Long-term Follow-up of Patients with Hirschsprung Disease: Unusual Late Complications After Pull-through

L. Mohajerzadeh, Ashkan Soltani, A. Zakeri, Ahmad Khaleghnejad Tabari, M. Rouzrokh, J. Ghoroubi, M. Sarafi, N. Dara, Farnoosh Rahimi, Sayeh Hatefi
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Abstract

Background: A large number of patients who underwent pull-through surgery due to Hirschsprung's disease (HD) were not followed up properly and they suffered from many complications such as fecal soiling, constipation, and etc. Although some of these complications may relief over time, it is rational to consider an evaluative protocol to identify anatomical or pathological complications in these patients. Objective: The aim of the present study is to evaluate and introduce these catastrophic complications. Method: In this historical cohort study, 193 patients with HD who had undergone pull- through surgery between 2006 to 2013 were considered. All files and questionnaires were used to collect patients' information and patients were physically examined individually. The mean duration of the follow-up was 96.4±17.2 months ranging from 60 to 144 months The follow-up performed for all patients via the outpatient clinics or by telephone. All statistical information was analyzed by SPSS software version 17. Results: Results: At first presentation, intestinal obstruction was more frequent than constipation. The most common involved segment was in rectosigmoid. The most common early postoperative complication was stricture in anal canal and the most common late complications were constipation and focal soiling. Conclusion: Although surgical advancements, a large number of patients underwent surgical procedures due to HD experience long term complications. Surgical treatment of HD generally present with high-quality outcome and the majority of children survive in satisfactory situation for long time but occasionally pediatric surgeons meet head-on catastrophic complication in these patients that require extended team work to be resolved
巨结肠病患者的长期随访:拔通后不寻常的晚期并发症
背景:大量因先天性巨结肠病(Hirschsprung's disease, HD)而行拉通手术的患者没有得到适当的随访,并且出现了粪便污染、便秘等并发症。虽然这些并发症中的一些可能会随着时间的推移而减轻,但考虑一种评估方案来识别这些患者的解剖或病理并发症是合理的。目的:本研究的目的是评估和介绍这些灾难性并发症。方法:在这项历史队列研究中,193例HD患者在2006年至2013年期间接受了拉通手术。采用所有档案和问卷收集患者信息,并对患者进行个体体检。随访时间60 ~ 144个月,平均96.4±17.2个月。所有患者均通过门诊或电话随访。所有统计资料采用SPSS软件17版进行分析。结果:结果:首次就诊时肠梗阻多于便秘。最常见的受累节段是直肠乙状结肠。术后早期最常见的并发症是肛管狭窄,晚期最常见的并发症是便秘和局灶性脏污。结论:尽管手术治疗取得了进展,但大量因HD而接受手术治疗的患者出现了长期并发症。HD的手术治疗通常具有高质量的结果,大多数儿童在长期满意的情况下存活,但偶尔儿科外科医生会遇到这些患者的正面灾难性并发症,需要延长团队合作才能解决
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