Kidney stone prevention
Prevention of recurrent calcium oxalate, uric acid and cystine kidney stones. Baseline measures: 2.5–3 L water/day, reduced salt and animal protein, normal dietary calcium. In patients with hypocitraturia, recurrent oxalate stones or distal renal tubular acidosis, potassium citrate raises urinary pH and binds calcium ions, reducing recurrence. Guidelines: AUA 2014, EAU 2024, Spanish AEU 2024.
Also known as: Urolithiasis, Stone disease prevention, Calcium oxalate stones, Uric acid stones
Drugs used for this condition
- APotassium citrateFirst line · Potassium salt with systemic alkalinising effect, used for kidney stone prevention and hypokalaemiaPotassium citrate is first-line for prevention of recurrent calcium oxalate, uric acid and cystine stones in patients with hypocitraturia, low urinary pH or recurrent urolithiasis. The Cochrane review 2015 pooled 7 RCTs with 477 patients and showed citrate salts reduce new-stone risk by 75 % versus placebo or control (RR 0.25, 95 % CI 0.14–0.44). Guidelines AUA 2014, EAU 2024 and Spanish AEU 2024 recommend potassium citrate 30–60 mEq/day as first-line after 24-hour urine assessment. Targets: urinary citrate above 320 mg/day, urinary pH 6.0–7.0. In gouty uric-acid nephropathy allopurinol adds benefit. AEMPS registered Acalka with this indication.
- BAllopurinolAdd-on therapy · Xanthine oxidase inhibitorsIn patients with frequent kidney stones and high uric acid in blood or urine, allopurinol lowers the recurrence risk. First-line care is high fluid intake and urine alkalinization with citrate (for uric acid stones); allopurinol is added when hyperuricosuria persists. In the Ettinger 1986 RCT, allopurinol reduced recurrence of calcium oxalate stones in hyperuricosuric patients; for uric acid stones the indication is on the AEMPS label and in the EAU guideline. It is an add-on to baseline prevention, not a replacement for fluid intake.
Marketing claims without evidence base
The drug is promoted for these uses outside international guidelines. Each entry below is analyzed against AEMPS, FDA, EMA, Cochrane and major RCTs.
How to read tiers A–F
Evidence tiers belong to the drug-indication pair, not to the drug as a whole: the same substance can be A for one condition and F for another.
- AStrong evidence – first or second line in international guidelines
- BRecommended in selected cases
- CStudy data contradict each other
- DBenefit not proven, no documented harm
- FDocumented harm, or risk without benefit