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先天性巨结肠再次拖出术的长期随访:经直肠拖出术的疗效

Long-term follow-up of redo pull-through procedures for Hirschsprung's disease: efficacy of the endorectal pull-through.

作者信息

van Leeuwen K, Teitelbaum D H, Elhalaby E A, Coran A G

机构信息

Department of Surgery, The University of Michigan Medical School and C.S. Mott Children's Hospital, Ann Arbor, USA.

出版信息

J Pediatr Surg. 2000 Jun;35(6):829-33; discussion 833-4. doi: 10.1053/jpsu.2000.6853.

Abstract

BACKGROUND/PURPOSE: The purpose of this study was to review the authors' 25-year experience with redo pull-through procedures for Hirschsprung's disease including surgical technique and long-term outcome.

METHODS

From 1974 to now, over 325 patients with Hirschsprung's disease have been treated at C.S. Mott Children's Hospital. This includes 30 patients referred after an unsuccessful pull-through at another hospital and 2 patients with an unsuccessful pull-through from C.S. Mott. All redo pull-throughs (n = 19) were performed in these patients, and their clinical courses are reviewed.

RESULTS

Twelve patients required reoperation secondary to a mechanical problem with their first pull-through. The other 7 patients had evidence of residual segments of dilated colon leading to functional failure of their initial operation including 5 patients with documented aganglionic bowel present at the second pull-through. Ten of the patients requiring reoperation initially had an endorectal pull-through (ERPT), 5 had a Duhamel procedure, 3 had a Swenson procedure, and 1 had a Rehbein procedure. Choice of revision was an ERPT in 8 patients in whom an adequate rectal cuff could be developed. Additional redo procedures included a Duhamel in 8 patients and a Swenson in 3 patients. Follow-up ranges from 3 months to 23 years (mean, 13.8 years). There were no deaths in the series, and 1 patient required a third pull-through. All patients who are not neurologically impaired and are over age 3 are continent except one (94%). Stools per day range from 1 to 10 (mean, 3.2).

CONCLUSIONS

Redo pull-through operations for Hirschsprung's disease appear to be as effective as primary procedures in terms of continence and stooling frequency. Distinct from other series, we found an ERPT to be the procedure of choice if an adequate rectal cuff was present.

摘要

背景/目的:本研究旨在回顾作者25年来对先天性巨结肠症再次拖出术的经验,包括手术技术和长期疗效。

方法

从1974年至今,超过325例先天性巨结肠症患者在C.S. 莫特儿童医院接受治疗。其中包括30例在其他医院初次拖出术失败后转诊而来的患者,以及2例在C.S. 莫特医院初次拖出术失败的患者。对这些患者均实施了再次拖出术(n = 19),并回顾了他们的临床病程。

结果

12例患者因初次拖出术出现机械性问题而需要再次手术。另外7例患者有扩张结肠残留段的证据,导致初次手术出现功能衰竭,其中5例在再次拖出术时发现有神经节缺如的肠段。需要再次手术的患者中,10例最初接受了经肛门直肠拖出术(ERPT),5例接受了杜哈梅尔手术,3例接受了斯文森手术,1例接受了雷贝恩手术。8例能够形成足够直肠袖带的患者选择了ERPT作为翻修手术。另外的再次手术包括8例杜哈梅尔手术和3例斯文森手术。随访时间为3个月至23年(平均13.8年)。该系列中无死亡病例,1例患者需要第三次拖出术。除1例患者外(94%),所有无神经功能障碍且年龄超过3岁的患者均能自主控制排便。每日排便次数为1至10次(平均3.2次)。

结论

先天性巨结肠症再次拖出术在控制排便和排便频率方面似乎与初次手术同样有效。与其他系列不同的是,我们发现如果存在足够的直肠袖带,ERPT是首选手术方式。

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