Specimen:
Collect
- Vaginal Swab in Aptima Kit-Multitest (Orange)
Submit
- Vaginal Swab in Aptima Kit-Multitest (Orange). Submit Refrigerated.
Special Handling
Rejection Criteria
- Patients under 14 years of age.
Swab transport tube with no swab, two swabs, a cleaning swab, or a swab not supplied by kit if aptima collection.
Stability
Ambient: 1 Month(s); Refrigerated: 1 Month(s); Frozen: 12 Month(s); Incubated: Unacceptable
Methodology
- Target Amplified Nucleic Acid Probe
Performed
Mon-Fri
Reported
1-3 Day(s)
CPT Codes
- 87491
- 87591
Interpretive Data
Please see report for interpretive data.
The Aptima Combo 2 Assay is a qualitative nucleic acid amplification test (NAAT) for the detection of Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC). The analytic performance characteristics have been determined by Interpath Laboratory for sources not FDA approved. Results depend on sufficient levels of DNA to be detected, absence of inhibitors and adequate sample collection. Results should be interpreted in conjunction with clinical findings and should not preclude additional studies if findings do not correlate.
The Aptima Combo 2 Assay is a qualitative nucleic acid amplification test (NAAT) for the detection of Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC). The analytic performance characteristics have been determined by Interpath Laboratory for sources not FDA approved. Results depend on sufficient levels of DNA to be detected, absence of inhibitors and adequate sample collection. Results should be interpreted in conjunction with clinical findings and should not preclude additional studies if findings do not correlate.
Components
- 1339 - N. GONORRHEA
- 1341 - CHLAMYDIA
- 1342 - SOURCE
Last Updated: May 19, 2025 @ 9:13 am
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