WebIncludes Chlamydia trachomatis RNA, TMA, Urogenital Neisseria gonorrhoeae RNA, TMA, Urogenital If Chlamydia trachomatis RNA, TMA, Urogenital is Detected, then Chlamydia trachomatis, TMA (Alternate Target), Urogenital will be performed at an additional charge (CPT code(s): 87491). If Neisseria gonorrhoeae RNA, TMA, Urogenital is Detected, then … Web1. Positive - C. trachomatis RNA detected and/or N. gonorrhoeae RNA detected and/or Trichomonas Vaginalis RNA detected Note: Positive Trichomonas results ALONE from ONLY pharyngeal or rectal sites should be disregarded for treatment. If Trichomonas is identified in urine, urethral or vaginal specimen, treatment should be provided. 2.
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WebDetecting Chlamydia trachomatis in non- US Food and Drug Administration -approved specimen types This test is not intended for use in medico-legal applications. This test is not useful for the detection of Chlamydia pneumoniae or other Chlamydia species Method Name Transcription Mediated Amplification NY State Available Yes Reporting Name WebSurePath™ fluid must be transferred to Aptima® tube within 4 days of collection. Send 0.5 mL of SurePath™ preservative fluid collected in Aptima® Vaginal collection kit (orange … raymonds seal coating
Monitoring therapy success of urogenital Chlamydia trachomatis …
WebC. trachomatis NAATs, including the APTIMA Combo 2 Assay. ... detection step, light emitted from the labeled RNA:DNA hybrids is measured as photon signals in a luminometer, and are reported as ... WebThis test is an in vitro nucleic acid amplification test for the detection of RNA from microorganisms associated with vulvovaginal candidiasis and trichomoniasis. The assay … WebC. trachomatis STIs are best identified in genital samples using nucleic acid amplification tests (NAATs) because these tests are more sensitive than cell culture and have less stringent sample handling requirements. Currently, 6 NAATs are approved by the U.S. Food and Drug Administration (FDA) for testing genital and urine specimens from adults and … simplify 77