Test Code LAB147 ANA Screen IFA
Clinical Information
Presence of antinuclear antibodies (ANA) is a hallmark feature of systemic autoimmune rheumatic diseases (SARD). However, ANA lacks diagnostic specificity and is associated with a variety of diseases (cancers, autoimmune, infectious, and inflammatory conditions) and may also occur in healthy individuals in varying prevalence. The lack of diagnostic specificity requires confirmation of positive ANA by more specific serologic tests. All positive patterns are reported to endpoint titers (1:2560). High-titered ANA is suggestive of connective tissue disease but should not be considered diagnostic. The ANA result should be considered in combination with other serological results as well as the overall clinical history of the patient. Reported patterns may help guide differential diagnosis, although they may not be specific for individual antibodies or diseases. Mitotic staining patterns not reported. Negative results do not necessarily rule out SARD.
Synonym
- ANAB
Profile Information
Reporting Name | Available Separately | Always Reported |
---|---|---|
ANA IFA | No | Yes |
ANA Pattern | No | No |
Specimen Required
Preferred Container/Tube: Gold SST Top
Acceptable Container/Tube: Gold SST Top
Specimen Volume: 3 mL
Specimen Minimum Volume: 1 mL
Specimen Stability Information
Ambient: 24 hours
Refrigerated: 7 days
Rejection Due To
- Improperly labeled specimens
- Microbially contaminated, heat-treated or specimens containing visible particulates
- Unacceptable container type
Testing Algorithm
If ANA screen is positive, then a quantitative ANA will be performed at an additional charge.
Reflex Tests
Reporting Name | Available Separately | Always Reported |
---|---|---|
Quant Antinuclear Antibody | No | No |
Interpretation
Negative
Cautions
Samples containing up to 10 mg/dL bilirubin, 200 mg/dL hemoglobin, 1000 mg/dL triglycerides, 224 mg/dL cholesterol, or 56 IU IgM rheumatoid factor did not show interference with the results generated with the NOVA Lite DAPI ANA Kit.
Method Description
Indirect immunofluorescence antibody
Performing Lab
Clinical Lab UH
Day(s) Performed
Monday through Friday (excludes OSU holidays)
Report Available
4 to 6 days
Reporting Name
ANA Screen IFA
CPT Code Information
86038
LOINC Code Information
13068-2