Epic Code LAB1230491 ANA Screen
Test Name Alias
ANA | Antinuclear Antibody | ANA Screen Double Reflex | ENA | Extractable Nuclear Antigens | ANA Screen Double Reflex | 184 | ANA (Antinuclear Antibodies) Screen, Double Reflex to ANA IFA Hep2 Titer and Pattern, and if positive to ANA antibodies | ANA Screen w/reflex
Interface Order Alias
1230491
Clinical Information
Initial ANA screen for autoimmune connective tissue diseases.
- The initial ANA screen if positive will reflex to a confirmatory ANA Hep2 IFA slide.
- The Hep2 slide patterns reported include Homogeneous, Speckled, Nucleolar, Centromere, and SSA Ro to a titer of 1:80 through 1:1280. All positive results are reported with endpoint titers.
- If the ANA Hep2 titer is ≥ 1:160 the following individual antinuclear antibodies will reflex. *Antibodies to: dsDNA, Smith, RNP, SSA, SSB, Scl 70, Centromere and Jo 1.
*Individual ANA antibodies reflexed at a titer of 1:160 due to more clinical significance.
ANA (antinuclear antibodies) occur in patients with a variety of autoimmune diseases, both systemic and organ-specific. They are particularly common in systemic rheumatic diseases, which include lupus erythematosus (LE), discoid LE, drug-induced LE, mixed connective tissue disease, Sjogren syndrome, scleroderma (systemic sclerosis), CREST (calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, telangiectasia) syndrome, polymyositis/dermatomyositis, and rheumatoid arthritis.
The diagnosis of a systemic rheumatic disease is based primarily on the presence of compatible clinical signs and symptoms. The results of tests for autoantibodies including ANA and specific autoantibodies are ancillary. Additional diagnostic criteria include consistent histopathology or specific radiographic findings.
Some patients without clinical evidence of an autoimmune disease or a systemic rheumatic disease may have a detectable level of antinuclear antibody (ANA). This finding is more common in women than men and the frequency of detectable ANA in healthy women over 40 years of age may approach 15% to 20%. ANA may also be detectable following viral illnesses, in chronic infections, or in patients treated with many different medications.
Collection Instructions
Specimen Collection: Blood
Container(s): Gold Top (Serum Separator-SST Gel)
Preferred Volume to Collect: 5.0 mL
Minimum Volume to Collect: 2.5 mL
Neonate Volume to Collect: 2.5 mL
Capillary collect ok: Yes
Microtainer acceptable: Yes
Collection Instructions:
- After collection, gently invert tube 8-10 times.
- Specimen should be processed within 2 hours – See Processing Instructions.
Processing Instructions (Laboratory, Outpatient or Off-site collection)
Processed Specimen: Serum
Centrifuge/Spin: Yes
Aliquot: No
Processing Instructions:
- Allow blood to clot for 30 minutes in a vertical position and centrifuge within 2 hours.
Transport Temperature: Refrigerate
Rejection Criteria
Specimen not centrifuged within 2 hours
Quantity not sufficient
Specimen Stability
Ambient: 8 hours
Refrigerate: 7 days
Frozen: aliquot serum for longer storage
Laboratory Retention: 7 days
Reflex Information
Reflex approved by Medical Executive Committee. Please see link: Reflex Testing Document
Test Frequency
Available M-F, usual TAT 1-3 days
Reference Range
ANA Screen: Negative
ANA Hep2 IFA: <1:80
Anti-dsDNA: <5 IU/ml
Antibodies to SSA, SSB, Sm, RNP, Scl 70, centromere, Jo 1: Negative
Performing Department
Immunochemistry
Performing Department Laboratory Location
Corewell Health Reference Laboratory, Grand Rapids, MI
Methodology
Multiplex flow immunoassay with reflex to indirect immunofluorescence (IFA), HE-p2000 substrate if positive
CPT
86038
CDM Code
3028603802
Epic Test ID
1230102113
Reviewed Date
12/13/2022
Updated Date
1/26/2024 - Reference Range and Methodology