Trichomonas vaginalis RNA, Qualitative, TMA, Pap Vial

Trichomonas vaginalis RNA, Qualitative, TMA, Pap Vial

Test Code

90521
87661
90521
87661
In-home collection is not available in your area through Quest Mobile.

Clinical Significance

Trichomonas vaginalis RNA, Qualitative, TMA, Pap Vial - Trichomonas vaginalis RNA, Qualitative Transcription- Mediated Amplification, Pap Vial test is a nucleic acid amplification test that uses transcription-mediated amplification for detection of T. vaginalis RNA, using a ThinPrep® or SurePath™ Pap sample as the specimen. It is used in the screening and diagnosis of trichomoniasis. When the clinical performance of this assay was evaluated, sensitivity was 100% in PreservCyt Solution liquid Pap specimens, while specificity was 98.6% [1,2].

Trichomoniasis is one of the most common sexually transmitted infections ...

Test Details

Methodology

Transcription-Mediated Amplification (TMA)

Reference Range(s)

Not detected

LOINC® Codes, Performing Laboratory

Methodology

Transcription-Mediated Amplification (TMA)

Reference Range(s)

Not detected

Preferred Specimen(s)

1 mL Liquid Cytology (PreservCyt®) Preservative (ThinPrep®) in Aptima® Transfer Tube or
0.5 mL SurePath™ Preservative Fluid in Aptima® Transfer Tube

Alternative Specimen(s)

20 mL PreservCyt® (ThinPrep®) • 10 mL SurePath™ Fluid

Minimum Volume

1 mL PreservCyt® (ThinPrep®) in Aptima® Transfer Tube • 0.5 mL SurePath™ Fluid in Aptima® Transfer Tube

Collection Instructions

PreservCyt® or SurePath™ material already processed for cytology or PAP are not acceptable.

Labs performing cytology: Aliquot PreservCyt® solution before performance of liquid based cytology testing.
PreservCyt®: Transfer 1 mL PreservCyt® solution into Aptima® Specimen Transfer Tube (green label).

SurePath™: SurePath™ fluid must be transferred to Aptima® tube within 4 days of collection. Transfer 0.5 mL SurePath™ solution into Aptima® Specimen Transfer Tube (green label).

Transport Container

Aptima® Vaginal Collection Kit

Transport Temperature

Room temperature

Specimen Stability

  • PreservCyt® (ThinPrep®) in Aptima® Transport
  • Room temperature: 14 days
  • Refrigerated: 30 days
  • Frozen: 12 months
  •  
  • SurePath™ Fluid in Aptima® Transport
  • Room temperature: 14 days
  • Refrigerated: 14 days
  • Frozen: Unacceptable
  •  
  • PreservCyt® (ThinPrep®)
  • Room temperature: 30 days
  • Refrigerated: 30 days
  • Frozen: 1 year
  •  
  • SurePath™ Fluid
  • Room temperature: 4 days
  • Refrigerated: 4 days
  • Frozen: Unacceptable

Reject Criteria

PreservCyt® or SurePath™ material previously processed for cytology • PreservCyt® with excess mucus

Setup Schedule

1 mL Liquid Cytology (PreservCyt®) Preservative (ThinPrep®) in Aptima® Transfer Tube or
0.5 mL SurePath™ Preservative Fluid in Aptima® Transfer Tube
20 mL PreservCyt® (ThinPrep®) • 10 mL SurePath™ Fluid
1 mL PreservCyt® (ThinPrep®) in Aptima® Transfer Tube • 0.5 mL SurePath™ Fluid in Aptima® Transfer Tube
PreservCyt® or SurePath™ material already processed for cytology or PAP are not acceptable.

Labs performing cytology: Aliquot PreservCyt® solution before performance of liquid based cytology testing.
PreservCyt®: Transfer 1 mL PreservCyt® solution into Aptima® Specimen Transfer Tube (green label).

SurePath™: SurePath™ fluid must be transferred to Aptima® tube within 4 days of collection. Transfer 0.5 mL SurePath™ solution into Aptima® Specimen Transfer Tube (green label).
Aptima® Vaginal Collection Kit
Room temperature
PreservCyt® (ThinPrep®) in Aptima® Transport
Room temperature: 14 days
Refrigerated: 30 days
Frozen: 12 months

SurePath™ Fluid in Aptima® Transport
Room temperature: 14 days
Refrigerated: 14 days
Frozen: Unacceptable

PreservCyt® (ThinPrep®)
Room temperature: 30 days
Refrigerated: 30 days
Frozen: 1 year

SurePath™ Fluid
Room temperature: 4 days
Refrigerated: 4 days
Frozen: Unacceptable
PreservCyt® or SurePath™ material previously processed for cytology • PreservCyt® with excess mucus
In-home collection is not available in your area through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

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