文章摘要
张莉,徐邦红,杨辉,等.脓毒症病儿肠内营养不耐受风险列线图模型的构建与验证[J].安徽医药,2025,29(10):2008-2012.
脓毒症病儿肠内营养不耐受风险列线图模型的构建与验证
Construction and validation of a column chart model for the risk of enteral nutrition intolerance in children with sepsis
  
DOI:10.3969/j.issn.1009-6469.2025.10.019
中文关键词: 脓毒症  肠道营养  儿童  肠内营养不耐受  列线图  危险因素  预测
英文关键词: Sepsis  Enteral nutrition  Child  Intestinal nutrition intolerance  Column chart  Risk factors  Prediction
基金项目:江苏省妇幼保健协会科研课题项目(FYX202033)
作者单位E-mail
张莉 南京医科大学附属儿童医院消化科江苏南京 210008  
徐邦红 南京医科大学附属儿童医院消化科江苏南京 210008  
杨辉 南京医科大学附属儿童医院消化科江苏南京 210008  
黄艳 南京医科大学附属儿童医院消化科江苏南京 210008 422852965@qq.com 
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中文摘要:
      目的探讨构建与验证脓毒症病儿肠内营养不耐受的列线图模型。方法选取 2021年 4月至 2023年 4月南京医科大学附属儿童医院收治的 421例脓毒症病儿作为研究对象,按照 7∶3比例大致估算,采用随机数字表法分为建模组(295例)与验证组(126),根据病儿是否发生肠内营养耐受情况将建模组病人分为耐受组(186例)和不耐受组(109例)。采用多因素 logistic回归分析脓毒症病儿的危险因素;采用 R软件和 rms程序包构建列线图模型,并评估模型预测效能。结果 295例脓毒症病儿有 109例发生肠内营养不耐受,发生率为 38.25%。耐受组和不耐受组在身体质量指数(BMI)、急性生理学和慢性健康状况评价Ⅱ(APACHEⅡ)评分、开始肠内营养时间、口服钾制剂、腹压、降钙素原(PCT)[(12.34±1.42)mg/L比(17.68±2.31)mg/L]、白蛋白[(14.67±3.02)g/L比(34.25±4.38)g/L]、C反应蛋白(CRP)[(38.14±3.89)mg/L比(58.34±5.62)mg/L]和前白蛋白[(64.35±10.32)mg/L比(129.67±13.57)mg/L]方面比较差异有统计学意义(P<0.05)。多因素 logistic回归分析 BMI≤16.8 kg/m2、APACHE Ⅱ评分>20分、开始肠内营养时间>48 h、口服钾制剂、腹压>15 mmHg、PCT、白蛋白、CRP和前白蛋白是脓毒症病儿发生肠内营养不耐受的危险因素(P<0.05)。建模组的验证结果显示,受试者操作特征曲线(ROC曲线)曲线下面积(AUC)为 0.90,区分度较好,H-L检验为 χ2=6.11,P=0.635,一致性良好。验证组 AUC为 0.96,区分度较好,H-L检验为 χ2=7.25,P=0.325,一致性良好。结论 BMI、APACHEⅡ评分、开始肠内营养时间、口服钾制剂、腹压、PCT、白蛋白、CRP和前白蛋白是脓毒症病儿肠内营养不耐受的危险因素,以此构建的列线图模型具有良好的区分度与一致性,能直观地预测脓毒症病儿发生肠内营养不耐受的风险。
英文摘要:
      Objective To explore the construction and validation of a columnar graphical model of enteral nutrition intolerance in children with sepsis.Methods A total of 421 children with sepsis admitted to Children's Hospital of Nanjing Medical University fromApril 2021 to April 2023 were selected as the research subjects. According to the 7∶3 ratio, the children were randomly assigned into a modeling group (n=295) and a validation group (n=126) by random number table method. Patients in the modeling group were separat-ed into a tolerance group (n=186) and an intolerance group (n=109) based on whether the child developed tolerance to enteral nutrition.Risk factors for children with sepsis were analyzed using multivariate logistic regression; R software and the rms package were used toconstruct the column-line graphical model and to assess the model predictive efficacy.Results In this study, 109 out of 295 childrenwith sepsis developed enteral nutrition intolerance, with an incidence rate of 38.25%. There were statistical differences between the tol-erance and intolerance groups in terms of body mass index (BMI), acute physiology and chronic health evaluation Ⅱ (APACHE Ⅱ)score, start of enteral nutrition, oral potassium preparation, abdominal pressure, procalcitonin (PCT) [(12.34±1.42) mg/L vs. (17.68± 2.31) mg/L], albumin [(14.67±3.02) g/L vs. (34.25±4.38) g/L], C-reactive protein (CRP) [(38.14±3.89) mg/L vs. (58.34±5.62) mg/L], and prealbumin [(64.35±10.32) mg/L vs. (129.67±13.57) mg/L] (P<0.05). The results of multivariate Logistic regression analysis indicated that BMI ≤ 16.8 kg/m2, APACHEⅡ score>20 points, start of enteral nutrition>48 hours, oral potassium preparation, abdominal pressure>15 mmHg, PCT, albumin, CRP, and prealbumin were risk factors for enteral nutrition intolerance in children with sepsis (P<0.05). Thevalidation results of the modeling group showed that the area under the ROC curve (AUC) was 0.90, with good discrimination, and theH-L test results were χ2=6.11, P=0.635, indicating good consistency. The AUC of the validation group was 0.96, with good discrimina-tion, and the H-L test showed χ2=7.25, P=0.325, indicating good consistency.Conclusion BMI, APACHEⅡ score, start of enteral nu-trition, oral potassium preparation, abdominal pressure, PCT, albumin, CRP, and prealbumin are risk factors for enteral nutrition intol-erance in children with sepsis, and the column-line graphical model constructed in this way has good discriminatory power and consis-tency, and can intuitively predict the risk of developing enteral nutrition intolerance in children with sepsis.
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