Non-variola orthopoxvirus (includes Mpox or monkeypox virus)




Test Mnemonic

OPXPCR

Primary CPT Codes

  • 87593 - QTY (1), Amplification, Orthopox virus

LOINC ®

104610-1

Aliases

  • Vaccinia virus
  • Non-variola orthopoxvirus
  • Monkeypox Virus Qualitative PCR
  • Monkey
  • Monkeypox
  • Mpox

Includes

  • Orthopoxvirus Source
  • Orthopoxvirus by PCR

Performing Laboratory

Cleveland Clinic Laboratories


Alternate Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
SwabFluid, lesionViral Transport Media RefrigeratedUsing a sterile swab, apply firm pressure to the lesion and swipe back and forth at least 2-3 times before rotating the swab and repeating using the other side of the swab. If the lesion ruptures while swabbing, ensure to collect the lesion fluid. Specimen source required.

Stability

Environmental Condition Description
Refrigerated7 days
Ambient48 hours
FrozenUnacceptable

Days Performed

Varies

Turnaround Time

Same day

Methodology

Name Description
Qualitative Polymerase Chain Reaction 

Reference Range

Monkeypox virus Clade II DNA
Sex Age From Age To Type Range Range Unit
       NormalNot Detected 

Special Info

Specimen source required. Calcium alginate swabs, wooden swabs and specimens without swabs will be rejected.

Clinical Info

This qualitative PCR test is used to detect both monkeypox virus clade II and non-variola Orthopoxvirus DNA. Detection of non-variola Orthopoxvirus DNA only most likely represents the presence of monkeypox virus clade II, however, there is a small chance this could represent the presence of a different non-variola Orthopoxvirus. Correlation with patient history is advised.

Clinical Limitation

This test is intended for the detection of both monkeypox virus clade II and non-variola Orthopoxvirus DNA. A negative result does not rule out the presence of PCR inhibitors in the patient specimen or assay specific nucleic acid in concentrations below the level of detection by the assay. Clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status.