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ADmark® Alzheimer's Evaluation
Test Code93798
CPT Codes
81401, 83520 (x3)<br /> Limited Access Code
Physician Attestation of Informed Consent
This germline genetic test requires physician attestation that patient consent has been received if ordering medical facility is located in AK, DE, FL, GA, IA, MA, MN, NV, NJ, NY, OR, SD or VT or test is performed in MA.
Includes
Phospho-Tau, Total-Tau, Ab42, ApoE
Athena does not perform ApoE testing for individuals under the age of 18. Patients must be symptomatic for Dementia
Athena does not perform ApoE testing for individuals under the age of 18. Patients must be symptomatic for Dementia
Preferred Specimen
8 mL whole blood collected in EDTA (lavender-top) tube(s), and 2 mL CSF collected in a polypropylene tube
Minimum Volume
6 mL whole blood • 0.5 mL CSF
Instructions
Informed Consent Required
Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
Whole blood-DNA yields and quality are better in fresh specimens. However, when necessary, most genetic tests are successful from DNA purified from whole blood that is several days old.
CSF-Tubes other than polypropylene are not acceptable
Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
Whole blood-DNA yields and quality are better in fresh specimens. However, when necessary, most genetic tests are successful from DNA purified from whole blood that is several days old.
CSF-Tubes other than polypropylene are not acceptable
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Whole blood
Room temperature: 10 days
Refrigerated: 10 days
Frozen: Call lab
CSF
Room temperature: 72 hours
Refrigerated: 21 days
Frozen: 4 months
Room temperature: 10 days
Refrigerated: 10 days
Frozen: Call lab
CSF
Room temperature: 72 hours
Refrigerated: 21 days
Frozen: 4 months
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
CSF samples that arrive in non-polypropylene tubes; CSF specimens with cell count > 500 erythrocytes/mm3
Methodology
Restriction Fragment Length Polymorphism, Enzyme-Linked Immunosorbent Assay
FDA Status
This test was developed and its analytical performance characteristics have been determined by Athena Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: Mon, Wed; Report available: 14-21 days
Reference Range
Report correlates levels of markers of Phosphorylated-Tau, Total-Tau, and Ab42; Presence of ApoE2, E3, E4 alleles is reported
Clinical Significance
Detection of ApoE2, E3, E4 alleles and levels of Phosphorylated-Tau protein, Total-Tau protein, and AB42.