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Order Code ORTHP Orthostatic Proteinuria, Random, Urine


Specimen Required


Patient Preparation: Specimens should be collected before fluorescein is given or not collected until at least 24 hour later.

Container/Tube: Plastic, 5-mL tube

Specimen Volume: 4 mL

Collection Instructions:

1. This is a nighttime (supine) collection.

2. Void immediately prior to lying down to sleep.

3. Collect an 8-hour (nighttime) urine specimen.

4. Upon awaking in the morning, the patient should immediately void into the specimen cup.

4. No preservative.

5. Invert well before taking 4-mL (maximum) aliquot.


Useful For

Diagnosis of orthostatic proteinuria

Profile Information

Test ID Reporting Name Available Separately Always Performed
PRCON Protein, Total, Random, U No Yes
RATO2 Protein/Creatinine Ratio No Yes
CRETR Creatinine, Random, U No Yes

Method Name

PRCON: Turbidimetry

CRETR: Enzymatic Colorimetric Assay

RATO2: Calculation

Reporting Name

Orthostatic Proteinuria, Random, U

Specimen Type

Urine

Specimen Minimum Volume

1 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Urine Refrigerated (preferred) 14 days
  Frozen  30 days
  Ambient  24 hours

Reject Due To

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

Reference Values

PROTEIN/CREATININE RATIO:

≥18 years: <0.18 mg/mg creatinine

 

CREATININE:≥18 years = 16-326 mg/dL

Reference values have not been established for patients younger than 18 years of age.

Method Description

Protein:

The sample is preincubated in an alkaline solution containing EDTA, which denatures the protein and eliminates interference from magnesium ions. Benzethonium chloride is then added, producing turbidity.(Package insert: Total Protein Urine/CSF. Roche Diagnostics; V13.0, 11/2018)

 

Creatinine:

The enzymatic method is based on the determination of sarcosine from creatinine with the aid of creatininase, creatinase, and sarcosine oxidase. The liberated hydrogen peroxide is measured via a modified Trinder reaction using a colorimetric indicator. Optimization of the buffer system and the colorimetric indicator enables the creatinine concentration to be quantified both precisely and specifically.(Package insert: Creatinine plus v2. Roche Diagnostics; V15.0, 03/2019)

 

The final result uses a calculation to provide the total protein per creatinine ratio. This calculation is performed by the laboratory information system, SCC Soft.

Day(s) Performed

Monday through Sunday

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

CRETR- 82570

PRCON- 84156