Department of Pediatric Nephrology, Free University of Brussels, Brussels, Belgium.
Urology. 2013 Sep;82(3):691-6. doi: 10.1016/j.urology.2013.03.041. Epub 2013 May 29.
To determine, in children with antenatally detected pelviureteric junction (PUJ) stenosis, what factors may be predictive for deterioration of differential renal function (DRF) in case of conservative treatment or improvement of DRF in case of pyeloplasty.
This study analyzed and compared the initial level of hydronephrosis, DRF, quality of renal drainage, and cortical transit with the late DRF outcome. We reviewed the medical charts of 161 consecutive children with antenatally diagnosed PUJ stenosis during a 10-year period (between 1997 and 2007). From this cohort, we retained 81 children with unilateral PUJ and strictly normal contralateral kidney, with a median follow-up of 67 months. Repeated ultrasounds, voiding cystourethrography, and radionuclide renograms were performed in all children.
Fifty patients never underwent a surgical intervention (62%), whereas surgical repair (Anderson-Hynes dismembered pyeloplasty) was performed in 31 (38%). During conservative follow-up, DRF deterioration was observed in 11% of patients. After pyeloplasty, DRF improvement was observed in 25% of patients. Abnormal cortical transit was the only predictive factor of DRF deterioration in case of conservative approach, whereas the initial degree of hydronephrosis, or renal drainage, and the initial DRF level were not predictive. In children who were operated on, only impaired cortical transit was predictive of DRF improvement postoperatively.
Conservative management of children with unilateral PUJ stenosis is a safe procedure. Impaired cortical transit although imperfect, seems the best criterion for identifying children for whom pyeloplasty is warranted.
在产前诊断为肾盂输尿管连接部(PUJ)狭窄的儿童中,确定哪些因素可能对保守治疗时 DRF 恶化或肾盂成形术后 DRF 改善具有预测价值。
本研究分析并比较了初始肾积水程度、DRF、肾引流质量和皮质转运与晚期 DRF 结果之间的关系。我们回顾性分析了 1997 年至 2007 年间 10 年间(1997 年至 2007 年间)接受产前诊断为 PUJ 狭窄的 161 例连续儿童的病历。在该队列中,我们保留了 81 例单侧 PUJ 且对侧肾脏完全正常的儿童,中位随访时间为 67 个月。所有儿童均接受了重复超声、排尿性膀胱尿道造影和放射性核素肾图检查。
50 例患者从未接受过手术干预(62%),而 31 例(38%)接受了手术修复(Anderson-Hynes 肾盂成形术)。在保守随访期间,11%的患者出现 DRF 恶化。行肾盂成形术后,25%的患者出现 DRF 改善。皮质转运异常是保守治疗时 DRF 恶化的唯一预测因素,而初始肾积水程度、肾引流和初始 DRF 水平均不是预测因素。对于接受手术的儿童,只有皮质转运异常是术后 DRF 改善的预测因素。
对单侧 PUJ 狭窄儿童进行保守治疗是一种安全的方法。虽然不完美,但皮质转运异常似乎是识别需要行肾盂成形术的儿童的最佳标准。