Geisinger Medical Laboratories/Geisinger Proven Diagnostics Test Catalog

Test Name: Sunquest Test Code Epic Procedure Code Or ID CPT Code:  

NEISSERIA AMPLIFIED

ORDERING INFORMATION:
Sunquest Test Code:
GCA      Geisinger Epic Procedure Code: 87591.02         Geisinger Epic ID: 20526

SPECIMEN COLLECTION
Specimen type:
Male urethral, female endocervical, male and female urine, vaginal
Preferred collection container:
Alternate Collection Container:
Aptima® Vaginal Swab Specimen Collection Kit
Special notes:
See GML GC CT Specimen Collection Guide. See Microbiology Collection Appendix for collection instructions. Check expiration date on transport device before use.

For specimens collected in listed collection devices/kits, follow instruction provided.
For Aptima® Unisex Swab Collection Kit (preferred device), use blue-shafted swab only. For Aptima® Vaginal Swab Specimen Collection Kit, use pink-shafted swab only. NOTE: The Aptima® Vaginal Swab Specimen Collection Kit is the only collection kit approved for vaginal specimens. This is not the primary collection device for GML.

This test cannot be added onto a urine specimen that has already been submitted to the laboratory for testing. A fresh urine collection is required. You can add on a CTA, GCA, or TVGA on a urine specimen that has either one of these tests already ordered.

SPECIMEN PROCESSING
Specimen processing instructions:
If a single urine specimen is collected and other testing is requested, the urine specimen must be transferred to an Aptima® urine collection kit before any other testing on the urine is performed. 
Transport temperature:
Swab Specimens: Room temperature (2-30°C is acceptable). Urine Specimens: Room temperature (2-30°C is acceptable) in Aptima® Urine Collection Kit. Room temperature (2-30°C is acceptable) collected in sterile specimen container, stable for only 24 hours.
Specimen stability:
Swabs: Stable for 60 days at 2-30°C
Urines: In Aptima® Urine Transport, stable 30 days at 2-30°C. In sterile container, stable for 24 hours at 2-30°C.
Rejection criteria:
Improperly labeled/identified specimens. Expired transport media. Collection swabs other than Aptima® supplied/approved collection swabs. More than one swab in collection device. White cleaning swab in collection device. No swab in collection device. Urine in preservatives. Urine collection tube underfilled/overfilled. Specimens stored or transported at incorrect temperature. Specimens which exceed stability limits. Frozen specimens (unless -70°C).

TEST DETAILS
Reference interval:
No Neisseria gonorrhoeae detected by transcription-mediated nucleic acid amplification
Critical values/courtesy alerts:
Neisseria gonorrhoeae detected by transcription-mediated nucleic acid amplification
CPT code(s):
87591
Note: The billing party has sole responsibility for CPT coding.  Any questions regarding coding should be directed to the payer being billed.  The CPT codes provided by GML are based on AMA guidelines and are for informational purposes only.
Test includes:
Molecular target amplification and detection of Neisseria gonorrhoeae
Methodology:
Target Capture
Transcription-Mediated Amplification (TMA)
Dual Kinetic Assay (DKA)
Synonyms:
Gen-Probe, DNA Probe, RNA Probe
Neisseria probe, Neisseria gonorrhoeae probe
GC probe, Amplified GC, Amplified Neisseria gonorrhoeae
GC culture, Neisseria gonorrhoeae, gonococcus
Probe
Gonorrhoeae probe
Clinical significance:
Neisseria gonorrhoeae is the causative agent of gonorrhea, a sexually transmitted disease.
Doctoral Director(s:)
Donna Wolk PhD, D(ABMM), Raquel Martinez, PhD, D(ABMM)    
Review Date: 05/06/2019

Performing Locations

Geisinger Medical Center

Performing laboratory: Microbiology
Technical Lead: Francis Tomashefski
Frequency: Monday-Friday, 1st shift
Performed stat? No
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