Hepatitis B Virus (HBV) Surface Antibody
Performed at multiple locations.
Hepatitis B Virus (HBV) Surface Antibody assay is a qualitative and quantitative enzyme immunoassay for the detection of antibody to hepatitis B surface antigen in human serum. The assay results may be used as an aid in the determination of susceptability to HBV infection prior to or following HBV vaccination or where vaccination status is unknown. Assay results may be used with other HBV serological markers for laboratory diagnosis of HBV disease associated with HBV infection. A reactive assay result will allow a differential diagnosis in individuals displaying signs and symptoms of hepatitis in whom etiology in unknown.
ProcedureThe MONOLISATM Anti-HBs EIA is an qualitiative ezyme immunoassay The test has been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.
Same day (within 8-12 hours from receipt of specimen), Monday through Friday. STAT testing is available. Call for more information.
| Specimen Type | Test Code | CPT Code | NY Approved | Volume | Assay Range | Special Instructions |
|---|---|---|---|---|---|---|
| plasma | 5218649 | 86706 | Yes | 1 mL | Positive/Negative |
|
| Serum | 5218649 | 86706 | Yes | 1 mL | Positive/Negative |
|
Positive/Negative
ShippingLee's Summit Lab: Ship Monday through Friday.
Ship specimens FedEx Priority Overnight® to:
Eurofins Viracor
18000 W 99th St. Ste, #10
Lenexa, KS 66219
Ph: (800) 305-5198
Los Angeles Lab: Ship Monday through Friday.
Ship specimens FedEx Priority Overnight® to:
Eurofins Viracor Serology
2100 West 3rd Street, Suite 301
Los Angeles, CA 90057
Ph: (213)229-3654
Label Friday shipments with Saturday delivery. All specimens must be labeled with patients name and collection date. A Eurofins Viracor test requisition form must accompany each specimen. Multiple tests can be run on one specimen.
Causes for RejectionSpecimens beyond their acceptable length of time from collection as listed in the specimen handling or specimen types other than those listed.
Specimens are approved for testing in New York only when indicated in the Specimen Information field above. The CPT codes provided are based on Eurofins Viracor's interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Eurofins Viracor assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.
ReferencesBio-RAD Laboratories, Inc.