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Test ID: SSAT
Supersaturation Profile, Urine

Secondary ID A test code used for billing and in test definitions created prior to November 2011

82029

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Useful For Suggests clinical disorders or settings where the test may be helpful

Diagnosis and management of patients with renal lithiasis:

-In patients who have a radiopaque stone, for whom stone analysis is not available, the supersaturation data can be used to predict the likely composition of the stone. This may help in designing a treatment program.

-Individual components of the supersaturation profile can identify specific risk factors for stones.

-During follow-up, changes in the urine supersaturation can be used to monitor the effectiveness of therapy by confirming that the crystallization potential has indeed decreased.

Profile Information A profile is a group of laboratory tests that are ordered and performed together under a single Mayo Test ID. Profile information lists the test performed, inclusive of the test fee, when a profile is ordered and includes reporting names and individual availability.

Test IDReporting NameAvailable SeparatelyAlways Performed
SUPSTSupersaturation, UNoYes
NAUPSodium, UYes, (order NAU)Yes
KUPPotassium, UYes, (order KUR)Yes
CALPCalcium, UYes, (order CAU)Yes
MGUPMagnesium, UYes, (order MGU)Yes
CLUPChloride, UYes, (order CLU)Yes
POUPPhosphorus, UYes, (order POU)Yes
SULFPSulfate, UYes, (order SULFU)Yes
CITPCitrate Excretion, UYes, (order CITR)Yes
OXUPOxalate, UYes, (order OXU)Yes
UPHPpH, UYes, (order PHU_)Yes
URCPUric Acid, UYes, (order URCU)Yes
CTUPCreatinine, UYes, (order CTU)Yes
UOSMPOsmolalityYes, (order UOSMU)Yes

Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test

Method Name A short description of the method used to perform the test

CITP/26355: Enzymatic

OXUP/26356: Enzymatic using Oxalate Oxidase

USOMP/26360: Freezing Point Depression

SULFP/26354: High-Performance Liquid Chromatography (HPLC)

CALP/26350, MGUP/26351: Inductively Coupled Plasma (ICP) Emission Spectroscopy

POUP/26353: Molybdic Acid

UPHP/26357: pH Meter

NAUP/26348, KUP/26349, CLUP/26352: Potentiometric, Indirect Ion-Selective Electrode (ISE)

CTUP/26359: Enzymatic Colorimetric Assay

URCP/26358: Uricase

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

Supersaturation, U

Aliases Lists additional common names for a test, as an aid in searching

Brushite Crystal
Calcium Oxalate Crystal
Hydroxyapatite Crystal
Kidney Stone Disease
Kidney Stone Profile
Sodium Urate Crystal
Stone Risk Profile
Uric Acid Crystals

Specimen Type Describes the specimen type needed for testing

Urine

Specimen Required Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.

Container/Tube: Plastic, 60-mL urine bottle

Specimen Volume: 35 mL

Collection Instructions:

1. Collect urine for 24 hours.

2. Add 30 mL of toluene as preservative at start of collection, or refrigerate specimen during and after collection.

3. Specimen pH should be between 4.5 and 8 and will stay in this range if kept refrigerated. Specimens with pH >8 indicate bacterial contamination, and testing will be cancelled. Do not attempt to adjust pH as it will adversely affect results.

Additional Information:

1. 24-Hour volume is required.

2. See Urine Preservatives in Special Instructions for multiple collections.

 

Urine Preservative Collection Options

Ambient

No

Refrigerated

Yes

Frozen

Yes

6N HCl

No

50% Acetic Acid

No

Na2CO3

No

Toluene

Preferred

6N HNO3

No

Boric Acid

No

Thymol

No

Forms: If not ordering electronically, submit a General Request Form (Supply T239) with the specimen.

Specimen Minimum Volume Defines the amount of specimen required to perform an assay once, including instrument and container dead space. Submitting the minimum specimen volume makes it impossible to repeat the test or perform confirmatory or perform reflex testing. In some situations, a minimum specimen volume may result in a QNS (quantity not sufficient) result, requiring a second specimen to be collected.

25 mL

Reject Due To Identifies specimen types and conditions that may cause the specimen to be rejected

Hemolysis

NA

Lipemia

NA

Icterus

NA

Other

Specimen pH >8.0

 

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.

Specimen TypeTemperatureTime
UrineRefrigerated (preferred)7 days
 Frozen 7 days

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Urine is often supersaturated, which favors precipitation of several crystalline phases such as calcium oxalate, calcium phosphate, and uric acid. However, crystals do not always form in supersaturated urine because supersaturation is balanced by crystallization inhibitors that are also present in urine. Urinary inhibitors include ions (eg, citrate) and macromolecules but remain poorly understood.

