Adenovirus Antigen, DFA

Adenovirus Antigen, DFA

Test Code

8355
87260
8355
87260
In-home collection is not available in your area through Quest Mobile.

Clinical Significance

Adenovirus Antigen, DFA - Respiratory viruses are responsible for a significant proportion of illness in human populations. Diagnosis may facilitate appropriate selection of specific antiviral drug therapy, prevent inappropriate use of antibiotics and guide patient management decisions.

Test Resources

None found for this test
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Test Details

Methodology

Direct Immunofluorescence Assay (DFA)

Reference Range(s)

See Laboratory Report

Alternative Name(s)

Adenovirus Direct Antigen Detection,Adenovirus Direct Exam

LOINC® Codes, Performing Laboratory

Methodology

Direct Immunofluorescence Assay (DFA)

Reference Range(s)

See Laboratory Report

Alternative Name(s)

Adenovirus Direct Antigen Detection,Adenovirus Direct Exam

Preferred Specimen(s)

3 mL nasopharyngeal aspirate/wash or nasopharyngeal swab in VCM medium or equivalent

Alternative Specimen(s)

3 mL bronchial lavage/wash in VCM medium or equivalent

Minimum Volume

1 mL

Collection Instructions

To maintain optimum viability, place swab or fluid into VCM (equal volumes of fluid and VCM) or equivalent and transport the specimen to the laboratory as soon as possible. Best recovery is obtained when the specimens are refrigerated at 2-8° C or kept on wet ice following collection and while in transit. If there will be a long delay before processing, specimens in VCM or equivalent should be frozen at -70° C or colder and transported on dry ice. Storage or transport at -20° C is not acceptable.

Transport Container

VCM medium tube or equivalent

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • VCM medium tube or equivalent
    Room temperature: Unacceptable
    Refrigerated: 4 days
    Frozen -20° C: Unacceptable
    Frozen -70° C: 30 days

Reject Criteria

Dry swabs • Nasal smear • Non-respiratory specimens • Received in formalin or other fixatives • Received in non-viral transport medium such as nucleic acid or bacterial transport media • Sputum • Throat swabs • Unpreserved samples

Setup Schedule

3 mL nasopharyngeal aspirate/wash or nasopharyngeal swab in VCM medium or equivalent
3 mL bronchial lavage/wash in VCM medium or equivalent
1 mL
To maintain optimum viability, place swab or fluid into VCM (equal volumes of fluid and VCM) or equivalent and transport the specimen to the laboratory as soon as possible. Best recovery is obtained when the specimens are refrigerated at 2-8° C or kept on wet ice following collection and while in transit. If there will be a long delay before processing, specimens in VCM or equivalent should be frozen at -70° C or colder and transported on dry ice. Storage or transport at -20° C is not acceptable.
VCM medium tube or equivalent
Refrigerated (cold packs)
VCM medium tube or equivalent
Room temperature: Unacceptable
Refrigerated: 4 days
Frozen -20° C: Unacceptable
Frozen -70° C: 30 days
Dry swabs • Nasal smear • Non-respiratory specimens • Received in formalin or other fixatives • Received in non-viral transport medium such as nucleic acid or bacterial transport media • Sputum • Throat swabs • Unpreserved samples
In-home collection is not available in your area through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

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