Sign in →

Catalog ID FARP Autoimmune Retinopathy Panel by Immunoblot (ARP)

Important Note

Order: Ref Misc Referral Lab Test

Comment: Autoimmune Retinopathy panel

Note: All orders for this test will undergo Pathology review for medical necessity.


Specimen Required


Submit the following required information with specimen:

1. Completed OHSU Ocular request form

2. Clinical history

3. Referring physician information (name & phone number)

-NOTE: Without this information, testing cannot be completed.

 

Submit only 1 of the following specimens:

 

Specimen Type: Serum

Collection Container/Tube:

Preferred: Red top

Acceptable: Serum gel

Submission Container/Tube: Plastic vial

Specimen Volume: 5 mL Serum

Collection Instructions:

1. Centrifuge and aliquot serum into a plastic vial.

2. Send refrigerate.

 

 

Specimen Type: Plasma

Collection Container/Tube: Lavender top (EDTA)

Submission Container/Tube: Plastic vial

Specimen volume: 5 mL Plasma

Collection Instructions:

1. Centrifuge and aliquot plasma into a plastic vial.

2. Send refrigerate.


WMCG Laboratory Test Catalog Note:

Collect 10.0 mL blood in Red top tube(s).

Secondary ID

75446

Special Instructions

Method Name

Immunoblot

Reporting Name

Autoimmune Retinopathy Panel (ARP)

Specimen Type

Varies

Specimen Minimum Volume

3 mL

Specimen Stability Information

Specimen Type Temperature Time
Varies Refrigerated 7 days

Reject Due To

Hemolysis Reject

Reference Values

An interpretive report will be provided.

Day(s) Performed

Batched

Report Available

16 to 35 days

Performing Laboratory

Ocular Immunology Laboratory OHSU

CPT Code Information

84182 x 8

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FARP Autoimmune Retinopathy Panel (ARP) Not Provided

 

Result ID Test Result Name Result LOINC Value
FARP Autoimmune Retinopathy Panel (ARP) Not Provided

Test Classification

This test was developed and its performance characteristics determined by Ocular Immunology Laboratory OHSU. It has not been approved by the U.S. Food and Drug Administration.