Test ID RZIKU Zika Virus, PCR, Molecular Detection, Random, Urine
Useful For
Qualitative detection of Zika virus RNA in paired urine and serum from individuals meeting CDC Zika virus clinical or epidemiologic criteria
Highlights
Provides qualitative detection of Zika virus RNA from urine collected during the acute phase of infection.
This test is intended for the evaluation of pregnant women and symptomatic nonpregnant individuals with potential exposure to Zika virus.
Due to similar clinical presentations, testing for RNA or IgM-class antibodies to dengue and chikungunya viruses, concurrently with Zika virus testing, is strongly recommended.
For the most up-to-date Zika epidemiology and testing recommendations, visit www.cdc.gov/zika/
Testing Algorithm
The FDA requires that urine specimens be tested in conjunction with a paired serum specimen; order RZIKS / Zika Virus, PCR, Molecular Detection, Serum for the paired serum specimen.
The following algorithms are available in Special Instructions:
Special Instructions
Method Name
Real-Time Reverse Transcription Polymerase Chain Reaction (PCR)/DNA Probe Hybridization
Reporting Name
Zika Virus, PCR, UrineSpecimen Type
UrineOrdering Guidance
Due to similar clinical presentations, testing for RNA or IgM-class antibodies to dengue and chikungunya viruses, concurrently with Zika virus testing, is strongly recommended.
Additional Testing Requirements
The FDA requires that urine specimens be tested in conjunction with a paired serum specimen; order RZIKS / Zika Virus, PCR, Molecular Detection, Serum for the paired serum specimen.
Necessary Information
Order questions and answers concerning pregnancy, exposure, and display of symptoms are required.
Specimen Required
Container/Tube: Sterile container
Specimen Volume: 1 mL
Collection Instructions:
1. Collect random urine in a sterile container.
2. Label specimen as urine.
Specimen Minimum Volume
0.3 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Refrigerated (preferred) | 7 days | |
Frozen | 7 days |
Reference Values
Negative
Day(s) Performed
Tuesday, Thursday
Report Available
5 to 8 daysPerforming Laboratory

Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
87662
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
RZIKU | Zika Virus, PCR, Urine | 85623-7 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
47916 | Zika Urine PCR Result | 85623-7 |
PREG1 | Is patient pregnant? | 11449-6 |
EXPO1 | Has patient had Zika exposure? | 88636-6 |
SYMP1 | Has patient been symptomatic? | 75325-1 |
48058 | Zika Urine Interpretation | 69048-7 |
NY State Approved
YesForms
If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.