Ehrlichia chaffeensis DNA, Real-Time PCR

Ehrlichia chaffeensis DNA, Real-Time PCR

Test Code

11353
87484
11353
87484
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

Ehrlichia chaffeensis DNA, Real-Time PCR - Ehrlichia chaffeensis DNA PCR is a highly sensitive method to detect the presence of ehrlichia chaffeensis DNA in clinical specimens.
The diagnosis of ehrlichia chaffeensis infection should not rely solely upon the result of PCR assay. A positive result should be considered in conjunction with clinical presentation and additional established clinical tests. Moreover, this assay cannot differentiate between viable and nonviable organisms. A negative PCR result indicates the absence of ehrlichia chaffeensis DNA at detectable levels in the sample tested and does not exclude the diagnosis of disease.

Test Details

Methodology

Real-Time Polymerase Chain Reaction

Assay Category

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

Reference Range(s)

Not detected

Alternative Name(s)

Tick borne,E chaffeensis,Ehrlichiosis

LOINC® Codes, Performing Laboratory

Methodology

Real-Time Polymerase Chain Reaction
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

Not detected

Alternative Name(s)

Tick borne,E chaffeensis,Ehrlichiosis

Preferred Specimen(s)

0.7 mL whole blood collected in an EDTA (lavender-top) or ACD (yellow-top) tube or
1 tick (in 70% ethanol) submitted in a sterile leak-proof container

Alternative Specimen(s)

1 mL CSF submitted in a sterile leak-proof container

Minimum Volume

0.3 mL

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Whole blood
    Room temperature: 48 hours
    Refrigerated: 7 days
    Frozen: 30 days

    Tick and CSF
    Room temperature: 48 hours
    Refrigerated: 7 days
    Frozen: 30 days

Reject Criteria

Hemolysis • Lithium heparin (green-top) tube • Sodium heparin (green-top) tube

Setup Schedule

0.7 mL whole blood collected in an EDTA (lavender-top) or ACD (yellow-top) tube or
1 tick (in 70% ethanol) submitted in a sterile leak-proof container
1 mL CSF submitted in a sterile leak-proof container
0.3 mL
Refrigerated (cold packs)
Whole blood
Room temperature: 48 hours
Refrigerated: 7 days
Frozen: 30 days

Tick and CSF
Room temperature: 48 hours
Refrigerated: 7 days
Frozen: 30 days
Hemolysis • Lithium heparin (green-top) tube • Sodium heparin (green-top) tube
In-home collection may be available in your area for purchase 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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