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短肠综合征患儿的治疗结果:一个多学科肠道康复单元二十年的经验

Outcomes of Children With Short Bowel Syndrome: Experiences in a Multidisciplinary Intestinal Rehabilitation Unit Over Two Decades.

作者信息

Tsang Jaime Tsz-Wing, Fung Adrian Chi-Heng, Lau Stephen Cheuk-Lam, Wong Kenneth Kak-Yuen

机构信息

Department of Surgery, School of Clinical Medicine, University of Hong Kong, Hong Kong.

Department of Paediatric and Adolescent Medicine, Queen Mary Hospital, Hong Kong.

出版信息

J Pediatr Surg. 2025 Feb;60(2):161646. doi: 10.1016/j.jpedsurg.2024.07.031. Epub 2024 Jul 24.

Abstract

BACKGROUND

Short bowel syndrome (SBS) is a rare but serious form of organ failure, and patients with SBS depend on total parenteral nutrition (PN) to maintain growth and development. The present study aimed to evaluate the experiences and outcomes of children with SBS managed by a multidisciplinary intestinal rehabilitation programme in a tertiary paediatric centre.

METHODS

A retrospective single-centre analysis of all paediatric patients with a clinical diagnosis of SBS between 2001 and 2022 was performed. Clinical outcomes and their predictors were extracted and analysed.

RESULTS

Of the 64 children included in the study, 43 (67%) had extensive necrotising enterocolitis. The median bowel length was 45 cm (interquartile range (IQR) = 18-65) and 18.9% (IQR = 10-28.5) of the expected length based on age. Over a mean follow-up period of 8.9 years, 57 patients (89%) survived, and 50 (78%) weaned off PN. The presence of intestinal failure-associated liver disease (IFALD) (OR = 6.375, p = 0.02) and patients managed before the introduction of fish oil-based PN in 2007 (OR = 5.895, p = 0.001) were significant predictors of mortality. There was an overall improvement in survival over time (p = 0.003). Ultrashort bowel length was not associated with significantly higher mortality (OR = 1.1, p = 0.65) but was a poor prognostic factor for weaning off PN (OR = 3.57, p = 0.004). Among all patients who weaned off PN, two had bowel lengthening procedures and one received a glucagon-like peptide 2 (GLP-2) analogue.

CONCLUSIONS

A multidisciplinary intestinal rehabilitation programme offers a comprehensive approach for patients with SBS and has been shown to be effective with favourable outcomes. Improvements in the choice of PN and the development of new treatment strategies potentially improved the survival and enteral autonomy of SBS patients.

LEVEL OF EVIDENCE

III.

摘要

背景

短肠综合征(SBS)是一种罕见但严重的器官衰竭形式,SBS患者依赖全胃肠外营养(PN)来维持生长发育。本研究旨在评估在一家三级儿科中心通过多学科肠道康复计划管理的SBS儿童的经验和结局。

方法

对2001年至2022年间所有临床诊断为SBS的儿科患者进行回顾性单中心分析。提取并分析临床结局及其预测因素。

结果

纳入研究的64名儿童中,43名(67%)患有广泛坏死性小肠结肠炎。中位肠长为45厘米(四分位间距(IQR)=18 - 65),占基于年龄预期长度的18.9%(IQR = 10 - 28.5)。在平均8.9年的随访期内,57名患者(89%)存活,50名(78%)停用了PN。存在肠道衰竭相关肝病(IFALD)(比值比(OR)=6.375,p = 0.02)以及在2007年引入基于鱼油的PN之前接受管理的患者(OR = 5.895,p = 0.001)是死亡率的显著预测因素。随着时间推移,总体生存率有所改善(p = 0.003)。超短肠长与显著更高的死亡率无关(OR = 1.1,p = 0.65),但对于停用PN是一个不良预后因素(OR = 3.57,p = 0.

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