426x Filetype PPT File size 1.54 MB Source: www.in.gov
Objectives
• Learn about specimen collections
• Learn about specimen submissions
• Learn about specimen ordering
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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
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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)
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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
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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
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