Liu D C, Rodriguez J, Hill C B, Loe W A
Children's Hospital of New Orleans, LA 70118, USA.
J Pediatr Surg. 2000 Feb;35(2):235-8. doi: 10.1016/s0022-3468(00)90016-2.
BACKGROUND/PURPOSE: Transanal mucosectomy of the aganglionic segment of colon is a critical step in minimally invasive surgery for Hirschsprung's disease. The purpose of this study was to examine the outcome of patients undergoing transanal mucosectomy.
From January 1979 to November 1998, 26 patients (ages 25 days to 17 years) underwent transanal mucosectomy for Hirschsprung's disease. Seventeen (65%) had partial transanal mucosectomy (PTM; 1979 to 1998) and 9 (35%) complete transanal mucosectomy (CTM; 1995 to 1998). In PTM, a 2- to 3-cm mucosal dissection was begun 1 cm above the dentate line in conjunction with transabdominal endorectal dissection (modified Soave). In CTM, the entire mucosal dissection was performed transanally as part of a laparoscopically assisted Soave procedure. Results were obtained by chart review and personal communication. Patients were assessed clinically for continence where age appropriate (>3 years) and for development of constipation, postoperative enterocolitis, and anal stricture.
One of 16 (6.2%) of the PTM group was incontinent versus none (4 patients) in the CTM group. Five of 17 (29.4%) of the PTM group were constipated versus 4 of 9 (44.4%) in the CTM group (t test, P = not significant). Postoperative enterocolitis developed in 4 of 17 (23.5%) of the PTM group versus 6 of 9 (66.6%) in the CTM group (t test, P<.05). Three of 6 (50%) of the CTM group versus none in the PTM group required hospitalization for bowel rest, rectal washouts, and antibiotics. All patients were well at the time of the report. Anal stricture was not seen in either group.
Constipation and postoperative enterocolitis are a significant feature of transanal mucosectomy for Hirschsprung's disease deserving close surveillance, especially in patients in whom the entire mucosal dissection was performed transanally. Continence appears to be satisfactorily preserved from these preliminary results.
背景/目的:经肛门切除结肠无神经节段黏膜是先天性巨结肠症微创手术的关键步骤。本研究旨在探讨接受经肛门黏膜切除术患者的治疗结果。
1979年1月至1998年11月,26例年龄在25天至17岁之间的患者因先天性巨结肠症接受了经肛门黏膜切除术。17例(65%)接受了部分经肛门黏膜切除术(PTM;1979年至1998年),9例(35%)接受了完全经肛门黏膜切除术(CTM;1995年至1998年)。在PTM中,于齿状线以上1 cm处开始进行2至3 cm的黏膜剥离,并联合经腹直肠内剥离术(改良Soave术)。在CTM中,作为腹腔镜辅助Soave手术的一部分,经肛门进行整个黏膜剥离。通过查阅病历和个人交流获取结果。对患者进行临床评估,评估其在适当年龄(>3岁)时的控便能力以及便秘、术后小肠结肠炎和肛门狭窄的发生情况。
PTM组16例中有1例(6.2%)出现大便失禁,而CTM组无(4例患者)。PTM组17例中有5例(29.4%)出现便秘,CTM组9例中有4例(44.4%)出现便秘(t检验,P值无统计学意义)。PTM组17例中有4例(23.5%)发生术后小肠结肠炎,CTM组9例中有6例(66.6%)发生术后小肠结肠炎(t检验,P<0.05)。CTM组6例中有3例(50%)因肠道休息、直肠冲洗和使用抗生素而需要住院治疗,PTM组则无。在报告时所有患者情况良好。两组均未发现肛门狭窄。
便秘和术后小肠结肠炎是先天性巨结肠症经肛门黏膜切除术的显著特征,值得密切监测,尤其是对于那些经肛门进行整个黏膜剥离的患者。从这些初步结果来看,控便能力似乎得到了令人满意的保留。