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唐氏综合征患儿的先天性巨结肠症:一项对比研究。

Hirschsprung's disease in children with Down syndrome: a comparative study.

作者信息

Travassos D, van Herwaarden-Lindeboom M, van der Zee D C

机构信息

University Medical Centre Utrecht, Pediatric Surgery, Utrecht, Netherlands.

出版信息

Eur J Pediatr Surg. 2011 Aug;21(4):220-3. doi: 10.1055/s-0031-1271735. Epub 2011 Feb 24.

Abstract

BACKGROUND AND AIM

There is controversy in the literature regarding the outcome after surgical treatment of Hirschsprung's disease in children with Down syndrome (DS). The aim of this study was to compare the outcome of our series of DS children with Hirschsprung's disease to our series of children without Down syndrome (NDS) with Hirschsprung's disease. The impact of laparoscopy within the DS group was analyzed.

MATERIAL AND METHODS

Between March 1987 and August 2008, 149 children were operated on for Hirschsprung's disease. 20 children of this group were additionally diagnosed with Down syndrome. All children underwent either an open or a laparoscopic Duhamel procedure. We evaluated postoperative hospital stay, short-term complications and the incidence of enterocolitis, constipation and incontinence.

RESULTS

20 patients (13.4%) in this series had Down syndrome. There were no significant differences in the extent of aganglionosis between children with or without Down syndrome. There were no intra-operative complications and no conversions. Postoperative leak occurred significantly more often in children with DS (n=5, 25%) compared to NDS children (n=1, 0.7%; p<0.0001). Postoperative leakage-related abscess formation was higher in the DS group (n=3, 15%) compared to the NDS group (0%). Within the DS group there was no significant difference between open or laparoscopic Duhamel procedure with regard to these postoperative complications. Postoperative hospital stay was significantly longer in the DS group compared to the NDS group (p<0.05). In the DS group there was a slightly shorter postoperative stay after laparoscopic Duhamel procedure. Mean long-term follow-up was 5.1 years. One death occurred in the DS group 9 months postoperatively due to sepsis and cardiomyopathy. Severe constipation was present significantly more often in DS children (n=11, 55%) compared to NDS children (n=29, 22.3%; p<0.01). There was no difference in incontinence between DS and NDS children. Enterocolitis occurred more frequently in DS patients after operation (40 [31% NDS] vs. 9 [45% DS]; p=0.038).

CONCLUSION

Compared to NDS children, children with DS have a higher rate of postoperative complications and a longer hospital stay. During long-term follow-up most patients with DS are severely constipated and have a higher incidence of enterocolitis.

摘要

背景与目的

关于唐氏综合征(DS)患儿先天性巨结肠症手术治疗后的结果,文献中存在争议。本研究的目的是比较我们收治的患先天性巨结肠症的DS患儿系列与患先天性巨结肠症的非唐氏综合征(NDS)患儿系列的治疗结果。分析了腹腔镜手术在DS组中的影响。

材料与方法

1987年3月至2008年8月期间,149例患儿接受了先天性巨结肠症手术。该组中有20例患儿还被诊断为唐氏综合征。所有患儿均接受了开放或腹腔镜Duhamel手术。我们评估了术后住院时间、短期并发症以及小肠结肠炎、便秘和大便失禁的发生率。

结果

本系列中有20例患者(13.4%)患有唐氏综合征。唐氏综合征患儿与非唐氏综合征患儿的无神经节细胞症范围无显著差异。术中无并发症,也无中转开腹情况。与NDS患儿(n = 1,0.7%;p < 0.0001)相比,DS患儿术后吻合口漏的发生率显著更高(n = 5,25%)。DS组术后与吻合口漏相关的脓肿形成率(n = 3,15%)高于NDS组(0%)。在DS组中,开放或腹腔镜Duhamel手术在这些术后并发症方面无显著差异。DS组的术后住院时间显著长于NDS组(p < 0.05)。在DS组中,腹腔镜Duhamel手术后的术后住院时间略短。平均长期随访时间为5.1年。DS组有1例患儿术后9个月因败血症和心肌病死亡。与NDS患儿(n = 29,22.3%;p < 0.01)相比,DS患儿中严重便秘的发生率显著更高(n = 11,55%)。DS患儿与NDS患儿在大便失禁方面无差异。DS患者术后小肠结肠炎的发生率更高(40例[31%为NDS] vs. 9例[45%为DS];p = 0.038)。

结论

与NDS患儿相比,DS患儿术后并发症发生率更高,住院时间更长。在长期随访中,大多数DS患者严重便秘,小肠结肠炎的发生率更高。

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