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Recommendations when to order or not order the test. May include related or preferred tests.
Not recommended for herpes simplex virus (HSV) testing; lacks adequate predictive value for acute infection. Preferred testing is Herpes Simplex Virus (HSV-1/HSV-2) Subtype by PCR (2010095).
New York DOH Approval Status
Indicates whether a test has been approved by the New York State Department of Health.
This test is not New York state approved. There are no New York state-approved laboratories available. The performing laboratory will submit an NYSDOH Single Use Permit (SUP) upon receipt of order. If SUP is approved by NYSDOH, testing will be performed.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
CSF
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
Transfer 1 mL CSF to an ARUP standard transport tube. (Min: 0.5 mL)
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Refrigerated.
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
Specimen types other than CSF. Contaminated, heat-inactivated, icteric, or hemolyzed specimens.
RemarksAdditional specimen collection, transport, or test submission information.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Ambient: 8 hours; Refrigerated: 2 weeks; Frozen: 1 year
Expected turnaround time for a result, beginning when ARUP has received the specimen.
1-2 days
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Test Number
Components
Reference Interval
HSV 1/2 Antibody Screen IgG, CSF
0.89 IV or less
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
Herpes Simplex Virus Type 1 and/or 2 Antibodies, IgG, CSF
0.89 IV or less: Negative. No significant level of detectable HSV IgG antibody. 0.90-1.09 IV: Equivocal. Questionable presence of IgG antibodies. Repeat testing in 10-14 days may be helpful. 1.10 IV or greater: Positive. IgG antibody to HSV detected which may indicate a current or past HSV infection.
Compliance Category
Laboratory Developed Test (LDT)
Note
Additional information related to the test.
If HSV 1/2 IgG, CSF is greater than or equal to 1.10 IV , then HSV 1 gG-specific IgG, CSF and HSV 2 gG-specific IgG, CSF will be added. Additional charges apply.
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
* 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.
Aliases
Other names that describe the test. Synonyms.
glycoprotein type-specific reactivity
Herpes Simplex Antibodies, IgG CSF
Herpes Simplex CSF
HSV 1, 2 IgG CSF
HSV 1,2
HSV 1,2 and glycoprotein reflex
HSV 1,2 glycoprotein CSF
HSV CSF antibody
HSV glycoprotein G CSF
HSV glycoprotein G-based type-specific CSF
Herpes Simplex Virus Type 1 and/or 2 Antibodies, IgG (CSF) With Reflex to Type 1 and 2 Glycoprotein G-Specific Ab, IgG
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