Pythiosis MVista® Pythium Canine and Feline Antibody IgG EIA
- Test Information
- Specimen Requirements
- Shipping Information
Test Code +
332
Clinical Significance +
- MVista® Pythium Canine and Feline Antibody IgG EIA, developed at MiraVista Diagnostics, aids in the diagnosis of pythiosis. It is highly accurate in both dogs and cats. This test can be used to help monitor treatment.
Methodology +
Sandwich Enzyme-Linked Immunoassay (EIA)
Turnaround Time +
- Testing performed Tuesday – Friday
- Reported next day
Reference Range +
Negative
Interpretative Information +
Positive ≥10.0 EU is Positive (Antibody Detected)
Negative <10.0 EU is Negative (Antibody Not Detected)
A positive test result (Antibody Detected) indicates the presence of anti-Pythium IgG antibodies. Based on IgG kinetics specifically with pythiosis, a positive test result is highly suggestive of active disease. Likewise, a negative test (Antibody Not Detected) result makes active pythiosis highly unlikely.
Additional Information +
This test was developed, and its analytical performance characteristics determined by MiraVista Diagnostics.
Specimen Collection +
Collect and allow blood to clot for 30 minutes, then centrifuge. Serum separator tube or any tube used for serum is acceptable. Can ship in serum separator tube or in transfer tube without additive.
Minimum Specimen Requirements +
- Serum: 0.25 mL
Specimen Stability +
- Room Temperature: 30 days
- Refrigerated: 30 days
- Frozen: 30 days
Specimen Rejection +
- For specimen submissions that do not meet these criteria, please call Laboratory Support (not customer service as is worded)
Transport Temperature +
Ambient or refrigerated with cold pack.
Shipping +
Overnight or Second Day delivery recommended.
* New positives may require confirmation.
** Turnaround times are provided as ranges, and may vary depending on daily testing volumes and specimen type.
*** Test set-up: Samples received by 10:30 AM are eligible for same-day testing. Same-day testing is not guaranteed and may vary based on daily test volume, sample receipt time, testing schedules, and sample type. Some samples may require pretreatment and/or confirmatory testing, which can extend turnaround time (TAT).
**** Patient's identification must be visible on the specimen container.
***** Specimens with particulate matter or viscosity that do not allow the specimen to be pipetted will be rejected.
