Hepatitis D Virus (HDV) IgM
Test Code: 30336
Cpt Code:86692 (x1)
Hepatitis D virus (HDV) is an incomplete RNA virus that requires the helper function of Hepatitis B virus (HBV) envelope proteins (HBSAg) to replicate. The presence of HDV IgM antibodies indicates recent exposure to HDV.
The Hepatitis D IgM Assay is an enzyme linked capture immunoassay. IgM contained in the sample is captured by monoclonal antibody against human IgM immobilized on the solid phase. Hepatitis D specific IgM is detected with an HRP conjugated HDV antigen complex. Positive samples will have OD values above the established cutoff. This test was developed and its performance characteristics determined by Viracor-IBT Laboratories. It has not been cleared or approved by the U.S. Food and Drug Administration. Results should be used in conjunction with clinical findings, and should not form the sole basis for a diagnosis or treatment decision.
The assay is specific for Hepatitis D.
Causes For Rejection
Sample types other than serum and plasma. Samples beyond their stability.
1-5 business days from receipt of specimen.
Ship Monday through Friday. Friday shipments must be labeled for Saturday delivery. All specimens must be labeled with patient's name and collection date. A Viracor-IBT test requisition form must accompany each specimen. Multiple tests can be run on one specimen. Ship specimens FedEx Priority Overnight® to: Viracor-IBT Laboratories, 1001 NW Technology Dr, Lee's Summit, MO 64086.
Collect 4-5 mL whole blood in red top tube, centrifuge and transfer 2 mL serum to sterile, screw top tube (minimum volume 0.5 mL) . Can be shipped at ambient or frozen temperature Monday through Friday. Specimens shipped at ambient temperature must be received within 7 days of collection.
Collect 4-5 mL whole blood in EDTA or sodium heparin tube, centrifuge and transfer 2 mLplasma to sterile, screw top tube (minimum volume 0.5 mL) . Can be shipped at ambient or frozen temperature Monday through Friday. Specimens shipped at ambient temperature must be received within 7 days of collection.
Specimens are approved for testing in New York only when indicated in the Specimen Information field above. The CPT codes provided are based on Viracor-IBT'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. Viracor-IBT assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.
Price, J. An update on Hepatitis B, D and E Viruses. (2014) Topics in Antiviral Medicine 21(5):157-163.