Epi proColon

2013906
copy
 

Copy Utility


emailprint
Example Reports
Negative
Positive

Ordering Recommendation

The Epi proColon test is indicated to screen adults of either sex, 50 years or older, defined as average risk for CRC, who have been offered and have a history of not completing CRC screening. Tests that are available and recommended in the USPSTF 2008 CRC screening guidelines should be offered and declined prior to offering the Epi proColon test. Patients with a positive Epi proColon test result should be referred for diagnostic colonoscopy. The Epi proColon test results should be used in combination with physician's assessment and individual risk factors in guiding patient management.

Mnemonic

EPIPRO

Methodology

Polymerase Chain Reaction

Performed

Sun, Wed

Reported

7-10 days

New York DOH Approval Status

This test is New York DOH approved.

Specimen Required

Patient Preparation
Collect

Lavender (K2EDTA). Collect 20 mL whole blood. (Min: 10 mL). Blood collection tubes should be allowed to complete the evacuated fill.

Specimen Preparation

Plasma preparation should be performed ASAP or within 4 hours of collection. Centrifuge for 12 min at 1350 ± 150 rcf. Transfer the plasma to a 15 mL conical tube and centrifuge for an additional 12 minutes at 1350 ± 150 rcf. Ensure a minimum of 8 mL plasma is obtained following centrifugation. Transfer 4 mL plasma into 2 cryovial tubes or freezable specimen transport tubes. (Min: 4 mL, no repeat testing)

Storage/Transport Temperature

Frozen. Also acceptable: Refrigerated.

Unacceptable Conditions

Serum, stool, or whole blood. Hemolyzed specimens.

Remarks
Stability

Ambient: Unacceptable; Refrigerated: 72 hours; Frozen: 2 weeks

Reference Interval

Interpretive Data

Refer to report.

Compliance Category

FDA

Note

This test is not intended to replace a colonoscopy. NOT recommended for pregnant women because of a potential for false-positive results in these individuals.

Accurate test performance requires following the specimen preparation instructions. Minimum volume of 4 mL is required for testing without repeats. If a repeat is necessary, an additional specimen will be requested.

Hotline History

N/A

CPT Codes

81327

Are you an ARUP Client? Click here for your pricing.

Components

Component Test Code* Component Chart Name LOINC
2013907 Epi proColon Result 65810-4
* 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

  • ColoVantage
  • mS9
  • Septin 9
  • Septin 9 methylation
Epi proColon