Universitas Gadjah Mada/Dr. Sardjito Hospital, Faculty of Medicine, Public Health and Nursing, Department of Surgery, Pediatric Surgery Division, Yogyakarta, Indonesia.
Universitas Gadjah Mada, Faculty of Medicine, Public Health and Nursing, Department of Child Health, Yogyakarta, Indonesia.
Med J Malaysia. 2024 Aug;79(Suppl 4):1-5.
Hirschsprung disease (HSCR) is a congenital disorder caused by the absence of ganglion cells, which leads to a functional obstruction in infants. HSCR is divided into short, long and total colon aganglionosis (TCA). However, post-operative outcome assessment of patients with long-segment and TCA is scarce. We determined the functional outcomes, Hirschsprung-associated enterocolitis (HAEC) and complications of long-segment and TCA HSCR's children following pull-through surgery.
Descriptive analysis research was done for children with HSCR long-segment and TCA who underwent an operation at our institutionfrom 2013 to 2020. We assessed the functional outcome and HAEC by the Krickenbeck and the HAEC scoring, respectively.
We ascertained 13 HSCR long-segment and six TCA. We performed the following surgical procedures: Duhamel (n=7), Martin (n=4), Kimura (n=1), transabdominal Yancey-Soave (n=3) and transanal endorectal pull-through (n=4). All long-segment patients revealed good functional outcomes, whereas two TCA children suffered soiling and failed to achieve voluntary bowel movement. HAEC was noted in three long-segment and four TCA patients. Furthermore, surgical site infection and diaper rash were noticed in 10 and two patients, respectively.
Long-segment patients might have better functional outcomes TCA group, whereas the frequency of HAEC is compatible among arms. Long-term follow-up is important and necessary to identify complications early and define the proper treatment. Our study comprehensively analyzes functional outcomes, HAEC and complications of children with HSCR long-segment and TCA after definitive surgery in a developing country.
先天性巨结肠(HSCR)是一种由神经节细胞缺失引起的先天性疾病,导致婴儿出现功能性肠梗阻。HSCR 分为短段、长段和全结肠无神经节细胞症(TCA)。然而,长段和 TCA 患者术后结果评估较为少见。我们确定了经肛门拖出术治疗长段和 TCA 型先天性巨结肠患儿的功能结果、巨结肠相关性结肠炎(HAEC)和并发症。
对 2013 年至 2020 年在我院接受手术的长段和 TCA 型先天性巨结肠患儿进行描述性分析研究。我们分别采用 Krickenbeck 和 HAEC 评分评估功能结果和 HAEC。
我们确定了 13 例长段和 6 例 TCA 型先天性巨结肠患儿。我们实施了以下手术:Duhamel 术(n=7)、Martin 术(n=4)、Kimura 术(n=1)、经腹 Yancey-Soave 术(n=3)和经肛门直肠内拖出术(n=4)。所有长段患者均表现出良好的功能结果,而 2 例 TCA 患儿存在大便失禁且未能实现自主排便。3 例长段和 4 例 TCA 患儿出现 HAEC。此外,10 例和 2 例患儿分别出现手术部位感染和尿布疹。
长段患者的功能结果可能优于 TCA 组,而 HAEC 的发生率在各组间相似。长期随访对于早期发现并发症并确定适当的治疗非常重要。本研究全面分析了发展中国家经根治性手术后长段和 TCA 型先天性巨结肠患儿的功能结果、HAEC 和并发症。