Cytomegalovirus by Qualitative PCR
Ordering Recommendation

Detects cytomegalovirus but does not quantify viral load. Potentially useful for specimen types other than blood. Cytomegalovirus by Quantitative PCR (0051813) on plasma is the preferred test for most clinical indications.

Qualitative Polymerase Chain Reaction
1-3 days
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
ARUP Consult®
Disease Topics
Specimen Required
Patient Preparation
Lavender (EDTA), Pink (K2EDTA), or Serum Separator Tube (SST). Also acceptable: Amniotic fluid, bronchoalveolar lavage (BAL), CSF, ocular fluid, tissue, urine, or dried blood spot (DBS). 
Specimen Preparation
Separate serum or plasma from cells. Transfer 1 mL plasma, serum, whole blood, bone marrow, amniotic fluid, BAL, CSF, ocular fluid, or urine to a sterile container.
(Min: 0.5 mL)
Dried Blood Spot: Whole blood collected on newborn screening card (3/16 inch punch). Transport punch in an ARUP Standard Transport Tube.
Tissue: Transfer to a sterile container and freeze immediately. 
Storage/Transport Temperature
Whole Blood or Bone Marrow: Refrigerated.
Dried Blood Spot: Room temperature. 
Unacceptable Conditions
Heparinized specimens. 
Specimen source is required. 
Ambient: 8 hours; Refrigerated: 72 hours; Frozen: 3 months
Whole Blood or Bone Marrow:
Ambient: 1 week; Refrigerated: 1 week; Frozen: 1 week
Dried Blood Spot:
Ambient: 28 days; Refrigerated: 8 days; Frozen: 8 days
Ambient: Unacceptable; Refrigerated: Unacceptable; Frozen: 3 months 
Reference Interval
Interpretive Data

Compliance Statement A: Analyte specific reagents (ASR) are used in many laboratory tests necessary for standard medical care and generally do not require U.S. Food and Drug Administration (FDA) approval or clearance. This test was developed and its performance characteristics determined by ARUP Laboratories. The U.S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions. This test should not be regarded as investigational or for research use.

CPT Code(s)
Component Test Code*Component Chart NameLOINC
0050103Cytomegalovirus Source31208-2
0060040Cytomegalovirus by Qualitative PCR5000-5
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
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