Wondemagegnehu Belachew Dejene, Asfaw Solomon Wubetu
College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
College of Medicine and Health Science, Jijiga University, Jijiga, Ethiopia.
Front Surg. 2025 Apr 24;12:1497644. doi: 10.3389/fsurg.2025.1497644. eCollection 2025.
Anorectal malformations (ARM) consist of a range of anomalies that occur in approximately 3.5 in 10,000 live births. Though variable, about half of these patients present with an associated genitourinary abnormality. Considering this high prevalence, this study aimed to assess the specific occurrence of urogenital anomalies in patients with anorectal malformations.
An institution-based observational study was conducted on 156 patients with anorectal malformation, all of whom were screened for urogenital anomalies. Data were collected using a pre-structured questionnaire and analyzed using SPSS (IBM) Version 26 software. Relevant statistical analysis was performed, and the results are presented in tables.
Of the 156 patients with ARM studied for associated urogenital anomalies, 91 (58.3%) were females with a male-to-female ratio of 0.7:1 and a median age of 12 months (IQR = 1-24). Forty-six of them (29.5%) had urogenital anomalies, of whom 22 (14.1%) had isolated urologic anomalies and 20 (12.8%) had both urologic and genital anomalies. Renal anomalies were found in 34 (21.8%) patients. The association between gender and genital anomalies was significant, (1), = 156 = 4.09, = 0.04. The type of ARM has a highly significant association with genital anomalies (11), = 156 = 21.95, = 0.009. Males were less likely to exhibit urogenital anomalies [OR = 0.386, 95% CI (0.15-0.995), = 0.048]. Children with complex ARM have 3.4 times genital and 2.3 times urinary anomalies than less complex forms. In summary, urogenital anomalies are the most common anomalies occurring in association with anorectal malformation. Genital anomalies have an association with gender with more occurrence in females. Children with complex anorectal malformations have a higher chance of urogenital anomalies.
肛门直肠畸形(ARM)是一系列发生率约为每10000例活产中有3.5例的异常情况。尽管情况各异,但这些患者中约有一半伴有泌尿生殖系统异常。鉴于这种高发生率,本研究旨在评估肛门直肠畸形患者泌尿生殖系统异常的具体发生率。
对156例肛门直肠畸形患者进行了一项基于机构的观察性研究,所有患者均接受了泌尿生殖系统异常筛查。使用预先构建的问卷收集数据,并使用SPSS(IBM)26版软件进行分析。进行了相关统计分析,结果以表格形式呈现。
在研究伴有泌尿生殖系统异常的156例ARM患者中,91例(58.3%)为女性,男女比例为0.7:1,中位年龄为12个月(IQR = 1 - 24)。其中46例(29.5%)有泌尿生殖系统异常,其中22例(14.1%)有孤立性泌尿系统异常,20例(12.8%)有泌尿系统和生殖系统异常。34例(21.8%)患者发现有肾脏异常。性别与生殖系统异常之间的关联具有显著性,(1),= 156 = 4.09,= 0.04。ARM的类型与生殖系统异常具有高度显著性关联(11),= 156 = 21.95,= 0.009。男性出现泌尿生殖系统异常的可能性较小[OR = 0.386,95% CI(0.15 - 0.995),= 0.048]。复杂ARM儿童出现生殖系统异常的几率是不太复杂形式的3.4倍,出现泌尿系统异常的几率是2.3倍。总之,泌尿生殖系统异常是与肛门直肠畸形相关的最常见异常。生殖系统异常与性别有关,女性发生率更高。复杂肛门直肠畸形儿童发生泌尿生殖系统异常的几率更高。