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Uric Acid, Body Fluid
0020513
Ordering Recommendation
 
Mnemonic
URIC-FL
Methodology
Quantitative Spectrophotometry
Performed
Sun-Sat
Reported
Within 24 hours  
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
 
Specimen Required
Patient Preparation
  
Collect
Body fluid.  
Specimen Preparation
Centrifuge to remove cellular material. Transfer 1 mL body fluid to an ARUP Standard Transport Tube. (Min: 0.2 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Breast milk and salivary fluid. Specimens too viscous to be aspirated by instrument.  
Remarks
Indicate source on test request form.  
Stability
After separation from cellular material: Ambient: 24 hours; Refrigerated: 5 days; Frozen: 6 months  
Reference Interval
A reference interval has not been established for body fluid specimens.  
Interpretive Data
Refer to report.

See Compliance Statement B: www.aruplab.com/CS
Statement B: This test was developed and its performance characteristics determined by ARUP Laboratories. The U.S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
 
Note
 
CPT Code(s)
84560
Components
Component Test Code*Component Chart NameLOINC
0020513Uric Acid, Body Fluid53612-8
0097114SR Source31208-2
* 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
  • Uric Acid, Synovial Fluid