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HelpTest Code UEBF Urea Nitrogen, Body Fluid
Additional Codes
Torrance Memorial Laboratories Test Code: 62872779
Reporting Name
Urea Nitrogen, BFUseful For
Identifying the presence of urine as a cause for accumulation of fluid in a body compartment
Assessing adequacy of peritoneal dialysis treatment protocols
Method Name
Photometric
Performing Laboratory
Mayo Clinic Laboratories in Rochester
Specimen Type
Body FluidNecessary Information
1. Date and time of collection are required.
2. Specimen source is required.
Specimen Required
Preferred Source:
-Peritoneal fluid (peritoneal, abdominal, ascites, paracentesis)
-Pleural fluid (pleural, chest, thoracentesis)
-Drain fluid (drainage, Jackson Pratt [JP] drain)
-Peritoneal dialysate (dialysis fluid)
-Pericardial
Acceptable Source: Write in source name with source location (if appropriate)
Collection Container/Tube: Sterile container
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Centrifuge to remove any cellular material and transfer into a plastic vial.
2. Indicate the specimen source and source location on label.
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Body Fluid | Refrigerated (preferred) | 7 days | |
| Frozen | 30 days | ||
| Ambient | 24 hours |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | Reject |
| Gross icterus | Reject |
| Cerebrospinal fluid Breast milk Saliva Nasal secretions Gastric secretions Bronchoalveolar lavage (BAL) or bronchial washings Colostomy/ostomy Feces Urine Sputum Vitreous fluid |
Reject |
Reference Values
An interpretive report will be provided.
Day(s) Performed
Monday through Sunday
Report Available
Same day/1 to 2 daysCPT Code Information
84520
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| UEBF | Urea Nitrogen, BF | 3093-2 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| UE_BF | Urea Nitrogen, BF | 3093-2 |
| FLD15 | Fluid Type, Urea Nitrogen | 14725-6 |
Test Classification
This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.Forms
If not ordering electronically, complete, print, and send a Renal Diagnostics Test Request (T830) with the specimen.