Heinrich M, Häberle B, von Schweinitz D, Stehr M
Dr von Haunersche Kinderspital, Pediatric Surgery, München, Germany.
Eur J Pediatr Surg. 2011 Oct;21(5):325-30. doi: 10.1055/s-0031-1284423. Epub 2011 Aug 30.
In some patients with Hirschsprung's disease (HD), the initial surgical procedure fails, and the patients suffer from repeated or persistent symptoms. These patients complain of severe inflammation, intestinal obstruction, fecal or urinary incontinence, abdominal pain or dystrophy. However, little data has been published on the long-term follow-up results after re-operations for HD.
We followed 8 cases between 2004 and 2006, of complicated HD requiring repeated surgery and recorded prior procedures, histological results, indications for re-operation, postoperative follow-up as well as long-term clinical outcomes including stool patterns, nutrition and micturition.
The follow-up period ranged from 3.0 to 5.5 years (mean: 4.4 years). Indications for repeat procedures were as follows: blind rectal pouch after a Duhamel operation (n = 2), persistent aganglionosis (n = 4), long-segment stenosis (n = 1) after a Rehbein operation, and anal stenosis following TERPT (transanal endorectal pull-through) (n = 1). In one patient who had a Duhamel-Martin operation, extirpation of the rectum and a definitive terminal ileostomy was necessary. A Duhamel procedure was performed in five patients with a primary Rehbein and 1 patient with a primary Duhamel operation. Complete stool continence was achieved in 4 patients. Partial fecal incontinence persisted in one patient with associated trisomy 21. 1 patient with total colonic aganglionosis and 1 patient with a pelvic fistula and a previous subtotal colectomy reported soiling 1-2 times per week after a repeat operation. 4 patients in our series experienced postoperative complications following repeated surgery [perianal ulceration (n = 2), repeated botulinum toxin injection for sphincter achalasia (n = 1) and functionally impaired colonic transit without stenosis (n = 1)]. Micturition was normal in 7 patients, 1 patient with associated trisomy 21 was partially continent, and 1 patient reported infrequent urge incontinence.
All patients improved after further surgical intervention. However, resolution of their symptoms was delayed and partial stool incontinence or soiling persisted in 3 patients. Most complications leading to repeat procedures are preventable, especially residual aganglionosis. Therefore, great efforts should be made to minimize complications when planning and performing the primary surgery.
在一些先天性巨结肠(HD)患者中,初次手术失败,患者出现反复或持续的症状。这些患者主诉有严重炎症、肠梗阻、大便或小便失禁、腹痛或营养不良。然而,关于HD再次手术后长期随访结果的资料报道较少。
我们对2004年至2006年间8例需要再次手术的复杂HD患者进行了随访,记录了之前的手术过程、组织学结果、再次手术的指征、术后随访以及包括排便模式、营养和排尿在内的长期临床结局。
随访期为3.0至5.5年(平均4.4年)。再次手术的指征如下:Duhamel手术后盲袋直肠(2例)、持续性无神经节细胞症(4例)、Rehbein手术后长段狭窄(1例)以及经肛门直肠内拖出术(TERPT)后肛门狭窄(1例)。1例接受Duhamel-Martin手术的患者需要切除直肠并进行确定性末端回肠造口术。5例初次行Rehbein手术和1例初次行Duhamel手术的患者接受了Duhamel手术。4例患者实现了完全大便自控。1例伴有21三体综合征的患者仍有部分大便失禁。1例全结肠无神经节细胞症患者和1例盆腔瘘且之前接受过次全结肠切除术的患者在再次手术后报告每周有1 - 2次便污。我们系列中的4例患者在再次手术后出现了术后并发症[肛周溃疡(2例)、因括约肌失弛缓症反复注射肉毒杆菌毒素(1例)以及无狭窄的功能性结肠传输障碍(1例)]。7例患者排尿正常,1例伴有21三体综合征的患者有部分控尿能力,1例患者报告有偶发的急迫性尿失禁。
所有患者在进一步手术干预后均有改善。然而,他们症状的缓解有所延迟,3例患者仍存在部分大便失禁或便污。导致再次手术的大多数并发症是可以预防的,尤其是残留无神经节细胞症。因此,在计划和实施初次手术时应尽最大努力将并发症降至最低。