Autologous Intestinal Reconstructive Surgery in the Management of Total Intestinal Aganglionosis.

IF 2.4 3区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Fabio Fusaro, Francesco Morini, Annika Mutanen, Paola De Angelis, Roberto Tambucci, Teresa Capriati, Dominique Hermans, Manila Candusso, Antonella Diamanti, Pietro Bagolan, Mikko Pakarinen
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引用次数: 7

Abstract

Objectives: Total/near total intestinal aganglionosis (TIA/NTIA) is the most uncommon and life-threatening form of Hirschsprung disease (HD). The management of TIA/NTIA is challenging and the role of autologous intestinal reconstructive (AIR) surgery is controversial. The objective is to evaluate the effectiveness of AIR in patients with TIA/NTIA.

Methods: Records from children affected by TIA and enrolled in the multicenter international Pediatric Intestinal Rehabilitation and Transplantation Registry were retrospectively reviewed.

Results: Fourteen patients with TIA were identified. TIA diagnosis was confirmed histologically at the median age of 14 days of life. All received a proximal decompressive jejunostomy. Two patients died, 4 patients had satisfactory stoma output with enteral tolerance without additional procedures, 8 underwent 10 AIR procedures (4 Ziegler myotomy-myectomy, 3 transposition of aganglionic ileum with or without myotomy, 2 simple tapering, 1 longitudinal lengthening and tailoring procedure with associated myotomy). AIR significantly reduced median stoma output, from 197 to 31 mL · kg · day (P = 0.0001). The reduction was seen in all patients. In addition, AIR improved enteral tolerance in the long term in 5 of 8 patients (63%), and temporarily in 1, leading to a reduction of parenteral nutrition requirement from 100% to 70% (P = 0.0231).

Conclusions: AIR surgery in carefully selected patients may be useful and effective way to enhance residual bowel absorptive function and to reduce parenteral nutrition requirements. AIR and intestinal transplantation are complementary surgical tools in the complex treatment algorithm of TIA/NTIA.

自体肠重建手术治疗全肠神经节病。
目的:全/近全肠神经节病(TIA/NTIA)是先天性巨结肠疾病(HD)中最罕见且危及生命的形式。TIA/NTIA的治疗具有挑战性,自体肠道重建(AIR)手术的作用也存在争议。目的是评估AIR在TIA/NTIA患者中的有效性。方法:回顾性分析多中心国际儿童肠道康复和移植登记处登记的TIA患儿的记录。结果:14例TIA患者被确诊。在出生14天的中位年龄组织学上证实TIA的诊断。所有患者均行近端空肠减压造口术。2例患者死亡,4例患者在没有额外手术的情况下获得满意的造口输出,8例患者接受了10例AIR手术(4例Ziegler肌切开术-肌切开术,3例有或没有肌切开术的腱鞘回转位,2例简单变细,1例纵向延长和剪裁手术合并肌切开术)。AIR显著降低中位造口量,从197 mL·kg·d降至31 mL·kg·d (P = 0.0001)。在所有患者中都观察到这种减少。此外,AIR改善了8例患者中5例(63%)的长期肠内耐受性,1例患者的短期肠外营养需求从100%降低到70% (P = 0.0231)。结论:对精心挑选的患者进行空气外科手术可能是增强残余肠吸收功能和减少肠外营养需求的有效方法。在TIA/NTIA的复杂治疗算法中,AIR和肠道移植是互补的手术工具。
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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来源期刊
CiteScore
5.30
自引率
13.80%
发文量
467
审稿时长
3-6 weeks
期刊介绍: ​The Journal of Pediatric Gastroenterology and Nutrition (JPGN) provides a forum for original papers and reviews dealing with pediatric gastroenterology and nutrition, including normal and abnormal functions of the alimentary tract and its associated organs, including the salivary glands, pancreas, gallbladder, and liver. Particular emphasis is on development and its relation to infant and childhood nutrition.
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