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Melatonin, Serum/Plasma

Test Summary

Measles (Rubeola) Virus, Qualitative Real-Time PCR, Nasopharyngeal/Throat - 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 mL serum (from Red Top, no gel tube) or 1 mL Plasma (from Lavender, EDTA tube)

Minimum Volume

0.4 mL

Instructions

Collect Red TopTube or EDTA lavender top tube. Centrifuge and transfer serum or plasma to a plastic pour off vial.

Patient Preparation

N/A

Storage

Refrigerated

Transport Temperature

Refrigerated

Specimen Stability

  • Room Temperature: 14 days
  • Refrigerated: 30 days
  • Frozen (-20 °C): 12 months

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Gel barrier tubes (SST or PST)

Order Code

MELASP

EPIC (Premier) Code

LAB6909

Includes

N/A

CPT Code

  • 80375

Billing Code

  • 670125

CPT Statement

Methodology

High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)

FDA Status

This test was developed and its performance characteristics determined by NMS Labs. It has not been cleared or approved by the US Food and Drug Administration.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

National Medical Services
200 Welsh Rd
Horsham PA, 19044

Department

Reference Testing

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Report available: 4 - 8 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum (from Red Top, no gel tube) or 1 mL Plasma (from Lavender, EDTA tube)

Minimum Volume

0.4 mL

Instructions

Collect Red TopTube or EDTA lavender top tube. Centrifuge and transfer serum or plasma to a plastic pour off vial.

Patient Preparation

N/A

Storage

Refrigerated

Transport Temperature

Refrigerated

Specimen Stability

  • Room Temperature: 14 days
  • Refrigerated: 30 days
  • Frozen (-20 °C): 12 months

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Gel barrier tubes (SST or PST)

Billing

CPT Code

  • 80375

Billing Code

  • 670125

CPT Statement

Result Information

Methodology

High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Report available: 4 - 8 days