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预测支原体肺炎病儿并发大叶性肺炎风险的列线图模型的建立
引用本文:郭晓茹,周巍玲.预测支原体肺炎病儿并发大叶性肺炎风险的列线图模型的建立[J].安徽医药,2023,27(10):1945-1948.
作者姓名:郭晓茹  周巍玲
作者单位:宝鸡市妇幼保健院儿科,陕西宝鸡 721000
基金项目:宝鸡市卫生健康委员会资助项目( 2021-GJ-LC021)
摘    要:目的探讨支原体肺炎病儿并发大叶肺炎的影响因素,并依此建立列线图预测模型。方法回顾性分析宝鸡市妇幼保健院 2019年 3月至 2022年 3月收治的 142例支原体肺炎病儿的临床资料,并将其作为模型组。比较模型组中并发组( 89例)和未并发组( 53例)两组病人的一般资料,采用多因素 logistic回归分析法分析模型组支原体肺炎病儿并发大叶肺炎的影响因素,并采用 R 3.4.3软件包绘制列线图模型,另收集 2016年 1月至 2019年 1月该院收治的 224例支原体肺炎病儿的临床资料,其作为验证组,绘制校准曲线图并采用 Bootstrap法检验预测列线图模型的校准度。结果多因素 logistic回归分析结果显示,将模型组年龄、发热时间、合并胸腔积液、发病至应用大环内酯类药物时间、 C-反应蛋白( CRP)和乳酸脱氢酶( LDH)表达水平升高均为影响支原体肺炎病儿并发大叶性肺炎的危险因素( OR=1.84、2.65、4.10、2.84、3.50、2.37,P<0.05)。将以上 6个影响因素作为预测指标,构建模型组支原体肺炎病儿并发大叶肺炎的风险预测列线图模型,经 Bootstrap法进行验证,模型组的其一致性指数( C-index)为 0.832,验证组的 C-index为 0.829,且校准曲线的校准度较好。结论年龄、发热时间、合并胸腔积液、发病至应用大环内酯类药物时间、 CRP和 LDH表达水平升高均是支原体肺炎病儿并发大叶肺炎的危险因素,基于以上危险因素构建的列线图模型具有良好的校准度,有助于临床预测并发大叶性肺炎的概率,为临床治疗提供更有力指导。

关 键 词:肺炎,支原体  大叶性肺炎  列线图  预测模型  儿童

Establishment of a risk prediction line chart model for lobar pneumonia in children with mycoplasma pneumonia
GUO Xiaoru,ZHOU Weiling.Establishment of a risk prediction line chart model for lobar pneumonia in children with mycoplasma pneumonia[J].Anhui Medical and Pharmaceutical Journal,2023,27(10):1945-1948.
Authors:GUO Xiaoru  ZHOU Weiling
Institution:Department of Pediatrics, Baoji Maternal and Child Health Hospital, Baoji, Shaanxi 721000, China
Abstract:Objective To explore the influencing factors of children with mycoplasma pneumonia complicated with lobar pneumonia, and to establish a line chart prediction model.Methods The clinical data of 142 children with mycoplasma pneumonia admittedto Baoji Maternal and Child Health Hospital from March 2019 to March 2022 were retrospectively analyzed as the model group. Thegeneral data of the concurrent group (89 cases) and the non-concurrent group (53 cases) in the model group were compared. Multivariate Logistic regression analysis was used to analyze the influencing factors of mycoplasma pneumonia complicated with lobar pneumonia. The R3.4.3 software package was used to draw the line graph model. The clinical data of 224 children with mycoplasma pneumoniaadmitted to the hospital from January 2016 to January 2019 were selected as validation group. The calibration curve was drawn and theBootstrap method was used to test the calibration degree of the predicted plot model.Results Multivariate logistic regression analysisshowed that age, fever time, pleural effusion, time from onset to application of macrolides, elevated levels of C-reactive protein (CRP)and lactate dehydrogenase (LDH) in the model group were risk factors for lobar pneumonia in children with mycoplasma pneumonia (OR =1.84, 2.65, 4.10, 2.84, 3.50, 2.37, P< 0.05). The above six influencing factors were used as the prediction indexes to construct the riskprediction line graph model of children with mycoplasma pneumonia complicated with lobar pneumonia in the model group. The Bootstrap method was used to verify the consistency index (C-index) of the model group was 0.832, and the C-index of the verification group was 0.829, and the calibration degree of calibration curve was better.Conclusion Age, fever time, pleural effusion, time from onset toapplication of macrolides and elevated levels of CRP and LDH are risk factors for children with mycoplasma pneumonia complicatedwith lobar pneumonia. The line graph model based on the above risk factors has good calibration, which is helpful to predict the probability of lobar pneumonia and provide more powerful guidance for clinical treatment.
Keywords:Pneumonia  mycoplasma  Lobar pneumonia  The column chart  Prediction model  Child
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