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Test Name:
StoneRisk® Diagnostic Profile


  • SBMF No:
    43141
  • Performance Lab Name:
    Quest Diagnostics Nichols Institute
  • Test Mnemonic:
    STONE RISK
  • ABN:
    Required – Not FDA-Approved
  • CPT Code:
    82140; 82340; 82507; 82570; 83735; 83945; 83986; 84105; 84133; 84300; 84392; 84560
  • LOINC Code:
    19146-0
  • Ref Lab Test No:
    5510
  • Test Includes:
    Ammonium
    Calcium
    Citrate
    Creatinine
    Magnesium
    Oxalate
    pH
    Phosphorus
    Potassium
    Sodium
    Sulfate
    Uric Acid
  • Spec Type:
    Urine, 24-hour
  • Spec Container:
    Quest 24-hour Urine Collection Kit specific for renal stone formation diagnosis
  • Pref Vol:
    Quest 24hr Urine Plain Kit: 60.0 mL
    Quest 24hr Urine Acid Kit: 50.0 mL
  • Min Vol:
    Quest 24hr Urine Plain Kit: 30.0 mL
    Quest 24hr Urine Acid Kit: 30.0 mL
  • Patient Prep:
    Follow instructions in the kit
  • Spec Collect:
    Use only Quest 24-hour Urine Collection Kits specific for renal stone formation diagnosis
    Follow instructions in the kit
  • Spec Process:
    Upon completion of 24-hour collection in the large orange collection container, tighten the cap on the container and mix contents in the container vigorously for one minute. A good mix will assure accurate test results.
    Carefully fill the two plastic white vials with urine collected in the large orange container. The two white vials must be filled within two to four hours of completion of 24-hour collection. Fill and cap vials one at a time. Cap both vials tightly, write patient's name on each vial and place in zip-lock bags provided (do not remove absorbent sheets).
    Complete the patient information section. Please provide the patient's weight (in pounds) if available.
    Place specimen in mailback box and return to the laboratory
  • Spec Store Transport:
    Room temperature or refrigerated
  • Spec Stability:
    10 days room temperature (20-30°C)
    10 days refrigerated (2-8°C)
  • Spec Remarks:
    Urine must only be collected and stored in the large orange collection container
    Do not remove sponge from the orange collection container
    Do not remove wool from white container
    Do not collect the first urination at the beginning of 24-hour collection
    During collection process store large orange container in a cool location
  • Methodology:
    Immunochemiluminometric Assay
    Inductively Coupled Plasma/Optical Emission Spectrometry (ICP-OES)
    pH Meter
    Spectrophotometry
  • Use:
    StoneRisk® Diagnostic Profile is for stone formers with a positive urine culture indicating Urinary tract infection (UTI), also for recurrent stone formers or when attending physician deems it medically necessary for the patient to have comprehensive metabolic evaluation.
  • Reference Range:
      Total Urine Volume
        > 2.00 L/day

      pH, Urine
        5.5-7.0

      Calcium, Urine
        < 250 mg/day

      Oxalate, Urine
        < 45 mg/day

      Uric Acid, Urine
        < 700 mg/day

      Citrate, Urine
        > 320 mg/day

      Sodium, Urine
        < 200 mEq/day

      Sulfate, Urine
        < 30 mmol/day

      Phosphorus, Urine
        < 1100 mg/day

      Magnesium, Urine
        > 60 mg/day

      Ammonium, Urine
        14-62 mEq/day

      Potassium, Urine
        19-135 mEq/day

      Creatinine, Urine
        Male: 800-2000 mg/day
        Female: 600-1800 mg/day
  • Additional Test Info:
    Citric Acid: This test(s) was performed using a kit that has not been cleared or approved by the FDA. The analytical performance characteristics of this test have been determined by Quest Diagnostics Nichols Institute, Valencia. This test should not be used for diagnosis without confirmation by other medically established means.
  • Day Run:
    Mon-Sat
  • Time Reported:
    Next day
    This is a sendout test. Please note that turnaround time is defined as the anticipated time from set up day to results release.
  • Test Type:
    URINE