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短肠综合征的手术治疗方法。160例患者的经验。

Surgical approach to short-bowel syndrome. Experience in a population of 160 patients.

作者信息

Thompson J S, Langnas A N, Pinch L W, Kaufman S, Quigley E M, Vanderhoof J A

机构信息

Department of Surgery, University of Nebraska Medical Center, Children's Hospital, USA.

出版信息

Ann Surg. 1995 Oct;222(4):600-5; discussion 605-7. doi: 10.1097/00000658-199522240-00016.

Abstract

OBJECTIVE

The authors reviewed their experience with short-bowel syndrome to define the surgical approach to this problem in 160 patients.

METHODS

Forty-eight adults and 112 children were evaluated over a 15-year period.

RESULTS

Seventy-one patients (44%) adapted to resection and took enteral nutrition alone. Forty-four patients (28%) were supported by parenteral nutrition (PN). Forty-five patients (28%) have had 49 surgical procedures. Fifteen patients with adequate intestinal length (> 120 cm in adults) but dilated dysfunctional bowel underwent stricturoplasty (n = 4) or tapering (n = 11). Thirteen patients (87%) demonstrated clinical improvement. Fourteen patients with shorter remnants (90-120 cm) and rapid transit time received an artificial valve (n = 2) or a reversed segment (n = 1). All patients' conditions improved initially, but the reversed segment was revised or taken down. Fourteen patients with short remnants and dilated bowel underwent intestinal lengthening. Twelve patients' conditions improved (86%), one underwent transplantation, and one died. Sixteen patients with very short remnants (< 60 cm) and complications of PN underwent solitary intestine (n = 4) or combined liver-intestinal transplantation (n = 13). One-year graft survival was 65%. There have been five deaths.

CONCLUSIONS

The surgical approach to short-bowel syndrome depends on the patient's age, remnant length and caliber, intestinal function, and PN-related complications. Nontransplant procedures have a role in the treatment of selected patients. Intestinal transplantation is emerging as a potential therapy for patients with significant PN-related complications.

摘要

目的

作者回顾了他们在短肠综合征方面的经验,以确定针对160例该疾病患者的手术治疗方法。

方法

在15年的时间里对48例成人和112例儿童进行了评估。

结果

71例患者(44%)适应了肠切除,仅接受肠内营养。44例患者(28%)接受肠外营养(PN)支持。45例患者(28%)接受了49次外科手术。15例肠长度足够(成人>120 cm)但肠管扩张功能不良的患者接受了狭窄成形术(n = 4)或肠管缩窄术(n = 11)。13例患者(87%)临床症状改善。14例残留肠管较短(90 - 120 cm)且肠传输时间较快的患者接受了人工瓣膜植入(n = 2)或肠段翻转术(n = 1)。所有患者病情最初均有改善,但肠段翻转术患者的肠段后来被修正或切除。14例残留肠管短且肠管扩张的患者接受了肠延长术。12例患者病情改善(86%),1例接受了移植,1例死亡。16例残留肠管极短(<60 cm)且有PN相关并发症的患者接受了单肠移植(n = 4)或肝肠联合移植(n = 13)。1年移植物存活率为65%。共有5例死亡。

结论

短肠综合征的手术治疗方法取决于患者的年龄、残留肠管长度和管径、肠道功能以及PN相关并发症。非移植手术在特定患者的治疗中具有作用。肠移植正逐渐成为治疗严重PN相关并发症患者的一种潜在疗法。

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