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Test Code CTGC C.trach/N.gonorr Amplified RNA

Performing Laboratory

Hunterdon Medical Center Laboratory

Useful For

Qualitative detection and differentiation of Chlamydia trachomatis (CT) and/or Neisseria gonorrhaeae (GC) by Nucleic Acid Amplification.

Specimen Required

 

Specimen Types
Vaginal
Cervix
Urethral
Rectal
Throat
Urine

 

Container Types
Gen-Probe® APTIMA Multitest Swab® (Orange)
Gen-Probe® APTIMA Unisex  Swab® (White)
Gen-Probe® APTIMA Urine Transport (Yellow) Volume must be between the two black lines on the tube.

 

Urine Collection and Handling

1. The patient should not have urinated for at least 1 hour prior to specimen collection.

2. Female patients: Do not clean labial area prior to collection.

3.  Collect urine in clean collection cup with no preservatives. Collect 20-30 mL from initial stream.

4. Handling of specimen: Remove cap and transfer 2mL of urine into the urine specimen transport tube using the disposable pipette provided. The correct volume of urine has been added when the fluid level is between the black fill lines on the urine specimen transport tube label.Recap the urine specimen transport tube tightly.

Specimen Stability Information

 

Temperature Time Frame
Ambient 15-25°C 30  Days
Refrigerated 2-8°C 30 Days

Specimen Transport Temperature

 

Temperature
Ambient 15-25°C
Refrigerated 2-8°C

Reject Due To

Expired collection kit.

Leaking specimen containers

No swab, two swabs, cleaning swab in collection container.

Incorrect container, unlabeled or mislabeled specimen.

Insufficient volume of specimen.

Day(s) Test Setup

Monday through Friday

Reference Values

Negative

Methodology

Nucleic Acid Amplification

CPT Code Information

CPT Codes  
C. trachomatis 87491
N. gonorrhaeae 87591

LOINC Code Information

LOINC Codes  
C. trachomatis 43304-5
N. gonorrhaeae 42205-2