Test Code VIP Vasoactive Intestinal Polypeptide, Plasma
Additional Codes
| Epic Ordering Code | LAB3040120 |
| NBS code | LBC01019 |
| Service code | 36940 |
Reporting Name
Vasoactive Intestinal Polypeptide,PSpecimen Type
Plasma EDTAOrdering Guidance
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube: Lavender top (EDTA)
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot plasma into a plastic vial. Freeze immediately.
NUH Outreach Laboratories:
Specimen Requirements
Submit the following:
Container: Purple Top
Processing Requirements
Centrifuge and aliquot plasma into a Mayo plastic tube. Freeze immediately.
Specimen type: Plasma
Volume: 1 mL
Storage/transport requirements: Frozen
Forms
If not ordering electronically, complete, print, and send an Oncology Test Request (T729) with the specimen.
Specimen Minimum Volume
0.55 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Plasma EDTA | Frozen | 90 days |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | Reject |
| Gross icterus | OK |
Method Name
Enzyme-Linked Immunosorbent Assay (ELISA)
Day(s) Performed
Monday, Thursday
Report Available
2 to 4 daysPlease note that this is a referral test requiring transport to the external testing facility and an additional 3-5 days is required.
Reference Values
<86 pg/mL
Performing Laboratory
Mayo Clinic Laboratories in Rochester
Useful For
Detecting vasoactive intestinal polypeptide-producing tumors in patients with chronic diarrheal diseases
CPT Code Information
84586
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| VIP | Vasoactive Intestinal Polypeptide,P | 3125-2 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 8150 | Vasoactive Intestinal Polypeptide,P | 3125-2 |
Secondary ID
8150Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.Last updated 17/08/2026