AutoICD API

81154-7

Laboratory

Dengue and Chikungunya and Zika virus panel by NAA with probe detection

Definition

This LOINC panel is used to report the qualitative detection and differentiation of Dengue, Chikungunya, and Zika viruses in human serum or CSF specimens, as well as for detecting Zika virus in human urine or amniotic fluid specimens. The panel is based on, but not limited in use to, the Centers for Disease Control and Prevention's Trioplex real time reverse transcriptase PCR assay, which is intended for use during the acute phase of infection when viral RNA is detectable for a limited period of time following onset of symptoms (approximately five days for Dengue, eight days for Chikungunya and seven days for Zika). Negative results do not rule out infection with Dengue, Chikungunya and/or Zika virus.

LOINC 6-Axis Classification

Component

Dengue & Chikungunya & Zika virus panel

Property

-

Time Aspect

Pt

System

^Patient

Scale Type

-

Method Type

Probe.amp.tar

Details

Class

PANEL.MICRO

Order/Observation

Order

Short Name

DENV + CHIKV + ZIKV Pnl NAA+pr

Display Name

DENV + CHIKV + ZIKV Pnl NAA+probe

Related Names

3 Self-Sustaining Sequence Replication3SR SRAmplifAmplificationAmplifiedDENV + CHIKV + ZIKV PnlDNA NUCLEIC ACID PROBEDNA probeIDInfectious DiseaseInfectiousDiseaseLATLCRLigase chain reactionLigation-activated transcriptionMicrobiologyNAA+probeNAATNASBANucleic acid sequence based analysisPanPANEL.MICROBIOLOGYPanlPCRPnlPoint in timePolymerase chain reactionProbe ampProbe with ampificationProbe with target amplificationQBRRandomSDAStrand Displacement AmplificationTMATranscription mediated amplificationZIKV

Frequently Asked Questions

What is LOINC code 81154-7?

LOINC code 81154-7 identifies "Dengue and Chikungunya and Zika virus panel by NAA with probe detection". This LOINC panel is used to report the qualitative detection and differentiation of Dengue, Chikungunya, and Zika viruses in human serum or CSF specimens, as well as for detecting Zika virus in human urine or amniotic fluid specimens. The panel is based on, but not limited in use to, the Centers for Disease Control and Prevention's Trioplex real time reverse transcriptase PCR assay, which is intended for use during the acute phase of infection when viral RNA is detectable for a limited period of time following onset of symptoms (approximately five days for Dengue, eight days for Chikungunya and seven days for Zika). Negative results do not rule out infection with Dengue, Chikungunya and/or Zika virus.

What does 81154-7 measure?

This code measures Dengue & Chikungunya & Zika virus panel in ^Patient. It belongs to the PANEL.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.