Ali Alaa, Haider Fayza, Alhindi Saeed
Pediatric Surgery, Salmaniya Medical Complex, Manama, BHR.
Cureus. 2021 Jan 4;13(1):e12480. doi: 10.7759/cureus.12480.
Background Hirschsprung's disease (HD) is a rare but important congenital pediatric disease of the colon, and its incidence varies widely between ethnic groups. Its incidence was first studied in Bahrain in 1980 using hospital-based data. Over a 16-month period, 10 cases were reported, representing a relatively high incidence rate: 1 per 4000 births. Even though the number of live births in Bahrain has increased dramatically over the last four decades (doubling from 10,000 to 20,000 per year), published studies about the incidence of HD are uncommon. In this research, we aimed to determine both the prevalence and the clinical characteristics of HD at a tertiary hospital in Bahrain. Methods This retrospective observational cross-sectional study included children diagnosed with HD at a tertiary hospital in Bahrain over the last seven years (2014-2020). Children over 10 years were excluded. Clinical data collected included gestational age, birth weight, gender, associated anomalies, clinical features at presentation, disease management, and complications. Results The prevalence of HD in Bahrain was found to be 1.3 per 10,000 live births, according to 18 patients qualified for inclusion in this study. The median age at diagnosis was 18 days; approximately 72% were males, and nearly 94% were Bahraini nationals. Three patients (16.7%) had associated anomalies including cardiac and urogenital malformations. Abdominal distention was the most common clinical presentation (83.3%) followed by constipation (77.8%). Half of the patients (50%) passed meconium within 48 hours of birth. Transanal full-thickness rectal biopsy was the method of diagnosis in most patients (83.3%). Seven patients (38.9%) were diagnosed comparatively late (beyond the neonatal period), at a mean age of 1-2 years. Significant associations between age at diagnosis and clinical presentation, initial management, or surgical intervention were not found. A total of 17 patients (94.4%) underwent the definitive surgery (transanal pull-through procedure). In this surgical group, initial colonic decompression was performed via rectal washout in six patients (35.3%) and via temporary stoma in three patients (17.8%). Laparotomy combined with the definitive surgery was necessary for six patients (35.3%). Most of the patients treated surgically had a short segment disease (70.5%). Conclusions The awareness of HD is highly important, especially with more than one-third of cases diagnosed outside the neonatal period and half of them passing meconium within 48 hours of birth. In addition, early detection of HD in the neonatal period would result in a less complicated course by reducing the number of patients requiring a multi-stage surgery and further laparotomies.
背景
先天性巨结肠症(HD)是一种罕见但重要的先天性小儿结肠疾病,其发病率在不同种族之间差异很大。1980年,巴林首次利用医院数据对其发病率进行了研究。在16个月的时间里,报告了10例病例,发病率相对较高:每4000例出生中有1例。尽管在过去四十年里,巴林的活产数量大幅增加(从每年10000例增加到20000例,翻了一番),但关于HD发病率的已发表研究并不常见。在本研究中,我们旨在确定巴林一家三级医院中HD的患病率和临床特征。
方法
这项回顾性观察性横断面研究纳入了过去七年(2014 - 2020年)在巴林一家三级医院被诊断为HD的儿童。10岁以上的儿童被排除在外。收集的临床数据包括孕周、出生体重、性别、相关畸形、就诊时的临床特征、疾病管理和并发症。
结果
根据本研究纳入的18例合格患者,巴林HD的患病率为每10000例活产中有1.3例。诊断时的中位年龄为18天;约72%为男性,近94%为巴林籍。3例患者(16.7%)有相关畸形,包括心脏和泌尿生殖系统畸形。腹胀是最常见的临床表现(83.3%),其次是便秘(77.8%)。一半的患者(50%)在出生后48小时内排出胎粪。大多数患者(83.3%)通过经肛门全层直肠活检进行诊断。7例患者(38.9%)诊断相对较晚(超过新生儿期),平均年龄为1 - 2岁。未发现诊断年龄与临床表现、初始治疗或手术干预之间存在显著关联。共有17例患者(94.4%)接受了根治性手术(经肛门拖出术)。在这个手术组中,6例患者(35.3%)通过直肠冲洗进行初始结肠减压,3例患者(17.8%)通过临时造口进行。6例患者(35.3%)需要开腹手术联合根治性手术。大多数接受手术治疗的患者患有短段型疾病(70.5%)。
结论
对HD的认识非常重要,尤其是超过三分之一的病例在新生儿期以外被诊断,且其中一半在出生后48小时内排出胎粪。此外,在新生儿期早期发现HD可减少需要进行多阶段手术和进一步开腹手术的患者数量,从而使病程不那么复杂。