,P=0.007)及发热持续时间≥6.5 d(OR=1.38,95%CI:1.03~1.84,P=0.029)为IVIg无应答危险因素。ROC曲线提示NLR≥3.78和发热≥6.5 d联合预测IVIg无应答的曲线下面积(AUC)为0.888,灵敏度0.867,特异度0.841。结论 0~5月龄组KD患儿大多临床表现不典型,iKD患儿CAL及IVIg无应答发生率更高。卡疤红肿与CAL的发生密切相关。NLR≥3.78联合发热≥6.5 d对IVIg无应答具有较高预测价值,结膜充血可能有助于6月龄以下IVIg无应答KD的早期识别与治疗。
李灿灿 , 朱雪萍 , 孙文强 , 张涵 , 耿海峰 . 6月龄以下婴儿川崎病的临床特征分析[J]. 临床儿科杂志, 2026 , 44(3) : 209 -216 . DOI: 10.12372/jcp.2026.25e1284
Objective This study aimed to analyze the clinical manifestations, coronary artery lesion (CAL) features, and independent risk factors/predictive indicators for intravenous immunoglobulin (IVIg) non-response in infants with Kawasaki disease (KD) under 6 months of age. Methods A retrospective analysis was performed on clinical data of 435 KD infants aged 0-12 months who were hospitalized January 2020 to December 2024. Patients were stratified into the 0-5 months group (under 6 months) and 6-12 months group; the 0-5 months group was further subdivided into incomplete KD (iKD) and complete KD (cKD) subgroups. Differences in core clinical characteristics between the 0-5 months and 6-12 months groups were analyzed, and phenotypic variations between the iKD and cKD subgroups were compared. Multivariate logistic regression was used to identify risk factors for CAL and IVIg non-response in the 0-5 months group. Receiver operating characteristic (ROC) curves were constructed to evaluate the predictive efficacy of candidate variables for IVIg non-response. Results A total of 179 patients (41.1%) were included in the 0-5 month group. Compared with the 6-12 months group, the 0-5 months group exhibited a significantly higher incidence of Bacille Calmette-Guérin (BCG) scar erythema/swelling and elevated inflammation-related markers such as platelet count, alongside lower frequencies of typical KD symptoms like conjunctival hyperemia and reduced albumin/hemoglobin levels. The incidence of CAL was also higher in the 0-5 months group (47.5%; all P<0.05). Within the 0-5 months group, 73 patients (40.8%) were diagnosed with iKD, presenting fewer typical symptoms, a higher CAL incidence (58.9%), and a higher IVIg non-response rate than the cKD subgroup (all P < 0.05). Multivariate regression revealed that BCG scar erythema/swelling was independently associated with an increased risk of CAL (OR=2.81, 95% CI: 1.44-5.48, P=0.002). Conjunctival hyperemia was inversely correlated with IVIg non-response (OR=0.15, 95% CI: 0.03-0.89, P=0.036), while a neutrophil-to-lymphocyte ratio (NLR)≥3.78 (OR=3.17, 95% CI: 1.37-7.31, P=0.007) and fever duration≥6.5 days (OR=1.38, 95% CI: 1.03-1.84, P=0.029) were identified as independent risk factors for IVIg non-response. The combined model of NLR≥3.78 and fever duration≥6.5 days yielded an area under the ROC curve (AUC) of 0.888 for predicting IVIg non-response, with a sensitivity of 0.867 and specificity of 0.841. Conclusions KD infants under 6 months of age often present with atypical manifestations. iKD in this age group is associated with a higher incidence of CAL and IVIg non-response. BCG scar erythema/swelling is closely linked to CAL development. The combination of NLR≥3.78 and fever duration≥6.5 days has robust predictive value for IVIg non-response, while conjunctival hyperemia may facilitate the early identification and management of IVIg-nonresponsive KD in infants under 6 months.
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