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Test ID NBLD0708 Porphyrins, Quantitative, Random, Urine

Reporting Name

Porphyrins, QN, Random, U

Useful For

Preferred test to begin assessment for congenital erythropoietic porphyria and porphyria cutanea tarda and during symptomatic periods for acute intermittent porphyria, hereditary coproporphyria, and variegate porphyria when specimen transport will not exceed 72 hours

Testing Algorithm

The following algorithms are available:

-Porphyria (Acute) Testing Algorithm

 

-Porphyria (Cutaneous) Testing Algorithm 

 

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Urine


Ordering Guidance


This random urine test should be ordered when the specimen will reach Mayo Clinic Laboratories within 72 hours. If transportation will take longer than 72 hours, order both PQNU / Porphyrins, Quantitative, 24 Hour, Urine and ALAUR / Aminolevulinic Acid, Urine and follow collection guidelines.



Shipping Instructions


Ship specimen in amber bottle 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 at least 24 hours before specimen collection.

Supplies: Urine Container - Amber, 60 mL (T596)

Container/Tube: Amber, 60-mL urine container

Specimen Volume: 20 to 50 mL

Collection Instructions:

1. Collect a random urine specimen.

2. No preservative necessary but pH must be above 5.0. If pH is below 5.0, specimen will be rejected.

3. Specimens should be protected from light and frozen immediately following collection.


Specimen Minimum Volume

15 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Urine Frozen 72 hours LIGHT PROTECTED

Reference Values

Uroporphyrins, Octacarboxyl:

≤3.1 mcmol/mol creatinine

 

Heptacarboxylporphyrins:

≤0.9 mcmol/mol creatinine

 

Hexacarboxylporphyrins:

≤0.3 mcmol/mol creainine

 

Pentacarboxyporphyrins:

≤1.2 mcmol/mol creatinine

 

Coproporphyrin, Tetra::

≤25.0 mcmol/mol creatinine

 

Porphobilinogen:

≤0.2 mmol/mol creatinine

 

Aminolevulinic Acid

≤ 2.3 mmol/mol creatinine

Day(s) Performed

Monday through Friday

Test 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.

CPT Code Information

84110-Porphobilinogen, quantitative

84120-Porphyrins, quantitation and fractionation

82135- ALA Delta Random Urine

Reject Due To

  All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Report Available

2 to 4 days

Method Name

High-Performance Liquid Chromatography (HPLC) with Fluorometric Detection/Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)

Secondary ID

60597
Sanford Laboratories - Fargo Additional Information:

 

Sanford Laboratories - Enterprise Additional Information:

SANFORD LABORATORY INTERFACE BUILD INFORMATION

 Result Code     Result Code Description   
 28373  Uroporphyrin, Octa
 28374  Heptacarboxylporphyrins
 28375  Hexacarboxylporphyrins
 28376  Pentacarboxylporphyrins
 28377  Coproporphyrin, Tetra
 28378  Porphobilinogen
 29374  Aminolevulinic Acid, U
 28379  Interpretation
 29375  Reviewed By