Trichomonas vaginalis, NAAT - Males

Message
USE THIS FOR MALES ONLY
FOR FEMALES ORDER IN-HOUSE TESTING


Test Code
LAB921


Alias/See Also
LAB921
LabCorp TC: 188052


CPT Codes
87661

Preferred Specimen
Urethral Swab


Other Acceptable Specimens
2 mL - First-void Urine transfered to an Aptima urine specimen transport vial


Instructions
For "Drity" urine collection: The patient should not have urinated for at least one hour prior to specimen collection. Direct patient to provide a first-catch urine (approximately 20-30 mL of the intial stream) into a urine collection cup free of any preservatives. Collection of larger volumes of urine may result in specimen dilution that may reduce test sensitivity; lesser volumes may not adequately rinse organisms into the specimen.


Transport Container
Aptima swab or Aptima Urine transport vial


Transport Temperature
Room Temperature


Specimen Stability
Roome Temperature: 30 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Specimen with incorrect patient identification; unlabeled specimen; inappropriate specimen transport conditions; specimens received after prolonged dealy (usually >72 hours); specimens leaked in transit; specimen in expired transport or incorrect transport device; specimens with inappropriate source for test requested; specimen with fixative or additives; Aptima Urine transport >30 days from collection; Aptima Urine transport with incorrect specimen volume; <15 mL urine submitted in sterile container; receipt of urine in steriel container >24 hours from collection; Aptima swab tranport >60 days from collection; Aptima swab specimens with incorrect specimen volume; Aptima swab specimen without a swab; cleaning swab (white-shaft) in Aptima swab transport; any non-Gen-Probe swab submitted in Aptima transport device; wooden-shaft swab in transport device; tranport device with multipe swabs; female urethral swab; bloody or grossly mucoid specimens; bacterial swabs; specimen in ProbeTec UPT transport; ProbeTec Q-swabs; UTM-RT; SurePath vial


Methodology
Nucleic Acid Amplification (NAA)

Clinical Significance
This test is used to detect Trichomonas vaginalis infection.
 


Performing Laboratory
LabCorp



The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.