Pediatric urolithiasis: Experience from a tertiary referral center - Abstract

OBJECTIVE: Pediatric urolithiasis can cause significant morbidity and damage to the kidney, or even renal failure.

We review our experience of the management of urolithiasis in pediatric patients at a tertiary referral center.

PATIENTS AND METHODS: We reviewed medical records of all children with urolithiasis who were diagnosed and managed at our center from August 2003 to October 2011. Management was planned according to stone burden and location. We noted and statistically analysed data about age, sex, stone burden, clinical features, management, metabolic abnormalities and recurrence.

RESULTS: There were 325 children with 378 stone sites. Age range was 3-17 (mean 8) years. The male to female ratio was 3:1. Most common presentation was abdominal pain in 257 children (79%), and the most common stone site was kidney in 215 (57%). Twenty-four (7%) children (stone burden ≤ 3 mm) were managed conservatively, while the rest received some form of intervention. Metabolic workup could be done in 154 (47%) children. A metabolic abnormality was seen in 67 (43%) children, normocalcemic hypercalciuria being the most common. Recurrence of urolithiasis was seen in 78 (24%) children after a mean follow-up of 3.2 (1-6) years, and was more common in those who had a metabolic abnormality or in whom small residual fragments were left in situ.

CONCLUSIONS: Availability of smaller instruments has led to safer use of percutaneous endoscopy and ureteroscopy in children, with results comparable to those in adults and an acceptable complication rate. The presence of a metabolic abnormality is quite common and is a cause of recurrence.

Written by:
Abhishek, Kumar J, Mandhani A, Srivastava A, Kapoor R, Ansari MS.   Are you the author?
Department of Urology and Renal transplantation, Sanjay Gandhi Postgraduate Institute of Medical Science, Raebreali Road, Lucknow 226014, U.P, India.

Reference: J Pediatr Urol. 2013 Jan 21. pii: S1477-5131(12)00258-6.
doi: 10.1016/j.jpurol.2012.11.003


PubMed Abstract
PMID: 23348148

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