Epic Code LAB3540 IFA ANA (Rheumatology)
Test Name Alias
ANA | IFA ANA Blood Level | RNAAutoantibodies | ANA Titer: ANA Pattern | 1122 | ANA Hep2 IFA |ANA (Antinuclear Antibodies), Hep2 Substrate IFA with reflex to Titer and Pattern if positive | Anti Nuclear Antibody Hep 2 Substrate with Reflex Titer and Pattern
Interface Order Alias
11778
Clinical Information
The ANA Hep2 IFA slide is screened at 1:80 dilution. If titer is ≥ 1:80 a titer and pattern will be reported. Patterns reported include Homogeneous, Speckled, Nucleolar, Centromere, and SSA Ro. All positive results are reported with endpoint titers.
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.
Cautions
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: 2.0 mL
Neonate Volume to Collect: 2.0 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: Yes
Processing Instructions:
- Allow blood to clot for 30 minutes in a vertical position and centrifuge within 2 hours.
- Aliquot serum into screw top plastic transport tube.
Transport Temperature: Refrigerated
Rejection Criteria
Specimen not centrifuged within 2 hours
Specimen Stability
Ambient: 8 hours
Refrigerate: 7 days
Frozen: aliquot serum for longer storage (-20°C or below)
Laboratory Retention: 7 days
Reflex Information
Reflex approved by Medical Executive Committee. Please see link: Reflex Testing Document
Test Frequency
Available Monday through Friday, usual TAT 1-3 days.
Reference Range
ANA Hep2 <1:80
Performing Department
Immunochemistry
Performing Department Laboratory Location
Corewell Health Reference Laboratory, Grand Rapids, MI
Methodology
ANA Hep2 slide IFA
CPT
86038
CDM Code
3028603801
Epic Test ID
1230100353
LOINC
Antinuclear Ab: 9423-5
ANA Titer: 5048-4
ANA Pattern: 13068-2
Mayo Access Code
SHO11778
Reviewed Date
12/13/2022