Sign in →

Test Code ARVNM Arginine Vasopressin, Plasma

Additional Codes

MAYO Test ID
AVP
EPIC Test ID
LAB1108

 

Reporting Name

Arginine Vasopressin, P

Useful For

Diagnosis and characterization of diabetes insipidus

 

Diagnosis of psychogenic water intoxication

 

As an adjunct in the diagnosis of the syndrome of inappropriate antidiuretic hormone secretion (SIADH), including ectopic arginine vasopressin production

Method Name

Radioimmunoassay (RIA)

Performing Laboratory

Mayo Medical Laboratories in Rochester

Specimen Type

Plasma EDTA


Advisory Information


 



Specimen Required


Patient Preparation:

1. This test should not be requested on patients who have recently received radioactive material.

2. Have patient fast and thirst for 6 hours (no liquids, including water, are allowed).

Specimen Type: Platelet-poor plasma

Collection Container/Tube: Lavender top (EDTA) iced tube

Submission Container/Tube: Plastic vial

Specimen Volume: 2 mL

Collection Instructions: Process 5 mL of EDTA whole blood as follows:

1. Spin down in a refrigerated centrifuge at approximately 1,000 x G (2,000 rpm for a 20-cm radius centrifuge) for 10 minutes.

2. Remove plasma, carefully avoiding the platelet/buffy coat.


Specimen Minimum Volume

1.15 mL

Specimen Stability Information

Specimen Type Temperature Time
Plasma EDTA Frozen (preferred) 14 days
  Refrigerated  24 hours

Reject Due To

Hemolysis

Mild OK; Gross reject

Lipemia

Mild OK; Gross OK

Icterus

Mild OK; Gross OK

Other

NA

Reference Values

Adults: <4.3 pg/mL

Reference values were determined on platelet-poor EDTA plasma from individuals fasting no longer than overnight.

Day(s) and Time(s) Performed

Wednesday; 1 p.m.

CPT Code Information

84588

LOINC Code Information

Test ID Test Order Name Order LOINC Value
AVP Arginine Vasopressin, P 3126-0

 

Result ID Test Result Name Result LOINC Value
80344 Arginine Vasopressin, P 3126-0

Analytic Time

3 days

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.