 

Urine supersaturation is calculated by measuring the concentration of all the ions that can interact (potassium, calcium, phosphorus, oxalate, uric acid, citrate, magnesium, sodium, chloride, sulfate, and pH). Once the concentrations of all the relevant urinary ions are known, a computer program can calculate the theoretical supersaturation with respect to the important crystalline phases, eg, calcium oxalate.(1)

 

Since the supersaturation of urine has been shown to correlate with stone type(2), therapy is often targeted towards decreasing those urinary supersaturations that are identified. Treatment strategies include alterations in diet and fluid intake as well as drug therapy, all designed to decrease the urine supersaturation.

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

SUPERSATURATION REFERENCE MEANS (DG)

Calcium oxalate: 1.77

Brushite: 0.21

Hydroxyapatite: 3.96

Uric acid: 1.04

Sodium urate: 1.76

 

INDIVIDUAL URINE ANALYTES

OSMOLALITY

0-11 months: 50-750 mOsm/kg

> or =12 months: 150-1,150 mOsm/kg

 

ALL REFERENCE RANGES BELOW ARE BASED ON 24-HOUR COLLECTIONS.

 

SODIUM

41-227 mmol/24 hours

 

POTASSIUM

17-77 mmol/24 hours

 

CALCIUM

Males: 25-300 mg/specimen*

Females: 20-275 mg/specimen*

Hypercalciuria: >350 mg/specimen

*Values are for persons with average calcium intake (ie, 600-800 mg/day).

 

MAGNESIUM

0-15 years: not established

> or =16 years: 75-150 mg/specimen

 

CHLORIDE

40-224 mmol/24 hours

 

PHOSPHORUS

<1,100 mg/specimen

 

SULFATE

7-47 mmol/specimen

 

CITRATE EXCRETION

0-19 years: not established

20 years: 150-1,191 mg/specimen

21 years: 157-1,191 mg/specimen

22 years: 164-1,191 mg/specimen

23 years: 171-1,191 mg/specimen

24 years: 178-1,191 mg/specimen

25 years: 186-1,191 mg/specimen

26 years: 193-1,191 mg/specimen

27 years: 200-1,191 mg/specimen

28 years: 207-1,191 mg/specimen

29 years: 214-1,191 mg/specimen

30 years: 221-1,191 mg/specimen

31 years: 228-1,191 mg/specimen

32 years: 235-1,191 mg/specimen

33 years: 242-1,191 mg/specimen

34 years: 250-1,191 mg/specimen

35 years: 257-1,191 mg/specimen

36 years: 264-1,191 mg/specimen

37 years: 271-1,191 mg/specimen

38 years: 278-1,191 mg/specimen

39 years: 285-1,191 mg/specimen

40 years: 292-1,191 mg/specimen

41 years: 299-1,191 mg/specimen

42 years: 306-1,191 mg/specimen

43 years: 314-1,191 mg/specimen

44 years: 321-1,191 mg/specimen

45 years: 328-1,191 mg/specimen

46 years: 335-1,191 mg/specimen

47 years: 342-1,191 mg/specimen

48 years: 349-1,191 mg/specimen

49 years: 356-1,191 mg/specimen

50 years: 363-1,191 mg/specimen

51 years: 370-1,191 mg/specimen

52 years: 378-1,191 mg/specimen

53 years: 385-1,191 mg/specimen

54 years: 392-1,191 mg/specimen

55 years: 399-1,191 mg/specimen

56 years: 406-1,191 mg/specimen

57 years: 413-1,191 mg/specimen

58 years: 420-1,191 mg/specimen

59 years: 427-1,191 mg/specimen

60 years: 434-1,191 mg/specimen

>60 years: not established

 

OXALATE

0.11-0.46 mmol/specimen

 

URIC ACID

Diet-dependent: <750 mg/specimen

 

CREATININE

15-25 mg/kg of body weight/24 hours

Reported in unit of mg/specimen

Interpretation Provides information to assist in interpretation of the test results

Delta G (DG), the Gibbs free energy of transfer from a supersaturated to a saturated solution is negative for undersaturated solutions and positive for supersaturated solutions. In most cases the supersaturation levels are slightly positive even in normal individuals but are balanced by an inhibitor activity.

 

While the DG of urine is often positive, even in the urine of nonstone formers, on average, the DG is even more positive in those individuals who do form kidney stones. The "normal" values are simply derived by comparing urinary DG values for the important stone-forming crystalline phases between a population of stone formers and a population of nonstone formers. Those DG values that are outside the expected range in a population of nonstone formers are marked "abnormal."

 

A normal or increased citrate value suggests that potassium citrate may be a less effective choice for treatment of a patient with calcium oxalate or calcium phosphate stones.

 

If the urine citrate is low, secondary causes should be excluded including hypokalemia, renal tubular acidosis, gastrointestinal bicarbonate losses (eg, diarrhea or malabsorption), or an exogenous acid load (eg, excessive consumption of meat protein).

