Order Code PTP Porphyrins, Total, Plasma
Additional Codes
Mayo Test ID: PTP
Reporting Name
Porphyrins, Total, PUseful For
Monitoring treatment of patients with porphyria cutanea tarda
Specimen Type
PlasmaShipping Instructions
Ship specimen in amber vial to protect from light.
Necessary Information
Include a list of medications the patient is currently taking.
Specimen Required
Patient Preparation: Patient must not consume any alcohol for 24 hours before specimen collection.
Supplies: Amber Frosted Tube, 5 mL (T915)
Collection Container/Tube:
Preferred: Green top (sodium or lithium heparin)
Acceptable: Lavender top (EDTA)
Submission Container/Tube: Amber vial
Specimen Volume: 3 mL
Collection Instructions:
1. Centrifuge specimen and aliquot plasma into amber vial.
2. Send plasma frozen.
Specimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Plasma | Frozen | 14 days | LIGHT PROTECTED |
Reject Due To
Gross hemolysis | OK |
Gross lipemia | OK |
Gross icterus | OK |
Reference Values
≤1.0 mcg/dL
Performing Laboratory
Mayo Clinic Laboratories in RochesterDay(s) Performed
Monday through Friday
Method Name
PTP: Extraction and Scanning Spectrofluorometry
PFP: High-Performance Liquid Chromatography (HPLC)
CPT Code Information
84311-Porphyrins, total
82542-Porphyrins, fractionation (if appropriate)
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
PFP | Porphyrins, Fractionation, P | No | No |
Testing Algorithm
If total porphyrins are above 1.0 mcg/dL, then porphyrin fractionation will be performed at an additional charge.
The following algorithms are available:
Special Instructions
Genetics Test Information
Plasma specimens from patients with active porphyria cutanea tarda, congenital erythropoietic porphyria, and erythropoietic protoporphyria may exhibit increased plasma porphyrin levels. However, a definitive diagnosis cannot be made by plasma analysis alone.
Method Description
The plasma porphyrins profile is performed as a 2-step analysis. First, the total plasma porphyrins concentration is determined by extracting the porphyrins from plasma with a mixture of ethyl acetate and acetic acid. The porphyrins are then back extracted into dilute hydrochloric acid. Total porphyrins are quantified on this extract via scanning spectrofluorometry. If the total plasma porphyrin concentration is elevated, the extract is submitted for high-performance liquid chromatography analysis, whereby the individual porphyrin analytes are separated by differential partitioning between a stationary aliphatic surface and a moving aqueous buffer solution. As the porphyrins emerge separately from the column, the quantity of each is monitored with a fluorescence detector.(Unpublished Mayo method)
Forms
If not ordering electronically, complete, print, and send a Biochemical Genetics Test Request (T798) with the specimen.