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