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. If youve been in a long-term, monogamous sexual relationship the same partner, you should still test for STDs once a year. Female patients should NOT cleanse the labial area prior to specimen collection. The final volume must be between the two black lines on the device (about 2 mL). Please provide SERVICE AREA INFORMATION to find available tests you can order. Female patients should not cleanse the labial area prior to providing the specimen. Reported: 4 days from receipt of the specimen. C trachomatis and N gonorrhoeae have been isolated from extra-genital sites in men who have sex with men and sexually active, heterosexuals who engage in unprotected oral or anal sex. 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. If the soft tip is touched, the swab is laid down, or the swab is dropped, use a new Aptima swab specimen collection kit. Aliquot removal from low-cellularity may leave insufficient material in the PreservCyt sample vial for preparation of a satisfactory ThinPrep Pap Test slide. Schillie S, Vellozzi C, Reingold A, et al. When doctors screen for gonorrhea, they may also screen for other STDs at the same time. Chlamydia/Neisseria requires use of a first catch (the initial stream of urine that will wash organisms out of the urethra of men or women). A full range of tests for STI screening and confirmation are available from ACL Laboratories. 9. CPT Code a. If an NAAT is positive for C trachomatis or N gonorrhoeae 3 or more weeks after the end of treatment,6 first ensure that the patient has complied with the prescribed therapy and that the patient denies having sex after treatment with an untreated or new sex partner. Testing schedules may vary. Chlamydia/Neisseria gonorrhoeae RNA, TMA, Urogenital Test Code 11363 CPT Code (s) 87491, 87591 CPT Code is subject to a Medicare Limited Coverage Policy and may require a signed ABN when ordering. The final volume must be between the two black lines on the device (about 2 mL). 8. Test code 11363 , 11361 , 11362 Question 1. CPT Code(s) 87491, 87591, 87661. Even better, they do not require a live bacterial sample. (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. Patient should not have urinated for at least 2 hours prior to collection. 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). Remove the cap from the swab specimen transport tube and immediately place the specimen collection swab into the specimen transport tube. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Note: Specimens cannot be collected and used for Chlamydia/Neisseria and routine chemistry or urine culture. (Min: 0.3 mL) Storage/Transport Temperature Room temperature Unacceptable Conditions Hemolyzed, Icteric, or lipemic specimens CPT Code 87110: Culture, Chlamydia, any source CPT Code 87270: Infectious agent antigen detection by immunofluorescent technique; Chlamydia trachomatis CPT Code 87320: Infectious agent antigen detection by enzyme immunoassay technique, qualitative or semiquantitative, multiple-step method; Chlamydia trachomatis Prevention of Hepatitis B Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices. Allow bleach to contact work surfaces and pipettors for at least one minute and then follow with a water rinse. Withdraw the swab carefully; avoid contact with the vaginal mucosa. The Xpert CT/NG Assay provides qualitative results. In the specimen transfer area, place a test tube rack containing a sufficient number of Aptima tubes to the number of ThinPrep Pap specimens being tested for Ct/Ng. 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). 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. Expected Turnaround Time 2 - 3 days Aliquot removal may leave insufficient material in the PreservCyt sample vial for performance of ancillary testing (ie, reflexive HPV testing) using the residual specimen following preparation of a ThinPrep Pap Test. These types of testing are sensitive to even very small amounts of bacterial DNA. Tests are available to detect chlamydia at home. Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. 3. If negative results from the specimen do not fit with the clinical impression, a new specimen may be necessary. Free fact sheets, free STI medications for patients and partner (s) who test positive for Chlamydia, call the Sexual Health Program, 721-7520 (or toll free 1 877 721-7520) For additional information and references, visit SMDHU Sexual Health AIDS & Sexual Health InfoLine, 416-392-2437 Other Resources Patient Self-Collection: Partially open the package of the Gen-Probe Aptima vaginal swab kit. Testing schedules may vary. Tightly screw on the cap. It is very essential to screen, and diagnose chlamydia in order to prevent its spread and possible long-term complications. Although much less commonly used, cell cultures can help diagnose a chlamydia infection. Gonorrhea is a sexually transmitted disease caused by the spread of the Neisseria gonorrhoeae bacteria. Chlamydia is a very common sexually transmitted disease. Tighten the cap on the ThinPrep container so that the torque line on the cap passes the torque line on the vial. Use: Updated 2/28/22. Tightly screw on the cap. 13. Direct