264x Filetype PPT File size 1.54 MB Source: www.in.gov
Objectives • Learn about specimen collections • Learn about specimen submissions • Learn about specimen ordering 2 CT/GC Testing • Gen-Probe/Hologic APTIMA Combo 2 Assay – A target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal urogenital disease. – FDA-cleared for male urethral and endocervical swab specimens, plus male and female first-catch urine (FCU) specimens, and in patient-and clinician-collected vaginal swab specimens. – Turnaround Time: 2-5 days 3 Specimen Collection • Acceptable Specimen Types – Urine (Male & Female) – Vaginal Swab – Unisex Swab • Endocervical • Male Urethral • Rectal • Must be collected using only APTIMA Specimen Collection Kits (see package insert for instructions) 4 CT/GC Testing: Specimen Transport • Specimen Transport – Store specimens in their collection systems and keep at 15-30°C until shipped to ISDH – Specimens must be transported to the ISDH Lab at 2‐ 30°C in Gen-Probe/Hologic urine, vaginal or unisex swab APTIMA Collection Kits. – Specimens MUST be received at the ISDH Lab in a timely manner: • Urine: within 30 days of collection • Swabs: within 60 days of collection 5 Common Causes of Specimen Rejection • Mismatch of patient name/ID – Name on specimen tube and LimsNet entry don’t match • Lack of patient identifier on specimen tube – Specimen tube is completely blank • Specimen tube is leaking or broken • Specimen received in Lab after: – 30 days for urine specimens – 60 days for swab specimens • Improper specimen type • Expired transport tube • Multiple swabs in specimen tube 6
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