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Fluoride Quantitative, Serum or Plasma
0091341
Ordering Recommendation
Mnemonic
FLUORIDE
Methodology
Quantitative Ion Chromatography
Performed
Varies
Reported
3-10 days
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
ARUP Consult®
Disease Topics
Specimen Required
Patient Preparation
 
Collect
Plain red, lavender (EDTA) or pink (K2EDTA). 
Specimen Preparation
Separate from cells within 2 hours. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL) 
Storage/Transport Temperature
Refrigerated. Also acceptable: Room temperature or frozen. 
Unacceptable Conditions
Gray (potassium oxalate/sodium fluoride) or separator tubes. 
Remarks
 
Stability
Ambient: 1 month; Refrigerated: 1 month; Frozen: 3 months 
Reference Interval
By report
Interpretive Data


Components
Component Test Code*Component Chart NameLOINC
0091340Fluoride Quantitative, Serum or Plasma5649-9
* 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
  • F

Performed at National Medical Services (NMS)