 

An increased urinary oxalate value may prompt a search for genetic abnormalities of oxalate production (ie, primary hyperoxaluria). Secondary hyperoxaluria can result from diverse gastrointestinal disorders that result in malabsorption. Milder hyperoxaluria could result from excess dietary oxalate consumption, or reduced calcium (dairy) intake, perhaps even in the absence of gastrointestinal disease.

 

The results can be used to determine the likely effect of a therapeutic intervention on stone-forming risk. For example, taking oral potassium citrate will raise the urinary citrate excretion, which should reduce calcium phosphate supersaturation (by reducing free ionic calcium), but citrate administration also increases urinary pH (because it represents an alkali load) and a higher urine pH promotes calcium phosphate crystallization. The net result of this or any therapeutic manipulation could be assessed by collecting a 24-hour urine and comparing the supersaturation calculation for calcium phosphate before and after therapy.

 

Important stone-specific factors:

-Calcium oxalate stones: urine volume, calcium, oxalate, citrate, and uric acid excretion are all risk factors that are possible targets for therapeutic intervention.

-Calcium phosphate stones (apatite or brushite): urinary volume, calcium, pH, and citrate significantly influence the supersaturation for calcium phosphate. Of note, a urine pH <6 may help reduce the tendency for these stones to form.

-Uric acid stones: urine pH, volume, and uric acid excretion levels influence the supersaturation. Urine pH is especially critical, in that uric acid is unlikely to crystallize if the pH is >6.

-Sodium urate stones: alkaline pH and high uric acid excretion promote stone formation.

 

A low urine volume is a universal risk factor for all types of kidney stones.

Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

The urine is often supersaturated with respect to the common crystalline constituents of stones, even in nonstone formers.

 

Individual interpretation of the supersaturation values in light of the clinical situation is critical. In particular, treatment may reduce the supersaturation with respect to 1 crystal type, but increase the supersaturation with respect to another. Therefore, the specific goals of treatment must be considered when interpreting the test results.

Clinical Reference Provides recommendations for further in-depth reading of a clinical nature

1. Werness PG, Brown CM, Smith LH, Finlayson B: EQUIL2: a BASIC computer program for the calculation of urinary saturation. J Urol 1985;134:1242-1244

2. Parks JH, Coward M, Coe FL: Correspondence between stone composition and urine supersaturation in nephrolithiasis. Kidney Int 1997;51:894-900

3. Finlayson B: Calcium stones: Some physical and clinical aspects. In Calcium in Renal Failure and Nephrolithiasis. Edited by DS David. New York, John Wiley and Sons, 1977, pp 337-382

Method Description Describes how the test is performed and provides a method-specific reference

The major analytes evaluated are potassium, calcium, phosphorus, oxalate, uric acid, citrate, magnesium, sodium, chloride, sulfate, and pH. Given the measured urine concentrations of these analytes and the known affinity constants of the ions for each other at the given pH, a computer program (EQUIL2) calculates a supersaturation for each ion pair of interest (eg, calcium oxalate)(1). Results are expressed as a Delta G (DG) value for each ion pair. DG is the Gibbs free energy of transfer from a supersaturated to a saturated solution.(Werness PG, Brown CM, Smith LH, Finlayson B: EQUIL2: a BASIC computer program for the calculation of urinary saturation. J Urol 1985;134:1242-1244)

Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.

Monday through Friday; 8 a.m.-4 p.m.

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

2 days; Excess capacity for this test is limited.

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

5 days

Specimen Retention Time Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

7 days

Performing Laboratory Location The location of the laboratory that performs the test

Rochester

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

82340-Calcium

82436-Chloride

82507-Citrate excretion

82570-Creatinine

83735-Magnesium

83935-Osmolality

83945-Oxalate

83986-pH

84105-Phosphorus

84133-Potassium

84300-Sodium

84392-Sulfate

84560-Uric acid

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.

Result IDReporting NameLOINC Code
UOSMPOsmolality2695-5
26350Calcium, U6874-2
CITRECitrate Excretion, U14650-6
CL24Chloride, U2079-2
CRETUCreatinine, U2162-6
K24UPotassium, U2829-0
26351Magnesium, U24447-5
NA24Sodium, U2956-1
OXLTOxalate, U (mmol/spec)14862-7
PHS_UPhosphorus, U2779-7
SULF_Sulfate Urine26889-6
21041Calcium Oxalate CrystalIn Process
UPHUpH, UIn Process
URACIUric Acid, U3087-4
21042Brushite CrystalIn Process
OXU2Oxalate, mg/spec2701-1
21043Hydroxyapatite CrystalIn Process
21044Uric Acid CrystalIn Process
21045Sodium Urate CrystalIn Process
21060Interpretation59462-2
CLDURCollection Duration13362-9
VL38Volume3167-4