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首页> 外文期刊>European journal of pediatric surgery = Zeitschrift fur Kinderchirurgie >Surgical Rehabilitation Techniques in Children with Poor Prognosis Short Bowel Syndrome
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Surgical Rehabilitation Techniques in Children with Poor Prognosis Short Bowel Syndrome

机译:预后较差的小肠综合征儿童的手术康复技术

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摘要

Intestinal failure (IF) requires a multidisciplinary management based on nutritional support, surgical and medical rehabilitation, and transplantation. The aim of this study is to review our experience with surgical rehabilitation techniques (SRTs: enteroplasty, Bianchi, Serial Transverse Enteroplasty Procedure [STEP]) in patients with short bowel syndrome (SBS) and poor prognosis due to complex abdominal pathology. We performed a single-center retrospective study of patients with IF evaluated for intestinal transplantation in the Intestinal Rehabilitation Unit who underwent an SRT. Nonparametric tests were used for statistical analysis. A total of 205 patients (107 males/98 females) with mean age of 25 +/- 7 months were assessed for IF. A total of 433 laparotomies were performed on 130 patients including intestinal resection, enteroplasties, adhesiolysis, and transit reconstruction. SRT were performed in 22 patients: 12 enteroplasties, 8 STEPs, and 4 Bianchi procedures. All patients were parenteral nutrition (PN) dependent with different stages of liver disease: mild (13), moderate (5), and severe (4). The adaptation rate for patients who underwent enteroplasty, STEP, and Bianchi were 70, 63, and 25%, respectively, although the techniques are not comparable. Overall, intestinal adaptation was achieved in nine (41%) patients, and four (18%) patients showed significant reduction of PN needs. One child did not respond to SRT and did not meet transplantation criteria. The remaining eight (36%) patients were included on the waiting list for transplant: four were transplanted, two are still on the waiting list, and two died. Better outcomes were observed in milder cases of liver disease (mild 77%, moderate 40%, severe 25%) (p<0.05). Conversely, a trend toward a poorer outcome was observed in cases with ultrashort bowel (p>0.05). One patient required reoperation after a Bianchi procedure due to intestinal ischemia and six needed further re-STEP or adhesiolysis procedure several months later. The median follow-up was 62 (3-135) months. Overall mortality was 19%, and was due to end-stage liver disease and/or central venous catheter-related sepsis. SRT led to intestinal adaptation in a significant number of patients with poor prognosis SBS referred for intestinal transplantation. However, SRT requires a multidisciplinary evaluation and should be attempted only in suitable cases. Careful assessment and optimal surgical timing is crucial to obtain a favorable outcome.
机译:肠衰竭(IF)需要基于营养支持,手术和医学康复以及移植的多学科管理。这项研究的目的是回顾我们的手术康复技术(SRT:肠成形术,Bianchi,连续横肠整形手术[STEP])在患有短肠综合征(SBS)且由于复杂的腹部病理而预后不良的患者中的经验。我们对接受SRT的肠道修复单元中经肠移植评估的IF患者进行了单中心回顾性研究。非参数检验用于统计分析。评估了平均年龄为25 +/- 7个月的205例患者(男性107例,女性98例)。 130例患者共进行了433例开腹手术,包括肠切除,肠成形术,黏附溶解和转运重建。在22例患者中进行了SRT:12例肠成形术,8步手术和4例Bianchi手术。所有患者均依赖肠外营养(PN),并具有不同阶段的肝病:轻度(13),中度(5)和重度(4)。尽管技术不具有可比性,但接受肠成形术,STEP和Bianchi的患者的适应率分别为70%,63%和25%。总体而言,有9名(41%)患者实现了肠道适应,而4名(18%)患者显示了PN需要量的显着减少。 1名儿童对SRT无反应,不符合移植标准。其余八名患者(36%)被列入等待移植名单:四名已移植,两名仍在等待名单中,两名死亡。在轻度肝病病例中观察到更好的预后(轻度77%,中度40%,重度25%)(p <0.05)。相反,在肠超短的患者中观察到了预后较差的趋势(p> 0.05)。一名患者由于肠缺血在Bianchi手术后需要再次手术,而六个月后几个月需要进一步的重新STEP或粘连溶解手术。中位随访时间为62(3-135)个月。总死亡率为19%,归因于末期肝病和/或中心静脉导管相关脓毒症。 SRT导致许多预后不良的患者发生肠道适应,SBS需进行肠移植。但是,SRT需要多学科评估,并且仅在适当情况下才应尝试。仔细评估和最佳手术时机对于获得良好结果至关重要。

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