Malformative uropathies in children: epidemiological, clinical, therapeutic and evolutive aspects in an ivoirian hospital setting

IF 0.7 Nephrologie & therapeutique Pub Date : 2024-08-01 Epub Date: 2024-08-19 DOI:10.1684/ndt.2024.88
Emmanuella Bouah-Kamon, Assamala Marielle Sophie Ehile-Kacou, Gnenefoly Diarrassouba, Tanoh Kassi François Eboua, Evelyne Lasme-Guillao
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Abstract

Introduction: Congenital anomalies of the kidney and the urinary tract are a major cause of chronic kidney failure in children. Prevalence in paediatrics varies according to studies. The data being rare in the ivorian context, this study aims to describe these defects' epidemiological, clinical, therapeutic and evolutionary aspects in children in a reference hospital setting.

Methods: We performed a retrospective and descriptive study held in the Yopougon's Teaching Hospital Pediatric Nephrology Unit from December 1st 2008 to December 31st 2020. It involved 152 children aged 0 to 15 years, admitted to the unit, with a congenital anomaly of the kidney and the urinary tract diagnosed with radiology.

Results: Socio-demographic characteristics: congenital anomalies of the kidney and urinary tract's prevalence was 11%. The median age at admission was 36 months. The median age at diagnosis of malformative uropathy was 17.5 months. The sex ratio (M/F) was 2.3. Clinical characteristics: posterior urethra valves were the most common malformative uropathy (38%). Malformative uropathy was associated with other defects in 4% of cases. The antenatal diagnosis involved 24% of patients. The average gestational age of discovery was 32 weeks of amenorrhea. In the postnatal period, abdominal pain was the main circumstance for discovery (39%). Therapeutic characteristics: surgery was indicated in 58% of patients and performed in 64% of cases. Evolutionary characteristics: evolution was better in patients who had received surgical treatment (asymptomatic in 83% of cases, occurrence of urinary tract infection in 35% of cases and chronic renal failure in 23% of cases). 72% of the study population was lost.

Conclusion: In Côte d'Ivoire, malformatives uropathies are late-discovered and are dominated by posterior urethra valves. Knowledge and management of these renal and urinary tract defects deserve to be improved through the development of antenatal diagnosis and training of practitioners in early recognition of clinical signs. The high rate of lost patients must be reduced by the implementation of an active patients' follow-up system.

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儿童畸形尿路病:科特迪瓦医院环境中的流行病学、临床、治疗和发展方面
导读:先天性肾脏和尿路异常是儿童慢性肾衰竭的主要原因。儿科的患病率因研究而异。数据是罕见的在科特迪瓦的背景下,本研究旨在描述这些缺陷的流行病学,临床,治疗和进化方面的儿童在参考医院设置。方法:我们于2008年12月1日至2020年12月31日在优坡贡教学医院儿科肾脏病科进行了回顾性和描述性研究。它涉及152名年龄在0到15岁之间的儿童,这些儿童都是通过放射学诊断出患有先天性肾脏和泌尿道异常的。结果:社会人口学特征:先天性肾、尿路异常患病率为11%。入院时中位年龄为36个月。诊断为畸形性尿病的中位年龄为17.5个月。性别比(M/F)为2.3。临床特点:后尿道瓣膜是最常见的畸形尿病(38%)。畸形性尿路病变在4%的病例中伴有其他缺陷。产前诊断涉及24%的患者。发现闭经的平均胎龄为32周。产后发现的主要情况为腹痛(39%)。治疗特点:58%的患者需要手术治疗,64%的病例需要手术治疗。进化特征:接受手术治疗的患者进化较好(83%的患者无症状,35%的患者发生尿路感染,23%的患者发生慢性肾衰竭)。72%的研究人群丢失了。结论:在Côte科特迪瓦,畸形性尿路病变发现较晚,以后尿道瓣膜为主。对这些肾脏和尿路缺陷的认识和管理值得通过产前诊断的发展和培训医生在早期识别临床症状来改善。必须通过实施积极的患者随访系统来降低高失诊率。
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