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Porphobilinogen, Quantitative, Random, Urine

Additional Codes

Orderable Codes:

Epic Code Atlas Code Mayo Test ID Order LOINC
LAB15612 LAB15612 PBGU 2811-8

Result Component(s):

Reporting Name Epic Code Atlas Code Mayo Test ID Result LOINC
Porphobilinogen, U. 12301013624 12301013624 29365 2811-8
Interpretation (PBGU) 12301013625 12301013625 29366 59462-2
Reviewed By 12301013645 12301013645 35032 18771-6

 

Reporting Name

Porphobilinogen, QN, Random, U

Useful For

First-order test for evaluating a suspected acute porphyria: acute intermittent porphyria, hereditary coproporphyria, and variegate porphyria

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Urine


Shipping Instructions


Ship specimen protected 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)

Specimen Volume: 20 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 (preferred) 7 days LIGHT PROTECTED
  Refrigerated  7 days LIGHT PROTECTED

Reference Values

≤0.2 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

LOINC Code Information

Test ID Test Order Name Order LOINC Value
PBGU Porphobilinogen, QN, Random, U 2811-8

 

Result ID Test Result Name Result LOINC Value
29365 Porphobilinogen, U 2811-8
29366 Interpretation (PBGU) 59462-2
35032 Reviewed By 18771-6

Report Available

2 to 4 days

Specimen Retention Time

1 week

Reject Due To

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

NY State Approved

Yes

Method Name

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