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Updated: May 8, 2026

Roux-en-Y Gastric Bypass Operation in Rats
Published on: June 11, 2012
Calcium oxalate supersaturation increases early after Roux-en-Y gastric bypass
Varun Agrawal1, Xiao J Liu2, Thomas Campfield3
1Division of Nephrology and Hypertension, Fletcher Allen Health Care, Burlington, Vermont.
The risk of calcium oxalate (CaOx) nephrolithiasis increases as early as 2 months after Roux-en-Y gastric bypass surgery (RYGB). This risk gradually rises within the first 6 months due to reduced urine volume and higher urinary oxalate.
Area of Science:
- Nephrology
- Bariatric Surgery Outcomes
- Urolithiasis Research
Background:
- Calcium oxalate (CaOx) nephrolithiasis is a known complication following Roux-en-Y gastric bypass (RYGB) surgery.
- The precise timing of the elevated risk for CaOx stone formation post-RYGB remains unclear.
Purpose of the Study:
- To determine the temporal relationship between RYGB and the development of CaOx nephrolithiasis risk.
- To investigate changes in urinary parameters contributing to CaOx stone risk after RYGB.
Main Methods:
- Prospective study of 13 morbidly obese adults undergoing RYGB.
- 24-hour urine collections were performed pre-surgery and at 1, 2, 4, and 6 months post-surgery.
- Calcium oxalate relative saturation ratio (CaOx RSR) was calculated using the EQUIL2 model.
Main Results:
- Urinary oxalate excretion significantly increased from baseline to 6 months post-RYGB (median 12.6 to 28.4 mg/24 hr).
- CaOx RSR showed a significant increase starting at 2 months post-RYGB (median 1.4 to 4.9) and continued to rise.
- Reduced urine volume and decreased sodium/potassium excretion were observed, while urinary pH, calcium, magnesium, and citrate remained unchanged.
Conclusions:
- The risk for CaOx nephrolithiasis, indicated by elevated CaOx RSR, emerges as early as 2 months after RYGB.
- The risk escalates gradually in the initial 6 months post-surgery, driven by diminished urine volume and increased oxalate excretion.
- Future interventions focusing on fluid intake and oxalate binding agents are warranted for patients at risk post-RYGB.
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