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先天性短结肠结肠成形术的技术与长期疗效

Technique and long-term results of coloplasty for congenital short colon.

作者信息

Wakhlu Ashish, Wakhlu Avtar Kishen

机构信息

Department of Pediatric Surgery, King George Medical University, Lucknow, India.

出版信息

Pediatr Surg Int. 2009 Jan;25(1):47-52. doi: 10.1007/s00383-008-2281-y. Epub 2008 Nov 1.

Abstract

PURPOSE

This paper aims to present the modified technique of coloplasty for congenital short colon (CSC) and analyse the long-term results of this operative procedure.

METHODS

A total of 310 patients of CSC have been admitted to out department between 1975 and 2007; 138 have been treated by the modified technique of coloplasty. Seven patients expired after coloplasty and nine are awaiting ileostomy closure. One hundred and twenty-two have completed all stages of surgery (study group). In these patients, three-stage surgical management (window colostomy, coloplasty with ileostomy and ileostomy closure) was performed. The range of follow-up is from 2 months to 18 years. The patients have been observed for: quality of muscle at the time of PSARP, Kelly's continence score, growth and development, schooling and social interactions and complications. Contrast study of the coloplasty tube has been done at different stages during follow-up with observation of colon diameter, evidence of peristalsis and colon emptying.

RESULTS

Ninety-seven patients from the study group have good quality of life, normal growth and development, where appropriate, they go to school and have normal social interactions. Using Kelly's scoring system, the results are good in 97 (stool frequency up to 3/day, no perineal excoriation, no soiling), fair in 9 (stool frequency 3-5/day, occasional perineal excoriation and occasional soiling) and poor in 16 (continuous stooling, soiling, perineal excoriation or complications). Complications include perineal dehiscence needing permanent colostomy (n=1), closure of the distal end of the coloplasty tube requiring revision (n=2), adhesive intestinal obstruction requiring re-exploration (n=2). Additionally intractable perineal excoriation (n=8), colonic dilatation requiring pouch excision and conversion to ileal 'S' pouch (n=2) and failure to thrive (n=4) were also seen.

CONCLUSIONS

Congenital short colon is the most severe colonic malformation barring cloacal exstrophy; however, good quality of life can be offered to these patients by coloplasty. The important technical step is to make the colonic tube long and small in diameter, so that it can propel stools and resist dilatation. These steps have been highlighted in the paper.

摘要

目的

本文旨在介绍先天性短结肠(CSC)结肠成形术的改良技术,并分析该手术的长期效果。

方法

1975年至2007年间,共有310例CSC患者入住我科;138例采用改良结肠成形术治疗。7例患者结肠成形术后死亡,9例等待回肠造口关闭。122例完成了所有手术阶段(研究组)。对这些患者实施了三阶段手术管理(开窗结肠造口术、带回肠造口的结肠成形术和回肠造口关闭术)。随访时间为2个月至18年。观察患者以下方面:肛门直肠成形术时的肌肉质量、凯利控便评分、生长发育、上学情况、社交互动及并发症。在随访的不同阶段对结肠成形管进行造影研究,观察结肠直径、蠕动迹象及结肠排空情况。

结果

研究组97例患者生活质量良好,生长发育正常,适龄上学,社交互动正常。采用凯利评分系统,结果为良好的97例(排便频率每天达3次,无会阴擦伤,无污粪),中等的9例(排便频率3 - 5次/天,偶尔会阴擦伤和偶尔污粪),差的16例(持续排便、污粪、会阴擦伤或有并发症)。并发症包括需要永久性结肠造口的会阴裂开(n = 1)、需要再次手术的结肠成形管远端闭合(n = 2)、需要再次探查的粘连性肠梗阻(n = 2)。此外,还观察到顽固性会阴擦伤(n = 8)、需要切除贮袋并改为回肠“S”贮袋的结肠扩张(n = 2)和发育不良(n = 4)。

结论

先天性短结肠是除泄殖腔外翻外最严重的结肠畸形;然而,通过结肠成形术可为这些患者提供良好的生活质量。重要的技术步骤是使结肠管长且直径小,以便能推动粪便并抵抗扩张。本文已突出强调了这些步骤。

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