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Sexually-Transmitted Infections (STIs)Pelvic Inflammatory Disease(PID)Panel
Test Code36965
CPT Codes
87491, 87591, 87661, 87563
Includes
Chlamydia/Neisseria gonorrhoeae RNA, TMA, Urogenital
Trichomonas vaginalis RNA, Qualitative, TMA
Mycoplasma genitalium, rRNA, TMA
Trichomonas vaginalis RNA, Qualitative, TMA
Mycoplasma genitalium, rRNA, TMA
Preferred Specimen
Vaginal or endocervical swab collected in an Aptima® transport tube or
2 mL urine collected in an Aptima® transport tube
2 mL urine collected in an Aptima® transport tube
Patient Preparation
Urine: Patient should not have urinated within one hour prior to collection. Female patients should not cleanse the labial area prior to providing the specimen.
Instructions
Female urine: Direct patient to provide 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 tube provided in the urine specimen collection kit . The fluid (urine plus transport media) level in the urine tube must fall within the clear pane on the tube label.
Preservcyt®: Transfer 1 mL of Preservcyt® solution into APTIMA® specimen transfer tube (green label) or APTIMA® vaginal collection tube (orange label) or Multitest Collection Tube (orange label) or Unisex swab specimen collection kit (white label).
Vaginal swab: Follow instructions in the APTIMA® Multitest Swab Specimen Collection Kit (orange label) or an APTIMA® Vaginal Swab Specimen Collection Kit (orange label).
Endocervical swab: Follow instructions in the APTIMA® Unisex Swab Specimen Collection Kit (white label). In females, to ensure collection of cells infected with N. gonorrhoeae/C. trachomatis, columnar epithelial cells lining the endocervix should be obtained. Excess mucus should be removed prior to sampling.
Preservcyt®: Transfer 1 mL of Preservcyt® solution into APTIMA® specimen transfer tube (green label) or APTIMA® vaginal collection tube (orange label) or Multitest Collection Tube (orange label) or Unisex swab specimen collection kit (white label).
Vaginal swab: Follow instructions in the APTIMA® Multitest Swab Specimen Collection Kit (orange label) or an APTIMA® Vaginal Swab Specimen Collection Kit (orange label).
Endocervical swab: Follow instructions in the APTIMA® Unisex Swab Specimen Collection Kit (white label). In females, to ensure collection of cells infected with N. gonorrhoeae/C. trachomatis, columnar epithelial cells lining the endocervix should be obtained. Excess mucus should be removed prior to sampling.
Transport Temperature
Room temperature
Specimen Stability
Room temperature: 14 days
Refrigerated: 14 days
Frozen: 30 days
Refrigerated: 14 days
Frozen: 30 days
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Transport tubes with two 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 black fill line • Urine submitted in non-APTIMA® transport container • Female specimens
Methodology
Transcription-Mediated Amplification (TMA)
Setup Schedule
Sets up 6 days a week.
Report Available
Reports in 3 to 5 days.
Clinical Significance
Pelvic inflammatory disease (PID) is an infection of the female reproductive organs and often due to sexually transmitted infections. It may be caused by Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis and/or Mycoplasma genitalium. Most women are asymptomatic. For those that present with symptoms, the symptoms may include pain in the lower abdomen and pelvis, heavy vaginal discharge with an unpleasant odor, abnormal vaginal bleeding, and pain during intercourse. A panel will help the clinician identify the cause of these symptoms.
