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合并先天性巨结肠症的小肠结肠炎患者的长期预后

Long-term outcome of patients with enterocolitis complicating Hirschsprung's disease.

作者信息

Menezes Maria, Puri Prem

机构信息

Children's Research Centre, Our Lady's Hospital for Sick Children, Crumlin, Dublin 12, Ireland.

出版信息

Pediatr Surg Int. 2006 Apr;22(4):316-8. doi: 10.1007/s00383-006-1639-2. Epub 2006 Feb 4.

Abstract

Enterocolitis remains the most serious complication of Hirschsprung's disease (HD). The purpose of this study was to evaluate the risk factors in the development of enterocolitis and the long-term outcome in these patients. The hospital records of 259 consecutive patients with HD during 1975-2003 were examined. The data was analysed for age at presentation, associated anomalies, level of aganglionosis, clinical features, number of episodes of enterocolitis, type of pullthrough, necessity for post-pullthrough sphincterectomy. Follow up was carried out by personal interviews and interviews over the telephone with patients/parents. Enterocolitis was diagnosed on the basis of clinical features of diarrhoea, pyrexia, abdominal distention and vomiting. Of the 259 patients with HD, 74 patients (28.5%) were found to have enterocolitis. Out of 39 patients with Down's syndrome and HD, 19 (48%) had enterocolitis. Fifteen (20%) patients had other associated anomalies. Fifty-six patients (75.6%) were male and 18 (24.3%) were female. In 30 patients enterocolitis was the presenting feature in the neonatal period, 22 of which presented in the first 2 weeks of life. Fifty-six patients (75.6%) had rectosigmoid disease and 18 (24.3%) had long segment disease or total colonic aganglionosis. Eighteen (24.3%) had only preoperative enterocolitis and 31(41.8%) had only postoperative enterocolitis. Twenty-five (33.7%) had both pre- and post-operative enterocolitis. Twenty (27%) patients had more than 2 episodes of enterocolitis. Various pullthrough procedures were performed. Twenty-six patients (35.1%) required internal sphinctermyectomy to treat the enterocolitis. At the time of follow-up, 16 patients were lost to follow-up. Of the remaining 58 patients, 3 patients died, 2 due to enterocolitis and 1 due to sepsis. Six patients remained with a stoma. Twenty-two patients were continent and were stooling normally, but 14 of these were on laxatives for several years after pullthrough procedure. The mean age at achieving full continence was 4.95 years in the 22 patients with normal bowel function. Nineteen patients are still on laxatives and 8 patients are soiling. Eight patients continue to have multiple recurrent episodes of enterocolitis at follow-up. Down's syndrome is an important risk factor in the development of enterocolitis. The majority of patients with enterocolitis complicating HD continue to have disturbances of bowel function many years after surgery for HD.

摘要

小肠结肠炎仍然是先天性巨结肠症(HD)最严重的并发症。本研究的目的是评估小肠结肠炎发生发展的危险因素以及这些患者的长期预后。对1975年至2003年间连续收治的259例HD患者的医院记录进行了检查。分析了患者就诊时的年龄、合并畸形、无神经节病变的范围、临床特征、小肠结肠炎发作次数、拖出术类型、拖出术后是否需要行括约肌切除术等数据。通过对患者/家长进行个人访谈及电话访谈进行随访。根据腹泻、发热、腹胀和呕吐等临床特征诊断小肠结肠炎。在259例HD患者中,74例(28.5%)被发现患有小肠结肠炎。在39例患有唐氏综合征和HD的患者中,19例(48%)患有小肠结肠炎。15例(20%)患者有其他合并畸形。56例(75.6%)患者为男性,18例(24.3%)为女性。30例患者小肠结肠炎为新生儿期首发症状,其中22例在出生后2周内发病。56例(75.6%)患者为直肠乙状结肠病变,18例(24.3%)患者为长段病变或全结肠无神经节症。18例(24.3%)患者仅术前发生小肠结肠炎,31例(41.8%)患者仅术后发生小肠结肠炎。25例(33.7%)患者术前和术后均发生小肠结肠炎。20例(27%)患者小肠结肠炎发作超过2次。实施了各种拖出术。26例(35.1%)患者需要行内括约肌切除术来治疗小肠结肠炎。随访时,16例患者失访。在其余58例患者中,3例死亡,2例死于小肠结肠炎,1例死于败血症。6例患者仍保留造口。22例患者大便自控且排便正常,但其中14例在拖出术后数年仍需使用泻药。22例肠道功能正常的患者实现完全自控的平均年龄为4.95岁。19例患者仍在使用泻药,8例患者存在大便失禁。8例患者在随访时小肠结肠炎仍多次复发。唐氏综合征是小肠结肠炎发生发展的一个重要危险因素。大多数合并HD的小肠结肠炎患者在HD手术后多年肠道功能仍有紊乱。

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