Banner Image

Test Directory

Porphobilinogen, Quantitative, Random Urine

Test Summary

Urinary Porphobilinogen is the first step in the diagnosis of acute porphyria's such as acute intermittent porphyria (AIP). AIP is an autosomal dominant disorder characterized by deficiency of porphobilinogen deaminase. An acute attack usually includes gastrointestinal disturbance and neuropsychiatric disorders.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

2 mL unpreserved urine collected in a plastic leak-proof container. Protect from light.

Minimum Volume

1 mL

Instructions

Urine should be refrigerated and protected from light.

Whenever possible, the specimen should be collected during an acute episode because porphobilinogen (PBG) may decrease rapidly upon remission. PBG may also degrade when samples are exposed to UV light for extended periods, or are transported at ambient temperature. If an amber collection jug/urine cup is not available, the sample must be protected from light by completely wrapping the container in aluminum foil. PBG is most stable at pH 6-7, but all samples may be sent with or without preservative. All results should be interpreted in the context of clinical findings, relevant history, and other laboratory data.

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Room temperature: Unacceptable
  • Refrigerated: 7 days
  • Frozen: 30 days

Limitations

N/A

Other Acceptable Specimens

Random clean-catch urine collected with 0.5g sodium carbonate (Na2CO3) per 100 mL of sample

Unacceptable Specimens

Not protected from light

Order Code

PORQNU

EPIC (Premier) Code

LAB3651

Includes

N/A

CPT Code

  • 84110

Billing Code

  • 670431

CPT Statement

Methodology

Chromatography/Mass Spectrometry

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
33608 Ortega Highway
San Juan Capistrano CA, 92675

Department

Reference Testing

Reference Range

≤17 Years<0.36 mg/g creat
≥18 Years<0.22 mg/g creat

Setup Schedule / Expected Turnaround Time

Tuesday, Thursday, Saturday; Report available: 4 - 7 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

2 mL unpreserved urine collected in a plastic leak-proof container. Protect from light.

Minimum Volume

1 mL

Instructions

Urine should be refrigerated and protected from light.

Whenever possible, the specimen should be collected during an acute episode because porphobilinogen (PBG) may decrease rapidly upon remission. PBG may also degrade when samples are exposed to UV light for extended periods, or are transported at ambient temperature. If an amber collection jug/urine cup is not available, the sample must be protected from light by completely wrapping the container in aluminum foil. PBG is most stable at pH 6-7, but all samples may be sent with or without preservative. All results should be interpreted in the context of clinical findings, relevant history, and other laboratory data.

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Room temperature: Unacceptable
  • Refrigerated: 7 days
  • Frozen: 30 days

Limitations

N/A

Other Acceptable Specimens

Random clean-catch urine collected with 0.5g sodium carbonate (Na2CO3) per 100 mL of sample

Unacceptable Specimens

Not protected from light

Billing

CPT Code

  • 84110

Billing Code

  • 670431

CPT Statement

Result Information

Methodology

Chromatography/Mass Spectrometry

Testing Laboratory

N/A

Reference Range

≤17 Years<0.36 mg/g creat
≥18 Years<0.22 mg/g creat

Setup Schedule / Expected Turnaround Time

Tuesday, Thursday, Saturday; Report available: 4 - 7 days