Virology Laboratory

Cytomegalovirus (CMV) PCR (Qualitative) - urine specimen

  • LIS Mnemonic: CMVPCR

    Collect

    Random Urine Container

    Volume Required

    5-10 ml of clean voided urine

    Minimum Required

    5 ml of clean voided urine

    Transport

    Keep specimen at 4C

    Processing

    For infants, a volume of 1 to 2 ml of urine is acceptable. If an extended delay in transport of specimens is anticipated, rapidly freeze the specimens to at least -60°C and transport to the laboratory on dry ice. Please consult the laboratory if necessary.

Days Performed

Daily

Reported

Same day

Reflex Testing

N/A

CPT

87496

Methodology

Amplification and detection of CMV DNA polymerase gene using TaqMan real-time PCR technology. This test is performed pursuant to an agreement with Roche Molecular Systems, Inc.

Interpretation

If positive, results are reported as cytomegalovirus DNA detected.

Reference Values

Negative or no cytomegalovirus DNA detected

Remarks

Clinical Utility: CMV infections are common and usually asymptomatic in otherwise healthy children and adults; however, the incidence and spectrum of disease in newborns and in immunocompromised hosts establish this virus as an important human pathogen. The detection of CMV DNA from urine, respiratory secretions, blood or other body fluids within the first 3 weeks of life is the traditional means of confirming the diagnosis of congenital CMV infection in newborns. PLEASE NOTE: When attempting to make a diagnosis of congenital CMV infection, infants not previously tested but found to be excreting virus after 3 weeks of age may have either congenital or acquired infection. Urine is the preferred specimen because it contains greater amounts of virus that can be readily detected. Detection of CMV DNA from maternal blood leukocytes and from amniotic fluid and fetal tissue by PCR may provide useful information for prenatal diagnosis of congenital CMV infection. While such prenatal testing is a sensitive indicator of maternal or fetal CMV infection, positive results do not predict which infants will have disease. CAUTION: In the evaluation of immunocompromised patients, detection of CMV in urine may be useful to monitor these patients for viral shedding, but finding CMV in the urine has limited utility for diagnosing disease since shedding of CMV in urine is common during asymptomatic infection and is usually not suggestive of more severe disease.

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