Test Code VMA Vanillylmandelic Acid, 24 Hour, Urine
Additional Codes
| Epic Ordering Code | LAB452 |
| NBS code | LBC01009 |
| Service code | 31987 |
Reporting Name
Vanillylmandelic Acid, 24 Hr, USpecimen Type
UrineOrdering Guidance
In the past, this test has been used to screen for pheochromocytoma. However, vanillylmandelic acid (VMA) is not the analyte of choice to rule out a diagnosis of pheochromocytoma. Recommended tests for that purpose include:
-PMET / Metanephrines, Fractionated, Free, Plasma
-METAF / Metanephrines, Fractionated, 24 Hour, Urine
-CATU / Catecholamine Fractionation, Free, 24 Hour, Urine
Necessary Information
1. Patient’s age is required.
2. Collection duration (in hours) and urine volume (in milliliters) are required.
3. All patients receiving L-dopa should be identified to the laboratory when this test is ordered.
4. Bactrim may interfere with detection of the analyte. All patients taking Bactrim should be identified to the laboratory when this test is ordered.
Specimen Required
Patient Preparation: Administration of L-dopa may falsely increase vanillylmandelic acid results. For 24 hours prior to specimen collection, the patient should not take L-dopa.
Supplies: Urine Tubes, 10 mL (T068)
Collection Container/Tube: Clean, plastic urine collection container
Submission Container/Tube: Plastic, 10-mL urine tube
Specimen Volume: 5 mL
Collection Instructions:
1. Add 25 mL of 50% acetic acid as preservative at the start of collection. Use 15 mL of 50% acetic acid for children younger than 5 years. If specimen is refrigerated during collection, preservative may be added up to 12 hours after collection. This preservative is intended to achieve a pH of between approximately 1 and 5.
2. Collect a 24-hour urine specimen.
3. If necessary, adjust urine pH to a level between 1 and 5 by adding 50% acetic acid or hydrochloric acid dropwise and checking the pH.
Additional Information: For multiple collections see Urine Preservatives-Collection and Transportation for 24-Hour Urine Specimens.
NUH Outreach Laboratories:
Specimen Requirements
Submit the following:
Container: 24 hr urine bottle with Acetic acid as preservative
Processing Requirements
Adjust pH to pH 1-5. Aliquot urine into a Mayo urine tube
Specimen type: Urine
Volume: 5 mL
Storage/transport requirements: Frozen
Forms
If not ordering electronically, complete, print, and send an Oncology Test Request (T729) with the specimen.
Special Instructions
Specimen Minimum Volume
2 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Urine | Refrigerated (preferred) | 28 days |
| Frozen | 180 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Method Name
Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)
Day(s) Performed
Monday through Friday
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
<1 year: <25.0 mg/g creatinine
1 year: <22.5 mg/g creatinine
2-4 years: <16.0 mg/g creatinine
5-9 years: <12.0 mg/g creatinine
10-14 years: <8.0 mg/g creatinine
≥15 years (adults): <8.0 mg/24 hours
Performing Laboratory
Mayo Clinic Laboratories in Rochester
Useful For
Screening children for catecholamine-secreting tumors using a 24-hour urine collection when requesting testing for vanillylmandelic acid only
Supporting a diagnosis of neuroblastoma
Monitoring patients with a treated neuroblastoma
CPT Code Information
84585
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| VMA | Vanillylmandelic Acid, 24 Hr, U | 43099-1 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 3580 | Vanillylmandelic Acid, Adult (>14y) | 3122-9 |
| 3581 | Vanillylmandelic Acid, Child (<15y) | 30571-4 |
| TM41 | Collection Duration | 13362-9 |
| VL39 | Urine Volume | 3167-4 |
Secondary ID
9454Test 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