HTLV-I/II Confirmation Panel

Also Known as (Alias) Anti-HTLV-I/II
Indications Confirmatory testing performed on an alternate manufactuer’s assay due to a reactive PRISM-HTLV-I/II result.
Method Avioq HTLV-I/II Microelisa System
Test Information Assay is a qualitative enzyme-linked, immunosorbent assay for the detection of antibodies to Human T-Lymphotropic Virus Type I and/or Human T-Lymphotropic Virus Type II in human serum or plasma.
Additional Test Information Although this assay is offered at Bloodworks as a screening test, when used as part of the confirmatory algorithm, it is performed at a referral laboratory.
Sample Requirements Serum or Plasma (EDTA, heparin, sodium citrate, CPD, and CPDA-1)
Requested Volume 6 mL
Minimum Volume or Pediatric volume 1 mL
Shipping Information Samples are acceptable at 2-8°C for 14 days; samples may be frozen at -20 °C
Requisition Form Donor Testing RFT
Transaction Code 3076-03
CPT Codes 86687 x 1, 86688 x 1
Test Schedule Referral Laboratory
Turn around Time (analytic time) Varied, dependent on Referral Laboratory schedule
Report/ Results Reactive or Nonreactive

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