Ordering Recommendation

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation

Patient should abstain from alcohol for 24 hours prior to collection.

Collect

Green (sodium or lithium heparin). Also acceptable: lavender (EDTA).

Specimen Preparation

Protect from light. Transfer 3 mL plasma to an ARUP amber transport tube. (Min: 1 mL)
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.

Storage/Transport Temperature

Frozen. Also acceptable: Refrigerated

Unacceptable Conditions

Separator tubes. Specimens not protected from light.

Remarks

Include a current list of patient medications.

Stability

Ambient: Unacceptable; Refrigerated: 2 weeks; Frozen: 2 weeks

Methodology

Quantitative Scanning Spectrofluorometry / Quantitative High Performance Liquid Chromatography (HPLC)

Performed

Varies

Reported

3-8 days

Reference Interval

Refer to report

Interpretive Data



Compliance Category

Performed by non-ARUP Laboratory

Note

If total porphyrins are greater than 1.0 mcg/dL, then fractionation will be performed. Additional charges apply.

Hotline History

N/A

CPT Codes

84311; if reflexed, add 82542

Components

Component Test Code* Component Chart Name LOINC
0092011 Porphyrins Total, Plasma 2815-9
2006594 Porphyins Total - Review 18771-6
2006595 Porphyrins Total - Interpretation 59462-2
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Congenital Erythropoietic Porphyria (CEP)
  • Coproporphyrin, EPP
  • Erythropoietic Protophyria (EPP)
  • Porphyria Cutanea Tarda (PCT)
  • Protoporphyrin, Uroporphyrin
  • Variegate Porphyria
  • X-linked Dominant Protoporphyria (XLDPP or XDP)
Porphyrins, Total with Reflex to Porphyrins Fractionation, Plasma

Mayo Clinic Laboratories