Test Code UCITXM Citrate Excretion, Random, Urine
Additional Codes
Mayo Test ID |
CITRA |
EPIC Test ID |
LAB3192 |
Ordering Guidance
A timed 24-hour collection is the preferred specimen for measuring and interpreting this urinary analyte. Order CITR / Citrate Excretion, 24 Hour, Urine.
Random collections normalized to urinary creatinine may be of some clinical use in patients who cannot collect a 24-hour specimen, typically small children.
Specimen Required
Patient Preparation: Any drug that causes alkalemia or acidemia may be expected to alter citrate excretion and should be avoided, if possible. The patient must avoid laxative use for 24 hours prior to collection.
Supplies: Sarstedt 5 mL Aliquot Tube (T914)
Container/Tube: Plastic, 5-mL tube
Specimen Volume: 4 mL
Collection Instructions:
1. Collect a random urine specimen.
2. No preservative.
Forms
If not ordering electronically, complete, print, and send a Renal Diagnostics Test Request (T830) with the specimen.
Useful For
Diagnosing risk factors for patients with calcium kidney stones using random urine specimens
Monitoring results of therapy in patients with calcium stones or renal tubular acidosis
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
CITR2 | Citrate Concentration, Random, U | No | Yes |
CRETR | Creatinine, Random, U | No | Yes |
RAT10 | Citrate/Creatinine Ratio | No | Yes |
Method Name
Enzymatic
Reporting Name
Citrate Excretion, Random, USpecimen Type
UrineSpecimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Refrigerated (preferred) | 14 days | |
Frozen | 14 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
No established reference values.
Day(s) Performed
Monday through Saturday
Report Available
Same day/1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
82507
82570
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
CITRA | Citrate Excretion, Random, U | 13722-4 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
CRETR | Creatinine, Random, U | 2161-8 |
CITR2 | Citrate Concentration, Random, U | 2128-7 |
RAT10 | Citrate/Creatinine Ratio | 13722-4 |