Urea Nitrogen, Fluid

0020183
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Example Reports
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Ordering Recommendation

Mnemonic

FL UN

Methodology

Spectrophotometry

Performed

Sun-Sat

Reported

Within 24 hours

New York DOH Approval Status

This test is New York DOH approved.

Specimen Required

Patient Preparation
Collect

Peritoneal fluid.

Specimen Preparation

Centrifuge and separate to remove cellular material. Transport 1 mL body fluid. (Min: 0.2 mL)

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Specimen types other than those listed.

Remarks

Indicate source on test request form.

Stability

Ambient: 24 hours; Refrigerated: 5 days; Frozen: 1 year

Reference Interval

Not established

Interpretive Data

Reference ranges for this assay have not been established for body fluid. Results should be interpreted in comparison to the concentration in blood and in conjunction with clinical context.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Compliance Category

Laboratory Developed Test (LDT)

Note

Hotline History

N/A

CPT Codes

84520

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Components

Component Test Code* Component Chart Name LOINC
0020183 Urea Nitrogen, Body Fluid 3093-2
0097114 SR Source 31208-2
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Blood Urea Nitrogen, Body Fluids
  • BUN, Body Fluids
  • Nitrogen, Body Fluids
  • Urea
  • Urea Nitrogen
Urea Nitrogen, Fluid