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发展中国家 1 岁后出现先天性巨结肠症的问题和结果。

Problems and outcome of Hirschsprung's disease presenting after 1 year of age in a developing country.

机构信息

Sub-Department of Paediatric Surgery, University of Nigeria Teaching Hospital, Enugu, Nigeria.

出版信息

World J Surg. 2011 Jan;35(1):22-6. doi: 10.1007/s00268-010-0828-2.

Abstract

BACKGROUND

The purpose of the present study was to evaluate the problems, treatment outcome, and contributory factors to delayed presentation in Hirschsprung's disease (HD) after 1 year of age in a resource-limited setting.

METHODS

This retrospective study included 41 children aged >1 year with HD managed at the University of Nigeria Teaching Hospital, Enugu, in south eastern Nigeria, between January 2000 and June 2009.

RESULTS

Complications of HD were evident at presentation in 38 (92.7%) of the 41 children. Late presentation was due to delayed referral in 27 cases (65.9%), parental ignorance in 11 (26.8%), and poverty in 3 (7.3%). The HD was rectosigmoid in 33 patients (80.5%) and was of ultra-short length variety in 8 patients (19.5%). Thirty-five patients (85.4%) required colostomy for decompression, and colostomy-related complications occurred in 24 of them (68.6%). The definitive surgical procedure was a Swenson pullthrough in 34 cases (82.9%) and posterior myectomy in 7 others (17.1%). Twenty patients (48.8%) experienced at least one postoperative complication. After follow-up of 7-64 months (mean: 31 months), 31 (75.6%) patients had a good outcome, 6 (14.6%) had persistent constipation, 3 had (7.3%) incontinence, and one child (2.4%) died from overwhelming infection.

CONCLUSIONS

Hirschsprung's disease presenting after 1 year of age may be associated with high colostomy rates and increased morbidity. Continued dissemination of updated information on HD to medical practitioners and a public awareness campaign may improve time to diagnosis.

摘要

背景

本研究旨在评估资源有限环境下 1 岁以后出现的先天性巨结肠(HD)的问题、治疗结果和延迟就诊的因素。

方法

本回顾性研究纳入了 2000 年 1 月至 2009 年 6 月期间在尼日利亚东南部恩古尼大学教学医院接受治疗的 41 名年龄>1 岁的 HD 患儿。

结果

41 名患儿中,38 名(92.7%)在就诊时存在 HD 并发症。27 例(65.9%)延迟就诊是由于转诊延迟,11 例(26.8%)是由于父母无知,3 例(7.3%)是由于贫困。33 例(80.5%)HD 为直肠乙状结肠型,8 例(19.5%)为超短段型。35 例(85.4%)患儿行结肠造口术减压,其中 24 例(68.6%)发生造口相关并发症。34 例行 Swenson 拖出术(82.9%),7 例行后肌切除术(17.1%)。20 例(48.8%)患儿至少发生 1 次术后并发症。术后随访 7-64 个月(平均 31 个月)后,31 例(75.6%)患儿结局良好,6 例(14.6%)持续便秘,3 例(7.3%)失禁,1 例(2.4%)死于感染性休克。

结论

1 岁以后出现的先天性巨结肠可能与较高的结肠造口率和较高的发病率有关。向医务人员和公众持续宣传 HD 的最新信息可能有助于改善诊断时间。

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