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For further information, see CMDT Part 25-05: Urinary Stone Disease

KEY FEATURES

Essentials of Diagnosis

  • Severe flank pain

  • Nausea and vomiting

  • Identification of urinary stone on noncontrast CT scan or ultrasonography

General Considerations

  • Five major types of urinary stones

    • Calcium oxalate

    • Calcium phosphate

    • Struvite (magnesium ammonium phosphate)

    • Uric acid

    • Cystine

  • Most urinary stones contain calcium (85%) and are radiopaque on plain abdominal radiographs

  • Uric acid stones may be radiolucent if pure, or partially radiopaque if mixed with calcium

  • Cystine and struvite stones are faintly radiopaque

  • Incidence is greatest during hot summer months

  • Contributing factors to urinary stone formation

    • Geographic factors

      • High humidity

      • Elevated temperatures

    • Genetic factors

      • Cystinuria

      • Distal renal tubular acidosis

    • Many commonly prescribed medications

      • Carbonic anhydrase inhibitors (topiramate, zonisamide, acetazolamide)

      • Systemic corticosteroids (prednisone)

      • Antiretroviral protease inhibitors (indinavir and others)

      • Gout medications (probenecid)

      • Diuretics (furosemide, bumetanide, torsemide, triamterene)

      • Decongestants (guaifenesin, ephedrine)

      • Laxatives (if abused for weight loss)

    • Dietary and other factors

      • Sedentary lifestyle

      • Obesity

      • Hypertension

      • Insulin resistance and poor glycemic control

      • Carotid calcification

      • Cardiovascular disease

      • High protein and salt intake

      • Inadequate hydration

  • Increasing evidence is revealing that urinary stone disease may be a precursor to subsequent cardiovascular disease

  • Hypercalciuric calcium nephrolithiasis (> 250 mg/24 h) can be caused by absorptive, resorptive, and renal disorders (eTable 25–1)

    • Absorptive hypercalciuria

      • Secondary to increased absorption of calcium at the level of the small bowel, predominantly in the jejunum

      • Can be diet-dependent, independent of calcium intake, or due to renal phosphate leak

    • Resorptive hypercalciuria

      • Primary hyperparathyroidism

      • Typically due to a parathyroid adenoma

      • Hypercalcemia, hypophosphatemia, hypercalciuria, and an elevated serum parathyroid hormone level are found

    • Renal hypercalciuria

      • Most common form of hypercalciuria

      • Occurs when the renal tubules are unable to efficiently reabsorb filtered calcium

      • Spilling calcium in the urine may result in secondary hyperparathyroidism with normal serum calcium

  • Hyperuricosuric calcium nephrolithiasis is secondary to dietary purine excess or uric acid metabolic defects

  • Hyperoxaluric calcium nephrolithiasis is usually due to primary intestinal disorders, including chronic diarrhea, inflammatory bowel disease, or steatorrhea

  • Hypocitraturic calcium nephrolithiasis is secondary to disorders associated with metabolic acidosis including chronic diarrhea, type I (distal) renal tubular acidosis, and long-term hydrochlorothiazide treatment

  • Uric acid calculi: Contributing factors include

    • Low urinary pH

    • Myeloproliferative disorders

    • Malignancy with increased uric acid production

    • Abrupt and dramatic weight loss

    • Uricosuric medications

  • Struvite calculi (magnesium-ammonium-phosphate, "staghorn" calculi)

    • Occur with recurrent urinary tract infections with urease-producing organisms, including Proteus, Pseudomonas, Providencia and, less commonly, Klebsiella, Staphylococcus, and Mycoplasma (but not Escherichia coli)

    • Urine pH ≥ 7.2

  • Cystine calculi: Inherited disorder with recurrent stone disease

eTable 25–1.Laboratory findings suggestive of systemic diseases presenting with kidney stones.

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