Human Immunodeficiency Virus 1 (HIV-1) PhenoSense Entry® (Monogram® Fuzeon Resistance)

CPT: 87903
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Synonyms

  • Fuzeon® Resistance
  • PhenoSense Entry®

Expected Turnaround Time

16 - 26 days




Specimen Requirements


Specimen

Plasma, frozen


Volume

3 mL


Container

Lavender-top (EDTA) or plasma preparation tube (PPT™).


Collection

Collect specimen in two lavender-top (EDTA) tubes or two PPT™ tubes. Do not use green-top (heparin) tubes. Centrifuge specimen within six hours of collection. Transfer plasma to one or more polypropylene screw-capped tube(s) and freeze. Ship specimen frozen. To avoid delays in turnaround time, when requesting multiple tests on frozen samples, please submit separate frozen specimens for each test requested.


Storage Instructions

Freeze


Causes for Rejection

PPT™ not centrifuged; insufficient volume; heparinized plasma; nonfrozen specimens


Test Details


Use

Determines phenotypic susceptibility to enfuvirtide (Fuzeon®) and assesses likely effectiveness before enfuvirtide is added to a patient's regimen or before changing a regimen that includes enfuvirtide


Limitations

This procedure should be used for patients with documented HIV-1 infection and viral loads ≥1000 copies/mL.


Methodology

Polymerase chain reaction (PCR) amplification and viral culture. PhenoSense Entry® is a trademark of Monogram Biosciences®.


LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
550240 PhenoSense Entry (R) 550247 PhenoSense Entry(R) PDF 51969-4
550240 PhenoSense Entry (R) 550248 PhenoSense Entry(R) 82719-6
550240 PhenoSense Entry (R) 550249 PhenoSense Entry(R) Interp. 77202-0

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