Ordering Recommendation

Refer to aruplab.com/bodyfluids for clinical indications and interpretive information.

Mnemonic
NA FL
Methodology

Quantitative Ion-Selective Electrode

Performed

Sun-Sat

Reported

Within 24 hours

New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect

CSF, Drain, Pancreatic, Pericardial, Peritoneal/Ascites or Pleural 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

Specimen types other than those listed. Specimens too viscous to be aspirated by instrument.

Remarks

Specimen source must be provided.

Stability

Ambient: 2 weeks; Refrigerated: 2 weeks; Frozen: 6 months

Reference Interval
Interpretive Data

For information on body fluid reference ranges and/or interpretive guidance visit https://aruplab.com/bodyfluids/

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

Modified FDA

Note
Hotline History
N/A
CPT Codes

84302

Components
Component Test Code* Component Chart Name LOINC
0020154 Sodium, Body Fluid 2950-4
2013037 Sodium Fluid 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
  • Na Body Fluids
  • Na+ Body Fluids
Sodium, Fluid