Sign in →

Trichomonas vaginalis PCR

Additional Codes

LAB3870

Performing Laboratory

Missouri Baptist Medical Center Molecular Lab

Methodology

Nucleic Acid Amplification Test (NAAT) for the detection of Trichomonas vaginalis genomic DNA using the following platforms:

  • Inpatient/ED: Cepheid Xpert® TV Assay performed on the GeneXpert System
  • Outpatient and ThinPrep (endocervical) samples: Roche cobas® TV Assay performed on the cobas 5800 System

Specimen Requirements

Acceptable Specimens:

Inpatient and ED:

Urine: Collected in Xpert Urine Specimen Collection Kit

Endocervical, Vaginal Swabs: Collected in Xpert Swab Specimen Collection Kit

 

Outpatient:

Urine:  

Specimen Volume: 30 mL

Collection Instructions:

1. Patient should not have urinated for at least 1 hour prior to specimen collection.

2. Patient should collect first portion of random voided urine (first part of stream) into a sterile, plastic, preservative-free container.

 

Endocervical, Vaginal Swabs: Collected in Cobas PCR Media Dual Swab Sample Kit

 

Endocervical ThinPrep:

Collected in ThinPrep PreserveCyt solution

Specimen Transport Temperature

Swabs - Ambient/Refrigerated OK

Urine - Ambient/Refrigerated OK

ThinPrep PreservCyt solution – Ambient OK

Day(s) Test Set Up

Monday through Sunday

Turnaround Time:
Cepheid Xpert Assay: Within 8 hours from receipt to the laboratory

Roche cobas Assay: Within 24 hours from receipt to the laboratory

Reference Values

Trichmonas vaginalis - Not Detected

Test Classification and CPT Coding

87661