Thakkar Hemanshoo S, Bassett Christopher, Hsu Andy, Manuele Riccardo, Kufeji Dorothy, Richards Catherine A, Agrawal Meena, Keshtgar Alireza S
Department of Paediatric Surgery, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, Westminster Bridge Road, London, SE1 7EH.
Department of Paediatric Surgery, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, Westminster Bridge Road, London, SE1 7EH.
J Pediatr Surg. 2017 Feb;52(2):277-280. doi: 10.1016/j.jpedsurg.2016.11.023. Epub 2016 Nov 14.
Hirschsprung disease (HD) is a chronic condition associated with long-term morbidity. We assessed the short and long-term functional outcomes of operated patients in a single institution over a 12-year period.
We conducted a retrospective review of all children operated for HD between 2002 and 2014. Postoperative functional outcomes were assessed using the Rintala Bowel Function Score (BFS, 0-20, 20=best score). We assessed hospital admissions, complications including Hirschsprung associated enterocolitis (HAEC) and the need for further surgical procedures.
72 (52 male) patients were studied, of whom, 6 (8%) had a positive family history, 5 (7%) had Trisomy 21 and 5 (7%) had total colonic HD. The median age at diagnosis was 6.5days (2 days-6.7 years) and median follow-up was 6years (1-12years). All patients except two underwent a Duhamel pull-through procedure. The median age at surgery was 4months (6days-90months). 37 (51%) procedures were performed single-stage and 7 (10%) were laparoscopically assisted. Our early complication rate was 15%; 11 (15%) patients were treated for HAEC and 43 (60%) did not require any further surgery. 12 (17%) underwent injection of botulinum toxin, 7 (10%) needed residual spur division and 4 (5%) required an unplanned, post pull-through enterostomy for obstructive defecation symptoms and HAEC. Two (3%) patients underwent an Antegrade Colonic Enema (ACE) stoma. The median BFS was 17 (5-20). There were two deaths both out of hospital.
Long-term functional outcomes following Duhamel Pull-Through surgery are satisfactory although 40% of patients needed some form of further surgical intervention. The management of anal sphincter achalasia has improved with the use of botulinum toxin and we advocate aggressive and early management of this condition for symptoms of obstructive defecation and HAEC.
III.
先天性巨结肠(HD)是一种与长期发病相关的慢性疾病。我们评估了一家机构在12年期间接受手术治疗的患者的短期和长期功能结局。
我们对2002年至2014年间所有因HD接受手术的儿童进行了回顾性研究。使用林塔拉肠功能评分(BFS,0 - 20分,20分为最佳评分)评估术后功能结局。我们评估了住院情况、包括先天性巨结肠相关小肠结肠炎(HAEC)在内的并发症以及进一步手术的必要性。
共研究了72例患者(52例男性),其中6例(8%)有家族史阳性,5例(7%)患有21三体综合征,5例(7%)患有全结肠型HD。诊断时的中位年龄为6.5天(2天至6.7岁),中位随访时间为6年(1至12年)。除2例患者外,所有患者均接受了杜哈梅尔拖出术。手术时的中位年龄为4个月(6天至90个月)。37例(51%)手术为一期进行,7例(10%)为腹腔镜辅助手术。我们的早期并发症发生率为15%;11例(15%)患者接受了HAEC治疗,43例(60%)患者无需进一步手术。12例(17%)患者接受了肉毒杆菌毒素注射,7例(10%)患者需要切除残留的吻合口嵴,4例(5%)患者因排便梗阻症状和HAEC需要在拖出术后进行计划外的肠造口术。2例(3%)患者接受了顺行结肠灌洗(ACE)造口术。中位BFS为17分(5至20分)。有2例患者均在院外死亡。
尽管40%的患者需要某种形式的进一步手术干预,但杜哈梅尔拖出术后的长期功能结局令人满意。肉毒杆菌毒素的使用改善了肛门括约肌失弛缓症的管理,我们主张对这种疾病的排便梗阻症状和HAEC进行积极和早期的管理。
III级