Trichomonas vaginalis RNA, Qualitative, TMA, Males

Trichomonas vaginalis RNA, Qualitative, TMA, Males

Test Code

90801
87661
90801
87661
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

Trichomonas vaginalis RNA, Qualitative, TMA, Males - The Trichomonas vaginalis RNA, Qualitative Transcription- Mediated Amplification, Males assay is a nucleic acid amplification test that uses TMA for detection of T. vaginalis RNA in male urethral swabs or urine. It is used in the screening and diagnosis of trichomoniasis [1].

Trichomoniasis is one of the most prevalent sexually transmitted infections (STIs) in the United States, with an estimated 1.1 million new cases each year [2]. It is curable. About 70% of people infected with T. vaginalis are asymptomatic, though symptoms may show up after ...

Test Details

Patient Preparation

Male urine: Patient should not have urinated within one hour prior to collection

Methodology

Transcription-Mediated Amplification (TMA)

Assay Category

The analytical performance characteristics of this assay have been determined by Quest Diagnostics. The modifications have not been cleared or approved by the FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

Not detected

Alternative Name(s)

T. vaginalis,Urine Trichomonas,Trichomonas Urine

LOINC® Codes, Performing Laboratory

Male urine: Patient should not have urinated within one hour prior to collection

Methodology

Transcription-Mediated Amplification (TMA)
The analytical performance characteristics of this assay have been determined by Quest Diagnostics. The modifications have not been cleared or approved by the FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

Not detected

Alternative Name(s)

T. vaginalis,Urine Trichomonas,Trichomonas Urine

Preferred Specimen(s)

1 male urethral swab in Aptima® Transport Tube or
2 mL male urine in Aptima® Transport Tube

Alternative Specimen(s)

Urine (no preservatives): 2 mL of urine, specimen must be transferred into the Aptima® Urine Transport Medium within 24 hours of collection and before being assayed

Minimum Volume

1 male urethral swab in Aptima® Transport • 2 mL random urine (male) in Aptima® Transport

Collection Instructions

For a complete list of limitations we recommend you review the manufacturers package insert: https://www.hologic.com/package-inserts/diagnostic-products/aptima-trichomonas-vaginalis-assay

Urethral swab: Follow instructions in the Aptima® Unisex Swab Specimen Collection Kit for Endocervical and Urethral Swab Specimens package insert.

Male urine: Direct patient to provide a first-catch urine (a maximum of 20-30 mL of the initial urine stream) into a urine collection cup free of any preservatives. 2 mL of urine specimen must be transferred into the Aptima® Specimen Transport within 24 hours of collection and before being assayed. Use the tube provided in the urine specimen collection kit. The fluid (urine plus transport media) level in the urine transport tube must fall within the clear pane of the tube label.

IMPORTANT: Please review the Specimen Collection instructions Specimen Collection guides for Aptima for this test

Transport Container

APTIMA® Unisex Swab Specimen Collection kit

Transport Temperature

Room temperature

Specimen Stability

  • Urine
  • Room temperature: 30 days
  • Refrigerated: 30 days
  • Frozen: 6 months
  •  
  • Swab
  • Room temperature: 60 days
  • Refrigerated: 60 days
  • Frozen: 6 months

Reject Criteria

Transport tubes with 2 swabs • Transport tubes with non-Aptima® swabs • Swab transport tubes with no swab • Specimens in broken containers • Swab submitted in viral transport media • Urine samples where the fluid level is not between the fill lines • Female specimens

Setup Schedule

1 male urethral swab in Aptima® Transport Tube or
2 mL male urine in Aptima® Transport Tube
Urine (no preservatives): 2 mL of urine, specimen must be transferred into the Aptima® Urine Transport Medium within 24 hours of collection and before being assayed
1 male urethral swab in Aptima® Transport • 2 mL random urine (male) in Aptima® Transport
For a complete list of limitations we recommend you review the manufacturers package insert: https://www.hologic.com/package-inserts/diagnostic-products/aptima-trichomonas-vaginalis-assay

Urethral swab: Follow instructions in the Aptima® Unisex Swab Specimen Collection Kit for Endocervical and Urethral Swab Specimens package insert.

Male urine: Direct patient to provide a first-catch urine (a maximum of 20-30 mL of the initial urine stream) into a urine collection cup free of any preservatives. 2 mL of urine specimen must be transferred into the Aptima® Specimen Transport within 24 hours of collection and before being assayed. Use the tube provided in the urine specimen collection kit. The fluid (urine plus transport media) level in the urine transport tube must fall within the clear pane of the tube label.
IMPORTANT: Please review the Specimen Collection instructions Specimen Collection guides for Aptima for this test
APTIMA® Unisex Swab Specimen Collection kit
Room temperature
Urine
Room temperature: 30 days
Refrigerated: 30 days
Frozen: 6 months

Swab
Room temperature: 60 days
Refrigerated: 60 days
Frozen: 6 months
Transport tubes with 2 swabs • Transport tubes with non-Aptima® swabs • Swab transport tubes with no swab • Specimens in broken containers • Swab submitted in viral transport media • Urine samples where the fluid level is not between the fill lines • Female specimens
In-home collection may be available in your area for purchase 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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