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Special Instructions
Contact the LabCorp supply department for collection kit.
Expected Turnaround Time
4 - 9 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
Related Information
Related Documents
Specimen Requirements
Specimen
Plasma with Trasylol®, frozen
Volume
2 mL
Minimum Volume
0.4 mL (Note: This volume does not allow for repeat testing.)
Container
Lavender-top (EDTA) tube
Collection
Trasylol® kits may be ordered through the PeopleSoft system (LabCorp N° 33328). Using a chilled 6-mL lavender-top (EDTA) tube taken from the kit, collect a whole blood specimen. Mix the specimen several times by inverting the EDTA collection tube. After removing the cap from the EDTA draw tube, take one of the sterile, Beral pipettes (from under the gray foam), and add 0.25 mL Trasylol® to the EDTA tube. Recap the EDTA tube and invert several times to mix well. Centrifuge the EDTA tube to separate the plasma from the cells, and immediately transfer the plasma into one of the brown screw-cap transfer tubes provided in the kit. There should be a "Trasylol® Added" label affixed to the brown transfer tubes. Cap and freeze the labeled transfer tube containing the EDTA plasma with Trasylol® added. To avoid delays in turnaround time when requesting multiple test on frozen samples, please submit separate frozen specimens for each test requested.
Storage Instructions
Freeze.
Patient Preparation
Patient must not have received radioactive substances 24 hours prior to test.
Causes for Rejection
Sample not collected with Trasylol®; sample not submitted in tube with Trasylol label, gross hemolysis; recently administered radioisotopes; specimen not received frozen; serum, sodium citrate, or heparinized plasma specimen; lipemia
Test Details
Use
Hypersecretion of VIP is observed in “pancreatic cholera syndrome,” Verner-Morrison syndrome or the watery diarrhea-hypokalemia-hypochlorhydria (WDHH) syndrome. It is characterized by hypermotility, watery diarrhea syndromes with hypokalemia and hypochlorhydria, dehydration and weakness; these symptoms can be reproduced by VIP. VIP can be secreted by pancreatic or ectopic islet cell tumors, and in islet-cell hyperplasia.
Limitations
Not all patients with the syndrome have increased VIP. Increased VIP can be found in healthy controls and in laxative abusers.
Results for this test are for research purposes only by the assay's manufacturer. The performance characteristics of this product have not been established. Results should not be used as a diagnostic procedure without confirmation of the diagnosis by another medically established diagnostic product or procedure.
Methodology
Radioimmunoassay (RIA)
Reference Interval
0.0−58.8 pg/mL
Additional Information
Other features of some cases of VIPoma have included hypercalcemia, flushing, and glucose intolerance.1 A study of islet cell tumors in patients with multiple endocrine neoplasia (MEN) included vasoactive intestinal polypeptide tumor (VIPoma) as well as Zollinger-Ellison syndrome and insulinoma.2 A VIP-producing tumor causing the pancreatic cholera syndrome was reported as a well differentiated mucinous adenocarcinoma which contained cells reactive for pancreatic peptide and VIP on immunocytochemistry.3 Normal levels of VIP have been reported in ulcerative colitis, Crohn's disease, cirrhosis, ascites, and diabetes.
Footnotes
1. Krejs GJ. Noninsulin-secreting tumors of the pancreatic islets. In: Wilson JD, Foster DW, eds. Williams Textbook of Endocrinology. 8th ed. Philadelphia, Pa: WB Saunders Co; 1992: 1567-1576.
2. Sheppard BC, Norton JA, Doppman JL, et al. Management of islet cell tumors in patients with multiple endocrine neoplasia: A prospective study. Surgery. 1989; 106(6):1108-1118. 2573957
3. Rood RP, DeLellis RA, Dayal Y, et al. Pancreatic cholera syndrome due to a vasoactive intestinal polypeptide-producing tumor: Further insights into the pathophysiology. Gastroenterology. 1988; 94(3):813-818. 2828145
References
Basson MD, Fielding LP, Bilchik AJ, et al. Does vasoactive intestinal polypeptide mediate the pathophysiology of bowel obstruction? Am J Surg. 1989 Dec; 157(1):109-114. 2910115
Deveney CW, Way LW. Regulatory peptides of the gut. In Greenspan FS, Forsham PH, eds. Basic and Clinical Endocrinology. 3rd ed. Los Altos, Calif: Lange Medical Publications; 1991: 569-591.
Fahrenkrug J, Emson PC. Vasoactive intestinal polypeptide: Functional aspects. Br Med Bull. 1982 Sep; 38(3):265-270 (review). 6129023
Fraker DL, Norton JA. The role of surgery in the management of islet cell tumors. Gastroenterol Clin North Am. 1989 Dec; 18(4):805-830. 2559034
Green DW, Gómez G, Greeley GH Jr. Gastrointestinal peptides. Gastroenterol Clin North Am. 1989 Dec; 18(4):695-733. 2693350
Jaffe BM. The diarrheogenic syndrome: Werner-Morrison, WDHA syndrome. In: Friesen SR, Bolinger RE, eds. Surgical Endocrinology. Philadelphia, Pa: JB Lippincott Co; 1978: 219-221.
Said SI. Vasoactive intestinal polypeptide (VIP): Current status. Peptides. 1984 Mar-Apr; 5(2):143-150 (review). 6147814
LOINC® Map
| Order Code | Order Code Name | Order Loinc | Result Code | Result Code Name | UofM | Result LOINC |
|---|---|---|---|---|---|---|
| 010397 | VIP, Plasma | 3125-2 | 010415 | VIP, Plasma | pg/mL | 3125-2 |
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The LOINC® codes are copyright © 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Permission is granted in perpetuity, without payment of license fees or royalties, to use, copy, or distribute the LOINC® codes for any commercial or non-commercial purpose, subject to the terms under the license agreement found at https://loinc.org/license/. Additional information regarding LOINC® codes can be found at LOINC.org, including the LOINC Manual, which can be downloaded at LOINC.org/downloads/files/LOINCManual.pdf