Recommended for the assessment of iodine nutritional status. This test reports total iodine from all iodine-containing species present in the specimen but does not determine the chemical form (species) of the iodine present. For determination of iodine excess and monitoring iodine overload in patients administered iodine-containing medications, refer to Iodine, Serum (2007463).
Quantitative Inductively Coupled Plasma-Mass Spectrometry
Tues, Thu, Sat
Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, nonessential over-the-counter medications for 48 hours (upon the advice of their physician). In addition, the administration of iodine-based contrast media and drugs containing Iodine may yield elevated results. Specimen must be collected in a plastic container and should be refrigerated after collection.
24-hour or random urine collection.
Transfer an 8 mL aliquot from a well-mixed collection to ARUP Trace Element-Free Tubes (ARUP supply #43116) available online through eSupply using ARUP Connect™ or contact ARUP Client Services at (800) 522-2787. (Min: 1 mL)
Acid preserved urine. Specimens collected within 72 hours after administration of iodinated or gadolinium-based contrast media. Specimens contaminated with blood or fecal material. Specimens transported in non-trace element-free transport tube (with the exception of the original device).
Record the total volume and collection time interval on transport tube and on test request form.
Ambient: 2 months; Refrigerated: 2 months; Frozen: 2 months
|Iodine, Urine - per volume||
|Iodine, Urine - per 24h||
|Iodine per gram of Creatinine||35.0-540.0 µg/g crt|
|0020473||Creatinine, Urine - per 24h||
Values greater than 1000 µg/L may indicate dietary excess, but more frequently suggest recent drug or contrast media exposure.
Compliance Statement B: For laboratory developed tests not using a RUO kit, and for FDA approved, cleared or 510(k) exempt assays with alterations. 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.
|Component Test Code*||Component Chart Name||LOINC|
|0020207||Creatinine, Urine - per volume||2161-8|
|0020208||Creatinine, Urine - per 24h||2162-6|
|2007466||Iodine, Urine - per volume||26842-5|
|2007467||Iodine, Urine - per 24h||2492-7|
|2007468||Iodine, per gram of CRT||55928-6|
- I urine
- Iodide urine
- Urinary Free Iodine
- Urinary Iodine