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体外膜肺氧合患儿早期肠内营养的安全性及临床疗效:一项回顾性队列研究

Safety and clinical efficacy of early enteral nutrition in children with extracorporeal membrane oxygenation: A retrospective cohort study.

作者信息

Hu Jinjiu, Liu Peng, Zhang Qiaoying, Wan Xin, Lu Qiufan, Zhu YangFan, Zhang Hui, Shen Qiao, Cai Ye, Weng Yonglin, Meng Yuqian, Zheng Xianlan

机构信息

Department of Nursing, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatric Metabolism and Inflammatory Diseases, Chongqing, China.

Pediatric Intensive Care Unit, Medicine Children's Hospital of Chongqing Medical University, Chongqing, China.

出版信息

Clin Nutr ESPEN. 2025 Oct;69:31-36. doi: 10.1016/j.clnesp.2025.06.045. Epub 2025 Jun 28.

Abstract

BACKGROUND AND AIMS

The benefits of enteral nutrition (EN) in pediatric patients undergoing extracorporeal membrane oxygenation (ECMO) are increasingly recognized; however, data on the safety and clinical effectiveness of early EN initiation in this population remain limited. We aimed to assess whether early EN would increase the incidence of feeding intolerance and ECMO-related complications, and improve clinical outcomes in pediatric ECMO patients.

METHODS

We conducted a retrospective analysis of clinical data from 45 pediatric patients who underwent ECMO for more than 48 h between January 2018 and October 2024. Patients were divided into early EN (initiated within 48 h post-ECMO) and delayed EN (initiated after 48 h post-ECMO) groups. A multivariate Cox proportional hazards regression model was used to calculate the adjusted hazard ratio (HR) and 95 % confidence interval (95 % CI).

RESULTS

Forty-five patients were enrolled in the study, of whom 30 (66.7 %) received early EN. On ECMO days 2, 5, and 7, the median energy intake from EN in the early EN group was 233 kcal (Inter quartile range (IQR): 120, 421), 368 kcal (IQR: 165, 568), and 358 kcal (IQR: 135, 758), respectively, representing 41.0 %, 56.9 %, and 66.7 % of the prescribed energy target. By ECMO day 7, 15 patients (50 %) in the early EN group achieved the target energy intake, compared with 26.7 % in the delayed EN group (P = 0.135). No significant differences were observed in ECMO-related complications (60 % vs 66.7 %, P = 0.664) and feeding intolerance (63.3 % vs 66.7 %, P = 0.826) between the two groups. Bleeding at the cannulation site was the most frequent ECMO-related complication (35.6 %), while gastrointestinal bleeding (24.4 %) and constipation (17.8 %) were the primary reasons for feeding intolerance. Successful ECMO weaning was achieved in 33 patients (73.3 %), with a higher rate in the early EN group than in the delayed EN group (86.7 % vs 46.7 %, P = 0.012). The early EN group had a higher survival rate (76.7 %) compared with the delayed EN group (40 %, P = 0.015). Early EN was associated with a significant reduction in mortality, with an adjusted HR of 0.13 (95 % CI: 0.03, 0.55).

CONCLUSIONS

Early EN demonstrated a favorable safety profile and effectively managed the increased intestinal load in pediatric patients, with the potential to reduce in-hospital mortality among children receiving ECMO. For pediatric patients undergoing ECMO, initiating EN at a low volume or low rate within 48 h of ECMO initiation is recommended.

摘要

背景与目的

肠内营养(EN)在接受体外膜肺氧合(ECMO)的儿科患者中的益处日益受到认可;然而,关于该人群早期开始EN的安全性和临床有效性的数据仍然有限。我们旨在评估早期EN是否会增加喂养不耐受和ECMO相关并发症的发生率,并改善儿科ECMO患者的临床结局。

方法

我们对2018年1月至2024年10月期间接受ECMO治疗超过48小时的45例儿科患者的临床资料进行了回顾性分析。患者分为早期EN组(ECMO后48小时内开始)和延迟EN组(ECMO后48小时后开始)。采用多变量Cox比例风险回归模型计算调整后的风险比(HR)和95%置信区间(95%CI)。

结果

45例患者纳入研究,其中30例(66.7%)接受早期EN。在ECMO第2天、第5天和第7天,早期EN组EN的中位能量摄入量分别为233千卡(四分位间距(IQR):120,421)、368千卡(IQR:165,568)和358千卡(IQR:135,758),分别占规定能量目标的41.0%、56.9%和66.7%。到ECMO第7天,早期EN组15例患者(50%)达到目标能量摄入量,而延迟EN组为26.7%(P = 0.135)。两组在ECMO相关并发症(60%对66.7%,P = 0.664)和喂养不耐受(63.3%对66.7%,P = 0.826)方面未观察到显著差异。插管部位出血是最常见的ECMO相关并发症(35.6%),而胃肠道出血(24.4%)和便秘(17.8%)是喂养不耐受的主要原因。33例患者(73.3%)成功撤机,早期EN组的成功率高于延迟EN组(86.7%对46.7%,P = 0.012)。早期EN组的生存率(76.7%)高于延迟EN组(40%,P = 0.015)。早期EN与死亡率显著降低相关,调整后的HR为0.13(95%CI:0.03,0.55)。

结论

早期EN显示出良好的安全性,有效应对了儿科患者增加的肠道负担,有可能降低接受ECMO儿童的住院死亡率。对于接受ECMO的儿科患者,建议在ECMO开始后48小时内以低容量或低速率开始EN。

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