Purpose

This is a qualitative in-vitro nucleic acid diagnostic test that utilizes real-time polymerase chain reaction (PCR) for the direct detection of Trichomonas vaginalis (TV) DNA in males or females.  This test is intended as an aid in the diagnosis of TV infections in individuals suspected to have TV infection.

Collect

Acceptable specimens:  Dirty urine, Endocervical, Genital, Vaginal, Thin Prep

Collection devices:
  • Endocervical swab specimens collected with cobas PCR Medial Dual Swab Sample Kit
  • Vaginal swab specimens collected with either cobas PCR Media Uni Swab Sample Kit or Dual Swab Sample Kit
  • Male and female urine collected with the cobas PCR Urine Sample Kit
  • Cervical specimens collected in PreservCyt Solution

Unacceptable Conditions

Samples visibly contaminated or stored at the wrong temperature

Storage/Transport Temperature

2 - 30oC

Stability (from collection to initiation)

Urine is stable for 24 hours before transfer to Roche Lysis Buffer.
Swabs and urine may be stored for up to 12 months once the specimens have been stabilized in Roche Lysis Buffer.

Cerner Orderable(s)

Trichomonas vaginalis PCR (Outreach)

Performed

BayCare Laboratories, LLC (Esoteric lab)

Performed daily

Methodology

Real-time PCR

Reported

TAT:  24 - 48 hours

Synonyms

  • TV

Reference Interval

Negative

Interpretive Data

This test is for the qualitative detection of Trichomonas vaginalis DNA in endocervical swabs, vaginal swabs, and male and female urine specimens.  This assay is performed using FDA-approved COBAS TV Test.  Presence of DNA is evidence of presumed infection with this organism.
Collection

Purpose

This is a qualitative in-vitro nucleic acid diagnostic test that utilizes real-time polymerase chain reaction (PCR) for the direct detection of Trichomonas vaginalis (TV) DNA in males or females.  This test is intended as an aid in the diagnosis of TV infections in individuals suspected to have TV infection.

Collect

Acceptable specimens:  Dirty urine, Endocervical, Genital, Vaginal, Thin Prep

Collection devices:
  • Endocervical swab specimens collected with cobas PCR Medial Dual Swab Sample Kit
  • Vaginal swab specimens collected with either cobas PCR Media Uni Swab Sample Kit or Dual Swab Sample Kit
  • Male and female urine collected with the cobas PCR Urine Sample Kit
  • Cervical specimens collected in PreservCyt Solution

Unacceptable Conditions

Samples visibly contaminated or stored at the wrong temperature

Storage/Transport Temperature

2 - 30oC

Stability (from collection to initiation)

Urine is stable for 24 hours before transfer to Roche Lysis Buffer.
Swabs and urine may be stored for up to 12 months once the specimens have been stabilized in Roche Lysis Buffer.
Ordering

Cerner Orderable(s)

Trichomonas vaginalis PCR (Outreach)

Performed

BayCare Laboratories, LLC (Esoteric lab)

Performed daily

Methodology

Real-time PCR

Reported

TAT:  24 - 48 hours

Synonyms

  • TV
Result Interpretation

Reference Interval

Negative

Interpretive Data

This test is for the qualitative detection of Trichomonas vaginalis DNA in endocervical swabs, vaginal swabs, and male and female urine specimens.  This assay is performed using FDA-approved COBAS TV Test.  Presence of DNA is evidence of presumed infection with this organism.
Administrative