TEST NAME. Lab Test - Chlamydia trachomatis / GC PCR Panel | Akron Children's Hospital Endocervical swab: Remove excess mucus from the cervical os and surrounding mucosa using the cleaning swab (white-shaft swab in the package with red printing). Your doctor might order a urine culture if you have symptoms of a UTI, which can . CPT Coding 87491 -Chlamydia trachomatis Amplified RNA 87591 -Neisseria gonorrhoeae Amplified RNA 87661 -Trichomonas vaginalis Amplified RNA Test Classification Female urine for CT/GC and male urine for Trich samples: This test has been modified from the manufacturer's instructions. TEST: 188070 CPT: 87491; 87529 (x2); 87591; 87661 Print Share Include LOINC in print Expected Turnaround Time 3 - 4 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. A gonorrhea test is performed in two different situations: Screening: Screening tests look for diseases when a person isnt experiencing symptoms in order to detect the disease earlier. Turnaround time is defined as the usual number of days from the date of pickup of a specimen for Recap the swab specimen transport tube tightly. The patient should not have urinated for at least one hour prior to specimen collection. LABupdate: Candida Species Identification by NAA, Microbiology Specimen Collection and Transport Guide, Patient Information: Chlamydia, Gonorrhea, and Trichomoniasis, Protect Your Patients From the Consequences of Untreated Chlamydia, Gonorrhea, and Trichomonas: Easily Detected and Easily Treated, Trichomonas vaginalis: Detect More Infections With Nucleic Acid Amplification. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. U.S. Department of Health and Human Service. Patient Self-Collection: Partially open the package of the Gen-Probe Aptima vaginal swab kit. Discard this swab. Uncap the vial and place it on the work surface with the threads facing up. As such, health plan access, test ordering, and billing processes may differ from those of Quest Diagnostics. For more information, please view the literature below. Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC 724344: Cadmium Std Profile, Blood/Ur: 085340: Cadmium, Blood: ug/L: 5609-3: 724344: Cadmium Std Profile, Blood/Ur: 072713: Cadmium, Urine: ug/L: 21130. Webcpt code for gc chlamydia urine test labcorp. allowed for additional confirmatory or additional reflex tests. Recommended Reading: Treatment For Chlamydia And Trichomoniasis. Urine specimen: The patient should not have urinated for at least one hour prior to specimen collection. Chlamydia/N. CPT: 87491; 87591 Print Share Include LOINC in print Synonyms Chlamydia/Gonococcus, Amplicor PCR Chlamydia/Gonococcus, Aptima TMA Chlamydia/Gonococcus, LCR Test Includes Detection of Chlamydia trachomatis and Neisseria gonorrhoeae by nucleic acid amplification technology Special Instructions Submit one specimen per test requested. Ordering Restrictions may apply. Female patients should not cleanse the labial area prior to providing the specimen. These days, bacterial DNA testing is considered a better option. The CDC currently recommends oral and anal testing of MSM who have had receptive oral or anal sex, respectively, within the previous year.4 Both C trachomatis and N gonorrhoeae testing are recommended on the anal specimens. Gently invert the tube two to three times to ensure complete mixing of the specimen. Hepatitis Panel, Acute with Reflex to Confirmation Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. Swirl the brush vigorously to release additional material. HIV p24 Antigen/Antibody With Reflex to Confirmation [083935] requires a dedicated, unopened, gel-barrier tube or red-top tube sent directly to the testing facility. If the soft tip is touched, the swab is laid down, or the swab is dropped, use a new Aptima Vaginal Swab Specimen Collection Kit. Additional information regarding LOINC codes can be found at LOINC.org, including the LOINC Manual, which can be downloaded at LOINC.org/downloads/files/LOINCManual.pdf. Tighten the cap on the ThinPrep container so that the torque line on the cap passes the torque line on the vial. Rectal and throat swabs are acceptable for C trachomatis and N gonorrhoeae NAAT testing. Chlamydia Gonorrhea & Trichomoniasis | Labcorp OnDemand Specimen with incorrect patient identification; unlabeled specimen; inappropriate specimen transport conditions; specimens received after prolonged delay (usually >72 hours); specimen leaked in transit; specimen in expired transport or incorrect transport device; specimens with inappropriate source for test requested; specimen with fixative or additives; Aptima urine transport >30 days from collection; Aptima urine transport with incorrect specimen volume; specimen in ProbeTec UPT transport; ProbeTec Q-swabs; urine in sterile container, Detect Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium. It is recommended to ask all patients who may be indicated for this test about biotin supplementation. . You should get tested for STDs, including chlamydia and gonorrhea, before and after every sexual encounter with new partners. Its my Answered by a verified OB GYN Doctor Does a positive leukocyte esterase urine test, in the absence of anything else being positive, indicate gonorrhea or chlamydia? All Rights Reserved. It is also common among African Americans. Cpt Code For Gc Chlamydia Urine Test Labcorp. Specimen with incorrect patient identification; unlabeled specimen; inappropriate