patient to provide a first-catch urine (approximately 20 mL to 30 mL of the initial urine stream) into a urine collection container free of any preservatives. Swirl the brush vigorously to release additional material. Recap the swab specimen transport tube tightly. Carefully break the swab shaft at the scoreline; use care to avoid splashing of the contents. gonorrhoeae and T. vaginalis RNA, Qualitative, TMA, Pap Vial - Diagnosis of the three most common sexually transmitted infections. allowed for additional confirmatory or additional reflex tests. Vaginal swab: 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 and rotating the swab for 10 to 30 seconds to absorb fluid. There is no evidence of degradation of cytology results by aliquot removal, however, this cannot be ruled out for all specimens. 2023 Laboratory Corporation of America Holdings. LabCorp Test #: 377036, CPT: 81001. Submit one specimen per test requested. When your order from Health Testing Centers there is no need to visit a std clinic, neighborhood health center or public health clinic. Turnaround time is defined as the usual number of days from the date of pickup of a specimen for Chlamydia Trachomatis And Neisseria Gonorrhoeae Detection - Test Code. WebCPT Code Description Start Date End Date Max Allowed 87320 Chlamydia trachomatis antigen detection using qualitative multiple step enzyme immunoassay technique 4/1/2022 3/31/2023 $18.00 87490 Chlamydia trachomatis detection by nucleic acid using direct probe technique 4/1/2022 3/31/2023 $30.00 81025 Urine pregnancy test using visual Specify the exact specimen source/origin (eg, endocervical). Quest Diagnostics offers throat- and anal -based testing: You May Like: Causes Of Chlamydia In Females, Introduction. Because cytology/HPV testing and STD testing address different clinical questions, aliquot removal may not be suitable for all clinical situations. Urine specimen: The patient should not have urinated for at least one hour prior to specimen collection. It is essential to have an early screening and diagnosis for both infections and, take the full course of prescribed antibiotics. Test Code CT/GC CHLAMYDIA TRACHOMATIS AND NEISSERIA GONORRHOEAE DETECTION BY NUCLEIC ACID AMPLIFICATION . This panel provides an assessment of sexual health by screening for three common sexually transmitted infections : For your urine test, its best not to urinate for two hours before your sample collection urinating within this period could affect the accuracy of your results. specifically Chlamydia trachomatis and Neisseria gonorrhoeae. Collection of larger volumes of urine may result in specimen dilution that may reduce test sensitivity; lesser volumes may not adequately rinse organisms into the specimen. If an at-home chlamydia test returns positive results, a doctor may suggest confirmation testing with a laboratory-based method. Vaginal, endocervical, or male urethral swab, first-void urine (patient should not have urinated for one hour prior to specimen collection), or cervical cells in liquid cytology vial. All Rights Reserved. Chlamydia/Gonococcus/Mycoplasma genitalium, NAA, Urine TEST: 180049 CPT: 87491; 87563; 87591 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. The final volume must be between the two black lines on the device (about 2 mL). If reflex test is performed, additional charges/CPT code(s) may apply. Carefully insert the swab into the vagina about 2" 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. Withdraw the swab carefully. Although the findings were not statistically significant, positivity appeared to. As such, health plan access, test ordering, and billing processes may differ from those of Quest Diagnostics. Regular screening for gonorrhea in heterosexual men without symptoms is not generally recommended. CPT Code(s): 87491; 87591; Specimen Requirements: . Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. Summary and Explanation of the Test . . The people you see wont know for what you are getting tested for. Browse our menu of tests. Specimen must be collected and transported with test-specific kit (ARUP supply #55224). 2020. testing to when the result is released to the ordering provider. 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. Chlamydia cell cultures may be used in children with a suspected chlamydia infection, when evaluating potential infections in the anus or rectum, and when initial treatment for chlamydia is unsuccessful. Urine specimen: The patient should not have urinated for at least one hour prior to specimen collection. 87491: Infectious Agent Detection by Nucleic Acid (DNA or RNA), Chlamydia . Remove the swab. Blood tests can be used to test for the following sexually transmitted diseases: Urine tests are typically used to detect the following sexually transmitted diseases: Whether testing is done via blood or urine samples, the lab that processes those samples is looking for key indicators of an STD infection. 