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The long-term outcomes of idiopathic hypercalciuria in children
1Ege University, School of Medicine, Department of Pediatric Nephrology, Bornova, Izmir, Turkey. yilmaztabel@yahoo.com
Insights
Idiopathic hypercalciuria (IH) is a common cause of urinary calcium stones. Determining the type of IH and using diet and thiazide therapies can help prevent new stone formation in affected patients.
Area of Science:
- Nephrology
- Pediatric Nephrology
- Metabolic Bone Diseases
Background:
- Idiopathic hypercalciuria (IH) is a significant metabolic risk factor in patients experiencing urinary calcium stones, contributing to 30%-50% of all such cases.
- Understanding the clinical manifestations and subtypes of IH is crucial for effective management and patient outcomes.
Purpose of the Study:
- To review the clinical manifestations and distribution of idiopathic hypercalciuria (IH) types in pediatric patients.
- To evaluate current treatment strategies and long-term outcomes for patients with IH.
- To identify risk factors and preventive measures for nephrolithiasis in IH patients.
Main Methods:
- A cohort of 131 pediatric patients (70 boys, 61 girls) aged 1-15 years with IH was studied.
- Patients were followed for 6 months to 16 years, with a mean follow-up of 4.1 years.
- Diagnosis of absorptive and renal types of IH was based on calcium challenge tests.
Main Results:
- Renal type IH was diagnosed in 40% of patients, and absorptive type in 39%.
- Nephrolithiasis was present on admission in 20% of patients and developed in an additional 6.1% during follow-up.
- Diet therapy normalized urinary calcium excretion in 65 patients, with definitive resolution in 26.7% and recurrence in 22.9%.
Conclusions:
- Idiopathic hypercalciuria (IH) can be associated with nephrolithiasis, necessitating type determination for appropriate management.
- Patients with absorptive type IH require close monitoring for nephrolithiasis.
- Dietary modifications and thiazide therapy show promise in preventing new stone formation in patients with IH.
Objective:
Idiopathic hypercalciuria (IH) is a metabolic risk factor in patients with urinary calcium stones and implicated in 30%-50% of all urinary stone diseases. Clinical manifestations and distribution of types of IH are reviewed, as well as current treatment methods and long-term outcomes.
Patients:
A total of 131 patients (70 boys and 61 girls), aged 1-15 years (mean 7.9+/-3.19 years), were studied. Follow up was between 6 months and 16 years (mean 4.1+/-6.8 years).
Results:
Fifty-three patients (40%) were diagnosed following calcium challenge as renal type, and 51 (39%) as absorptive type of hypercalciuria. Whereas 72 patients (54.9%) had a family history of nephrolithiasis, 59 patients did not. Nephrolithiasis was found in 27 patients (20%) on admission (absorptive=9.9%, renal=4.5%, undetermined=6.1%), but developed in eight other patients (6.1%) (absorptive=2.2%, renal=0.7%, undetermined=3.8%). Urinary calcium excretion reversed in 65 patients with the suggested diet therapy; it recurred in 30 patients (22.9%) (absorptive=9.1%, renal=11.4%, undetermined=2.2%) but 35 returned to normal definitively (26.7%) (absorptive=11.4%, renal=12.9%, undetermined=2.2%). No change was seen in the status of 50 patients (38.1%) (absorptive=18.3%, renal=16%, undetermined=3.8%).
Conclusion:
IH may be accompanied by nephrolithiasis; type must be determined and those patients with absorptive type should be followed for nephrolithiasis. Our results suggest that formation of new stones could be prevented with diet and thiazide therapies in IH.
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