specimen transport conditions; specimen leaked in transit; specimen in expired transport or incorrect transport device; specimens with inappropriate source for test requested; specimen with fixative or additives; APTIMA urine transport >30 days from collection; APTIMA urine transport with incorrect specimen volume; <15 mL urine submitted in sterile container; receipt of urine in sterile container >72 hours from collection; APTIMA swab transport >60 days from collection; APTIMA swab specimens with incorrect specimen volume; APTIMA swab specimen without a swab; cleaning swab (white-shaft swab) in APTIMA swab transport; any non-Gen-Probe swab submitted in APTIMA transport device; wooden-shafted swab in transport device; transport device with multiple swabs; female urethral swab; bloody or grossly mucoid specimens; bacterial swabs; specimen in ProbeTec UPT transport; ProbeTec Q-swabs; BD ProbeTec ET male urethral swab; swab specimen in universal transport media or viral transport media; SurePath vial, Detect Chlamydia trachomatis and Neisseria gonorrhoeae. Turnaround time is defined as the usual number of days from the date of pickup of a specimen for Recap the swab specimen transport tube tightly. (Press Enter or Space to Go to Landing Page or Press Down to expand Menu), Federally Qualified Health Centers (FQHCs), Combatting Modern Slavery and Human Trafficking Statement. It is recommended to use powder-free gloves and an individually wrapped, disposable pipetting device with an aerosol barrier tip that is sized appropriately for the volume being withdrawn and dispensed. Rinse the collection device in the PreservCyt solution by pushing the brush into the bottom of the vial 10 times, forcing the bristles to bend apart to release the cervical material. Recap the swab specimen transport tube tightly. Top 3Reference Laboratory Test Catalogs for MiscellaneousLab TestOrders: As of 23 February 2023, NorDx is transitioning to Aptima collection devices for this test. C. trachomatis; PDF Labcorp Drug Test Requisition Form - annualreport.psg.fr Carefully dispense the aliquot into the appropriately labeled Aptima tube. Remove the cap from the swab specimen transport tube and immediately place the specimen collection swab into the specimen transport tube. Aliquot removal from low-cellularity may leave insufficient material in the PreservCyt sample vial for preparation of a satisfactory ThinPrep Pap Test slide. Add urine to the Aptima COMBO 2 urine collection device. The FDA has determined that such clearance or approval is not necessary. testing to when the result is released to the ordering provider. Most at-home chlamydia tests are self-collection kits, which allow you to obtain a swab or sample of urine at home and return it to a laboratory by mail. 6. Testing schedules may vary. Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. Tests are available to detect chlamydia at home. One swab, 2 mL of a 20 mL to 30 mL urine collection, or entire liquid cytology vial, Gen-Probe Aptima swab or Aptima urine specimen transport; ThinPrep liquid cytology vial. Accessed March 2022 at https://www.hhs.gov/sites/default/files/STI-National-Strategic-Plan-2021-2025.pdf. Vaginal swab collection: Care provider specimen: Collect vaginal fluid sample using the Gen-Probe Aptima Vaginal Swab Kit by contacting the swab to the lower third of the vaginal wall, rotating the swab for 10 to 30 seconds to absorb the fluid. When you have symptoms of chlamydia, such as pain during urination, vaginal discharge and abdominal pain or unusual discharge from the penis, pain on urination or painful, swollen testicles, Having an STD in the past or a sex partner recently treated for an STD. Labs & Appointments Toggle Labs & Appointments, Billing & Insurance Toggle Billing & Insurance, Diseases & Conditions Toggle Diseases & Conditions, OnDemand Testing Toggle OnDemand Testing, Testing by Disease & Condition Toggle Testing by Disease & Condition, Testing & Services For Toggle Testing & Services For, Hospitals & Physician Systems Toggle Hospitals & Physician Systems, Managed Care Health Plans Toggle Managed Care Health Plans, Lab Data Integrations & Tools Toggle Lab Data Integrations & Tools, Employee Wellness & Testing Toggle Employee Wellness & Testing, Government & Education Toggle Government & Education, Therapeutic Indications Toggle Therapeutic Indications, Development Phase Toggle Development Phase, Compounds & Molecules Toggle Compounds & Molecules, Detection of Chlamydia trachomatis and Neisseria gonorrhoeae by nucleic acid amplification technology. Female patients should not cleanse the labial area prior to providing the specimen. It works differently than a bacterial culture. Carefully insert the swab into the vagina about two inches past the introitus and gently rotate the swab for 10 to 30 seconds, making sure the swab touches the walls of the vagina so that moisture is absorbed by the swab. Chlamydia/Neisseria gonorrhoeae RNA, TMA, Urogenital No Chlamydia trachomatis or Neisseria gonorrhoeae detected. The final volume must be between the two black lines on the device (about 2 mL). Store in a specimen transport tube at 2C to 30 . female and male urine specimens. Routine chemistry and bacterial or fungal culture require use of the clean catch midstream collection technique. Dispose of the pipette tip into a biohazard bag containing absorbent material soaked with bleach.