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比较腹裂和肠扭转患儿中需要长期/家庭静脉营养的短肠综合征的长期结局。

Long-term outcomes of short bowel syndrome requiring long-term/home intravenous nutrition compared in children with gastroschisis and those with volvulus.

作者信息

Sala D, Chomto S, Hill S

机构信息

Department of Gastroenterology, Great Ormond Street Hospital for Children, London, UK.

出版信息

Transplant Proc. 2010 Jan-Feb;42(1):5-8. doi: 10.1016/j.transproceed.2009.12.033.

Abstract

INTRODUCTION

Short bowel syndrome (SBS) is a malabsorptive state that occurs following extensive small intestinal resection. The most severely affected children require intravenous feeding/parenteral nutrition (PN). Two common causes in infancy/early childhood are intestinal resection for volvulus and resection of necrotic small intestine in infants with gastroschisis. The aim of this study was to review the long-term outcomes of children with severe intestinal failure who remained dependent on PN for many months or years. We evaluated the outcomes among gastroschisis cases versus those following resection of mid-gut volvulus or congenital short gut.

METHODS

We reviewed the case records over a 10-year period from 1997 of children presenting by 5 years of age with volvulus and/or congenital short gut or gastroschisis and who were dependent on long-term/home PN. We obtained data regarding the diagnosis, the small intestinal length, the presence of the ileo-cecal valve, the survivals, and the incidences of weaning from PN.

RESULTS

Six children underwent resection following volvulus or congenital short gut syndromes and 7 had gastroschisis. Ten of the 13 children underwent surgery as neonates and 3 from 2-5 years of age. The residual small intestinal length was <10 cm in 1, 10-25 cm in 4, 25-50 cm in 5, 50-100 cm in 2, and >100 cm in 1 case. The ileo-cecal valve was removed in 8 children. All children were treated with PN after surgery for at least 7 months. All 7 children with gastroschisis and 1 with <10 cm small intestine after intestinal resection for volvulus still required PN after 14-120 months. Three with gastroschisis died. All 5 children with volvulus and >10 cm small intestine were weaned from PN, thriving at our review 7 months-7 years later.

CONCLUSIONS

Infants and young children with short gut and >10 cm small intestine gain intestinal autonomy. In contrast, those with gastroschisis have poor outcomes and should be referred for intestinal transplantation assessment more readily than those with after intestinal resection for volvulus short gut.

摘要

引言

短肠综合征(SBS)是一种在广泛小肠切除术后出现的吸收不良状态。受影响最严重的儿童需要静脉喂养/肠外营养(PN)。婴儿期/幼儿期的两个常见病因是肠扭转的肠切除和腹裂婴儿坏死小肠的切除。本研究的目的是回顾严重肠衰竭且数月或数年依赖PN的儿童的长期预后。我们评估了腹裂病例与中肠扭转或先天性短肠切除术后病例的预后。

方法

我们回顾了1997年以来10年间5岁前因肠扭转和/或先天性短肠或腹裂就诊且依赖长期/家庭PN的儿童的病例记录。我们获取了有关诊断、小肠长度、回盲瓣的存在情况、生存率以及停止PN的发生率的数据。

结果

6名儿童因肠扭转或先天性短肠综合征接受了手术切除,7名患有腹裂。13名儿童中有10名在新生儿期接受了手术,3名在2至5岁时接受手术。残余小肠长度<10 cm的有1例,10 - 25 cm的有4例,25 - 50 cm的有5例,50 - 100 cm的有2例,>100 cm的有1例。8名儿童的回盲瓣被切除。所有儿童术后接受PN治疗至少7个月。7名腹裂儿童和1名肠扭转肠切除术后小肠长度<10 cm的儿童在14 - 120个月后仍需要PN。3名腹裂儿童死亡。所有5名小肠长度>10 cm的肠扭转儿童均停止了PN,在我们随访7个月至7年后情况良好。

结论

小肠长度>10 cm的短肠婴幼儿可实现肠道自主。相比之下,腹裂患儿预后较差,应比肠扭转短肠切除术后患儿更易被转诊进行肠道移植评估。

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