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Published on: October 12, 2017
Pelvi-ureteric junction obstruction in children
Insights
This study reviewed 100 children with hydronephrosis due to pelvi-ureteric obstruction. Pyeloplasty yielded satisfactory long-term results, highlighting the infant kidney
Area of Science:
- Pediatric Urology
- Nephrology
- Surgical Pediatrics
Background:
- Pelvi-ureteric junction obstruction is a common cause of congenital hydronephrosis in children.
- Early diagnosis and intervention are crucial for preserving renal function.
- Surgical management aims to restore urine flow and prevent further kidney damage.
Purpose of the Study:
- To review outcomes of surgical management for pelvi-ureteric junction obstruction in pediatric patients.
- To evaluate the efficacy of different surgical techniques, including pyeloplasty.
- To assess the long-term clinical, radiological, and renographic results following surgical correction.
Main Methods:
- Retrospective review of 100 pediatric patients with hydronephrosis secondary to pelvi-ureteric obstruction over 13 years.
- Analysis of symptomatology, pre-operative investigations, and post-operative assessments.
- Evaluation of surgical techniques, including dismembered pyeloplasty, nephrostomy, splintage, and vessel hitching for aberrant vessels.
Main Results:
- Overall satisfactory long-term outcomes were achieved following pyeloplasty, assessed clinically, radiologically, and renographically.
- Dismembered pyeloplasty was the favored technique, with variations based on abnormality severity.
- Simple vessel hitching provided good results in 12 patients with aberrant lower pole vessels.
Conclusions:
- Pyeloplasty is an effective treatment for pediatric hydronephrosis secondary to pelvi-ureteric obstruction, with excellent long-term results.
- The infant kidney demonstrates significant recuperative potential, supporting a conservative surgical approach.
- Surgical technique should be tailored to the specific nature and severity of the obstruction.
Abstract:
Hydronephrosis secondary to pelvi-ureteric obstruction affecting one hundred children and derived from a 13 year period were reviewed. Particular attention was paid to symptomatology in infancy and childhood, pre-operative investigations and postoperative assessment. Following pyeloplasty the late results assessed clinically, radiologically and renographically were entirely satisfactory. The operative technique varied satisfactory. The operative technique varied according to the nature and severity of the abnormality but dismembered pyeloplasty and nephrostomy and splintage was favoured. Twelve patients with aberrant lower pole vessels had simple hitching of vessels alone with good results. Our experience suggests that the recuperative power of the kidney in the infant is unpredictable and surprising. For this reason a plea is made for extreme conservatism.
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