Neuromyotonia Evaluation

Test Code
92822


CPT Codes
83519, 86255<br>Restricted Client Code

Physician Attestation of Informed Consent
This germline genetic test requires physician attestation that patient consent has been received if ordering medical facility is located in AK, DE, FL, GA, IA, MA, MN, NV, NJ, NY, OR, SD or VT or test is performed in MA.


Preferred Specimen
2 mL serum


Minimum Volume
0.5 mL


Instructions
Specimens shipped at room temperature must be received within 48 hours of draw.

Note: Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.


Transport Container
Tranpsort tube


Transport Temperature
Room temperature


Specimen Stability
Room temperature: 72 hours
Refrigerated: 21 days
Frozen: 28 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Hemolysis • Lipemia • Icteric • Turbid • Bacterial contamination


Methodology
Immunofluorescence Assay (IFA) • Radioimmunoassay (RIA)

FDA Status
This test was developed and its analytical performance characteristics have been determined by Athena Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Setup Schedule
Set up: Mon, Thurs; Report available: 7-10 days


Report Available
10 Days


Reference Range
See Laboratory Report


Clinical Significance
Anti- voltage gated potassium channels (VGKC) and anti-CASPR2 antibodies are found in patients with progressive muscle stiffness, myokymia, autonomic dysfunction, and delayed muscle relaxation.




The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.