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 Iodide Quantitative, Serum or Plasma
0090695
Ordering Recommendation

This test reports iodide, a subset of the total iodine present and is recommended for determination of toxic exposures to iodide containing compounds. This test is not recommended for the assessment of iodine status. Order Iodine, Urine (2007465) for the assessment of iodine nutritional status.

Mnemonic
IODIDE SP
Methodology
Quantitative Ion Exchange Chromatography
Performed
Varies
Reported
3-9 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
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
Separator tubes. 
Remarks
 
Stability
Ambient: 2 weeks; Refrigerated: 2 weeks; Frozen: 8 months 
Reference Interval
By report
Interpretive Data


Components
Component Test Code*Component Chart NameLOINC
0090693Iodide Quantitative, Serum or Plasma59697-3
* 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
  • White Cross

Performed at National Medical Services (NMS)