2. Carefully dispense the aliquot into the appropriately labeled Aptima tube. It affects both men and women, of all ages. In some cases, additional time should be Tightly screw on the cap, Amphetamine Confirmation, Ur Amylase, Body Fluid Anabolic Steroid Screen Analyze 20-25 cells ANCA Panel Androstenedione LCMS Chlamydia trachomatis, NAA Chlamydia/GC Amplification Chromogranin A Chromosome Analysis, BM Chromosome, Leukemic Blood Chromosomes Leuk/Lymph. Transfer the specimen to the Aptima urine specimen collection kit if 14 years of age or older Urine Specimen Collection Instructions: 1. Assay interference may be observed in the presence of blood, mucin, bilirubin, or Vagisil feminine powder with urine specimens. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Permission is granted in perpetuity, without payment of license fees or royalties, to use, copy, or distribute the LOINC codes for any commercial or non-commercial purpose, subject to the terms under the license agreement found at https://loinc.org/license/. Recap the swab specimen transport tube tightly. Risk factors that impact the frequency of gonorrhea screening include: You May Like: How Common Is It For Chlamydia To Come Back, Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC 183198: Ct/Ng NAA rfx Tv NAA: 188106: Chlamydia by NAA: 43304-5: 183198: Ct/Ng NAA rfx Tv NAA: 188107: Gonococcus by NAA: 43305-2: 183198: Ct/Ng NAA rfx Tv NAA: 183199: Trich vag by NAA Rfx: N/ Vaginal swab: Collect vaginal fluid sample using the Gen-Probe Aptima swab by contacting the swab to the lower third of the vaginal wall and rotating the swab for 10 to 30 seconds to absorb fluid. Test Code: GCAT, CHAT, GCCAT (Battery for both tests) CPT 4 Code: 87491 (Chlamydia) 87591 (GC) Specimen Requirements: Urine: First catch urine (approximately 20 to 30 ml of initial urine stream) into urine collection cup free of any preservatives. Men, on the other hand, may show symptoms like pain and swelling of the testicles, painful urination, and burning, itching and cloudy discharges at the tip of the penis. Testing schedules may vary. - GC NGC : 3 x 1.7 mL : Non-infectious . (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. If not diagnosed and treated, it can cause severe health problems. Remove the cap from the swab specimen transport tube and immediately place the specimen collection swab into the transport tube. This training should be provided by Hologic. Chlamydia trachomatis/Neisseria gonorrhoeae RNA, TMA. Chlamydia trachomatis / Neisseria gonorrhoeae DNA, SDA Test code (s) 17305 Question 1. Please provide SERVICE AREA INFORMATION to confirm Test Code for the lab that services your account or to find available tests you can order. Chlamydia trachomatis : Symptoms, Diagnosis and Treatments. Withdraw the swab without touching the skin. Withdraw the swab without touching the skin. Gen-Probe Pace transport system; bacterial swab specimen; transport with multiple swabs; specimen received in grossly leaking transport container; specimen submitted in fixative or additives; specimen received in expired transport media or incorrect transport device; inappropriate specimen transport conditions; specimen received after prolonged delay in transport (usually more than 72 hours); swab in transport device; unlabeled specimen or name discrepancy between specimen and request label; prequot specimens with more than 1 mL of PreservCyt added, Detect Chlamydia trachomatis and/or Neisseria gonorrhoeae. Chlamydia trachomatis is a type of gram-negative bacteria that is responsible for causing Chlamydia infection. Dispose of the pipette tip into a biohazard bag containing absorbent material soaked with bleach. 5. download here chlamydia gc screening requisition form supply order form of america llc home healthcare supply A complete menu in microbiology, serology, and cytology to meet CGPT Chlamydia/GC Amplified Probe Chlamydia trachomatis, Gonorrhea CGLP Chlamydia/GC Amplified Probe, from ThinPrep vial NAA TVLP Trichomonas Vaginalis from ThinPrep vial TPS. People at risk of getting chlamydia need to be tested, regularly. 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? CPT Code: 87491, 87591. 91448. All Rights Reserved. If the soft tip is touched, the swab is laid down, or the swab is dropped, use a new Aptima swab specimen collection kit. Patient self-collection instructions: Partially open the package. TEST CODE. U.S. Preventive Services Task Force: Screening for Hepatitis B Virus Infection in Pregnant Women: Recommendation Statement. Sexually Transmitted Infections: National Strategic Plan for the United States 2021-2025. Option 2: Urine Specimen: The patient should not have urinated for at least one hour prior to specimen collection. When opting for concurrent cytologic and STD testing, providers should consider risk and clinical history (eg, disease prevalence, patient age, sexual history, or pregnancy) as well as specimen suitability (ie, exudates of bleeding) that can impact diagnostic reliability.1,2. Most persons with C trachomatis detected at oropharyngeal sites do not have oropharyngeal symptoms. 