|87491; 8759187491; 87591|
Submit one specimen per test requested. Specify the exact specimen source/origin (e.g., rectal). Indicate a specific test number on the test request form.
Submit one specimen per test requested. Specify the exact specimen source/origin (e.g.,
Submit one specimen per test requested. Specify the exact specimen source/origin (e.g., al). Indicate a specific test number on the test request form.
2 - 3 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
Rectal specimen collected with Aptima® Unisex collection swab and submitted in the Aptima® swab specimen transport tube
1 swab (rectal)
1 swab (rectal)
Aptima® swab specimen transport tube
Insert the blue-shafted swab, labeled "unisex collection swab for endocervical and male urethral specimens," 2 inches to 4 inches into the rectum and rotate to sample the mucosal surfaces. Do not use the white-shafted swab; discard this swab. Remove the cap from the swab specimen transport tube and immediately place the specimen collection swab into the transport tube. Carefully break the swab shaft at the scoreline; use care to avoid splashing of the contents. Recap the swab specimen transport tube tightly.
Maintain specimen at room temperature or refrigerate (2°C to 30°C).
Inappropriate transport conditions; bacterial swabs; swabs from sites other than rectal; unlabeled specimens or those with a discrepancy between the specimen label and the test request form; Aptima swab transport tube with no swab, two swabs or swab not supplied by Hologic; Aptima swabs greater than 60 days from collection; any transport device other than an Aptima swab transport
This test is used for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae in patients who are eligible for or who are receiving pre-exposure prophylaxix for HIV (PrEP).
This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.
Nucleic acid amplification (NAA)
|Order Code||Order Code Name||Order Loinc||Result Code||Result Code Name||UofM||Result LOINC|
|188725||PrEP: Ct/GC NAA, Rectal||188608||C. trachomatis, NAA, Rectal||80363-5|
|188725||PrEP: Ct/GC NAA, Rectal||188632||N. gonorrhoeae, NAA, Rectal||80366-8|
|188725||PrEP: Ct/GC NAA, Rectal||019054||N/A|
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