AutoICD API

80387-4

Laboratory

HIV 1+2 Ab [Presence] in Serum, Plasma or Blood by Rapid immunoassay

Definition

This term should be used for assays that detect the presence of antibodies to HIV-1 and/or -2 but do not differentiate between the two. This term was created for, but is not limited in use to, the bioMerieux VIKIA HIV 1/2 assay for the qualitative detection of antibodies to HIV-1 and HIV-2 in human serum, plasma, or whole blood. The VIKIA HIV 1/2 assay result should be read 30 minutes after the sample is applied to the sample well.

LOINC 6-Axis Classification

Component

HIV 1+2 Ab

Property

PrThr

Time Aspect

Pt

System

Ser/Plas/Bld

Scale Type

Ord

Method Type

IA.rapid

Details

Class

MICRO

Order/Observation

Both

Short Name

HIV1+2 Ab SerPlBld Ql IA.rapid

Display Name

HIV 1+2 Ab IA.rapid Ql (S/P/Bld)

Related Names

ABSAbyAIDSAntbyAntiAntibodiesAntibodyAutoantibodiesAutoantibodyBloodEIAELFAELISAEnzyme immunoassayHIV 1 & 2HIV 1 and 2 AbHIV type 1HIV type IHIV1HIV1+2Human immunodeficiency virusiIAAIDIIInfectious DiseaseInfectiousDiseaseMEIAMicrobiologyOrdinalPlPlasBldPlasmaPlsmPoint in timePRQLQualQualitativeRandomScreenSerPSerPlSerPlasSerPlBldSerumSerum or plasmaSerum, plasma or whole bloodSRSUDSWBWhole blood

Frequently Asked Questions

What is LOINC code 80387-4?

LOINC code 80387-4 identifies "HIV 1+2 Ab [Presence] in Serum, Plasma or Blood by Rapid immunoassay". This term should be used for assays that detect the presence of antibodies to HIV-1 and/or -2 but do not differentiate between the two. This term was created for, but is not limited in use to, the bioMerieux VIKIA HIV 1/2 assay for the qualitative detection of antibodies to HIV-1 and HIV-2 in human serum, plasma, or whole blood. The VIKIA HIV 1/2 assay result should be read 30 minutes after the sample is applied to the sample well.

What does 80387-4 measure?

This code measures HIV 1+2 Ab in Ser/Plas/Bld. It belongs to the MICRO class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.