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Epic Code LAB1230628 Trichomonas Vaginalis RNA, Qualitative TMA, Urine, Males (Send Out)

Important Note

Only to be ordered on patients <14 years old or CPS patients.

Additional Test Codes

Quest: 90801

Clinical Information

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.

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. It is curable. About 70% of people infected with T. vaginalis are asymptomatic, though symptoms may show up after the infection has been present for some time. In men, symptoms include genital itching or irritation, burning after urination or ejaculation, and penile discharge.

In men, T. vaginalis is associated with nongonococcal urethritis and chronic prostatitis. T. vaginalis is also a risk factor for HIV transmission and infection in men, as it increases HIV excretion in semen. Because of the high rate of reinfection, individuals infected with T. vaginalis should return 3 months post-treatment to be retested.

Men with urethritis and other symptoms of T. vaginalis, as well as those who are clinically suspected of having T. vaginalis, should be tested. In a study of 298 men, TMA-based testing for T. vaginalis had a sensitivity of 91.7%, using either urine or urethral swab specimens; specificity was 91.9% for urine and 86.7% for urethral swab specimens.

A "detected" result is consistent with T. vaginalis infection. False-positive results could be obtained from sampling less than 2 weeks after cessation of therapy, since TMA-based tests can detect nucleic acids from dead organisms. A "not detected" result is consistent with the absence of T. vaginalis infection. False-negative results could be obtained due to an organism concentration below the assay detection limit.

Icons & Photos

Urine collection kit

Collection Instructions

Specimen Collection: Urine

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

Processing Instructions (Laboratory, Outpatient or Off-site collection)

Processed Specimen: Urine sample must be poured over within 24 hours into Aptima urine transport tube.

Transport Temperature: Ambient

Rejection Criteria

• Specimens in broken containers 

• Urine samples where the fluid level is not between the fill lines

• Non-Aptima® transport tubes

Specimen Stability

Ambient: 24 hours (before poured over). 30 days after poured over.

Test Frequency

Set up: Daily; Report available: 3-5 days.

Performing Department

REFERRAL SEND OUTS

Performing Department Laboratory Location

Send Out to QUEST CHANTILLY REF LAB

Methodology

Transcription-Mediated Amplification (TMA)

CPT

87661

CDM Code

80106093

Epic Test ID

1230102247

LOINC

46154-1

Reviewed Date

6/9/2023