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Management of stones in childhood
1Consultant Urological Surgeon Scottish Lithotripter Centre, Western General Hospital, Crewe Road, Edinburgh, UK. bthomas2@nhs.net
Insights
Paediatric stone disease diagnosis requires high suspicion, especially in young children. Metabolic evaluation aids management and recurrence prevention, though treatment consensus remains challenging due to limited data.
Area of Science:
- Pediatric Nephrology
- Urology
- Pediatric Stone Disease Management
Background:
- Paediatric stone disease literature is limited, primarily comprising single-centre case series.
- Variations in diagnostic criteria and treatment techniques hinder direct comparisons.
- Recent trends indicate shifts in stone disease incidence, particularly among female pediatric patients.
Purpose of the Study:
- To review the latest global literature on paediatric stone disease.
- To highlight current understanding and challenges in managing pediatric urolithiasis.
- To identify gaps in evidence for treatment efficacy and long-term outcomes.
Main Methods:
- Systematic review of recent world literature on paediatric urolithiasis.
- Analysis of case series and available data on treatment safety and efficacy.
- Identification of trends in incidence, diagnosis, and management strategies.
Main Results:
- Metabolic abnormalities are common in children with stones and necessitate follow-up.
- Evidence for the safety and efficacy of pediatric stone treatments is growing.
- Long-term follow-up data on treatment adverse effects are still needed.
- Increased incidence noted, especially in female pediatric patients.
Conclusions:
- Early diagnosis of paediatric stones requires a high index of suspicion.
- Metabolic evaluation is crucial for management and preventing recurrence after excluding anatomical issues.
- Expanding treatment options contrast with difficulties in achieving treatment consensus due to small patient numbers and technological variations.
Purpose Of Review:
The purpose of this review was to report on the latest world literature relating to paediatric stone disease. Inevitably, because of the small numbers, the literature is limited and consists mainly of case series from individual centres. There is also a wide variation in criteria and techniques, making direct comparison limited.
Recent Findings:
Changes in the incidence of stone disease are becoming more apparent particularly in female patients. Metabolic abnormalities can be identified in the majority of children with stones, and even in the absence of obvious physical stone, if detected warrant further follow-up. Data supporting the safety and efficacy of treatments for stones in children is improving constantly, but choosing the best option may be difficult on current evidence. Better long-term follow-up is still needed regarding adverse effects of treatment.
Conclusion:
A high index of suspicion is required for the diagnosis of stone disease in children, especially in the very young. After exclusion of anatomical abnormalities, metabolic evaluation is important in management and prevention of recurrence. Modalities for treatment are expanding all the time, but due to overall small numbers, and variations in the availability of technology, consensus views about treatment are difficult to agree.
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