Epic Code LAB3522 Discontinued: APTIMA Chlamydia Gonococcus
Interface Order Alias
11777
Clinical Information
Chlamydia trachomatis (CT) is the major cause of genital chlamydial infections in men and women. CT can cause nongonococcal urethritis, epididymitis, proctitis, cervicitis, acute salpingitis, and Pelvic Inflammatory Disease (PID). CT infections are often asymptomatic in both males and females. Children born to infected mothers are at significantly higher risk for inclusion conjunctivitis and chlamydial pneumonia.
N. gonorrhoeae is the causative agent of gonococcal (GC) infections, the majority of which are uncomplicated lower genital tract infections and may be asymptomatic. However, if left untreated in women, infections can ascend and cause PID which can manifest as endometriosis, salpingitis, pelvic peritonitis, and tubo-ovarian abscesses. A smaller percentage of persons with gonococcal infections may develop disseminated Gonococcal Infection.
Cervical specimens in ThinPrep Pap Test vials containing PreservCyt Solution, APTIMA vaginal swabs, APTIMA endocervical unisex swabs, and male and female urine specimens from symptomatic and asymptomatic individuals are approved for testing. Other specimen types are not acceptable.
Improper collection of the specimen may results in invalid results. If the lab receives a swab specimen transport tube with no swabs, two swabs, a cleaning swab, or a swab not supplied by Hologic the specimen must be rejected.
A negative test result does not preclude the presence of a CT or GC infection because results are dependent on adequate specimen collection, absence of inhibitors, and sufficient rRNA to be detected.
If a specimen has small numbers of CT and GC cellular material, uneven distribution may occur which may affect the ability to detect small numbers of organisms in the collected material. If negative results from the specimen do not fit with the clinical impression, a new specimen may be necessary.
Results for CT and/or GC will be reported as Positive, Negative (presumed negative for CT and/or GC rRNA) or Equivocal. For specimens giving an Equivocal (indeterminate) result, a new specimen should be collected.
Reference Range
Negative
Performing Department
Formerly
Cytology or Molecular Diagnostics
Performing Department Laboratory Location
Corewell Health Reference Laboratory, Grand Rapids, MI
Corewell Health Advanced Technology Laboratory, Grand Rapids, MI
Methodology
The APTIMA Nucleic Acid Amplification Test (NAAT) utilizes target capture, Transcription-Mediated Amplification (TMA) and Dual Kinetic Assay (DKA) technologies for the detection of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC).
CPT
87591, 87491
CDM Code
3068759104, 3068749101
Epic Test ID
1230100359
LOINC
CHLAMYDIA NAAT APTIMA: 43304-5
GONOCOCCUS NAAT APTIMA: 43305-2
Mayo Access Code
SHO11777
Reviewed Date
3/23/2022
Updated Date
8/27/24 - Discontinued