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Test ID VRERP Vancomycin-Resistant Enterococcus, Molecular Detection, PCR

Useful For

Identifying carriers of vancomycin-resistant enterococci

Method Name

Real-Time Polymerase Chain Reaction (PCR)

(PCR is utilized pursuant to a license agreement with Roche Molecular Systems, Inc.)

Reporting Name

VRE PCR

Specimen Type

Varies

The high sensitivity of amplification by PCR requires the specimen to be processed in an environment in which contamination of the specimen by Vancomycin-Resistant Enterococcus DNA is unlikely.

 

Forms: If not ordering electronically, complete, print, and send a Microbiology Test Request Form (T244) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/microbiology_test_request_form.pdf).

 

Specimen source is required.

 

Submit only 1 of the following specimens:

 

Preferred:

Specimen Type: Perianal, perirectal, rectal

Container/Tube: Culture transport swab

Specimen Volume: Swab

 

Acceptable:

Specimen Type: Preserved Stool

Container/Tube: Commercially available transport system specific for recovery of enteric pathogens from fecal specimens (15 mL of non-nutritive transport medium containing phenol red as a pH indicator, either Cary-Blair, Para-Pak C and S)

Specimen Volume: Representative portion of stool

 

Specimen Type: Unpreserved stool

Container/Tube: Stool container (Supply T288)

Specimen Volume: Representative portion of stool

Specimen Stability Information

Specimen Type Temperature Time
Varies Refrigerated (preferred) 7 days
  Ambient  7 days
  Frozen  7 days

Clinical Information

Vancomycin-resistant enterococci (VRE) are major nosocomial pathogens. Patients who are particularly vulnerable to fatal disease from VRE include those with hematologic malignancies and liver transplants. Nosocomial spread of VRE occurs as the result of fecal carriage. Risks for both colonization and infection include prolonged hospitalization, intensive care unit stay, transplantation, hematologic malignancies, and prolonged exposure to antibiotics.

 

The Centers for Disease Control and Prevention provides recommendations to prevent the spread of VRE in institutional settings. These recommendations include isolation of patients experiencing active VRE infection, screening of patients by perianal swab or fecal testing to identify carriers of VRE, and subsequent isolation or cohorting of VRE carriers. Identification and isolation of VRE carriers has been shown to be cost-effective.

 

In Enterococcus faecalis or Enterococcus faecium, vancomycin resistance is usually associated with the presence of the vanA or vanB genes. The presence of these genes is detected by a molecular method in this assay.

Reference Values

Not applicable

Cautions

A positive result does not imply the presence of vancomycin-resistant enterococci (VRE) disease; the presence of vanA or vanB genes correlates with colonization by VRE. Colonization with VRE is not associated with any signs or symptoms.

 

vanA or vanB genes may occasionally be found in organisms other than enterococci.

Day(s) Performed

Monday through Friday

Report Available

1 day

Performing Laboratory

Mayo Medical Laboratories in Rochester

Test Classification

This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.

CPT Code Information

87500

NY State Approved

Yes