Herpes Simplex Virus (HSV) Types 1 and 2, NAA
Code:18041|CPT:87529|LOINC:16130-7, 16131-5
| Includes | HSV 1 NAA HSV 2 NAA |
|---|
Analysis details
Methodology
- Nucleic acid amplification (NAA)
- Real-time polymerase chain reaction (RT-PCR)
Expected Turnaround Time
1–2 days
Special Instructions
- For oropharyngeal swabs, do not eat, drink, brush teeth, rinse the mouth or throat, chew gum, or smoke for 3–4 hours before sampling; the preferred time is morning after overnight sleep.
- Women: collect a urethrogenital swab or urine sample before menses or 2–3 days after menses ends.
- Avoid smoking for 30 minutes prior to specimen collection.
- Men: avoid urination for 3 hours before urethrogenital swab collection.
- Men: avoid both urination and genital hygiene for 6 hours before urine collection.
How to use
Herpes Simplex Virus (HSV) Types 1 and 2, NAA is used to confirm HSV infection and determine type when viral shedding is present, aiding evaluation of oral, cutaneous, and anogenital disease. The test supports assessment of suspected genital herpes in women and men, risk-based testing during pregnancy, and documentation of therapeutic response when molecular evidence of shedding is required. Common synonyms include HSV DNA PCR and HHV-1/HHV-2 nucleic acid testing.
Limitations
Real-time PCR identifies HSV DNA at low copy numbers and is independent of the timing of seroconversion. HSV-1 most often involves oral and perioral sites, whereas HSV-2 more commonly affects the anogenital region; either type can infect either location, and transmission may occur with or without visible lesions. Primary infection typically presents with painful vesicles and systemic symptoms, after which latency is established with potential reactivation triggered by stress or immunosuppression. A negative HSV nucleic acid amplification result indicates no detectable shedding at the time of collection but does not exclude prior infection. Severe disease can occur in neonates and in immunocompromised individuals; antiviral therapy suppresses replication and shortens the acute illness but does not eradicate latent virus.
| Unit | qualitative |
|---|---|
| Reference interval | — |
| Indications | Assessment of suspected genital herpes due to HSV-1 or HSV-2 infection |
Possible Causes of Abnormal Results
Decreased levels
- antiviral therapy
- improper specimen collection
Specimen Requirements
| Specimen | Whole blood |
|---|---|
| Container | Lavender Top (K3 EDTA) |
| Storage Instructions | Room temperature, Refrigerated |