Anaplasma phagocytophilum Antibodies (IgG, IgM) with Reflex to Titers
ANAPHR
Test Summary
This test is for the detection of IgG and IgM antibodies against Anaplasma phagocytophilum to aid in the diagnosis of Anaplasmosis (human granulocytic anaplasmosis). Anaplasmosis is a tickborne disease caused by transmission of the bacteria via the bite of an infected tick. It is most common in the Northeastern and upper Midwestern United States during warmer months. Testing for Anaplasmosis is based on a clinical evaluation and risk of tick exposure with consideration to the geographic region. Symptoms may be nonspecific, including headache, fever/chills, malaise, myalgia, gastrointestinal symptoms, and rash (less common). Infection can have similarities with other tickborne illnesses with overlapping vectors, geographic endemicity, and similar clinical signs and symptoms, including Ehrlichia spp, Borrelia burgdorferi (Lyme disease) and Babesia microti. Negative results can occur early in infection. Nucleic acid amplification tests are the preferred method for diagnosis during acute infection. Seroconversion or a four-fold increase between acute and convalescent sera can be used to support a diagnosis. The presence of IgG alone may indicate past infection, and IgM may persist for many months after infection has resolved. Antibody levels may remain elevated for several years after acute illness. Cross-reactivity between related organisms Anaplasma and Ehrlichia spp, can occur. Therefore, interpretation of serologic results is done in the context of pertinent clinical picture, including timing from symptom onset.
Aliases
- HE
- Anaplasma Ab IgG
- IgM
- Human Granulocytic Ehrlichiosis Ab
Specimen Collection
Special Instructions
Preferred Specimen
Minimum Volume
0.2 mL
Instructions
Patient Preparation
Storage
Transport Temperature
Specimen Stability
- Room temperature: 7 days
- Refrigerated: 14 days
- Frozen: 30 days
Limitations
Other Acceptable Specimens
Unacceptable Specimens
Order Code
ANAPHR
EPIC (Premier) Code
Includes
CPT Code
- 86666 (x2)
Billing Code
- 670921
CPT Statement
Methodology
FDA Status
Physician Attestation of Informed Consent
Testing Laboratory
14225 Newbrook Drive
Chantilly VA, 20153
Department
Reference Range
Setup Schedule / Expected Turnaround Time
Specimen Collection
Special Instructions
Preferred Specimen
Minimum Volume
0.2 mL
Instructions
Patient Preparation
Storage
Transport Temperature
Specimen Stability
- Room temperature: 7 days
- Refrigerated: 14 days
- Frozen: 30 days