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Specimen Collection Manual and Test Catalog

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ANCA, IFA

Geisinger Epic Procedure Code:  LAB5192    Geisinger Epic ID:  196775

SPECIMEN COLLECTION
Specimen type: 
Preferred collection container: 
Alternate collection container: 
6 mL red-top (plain, non-serum separator) tube
Specimen required: 

0.5 mL serum; minimum 0.2 mL



SPECIMEN PROCESSING
Processing instructions: 

Allow to clot. Centrifuge and submit 0.5 mL serum.


Transport temperature: 

Refrigerated (preferred). Room temperature (stable 8 hours) and frozen specimens also acceptable.


Specimen stability: 

Room temperature: 8 hours. 2-8°C: 48 hours. Frozen: 6 months.


Rejection criteria: 

Specimen stability exceeded; specimen grossly hemolyzed.



TEST DETAILS
Reference interval: 

C-ANCA negative, P-ANCA negative.


Interpretation guide: 

A sample is considered negative if specific neutrophil staining is equivalent to or less than the negative control well. A sample is considered positive if cytoplasmic or perinuclear staining is observed.


CPT code(s):  86036
Note: The billing party has sole responsibility for CPT coding.  Any questions regarding coding should be directed to the payer being billed.
The CPT codes provided by GML are based on AMA guidelines and are for informational purposes only.

Test includes: 

C-ANCA, P-ANCA antibody detection.


Methodology: 
Indirect Immunofluorescent Antibody (IFA)
Synonyms: 

ANCA, Anti-neutrophil cytoplasmic antibody


Clinical significance: 

For initial evaluation of suspected autoimmune vasculitis, Systemic Vasculitis Screen (LAB5191) should be used. In rare cases, ANCA-associated vasculitides (AAV) such as Microscopic Polyangiitis, Granulomatosis with Polyantiitis, pauciimmune-necrotizing crescentic glomerulonephritis, and Churg-Strauss syndrome, may present with positive ANCA testing by immunofluorescence (ANCA-IFA) and negative anti-MPO/PR3 antibodies. ANCA-IFA may be useful in conjunction with other tests and clinical findings in the evaluation of patients where anti-MPO/PR3 are negative but strong clinical suspicion of autoimmune vasculitis remains, or follow-up of known MPO/PR3-negative, ANCA-positive vasculitis. ANCA-IFA positivity is also seen in some patients with other autoimmune conditions such as IBD, PSC, and RA.


Doctoral Director(s): 
Benjamin Andress, PhD, DABCC
Hoi-Ying Elsie Yu, PhD, DABCC, FADLM
Review Date:  05/21/2025

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