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Measles (Rubeola) Virus, Qualitative Real-Time PCR

Test Summary

Measles is a highly contagious, acute viral respiratory illness. The disease starts with high fever, malaise, cough, coryza (runny nose), conjunctivitis and Koplik spots, followed by a spreading maculopapular rash which appears about 14 days after exposure. Infants and children <5 years of age, adults older than 20, pregnant women and those who are immunocompromised are at risk for severe complications which include pneumonia or encephalitis. Measles outbreaks occur in unvaccinated or not properly vaccinated individuals. Testing for acute Measles infection is recommended by the CDC using Real-Time PCR from respiratory specimens (throat and nasopharyngeal swabs) as well as testing for Measles IgM in serum. IgM antibodies may be detected three days after rash onset whereas detection of Measles RNA by RT-PCR may be detected prior to antibody development, and as late as 10 to 14 days after rash onset. The optimal time for collecting acute blood for serology is at least 72 hours after rash onset. Serum collected before then may be falsely negative.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 nasopharyngeal (NP) or throat swab in liquid Amies elution swab (ESwab), VCM, M4, or equivalent (UTM)

Minimum Volume

N/A

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Refrigerated

Specimen Stability

  • Room temperature: 48 hours
  • Refrigerated: 7 days
  • Frozen: 30 days

Limitations

N/A

Other Acceptable Specimens

EDTA plasma (lavender-top)

Unacceptable Specimens

Transport container without a swab • Dry swab • Swab in gel amies

Order Code

MEASLP

EPIC (Premier) Code

LAB6828

Includes

N/A

CPT Code

  • 87798

Billing Code

  • 671293

CPT Statement

Methodology

Reverse Transcriptase Real-Time Polymerase Chain Reaction (RT-PCR)

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 FDA. 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
14225 Newbrook Drive
Chantilly VA, 20153

Department

Reference Testing

Reference Range

Not detected

Setup Schedule / Expected Turnaround Time

Tuesday-Saturday morning Report available: 2 Days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 nasopharyngeal (NP) or throat swab in liquid Amies elution swab (ESwab), VCM, M4, or equivalent (UTM)

Minimum Volume

N/A

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Refrigerated

Specimen Stability

  • Room temperature: 48 hours
  • Refrigerated: 7 days
  • Frozen: 30 days

Limitations

N/A

Other Acceptable Specimens

EDTA plasma (lavender-top)

Unacceptable Specimens

Transport container without a swab • Dry swab • Swab in gel amies

Billing

CPT Code

  • 87798

Billing Code

  • 671293

CPT Statement

Result Information

Methodology

Reverse Transcriptase Real-Time Polymerase Chain Reaction (RT-PCR)

Testing Laboratory

N/A

Reference Range

Not detected

Setup Schedule / Expected Turnaround Time

Tuesday-Saturday morning Report available: 2 Days