Specimen Requirements

Alternate Specimen Requirements

Minimum Specimen Requirements

Stability

Days Performed

Mon - Sun

Turnaround Time

8 - 11 days

Methodology

Reference Range

Special Info

Reflex Algorithm: If indirect immunofluorescence assay (IFA) patterns suggest amphyphysin Ab, amphiphysin immunoblot (IB) is performed at an additional cost. If IFA patterns suggest ANNA-1 Ab, ANNA-1 IB and ANNA-2 IB are performed at an additional cost. If IFA patterns suggest PCA-1 Ab, PCA-1 IB is performed at an additional cost. If IFA patterns suggest Purkinje Cell Cytoplasmic Ab, the appropriate antibody will be performed at an additional cost.. If IFA patterns suggest CRMP-5-IgG, CRMP-5-IgG Western blot is performed at an additional cost. If IFA patterns suggest NMDA-R, NMDA-R cell-binding assay (CBA) and NMDA-R titer are performed at an additional cost. If IFA patterns suggest AMPA-R, AMPA-R CBA and AMPA-R titer are performed at an additional cost. If IFA patterns suggest GABA-B-R, GABA-B-R CBA and GABA-B-R titer are performed at an additional cost. If IFA patterns suggest DPPX Ab, then DPPX Ab CBA and DPPX titer are performed at an additional cost. Neuron-restricted patterns of IgG staining that do not fulfill criteria for ANNA-1, CRMP-5-IgG, or PCA-2 may be reported as "unclassified anti-neuronal IgG." Complex patterns that include nonneuronal elements may be reported as "uninterpretable." Include ordering provider name, number, address, and email. Include relevant clinical information. Patient Prep: For optimal antibody detection, collection of specimen before initiation of immunosuppressant medication is recommended. This test should not be requested in patients who have recently received radioisotopes, therapeutically or diagnostically, because of potential assay interference. The specific waiting period before specimen collection will depend on the isotope administered, the dose given, and the clearance rate in the individual patient. Specimens will be screened for radioactivity prior to analysis. Radioactive specimens received in the laboratory will be held 1 week and assayed if sufficiently decayed, or canceled if radioactivity remains. Patient should have no general anesthetic or muscle-relaxant medications in the previous 24 hours. Grossly hemolyzed, grossly lipemic, or grossly icteric specimens will be rejected.

Clinical Info

Investigation of idiopathic dysautonomic symptoms. In patients with idiopathic dysautonomia, directing a focused search for cancer. Investigation of autonomic symptoms that appear in the course or wake of cancer therapy and are not explainable by recurrent cancer or metastasis; detection of autoantibodies in this profile helps differentiate autoimmune dysautonomia from the effects of chemotherapy. Caution: Negative results do not exclude autoimmune dysautonomia or cancer. Note: CRMP-5 titers < 1:240 are detectable by recombinant CRMP-5 Western blot analysis, which can be done upon request on stored serum (held 4 weeks). This supplemental testing is recommended in cases of chorea, vision loss, cranial neuropathy, and myelopathy.