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Test Directory

Hantavirus Antibody (IgG, IgM)

Test Summary

This immunoassay is for the detection of IgM and IgG antibodies against Sin Nombre virus (SNV), a New World Hantavirus species endemic in the United States. Laboratory testing can aid in the diagnosis of Hantavirus Pulmonary Syndrome (HPS) in a patient with consistent signs and symptoms of infection. 

HPS is caused primarily via inhalation of Hantavirus from contaminated rodent urine, droppings, or saliva. Symptoms may include fatigue, fever, muscle aches, with rapid progression to coughing and shortness of breath, which may be severe and life-threatening. Testing may be considered in patients with HPS-compatible symptoms who may have had contact with rodents or infested areas.

In addition to New World Hantavirus, there are Old World Hantaviruses (e.g. Seoul, Hantaan, Dobrava, and Puumala) endemic to Asia and Europe that cause hemorrhagic fever with renal syndrome, a condition not typically seen in the United States. This assay may or may not detect antibodies against these Old World Hantaviruses due to variable cross-reactivity with the target antigen. Negative antibody results may also occur early in infections, prior to seroconversion. Antibodies can be detected as early as the prodromal phase of infection (3-7 days). IgM results may be detected for months and IgG for up to several years after acute infection. Cross-reactivivty with autoimmune conditions can occur. Therefore, the results of this test should be interpreted in the context of pertinent clinical and physical findings.


Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

0.5 mL serum

Minimum Volume

0.1 mL

Instructions

Please note: IgM positives will be reported to public health.

Patient Preparation

N/A

Storage

Plastic screw-cap vial

Transport Temperature

Room temperature

Specimen Stability

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

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Grossly hemolyzed, icteric, or lipemic samples

Order Code

HANTA

EPIC (Premier) Code

LAB5234

Includes

IgM positives will be reported to public health

CPT Code

  • 86790 (x2)

Billing Code

  • 671004

CPT Statement

Methodology

Immunoassay (IA)

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. The FDA has determined that such clearance or approval is not necessary. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

N/A

Department

Reference Testing

Reference Range

Hantavirus Ab (IgG) Negative
Hantavirus Ab (IgM) Negative

Setup Schedule / Expected Turnaround Time

Wednesday; Report available: 1 - 7 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

0.5 mL serum

Minimum Volume

0.1 mL

Instructions

Please note: IgM positives will be reported to public health.

Patient Preparation

N/A

Storage

Plastic screw-cap vial

Transport Temperature

Room temperature

Specimen Stability

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

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Grossly hemolyzed, icteric, or lipemic samples

Billing

CPT Code

  • 86790 (x2)

Billing Code

  • 671004

CPT Statement

Result Information

Methodology

Immunoassay (IA)

Testing Laboratory

N/A

Reference Range

Hantavirus Ab (IgG) Negative
Hantavirus Ab (IgM) Negative

Setup Schedule / Expected Turnaround Time

Wednesday; Report available: 1 - 7 days