Kommareddy Anirudh, Vagha Keta, Vagha Jayant D, Javvaji Chaitanya Kumar, Taksande Amar, Meshram Revat J, Wandile Shailesh, Wazurkar Ajinkya
Pediatrics, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Cureus. 2024 Jul 3;16(7):e63766. doi: 10.7759/cureus.63766. eCollection 2024 Jul.
Background Congenital anomalies of the kidney and urinary tract (CAKUT) encompass a diverse array of disorders arising from developmental irregularities in the renal parenchymal development, disrupted embryonic migration of the kidneys, and the urinary collecting system. This study aimed to investigate the clinical presentations, patterns of obstructive and non-obstructive CAKUT, and associated extrarenal manifestations in affected children. Methods This observational study was conducted in the Department of Pediatrics, Acharya Vinoba Bhave Rural Hospital, Wardha. Ethical clearance was obtained, and the study included 105 diagnosed CAKUT patients aged from birth to 18 years. Data collection spanned from June 2022 to May 2024. Clinical features, antenatal findings, associated anomalies, estimated glomerular filtration rate (eGFR), and serum creatinine levels were recorded. Descriptive and inferential statistical analyses were performed using Stata software. Results Among the 105 participants, 81 (77.14%) were males, with a male-to-female ratio of 3.37:1. The mean age was 42.49 months. Forty-two individuals (40%) were asymptomatic, while the most common symptomatic presentation was the ventral opening of the urethra (24.76%). Extrarenal malformations were present in 35 subjects (33.33%), with undescended testis (25.71%) and congenital heart disease (CHD) (20%) being the most common. The antenatal diagnosis was made in 63.8% of cases. Obstructive uropathy was present in 42.86% of subjects, with a significant association between antenatal diagnosis and bilateral hydronephrosis. Medical management was provided to 41.9% of subjects, while 58.1% underwent surgical interventions. Conclusion The study highlights the clinical variability and diverse presentations of CAKUT in children, with a substantial proportion being asymptomatic. Early detection through antenatal screening and prompt intervention can potentially prevent or delay the progression to ESRD. The findings underscore the importance of comprehensive evaluation and targeted management strategies to address both renal and extrarenal manifestations of CAKUT.
背景 先天性肾脏和尿路异常(CAKUT)包括一系列因肾实质发育异常、肾脏胚胎迁移受阻以及泌尿系统收集系统异常而引发的疾病。本研究旨在调查受影响儿童的临床表现、梗阻性和非梗阻性CAKUT的模式以及相关的肾外表现。方法 本观察性研究在沃德哈阿查里亚·维诺巴·巴韦农村医院儿科进行。获得了伦理批准,研究纳入了105例年龄从出生至18岁的确诊CAKUT患者。数据收集时间为2022年6月至2024年5月。记录了临床特征、产前检查结果、相关异常、估计肾小球滤过率(eGFR)和血清肌酐水平。使用Stata软件进行描述性和推断性统计分析。结果 在105名参与者中,81名(77.14%)为男性,男女比例为3.37:1。平均年龄为42.49个月。42人(40%)无症状,最常见的症状表现是尿道下裂(24.76%)。35名受试者(33.33%)存在肾外畸形,其中隐睾(25.71%)和先天性心脏病(CHD)(20%)最为常见。63.8%的病例进行了产前诊断。42.86%的受试者存在梗阻性肾病,产前诊断与双侧肾积水之间存在显著关联。41.9%的受试者接受了药物治疗,58.1%接受了手术干预。结论 该研究突出了儿童CAKUT的临床变异性和多样表现,其中很大一部分为无症状患者。通过产前筛查早期发现并及时干预可能预防或延缓向终末期肾病的进展。研究结果强调了全面评估和针对性管理策略对于解决CAKUT的肾脏和肾外表现的重要性。