Sign in →

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

620554

Useful 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, U

Specimen Type

Urine

Specimen 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 day

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test 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 Laboratories - Bismarck Additional Information:

SANFORD LABORATORY INTERFACE BUILD INFORMATION

 Result Code     Result Code Description   
 27693  Hemosiderin, Random U