首页|儿童川崎病并发胸腔积液的临床特点及风险预测模型构建

儿童川崎病并发胸腔积液的临床特点及风险预测模型构建

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目的 探讨儿童川崎病(KD)并发胸腔积液(PE)的临床特点并构建临床预测模型.方法 回顾性收集462例KD患儿的临床资料,以并发PE的11例患儿为KD-PE组,采用倾向性评分匹配选取未并发PE的KD患儿118例为KD对照组.分析患儿临床表现、辅助检查、治疗经过及预后等临床资料,采用单因素及Lasso-Logistic回归分析KD患儿并发PE的影响因素.构建预测KD-PE的列线图模型,并评价模型的预测效能.结果 KD-PE组患儿呼吸道症状均较轻,10例为少量PE.Lasso-Logistic回归筛选出C反应蛋白(CRP,OR=1.045,95%CI:1.009~1.082)及白蛋白(ALB,OR=0.755,95%CI:0.591~0.964)2个变量构建预测模型,回归方程为Logit(P)=2.221+0.044×CRP-0.281×ALB.预测模型受试者工作特征(ROC)曲线下面积为0.957(95%CI:0.911~1.000).Hosmer-Lemeshow检验显示校准模型曲线与实际模型曲线重合良好(χ2=4.320,P=0.827),具有较好的区分度和校准度,采用临床决策曲线及临床影响曲线评估模型具有良好的临床适用性.结论 CRP升高是KD并发PE的危险因素,ALB升高是保护因素,本模型准确度、辨识能力及净获益均较高.
Clinical characteristics and risk prediction model construction of children with Kawasaki disease complicated with pleural effusion
Objective To investigate the clinical features of pediatric Kawasaki disease(KD)complicated with pleural effusion(PE)and construct a clinical prediction model.Methods A retrospective review was conducted on clinical data of 462 children with KD from June 2017 to June 2023.Eleven KD children with PE were selected as the KD-PE group,and 118 patients without PE were selected as the KD control group.Using propensity score matching,the clinical data including clinical manifestation,auxiliary examination,treatment process and complications were collected and analyzed.Univariate and Lasso-Logistic regression were used to analyze influence factors of PE in children with KD.A line chart model for predicting KD-PE was constructed,and the prediction efficiency of the model was evaluated.Results The respiratory symptoms were generally mild in the KD-PE group,with 10 cases exhibiting mild PE.Two variables of C-reactive protein(CRP,OR=1.045,95%CI:1.009-1.082)and albumin(ALB,OR=0.755,95%CI:0.591-0.964)were screened out by Lasso regression and multi-factor Logistic regression to construct the prediction model.The regression equation was Logit(P)=2.221+0.044×CRP-0.281×ALB.The area under the ROC curve of the prediction model was 0.957(95%CI:0.911-1.000),and the Hosmer-Lemeshow test showed that the curve of the calibration model was well coincident with the curve of the actual model(χ2=4.320,P=0.827).The evaluation model using clinical decision curve and clinical impact curve had good clinical applicability.Conclusion KD complicated with PE in children is rare,elevated CRP is a risk factor for KD-complicated PE,and elevated ALB is a protective factor.The model has higher accuracy,discriminatory power and net benefit.

mucocutaneous lymph node syndromepleural effusionC-reactive proteinserum albuminnomograms

杨湖、雷君、杨丽、彭小铜

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邵阳市中心医院儿科(邮编 422000)

南华大学附属邵阳医院儿科

黏膜皮肤淋巴结综合征 胸腔积液 C反应蛋白质 血清白蛋白 列线图

2024

天津医药
天津市医学科学技术信息研究所

天津医药

CSTPCD
影响因子:1.107
ISSN:0253-9896
年,卷(期):2024.52(10)