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Multidimensional Analysis of Urinary Stone Diseases in Pediatric Patients
Ayhan Dalkılınç1, Hasan Demirkan2, Gül Özçelik3
1Department of Urology, Health Sciences University, Şişli Etfal Health Application Research Center, İstanbul, Turkey.
Insights
Pediatric urinary stone disease requires metabolic evaluation and stone analysis for effective treatment and prevention of recurrence. Lifelong follow-up is crucial for children diagnosed with kidney stones.
Area of Science:
- Pediatric Nephrology
- Urology
- Metabolic Disorders
Background:
- Urinary tract stones are less frequent in children compared to adults.
- Identifying the underlying cause of pediatric urinary stones is essential for successful management and preventing recurrence.
Purpose of the Study:
- To investigate the clinical characteristics of pediatric urinary stone disease.
- To identify potential risk factors associated with urinary stone formation in children.
Main Methods:
- Retrospective analysis of 126 pediatric patients (2000-2014) treated for urinary stones.
- Comprehensive evaluation including urinalysis, urine culture, 24-hour urine collection for metabolic parameters, serum analysis, and urinary ultrasound.
- Stone analysis using X-ray diffraction.
Main Results:
- 41% of patients had hypercalciuria, 30% hypocitraturia, 14% hyperoxaluria, 10% hyperuricosuria, and 5% cystinuria.
- Calcium oxalate (45%) and calcium phosphate (35%) were the most common stone compositions.
- 81% of patients presented with kidney stones, with extracorporeal shock wave lithotripsy and surgical treatment being common interventions.
Conclusions:
- Metabolic evaluation and detailed stone analysis are critical for managing pediatric urinary stone disease.
- Lifelong follow-up is recommended for children to prevent recurrent stone formation.
Objectives:
Urinary tract stones are less common in children than in adults. Determining the etiology is the most important step to achieve successful treatment and prevent future recurrence. The aim of this study was to investigate the clinical characteristics and possible risk factors for urinary stone disease in pediatric patients.
Methods:
The data of 126 patients with urinary stone disease who were treated in a pediatric nephrology clinic between 2000 and 2014 were analyzed retrospectively. A total 126 patients were enrolled in the study: 70 (55%) male and 56 (45%) female patients were included. The complaints, age of diagnosis, family histories, and stone location were examined. Direct urine microscopic examination, complete urinalysis, and urine culture were performed for all of the patients. Calcium, uric acid, oxalate, citrate, magnesium, and cystine levels were measured in urine collected in a 24-hour period. Serum electrolyte, blood urea nitrogen, creatinine, calcium, phosphorus, uric acid, and albumin levels were measured. Urinary ultrasound was performed. Stone analysis was conducted using the X-ray diffraction method. The mean age of the patients was 55 months (range: 1-162 months) at presentation.
Results:
In all, 34% of the patients had a family history of urinary stone disease. The rate of previous urinary tract infection was 26%. It was determined that 34% of the patients had been taking vitamin D and 5% had been taking a high dose. Metabolic risk factors determined were: hypercalciuria in 41%, hypocitraturia in 30%, hyperoxaluria in 14%, hyperuricosuria in 10%, and cystinuria in 5%. Among the group, 81% of the patients had kidney stones, 6.5% had ureter stones, and 2.5% had bladder stones. Furthermore, it was determined that 45% of the stones were composed of calcium oxalate, 35% had calcium phosphate stones, 14.2% had uric acid stones, and 13.3% had cystine stones. In 52% of the cases, extracorporeal shock wave lithotripsy was performed, and 71% underwent surgical treatment.
Conclusion:
Metabolic evaluation and stone analysis should be performed to prevent future recurrences in children with urinary stone disease and lifelong follow-up should be emphasized.
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