Outcomes Of Children With Short Bowel Syndrome: Experiences In A Multidisciplinary Intestinal Rehabilitation Unit Over Two Decades

IF 2.4 2区 医学 Q1 PEDIATRICS
Jaime Tsz-wing Tsang MBBS, Adrian Chi-heng Fung MBBS, Stephen Cheuk-lam Lau MBBS, Kenneth Kak-yuen Wong PhD
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Abstract

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. 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. 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, = 0.02) and patients managed before the introduction of fish oil-based PN in 2007 (OR = 5.895, = 0.001) were significant predictors of mortality. There was an overall improvement in survival over time ( = 0.003). Ultrashort bowel length was not associated with significantly higher mortality (OR = 1.1, = 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. 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. III
短肠综合征患儿的疗效:多学科肠道康复小组二十年来的经验
短肠综合征(SBS)是一种罕见但严重的器官功能衰竭,SBS 患者依赖全肠外营养(PN)来维持生长和发育。本研究旨在评估一家三级儿科中心通过多学科肠道康复计划治疗 SBS 患儿的经验和效果。本研究对 2001 年至 2022 年期间临床诊断为 SBS 的所有儿科患者进行了单中心回顾性分析。研究人员提取并分析了临床结果及其预测因素。在纳入研究的64名患儿中,43名(67%)患有广泛坏死性小肠结肠炎。肠道长度的中位数为 45 厘米(四分位距 (IQR) = 18-65),为年龄预期长度的 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 名患者(78%)脱离了 PN。肠功能衰竭相关肝病(IFALD)(OR = 6.375,= 0.02)和在 2007 年引入鱼油 PN 之前接受治疗的患者(OR = 5.895,= 0.001)是预测死亡率的重要因素。随着时间的推移,总体生存率有所提高(= 0.003)。超短肠长度与死亡率明显升高无关(OR = 1.1,= 0.65),但却是断离 PN 的不良预后因素(OR = 3.57,p = 0.004)。在所有停用 PN 的患者中,有两人接受了肠道延长术,一人接受了胰高血糖素样肽 2 (GLP-2) 类似物治疗。多学科肠道康复计划为 SBS 患者提供了一种全面的方法,并已被证明是有效的,效果良好。PN 选择的改进和新治疗策略的开发可能会提高 SBS 患者的生存率和肠道自主能力。三
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来源期刊
CiteScore
1.10
自引率
12.50%
发文量
569
审稿时长
38 days
期刊介绍: The journal presents original contributions as well as a complete international abstracts section and other special departments to provide the most current source of information and references in pediatric surgery. The journal is based on the need to improve the surgical care of infants and children, not only through advances in physiology, pathology and surgical techniques, but also by attention to the unique emotional and physical needs of the young patient.
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