Epic Code LAB744 Abbott multi-Collect Chlamydia Gonococcus, PCR, Urine
Test Name Alias
Chlamydia trachomatis | CT GC | 8446
Interface Order Alias
10841
Clinical Information
The predictive value of an assay depends upon the prevalence of disease in any population. In populations where the prevalence of sexually transmitted diseases (STD) are high, a positive test result is more likely to be a true positive than in populations of low prevalence of disease.
In cases where a patient’s clinical symptoms or risk factors are inconsistent with GC or CT urogenital infection, positive results should be carefully assessed and retesting using another procedure such as culture may be necessary. Additional testing is recommended in any circumstance when a false positive or false negative result could lead to adverse medical, social or psychological consequences. Samples containing blood may give false positive results.
A negative test result does not exclude the possibility of infection which may be due to improper specimen collection, specimen mix-up, technical error, concurrent or previous antimicrobial therapy or a low number of organisms present in the specimen below the sensitivity of the test. The presence of inhibitors to polymerase chain reactions such as lubricants and cervical secretions may result in a false negative test result.
This method is approved only for male and female urines, female endocervical swabs, female vaginal swabs and male urethral swabs. Specimens from the respiratory tract, eyes, and rectum are not acceptable.
This method is not approved for use in young children.
In medical-legal cases, culture for GC and CT should also be done.
Collection Instructions
Specimen Collection: Urine (First void)
Container(s): Sterile urine cup (with lid) or Abbott multicollect kit
Preferred Volume to Collect: 30.0 mL
Minimum Volume to Collect: 10.0 mL
Neonate Volume to Collect: 10.0 mL
Collection Instructions:
- First void ("dirty") urine is included in this collection, this is collected before a UA specimen, if both are needed.
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Do not cleanse the genital area prior to specimen collection.
- Patient should not have urinated for at least one hour prior to sample collection
- Patient Collection Instructions are located in the menu on the left.
- Specimen should not be submitted with orders for culture.
Abbott multicollect kit instructions
- Follow directions above to obtain a first void urine specimen.
- Discard specimen collection swab, it is not required for urine specimen collection.
- Unscrew the transport tube cap, taking care not to spill the transport buffer within.
- Handle the cap and tube carefully to avoid contamination.
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Use the plastic transfer pipette to transfer urine from the collection cup into the transport tube until the liquid level in the tube falls within the clear fill window of the transport tube label or else a new specimen should be collected.
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Do not overfill. Slightly more than one full squeeze of the transfer pipette bulb may be required to transfer the necessary volume of urine specimen.
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Recap the transport tube carefully. Ensure the cap seals tightly.
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Label the transport tube with sample identification information, including date of collection. Take care not to obscure the fill window on the transport tube.
NOTE (for either collection): Failure to collect a urine specimen, including the first part of the voiding, may decrease the sensitivity of this test. If the specimen cannot be delivered to the laboratory within a few hours after collection it should be stored and refrigerated until it can be delivered. Specimen must be received in laboratory for analysis within 24 hours of collection.
Transport Temperature: Refrigerate
Specimen Stability
If the urine is put directly in the Abbott collection tube, the following applies:
Ambient: 14 days 2oC – 30oC in Abbott multi-collect specimen container
Refrigerate: 14 days 2oC -30oC in Abbott multi-collect specimen container
Laboratory Retention: 7 days
If only a urine cup is received Refrigerate: 24 hours
Laboratory Retention: 24 hours
Test Frequency
Available Monday - Friday, usual TAT 2 - 5 days
Reference Range
Negative
Performing Department
IMMUNOCHEMISTRY
Performing Department Laboratory Location
Spectrum Health Regional Laboratory, Grand Rapids, MI
Methodology
Polymerase chain reaction (PCR)
CPT
87491, 87591
CDM Code
4088885, 4088884
Epic Test ID
1230100475
Beaker LOINC
CHLAMYDIA MDI RESULT: N/A
CHLAMYDIA PCR URINE: 6357-8
GONOCOCCUS MDI RESULT: N/A
GONOCOCCUS PCR URINE: 21416-3
Mayo Access Code
SHO8446
Reviewed Date
12/13/2021
Beaker Names
Beaker Procedure Name: CHLAMYDIA/GC DNA URINE
Beaker Display Name: Chlamydia Gonococcus, PCR, Urine
BEAKER TEST NAME: CHLAMYDIA/GONOCOCCUS PCR, URINE
BEAKER TEST REPORT NAME: Chlamydia/Gonococcus PCR, Urine
Beaker Synonyms
No synonym on file
Beaker Location, Container and Temperature
BW IMMUNOCHEM: URINE CUP R (Preferred)-Refrigerated