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巨结肠同源病的再次手术:我们学到了什么?70 例单中心经验。

Redo surgery in Hirschsprung disease: what did we learn? Unicentric experience on 70 patients.

机构信息

Department of Pediatric Surgery - G. Gaslini Institute, Largo G. Gaslini, 5, 16147 Genoa, Italy.

出版信息

J Pediatr Surg. 2010 Apr;45(4):747-54. doi: 10.1016/j.jpedsurg.2009.08.001.

Abstract

PURPOSE

This article is aimed at describing a series of 70 patients who underwent a redo pull-through in the period between January 1991 and January 2007 and to compare them with a series of consecutive patients with Hirschsprung disease who underwent a single pull-through.

METHODS

The notes were reviewed, and a comprehensive interview based on a disease-specific questionnaire for continence and quality of life was submitted to all eligible patients. We used a number of consecutive patients who underwent a single pull-through for Hirschsprung disease as control group.

RESULTS

Seventy patients were included. Residual aganglionosis in pulled-through bowel or retained aganglionic rectum represented the indications to reoperation in most cases. Intestinal obstruction represented the leading symptom in more than 60% of patients. We adopted either the endorectal pull-through, the Duhamel, or the Swenson procedure. Thirty-six patients were assessed for long-term outcome. One third experienced complications. Long-term continence was satisfactory in 70%. Enterocolitis, soiling, and perineal excoriations were complained by 30%. Excellent to good perspectives were described by 94%, and excellent to good cosmetic results by 22%. The only significant difference with control group (109 patients) involved cosmetic appearance, whereas soiling, although more frequent, could not be considered significantly increased.

CONCLUSIONS

Patients who experience failure of a pull-through must go through multiple procedures to achieve definitive results. Although overall outcome does not significantly differ from that of a single effective pull-through, great efforts should be made to minimize complications and avoid the need for a redo, which requires experienced surgeons and highly committed families for a longer course of the disease.

摘要

目的

本文旨在描述 70 例 1991 年 1 月至 2007 年 1 月间接受再次拖出手术的患者,并与同期接受单次拖出手术的先天性巨结肠患者进行比较。

方法

回顾病历,并对所有符合条件的患者进行基于特定疾病的控便和生活质量问卷的综合访谈。我们将同期接受单次拖出手术的先天性巨结肠患者作为对照组。

结果

70 例患者入选。在大多数情况下,拖出肠段中残留的无神经节细胞组织或保留的无神经节细胞直肠是再次手术的指征。肠梗阻是超过 60%患者的主要症状。我们采用经肛门直肠拖出术、Duhamel 或 Swenson 手术。36 例患者进行了长期结局评估。三分之一的患者发生了并发症。70%的患者长期控便满意。30%的患者抱怨结肠炎、大便失禁和会阴部皮肤皲裂。94%的患者描述为良好至极好的前景,22%的患者描述为良好至极好的美容效果。与对照组(109 例)唯一显著的差异涉及美容外观,尽管大便失禁更为常见,但不能认为显著增加。

结论

经历拖出术失败的患者必须经过多次手术才能获得确定性结果。尽管总体结局与单次有效的拖出术无显著差异,但应努力最大程度地减少并发症,并避免需要再次手术,这需要有经验的外科医生和高度投入的家庭,以应对更长时间的疾病。

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