Cobalt, Serum or Plasma




Test Mnemonic

COBALT

CPT Codes

  • 83018 - QTY (1)

LOINC ®

5627-5

Aliases

  • Cobalt, Plasma

Performing Laboratory

ARUP

FDA Category

Laboratory Developed Test


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
2 mLSerumNo additive (Navy Blue) AmbientPatient Prep: Diet, medication and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals and non-essential over-the-counter medications (upon the advice of their physician). Do not use serum separator tubes. Remove serum from cells ASAP or within 2 hours of collection and aliquot into a trace metal-free transport tube (ARUP #43116).

Alternate Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
2 mLPlasmaEDTA (Royal blue) AmbientPatient Prep: Diet, medication and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals and non-essential over-the-counter medications (upon the advice of their physician). Remove plasma from cells ASAP or within 2 hours of collection and aliquot into a trace-metal free transport tube (ARUP #43116).

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
0.5 mL     

Stability

Environmental Condition Description
AmbientIndefinitely
RefrigeratedIndefinitely
FrozenIndefinitely

Days Performed

Sun - Sat

Turnaround Time

2 - 4 days

Methodology

Name Description
Inductively Coupled Plasma / Mass Spectrometry (ICP-MS) 

Reference Range

Cobalt, Serum
Sex Age From Age To Type Range Range Unit
       Normal< or =1.0ug/L

Special Info

Patient Prep: Diet, medication and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals and non-essential over-the-counter medications (upon the advice of their physician). Unacceptable conditions: Non-certified metals-free tubes. Specimens collected and/or transported in containers other than specified will be rejected. This test is New York DOH approved.

Clinical Info

Occupational exposure or toxic ingestion monitoring. Whole blood is the preferred test for evaluating metal ion release from metal-on-metal joint arthroplasty. Serum levels may be increased in asymptomatic patients with metal-on-metal prosthetics and should be considered in the context of the overall clinical scenario. Symptoms associated with cobalt toxicity vary based on route of exposure, and may include cardiomyopathy, allergic dermatitis, pulmonary fibrosis, cough and dyspnea.