鉴定乌干达西南部与肛门直肠畸形相关的泌尿系统异常:局限与机遇

IF 2 3区 医学 Q2 PEDIATRICS Journal of Pediatric Urology Pub Date : 2024-08-07 DOI:10.1016/j.jpurol.2024.07.027
Felix Oyania, Nnaemeka Eze, Mercy Aturinde, Sarah Ullrich, Marvin Mwesigwa, Doruk E. Ozgediz
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引用次数: 0

摘要

肛门直肠畸形(ARMs)可能与影响其他身体部位(即脊椎、肛门直肠、心脏、气管食管、肾脏和肢体(VACTERL))的先天性畸形有关,发生率在 7%-60% 之间 [1-10]。在所有肛门直肠畸形患者中,约有 50% 的患者可能存在泌尿生殖系统缺陷 [11],因此应从出生时就对患者进行评估,以排除这些缺陷。为了确定乌干达西南部与肛门直肠畸形相关的泌尿系统异常。这是一项描述性回顾性队列研究,在乌干达西南部的地区转诊医院进行,涉及 2021 年 6 月至 2023 年 7 月期间接受过肛门直肠畸形手术矫正的患者。在我们的研究对象中,肾脏异常的总发病率为 18.05%。在与 ARM 相关的肾脏异常患者中,特定异常包括:肾脏缺如(6.8%)、肾积水(4.5%)、双肾集合系统(3.8%)、交叉融合肾(1.5%)和异位肾(0.75%)。(我们发现与 ARM 相关的肾脏异常发生率为 18.05%,最常见的异常是单侧肾缺如(6.8%),这与其他研究结果类似[12]。之前的数据显示,肾脏异常是 ARM 中常见的异常[13]。虽然不同研究的确切数值各不相同,但它们都得出结论,ARM 相关异常的发生率极高,因此一旦发现 ARM,就应进行彻底的术前检查。因此,这一发现强调了彻底评估和多学科护理方法以及包括泌尿科医生在内的 ARM 管理随访系统的重要性,即使患儿现在没有症状也是如此。我们研究的主要局限是缺少患者病历资料,由于大多数患者在评估时没有出院表,因此我们无法获得诊断结果。与肾脏异常相关的 ARM 可能仍未被诊断出来,也可能没有症状。对于那些被确定为无症状的患者,需要包括儿科泌尿科医生在内的多学科人员进行随访。
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Identification of urological anomalies associated with anorectal malformation in southwestern Uganda: Limitations and opportunities
Anorectal malformations (ARMs) may be associated with congenital anomalies affecting other body parts namely vertebral, anorectal, cardiac, tracheoesophageal, renal, and limb (VACTERL) with varying incidences of 7%–60% [1–10]. Genitourinary defects might occur approximately in 50% of all patients with anorectal malformations [11] hence patients should be evaluated from birth to rule out these defects. To identify urological anomalies associated with anorectal malformation in southwestern Uganda. This was a descriptive retrospective cohort study conducted at our regional referral hospital in Southwestern Uganda involving patients who have undergone surgical correction of ARMs between June 2021 and July 2023. The overall prevalence of renal anomalies in our study patient population was 18.05%. Of those with ARM-associated renal anomalies, Specific anomalies included; renal agenesis (6.8%), hydronephrosis, (4.5%), duplex collecting system (3.8%), crossed fused kidney (1.5%), and ectopic kidney (0.75%). () We found that the prevalence of ARM-associated renal anomalies was 18.05%, and the commonest anomaly was unilateral agenesis (6.8%) similar to other studies [12]. Previous data have shown renal anomalies are common anomalies in ARM [13]. While the exact values vary across studies, they all concluded that the rate of associated anomalies is extremely high in ARMs and warrants a thorough preoperative investigation once the ARMs are detected. This finding therefore underscores the importance of thorough evaluation and a multidisciplinary approach of care and follow-up system for ARM management including urologists even when the children are asymptomatic now. The main limitation of our study was missing information on patients' charts, we were not able to get the diagnosis since most patients didn't have their discharge forms at the time of evaluation. ARM associated with renal anomalies may remain undiagnosed and asymptomatic. Those identified as asymptomatic need to be followed in a multidisciplinary fashion including pediatric urologists.
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来源期刊
Journal of Pediatric Urology
Journal of Pediatric Urology PEDIATRICS-UROLOGY & NEPHROLOGY
CiteScore
3.70
自引率
15.00%
发文量
330
审稿时长
4-8 weeks
期刊介绍: The Journal of Pediatric Urology publishes submitted research and clinical articles relating to Pediatric Urology which have been accepted after adequate peer review. It publishes regular articles that have been submitted after invitation, that cover the curriculum of Pediatric Urology, and enable trainee surgeons to attain theoretical competence of the sub-specialty. It publishes regular reviews of pediatric urological articles appearing in other journals. It publishes invited review articles by recognised experts on modern or controversial aspects of the sub-specialty. It enables any affiliated society to advertise society events or information in the journal without charge and will publish abstracts of papers to be read at society meetings.
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