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本文引用的文献

1
[Establishment of a nomogram model for predicting the risk of early-onset sepsis in very preterm infants].[建立预测极早产儿早发型败血症风险的列线图模型]
Zhongguo Dang Dai Er Ke Za Zhi. 2023;25(9):915-922. doi: 10.7499/j.issn.1008-8830.2302002.
2
Nasogastric decompression after intestinal surgery in children: a systematic review and meta-analysis.儿童肠道手术后的鼻胃减压:一项系统评价和荟萃分析。
Pediatr Surg Int. 2021 Mar;37(3):377-388. doi: 10.1007/s00383-020-04818-6. Epub 2021 Feb 10.
3
Determining Optimal Outcome Measures in a Trial Investigating No Routine Gastric Residual Volume Measurement in Critically Ill Children.探讨危重症儿童中不常规进行胃残余量测量的试验中最佳结局指标的确定。
JPEN J Parenter Enteral Nutr. 2021 Jan;45(1):79-86. doi: 10.1002/jpen.1817. Epub 2020 Mar 6.
4
Definitions, predictors and outcomes of feeding intolerance in critically ill children: A systematic review.定义、预测因素和危重症儿童喂养不耐受的结局:系统评价。
Clin Nutr. 2020 Mar;39(3):685-693. doi: 10.1016/j.clnu.2019.03.026. Epub 2019 Mar 30.
5
Early mobilization in the pediatric intensive care unit.儿科重症监护病房中的早期活动
Transl Pediatr. 2018 Oct;7(4):308-313. doi: 10.21037/tp.2018.09.02.
6
Prevalence and duration of reasons for enteral nutrition feeding interruption in a tertiary intensive care unit.三级重症监护病房中肠内营养喂养中断的原因及其持续时间。
Nutrition. 2018 Sep;53:26-33. doi: 10.1016/j.nut.2017.11.014. Epub 2018 Jan 31.
7
Conceptualizing Post Intensive Care Syndrome in Children-The PICS-p Framework.儿童重症监护后综合征的概念化- PICS-p 框架。
Pediatr Crit Care Med. 2018 Apr;19(4):298-300. doi: 10.1097/PCC.0000000000001476.
8
Guidelines for the Provision and Assessment of Nutrition Support Therapy in the Pediatric Critically Ill Patient: Society of Critical Care Medicine and American Society for Parenteral and Enteral Nutrition.《儿科危重症患者营养支持治疗的提供与评估指南:危重症医学会和美国肠外肠内营养学会》
Pediatr Crit Care Med. 2017 Jul;18(7):675-715. doi: 10.1097/PCC.0000000000001134.
9
[Risk Prediction of Feeding Intolerance in Preterm Infants].[早产儿喂养不耐受的风险预测]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2016 Sep;47(5):749-754.
10
Gut Microbiota Mediates Protection Against Enteropathy Induced by Indomethacin.肠道微生物群介导对吲哚美辛诱导的肠病的保护作用。
Sci Rep. 2017 Jan 9;7:40317. doi: 10.1038/srep40317.

[危重症儿童肠内营养不耐受的危险因素及预测模型的建立]

[Risk factors and development of a prediction model of enteral feeding intolerance in critically ill children].

作者信息

Zhou Xia, Gao Hong-Mei, Huang Lin, Han Hui-Wu, Hu Hong-Ling, Li You, Yu Ren-He

机构信息

Department of Clinical Nursing, Xiangya Hospital, Central South University, Changsha 410008, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2025 Mar 15;27(3):321-327. doi: 10.7499/j.issn.1008-8830.2409102.

DOI:10.7499/j.issn.1008-8830.2409102
PMID:40105078
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11928032/
Abstract

OBJECTIVES

To explore the risk factors of feeding intolerance (FI) in critically ill children receiving enteral nutrition (EN) and to construct a prediction nomogram model for FI.

METHODS

A retrospective study was conducted to collect data from critically ill children admitted to the Pediatric Intensive Care Unit of Xiangya Hospital, Central South University, between January 2015 and October 2020. The children were randomly divided into a training set (346 cases) and a validation set (147 cases). The training set was further divided into a tolerance group (216 cases) and an intolerance group (130 cases). Multivariate logistic regression analysis was used to screen for risk factors for FI in critically ill children receiving EN. A nomogram was constructed using R language, which was then validated on the validation set. The model's discrimination, calibration, and clinical net benefit were evaluated using receiver operating characteristic curves, calibration curves, and decision curves.

RESULTS

Duration of bed rest, shock, gastrointestinal decompression, use of non-steroidal anti-inflammatory drugs, and combined parenteral nutrition were identified as independent risk factors for FI in critically ill children receiving EN (<0.05). Based on these factors, a nomogram prediction model for FI in critically ill children receiving EN was developed. The area under the receiver operating characteristic curve for the training set and validation set was 0.934 (95%: 0.906-0.963) and 0.852 (95%: 0.787-0.917), respectively, indicating good discrimination of the model. The Hosmer-Lemeshow goodness-of-fit test showed that the model had a good fit (χ 2=12.559, =0.128). Calibration curve and decision curve analyses suggested that the model has high predictive efficacy and clinical application value.

CONCLUSIONS

Duration of bed rest, shock, gastrointestinal decompression, use of non-steroidal anti-inflammatory drugs, and combined parenteral nutrition are independent risk factors for FI in critically ill children receiving EN. The nomogram model developed based on these factors exhibits high predictive efficacy and clinical application value.

摘要

目的

探讨接受肠内营养(EN)的危重症儿童发生喂养不耐受(FI)的危险因素,并构建FI的预测列线图模型。

方法

进行一项回顾性研究,收集2015年1月至2020年10月期间在中南大学湘雅医院儿科重症监护病房收治的危重症儿童的数据。将这些儿童随机分为训练集(346例)和验证集(147例)。训练集进一步分为耐受组(216例)和不耐受组(130例)。采用多因素logistic回归分析筛选接受EN的危重症儿童发生FI的危险因素。使用R语言构建列线图,然后在验证集上进行验证。采用受试者工作特征曲线、校准曲线和决策曲线评估模型的区分度、校准度和临床净效益。

结果

卧床时间、休克、胃肠减压、使用非甾体类抗炎药和联合肠外营养被确定为接受EN的危重症儿童发生FI的独立危险因素(<0.05)。基于这些因素,建立了接受EN的危重症儿童FI的列线图预测模型。训练集和验证集的受试者工作特征曲线下面积分别为0.934(95%:0.906 - 0.963)和0.852(95%:0.787 - 0.917),表明模型具有良好的区分度。Hosmer-Lemeshow拟合优度检验显示模型拟合良好(χ2 = 12.559,P = 0.128)。校准曲线和决策曲线分析表明该模型具有较高的预测效能和临床应用价值。

结论

卧床时间、休克、胃肠减压、使用非甾体类抗炎药和联合肠外营养是接受EN的危重症儿童发生FI的独立危险因素。基于这些因素建立的列线图模型具有较高的预测效能和临床应用价值。