Test ID NBLD0369 Hemosiderin, Random, Urine
Specimen Required
Container/Tube: Plastic urine container
Specimen Volume: 13 mL
Collection Instructions:
1. Collect a random urine specimen.
2. No preservative.
Secondary ID
620554Useful For
Detecting hemosiderinuria, secondary to excess hemolysis, as in incompatible blood transfusions, severe acute hemolytic anemia, or hemochromatosis for external patients.
Method Name
Rous Method
Reporting Name
Hemosiderin, Random, USpecimen Type
UrineSpecimen Minimum Volume
12 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Refrigerated (preferred) | 7 days | |
Frozen | 7 days | ||
Ambient | 2 hours |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
Negative
Day(s) Performed
Monday through Sunday
Report Available
1 dayPerforming 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
83070
SANFORD LABORATORY INTERFACE BUILD INFORMATION
Result Code | Result Code Description |
---|---|
27693 | Hemosiderin, Random U |