Sign in →

Order Code HIAAP 5-Hydroxyindoleacetic Acid, Plasma


Ordering Guidance


This test quantifies 5-hydroxyindoleacetic acid in plasma specimens and is comparable to testing on 24-hour and random urine specimens for the diagnosis and monitoring of intestinal carcinoid syndrome.



Necessary Information


Patient's age is required.



Specimen Required


Patient Preparation:

1. Some medications could interfere with test results. The ordering provider should decide if any medications should be stopped and when they should be restarted. If clinically feasible, discontinue the following medications at least 24 hours prior to specimen collection:

-Acetaminophen (Tylenol or generic versions)

-Tryptophan containing supplements.

2. For 24 hours prior to the collection, the patient should:

Limit the following to one serving per day:

-Fruits

-Vegetables

-Caffeinated beverages or foods

Abstain from the following:

-Nuts, especially walnuts. Plasma 5-hydroxyindoleacetic acid levels revert to baseline levels when walnuts are ingested after other foods.

 

Collection Container/Tube:

Preferred: Green top (sodium heparin)

Acceptable: Lavender top (EDTA)

Submission Container/Tube: Plastic vial

Specimen Volume: 0.5 mL

Collection Instructions:

1. Centrifuge at 4° C.

2. Aliquot plasma into plastic vial.

3. Send plasma frozen.


Useful For

Biochemical diagnosis and monitoring of intestinal carcinoid syndrome using a plasma specimen

Method Name

Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)

Reporting Name

5-Hydroxyindoleacetic Acid, P

Specimen Type

Plasma

Specimen Minimum Volume

0.2 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Plasma Frozen (preferred) 60 days
  Refrigerated  72 hours

Reject Due To

Gross hemolysis OK
Thawing** Cold OK; Warm reject
Gross lipemia OK
Gross icterus OK

Reference Values

≤6 months: ≤130 ng/mL

>6 months: ≤30 ng/mL

Method Description

Plasma is mixed with deuterium labeled hydroxyindoleacetic acid (HIAA) as internal standard in acetonitrile. After centrifugation and filtration, the sample is reconstituted in mobile phase. Liquid chromatography tandem mass spectrometry is performed by injecting the reconstituted specimen onto a reverse phase high-performance liquid chromatography column. HIAA is quantitated using the stable isotope-labeled internal standard from calibration over a concentration range of 0 to 1000 ng/mL.(Unpublished Mayo method)

Day(s) Performed

Monday, Wednesday, Friday

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

83497