Segmental intestinal reconfiguration (SIR) in combined reconstructions for ultrashort bowel syndrome

Vasily V. Nikolaev , Julia Averyanova
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引用次数: 0

Abstract

Background

Ultrashort bowel syndrome represents the most rare and complex variant of the short bowel syndrome. Autologous intestinal reconstructions for ultrashort bowel syndrome is typically reserved for severe cases characterized by symptomatic dysmotility within the ultrashort dilated segments. Limited surgical techniques are available to substantially increase the length of ultrashort bowels with asymmetric and highly dilated segments.

We present a case series detailing the application of a technique for lengthening and tapering significantly dilated ultrashort bowels – segmental intestinal reconfiguration (SIR), based on the Yang-Monti principle. Our analysis delves into the technical features across various anatomical variants and provides mid-term results.

Methods

From 2021 to 2022, patients experiencing dysmotility in dilated ultrashort bowel segments with a preserved colon underwent sequential combined intestinal reconstructions. Assessments were conducted 18–24 months post-surgery, and statistical calculations employed nonparametric methods to compare pre- and postoperative results.

Results

Six patients, with a median age of 48.5 months, underwent autologous intestinal reconstructions, including SIR. The serial transverse enteroplasty (STEP) was performed on the dilated duodenum in five children, and colon interposition in two. The length of the small bowel exhibited a significant difference before and after surgery (p = 0.031). No complications were observed in the postoperative period. The postoperative group demonstrated a lower dependence on parenteral nutrition (NPEI/REE < 80 % in 6 (100.0 %); p = 0.007). Enteral autonomy was restored in two children.

Conclusions

The results of SIR technique in combined reconstructions for ultrashort bowel syndrome in a carefully selected cohort of children demonstrate feasibility and reliability, as well as the restoration of intestinal transport function at midterm evaluation. This comprehensive approach resulted in increased enteral tolerance and reduced parenteral requirements.

超短肠综合征联合重建中的节段性肠重组(SIR)
背景超短肠综合征是短肠综合征中最罕见、最复杂的变异。针对超短肠综合征的自体肠道重建术通常只适用于以超短扩张肠段内出现症状性运动障碍为特征的严重病例。我们展示了一个病例系列,详细介绍了一种基于杨-蒙蒂原理的技术--节段性肠重组(SIR)--的应用,用于延长和缩窄明显扩张的超短肠。我们的分析深入探讨了各种解剖变异的技术特点,并提供了中期结果。方法从 2021 年到 2022 年,对保留结肠的扩张超短肠段出现运动障碍的患者进行了连续的联合肠道重建。术后 18-24 个月进行评估,统计计算采用非参数方法比较术前术后结果。结果六名患者接受了自体肠道重建术,包括 SIR,中位年龄为 48.5 个月。五名患儿在扩张的十二指肠上进行了连续横向肠成形术(STEP),两名患儿进行了结肠插置术。小肠长度在手术前后有显著差异(P = 0.031)。术后未发现并发症。术后组对肠外营养的依赖性较低(NPEI/RE <;6 例为 80%(100.0%);p = 0.007)。结论在精心挑选的儿童群体中采用 SIR 技术对超短肠综合征进行联合重建的结果表明,该技术是可行的、可靠的,而且在中期评估时恢复了肠道转运功能。这种综合方法提高了肠道耐受性,减少了肠外治疗需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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