Mumps Virus Antibody (IgM), (NY)

Test Code

901435

CPT Codes
86735<br /> **For non-New York patient testing, see test code 36565.**

Preferred Specimen

1 mL serum

Minimum Volume

0.2 mL

Transport Container

Plastic screw-cap vial

Transport Temperature

Room temperature

Specimen Stability

Room temperature: 7 days
Refrigerated: 14 days
Frozen: 30 days

Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)

Gross hemolysis • Gross lipemia

Methodology
Immunofluorescence Assay (IFA)

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

Setup Schedule

Set up: Mon-Fri; Report available: 4 days

Reference Range

Mumps Virus Antibody (IgM)

Titer	Interpretation
<1:20	Antibody not detected
≥1:20	Antibody detected

The presence of IgM antibody to mumps typically indicates recent or current mumps infection; however, false positive results may occur due to antibody cross reactivity to parainfluenza virus.

Performing Laboratory

Quest Diagnostics Nichols Institute-San Juan Capistrano, CA

33608 Ortega Highway

San Juan Capistrano, CA 92675-2042

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.