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). Microbiology Specimen Collection and Transport Guide, PreservCyt fluid (removed prior to processing of the vial on the ThinPrep processor) placed in the Gen-Probe Aptima swab transport tube, 1 mL; although up to 4 mL may be removed from the ThinPrep vial, only 1 mL of PreservCyt will be placed in the transport device, Gen-Probe Aptima swab transport or Gen-Probe Aptima specimen transfer kit with 1 mL of PreservCyt fluid (do not use swabs provided with Aptima kit), ThinPrep preservative vial processing: ThinPrep instructions for removal of material are specifically listed in the ThinPrep 2000 and ThinPrep 3000 System Operator's manual Addenda. Please note ReproSource is not a Medicare/Medicaid provider. in juliet papa 1010 wins. C. trachomatis; 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. Chlamydia/Neisseria Gonorrhoeae RNA, TMA, Urine Test Code 36341 This test is not available in all locations. Nucleic acid amplification testing is recommended for detection of Chlamydia trachomatis from endocervical or urethral specimens. Hepatitis B. CDC website: www.cdc.gov/hepatitis/hbv/index.htm. Note: For testing, aliquots must be transferred to Aptima specimen transport tubes or Aptima Unisex specimen transport tubes (both referred to as Aptima tube in the following procedure) from ThinPrep vials within seven days of specimen collection when ThinPrep vials are stored at 15C to 30C. Both men and women can experience fertility problems after a chlamydia infection. For more information, please view the literature below. This type of test detects the genetic material of Chlamydia trachomatis. Routine chemistry and bacterial or fungal culture require use of the clean catch midstream collection technique. Infected women report abnormal vaginal discharges, bleeding between periods, pain during period, when urinating and while having sex, as well as itching and burning around the area of the vagina. Screening and Referral Algorithm for Hepatitis B Virus (HBV) Infection Among Pregnant Women. Testing Performed: Monday - Saturday; Results in 1-3 days. If reflex testing is performed, additional charges/CPT code(s) may apply. Maintain specimen at room temperature or refrigerate (2C to 30C). Aliquots must be transferred to the Aptima tube within seven days of collection. Prior to sampling the patient should not have urinated for at least 1 hour. It is essential in preventing its complications, which could be very drastic, ranging from septicemia and joints infection, to a disseminated gonococcal infection that could infect our heart, brain and spinal cord. First-void urine in Aptima urine transport, 2 mL aliquot of a 20 to 30 mL urine collection. Centers for Disease Control and Prevention (CDC). (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. Direct patient to provide a first-catch urine (approximately 20 to 30 mL of the initial urine stream) into a urine collection cup free of any preservatives. Test Code M14 Chlamydia/GC PCR, Urine Important Note. 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. A urine culture test detects and identifies bacteria and yeasts in the urine, which may be causing a UTI. Put on clean gloves before proceeding to specimen transfer. Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC 180049: Ct Ng M genitalium NAA, Urine: 180024: Mycoplasma genitalium NAA: 88226-6: 180049: Ct Ng M genitalium NAA, Urine: 180050: Chlamydia trachomatis, NAA: 42931-6: 180049: Ct Ng M genitalium NAA, Urine: 180052: Neisseria gonorrhoeae, NAA: 60256-, Read Also: What Medication Do You Take For Chlamydia. female and male urine specimens. A chlamydia and gonorrhea urine test, random detects chlamydia trachomatis and neisseria gonorrhoeae which is generally transmitted through sexual contact with an infected partner. Testing schedules may vary. Tightly screw on the cap. (Press Enter or Space to Go to Landing Page or Press Down to expand Menu), 86592; 86704; 86706; 86803; 87340; 87389; 87491; 87591, Federally Qualified Health Centers (FQHCs), Combatting Modern Slavery and Human Trafficking Statement. The assay may be used to test . Wipe down work surfaces and pipettors with 1:1 bleach:water solution. 6. NorDx Respiratory Panel Quick Guide (non MidCoast), NorDx Respiratory Panel Quick Guide (MidCoast only), 2022 Acceptable Tan Top Usage for Hematology, 2022 Acceptable Alternate Tube Types for Chemistry, 2019 Scarborough NorDx Urine Toxicology Guide, Tick-Bourne Disease Pathogen Testing Information, Individually Orderable IGE Allergens Chart with Test Codes, Biotin Interference Thresholds--Scarborough site, Biotin Interference Thresholds--non-Scarborough sites, Laboratory Corporation of America (LabCorp) Test Menu, Critical Laboratory Values - Scarborough & MMC, Critical Laboratory Values - Mid Coast Hospital, CHLAMYDIA TRACHOMATIS AND NEISSERIA GONORRHOEAE DETECTION BY NUCLEIC ACID AMPLIFICATION, Infectious Agent Detection by Nucleic Acid (DNA or RNA), Chlamydia trachomatis, Amplified Probe Technique, Infectious Agent Detection by Nucleic Acid (DNA or RNA), Neisseria gonorrhoeae, Amplified Probe Technique. Accessed March 2022. Clinical Significance: This assay may be used to test specimens from symptomatic and asymptomatic individuals to aid in the diagnosis of gonococcal and/or chlamydial urogenital disease. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. 15. These instructions include the following statement. These days, bacterial DNA testing is considered a better option. The labs that we utilize are the same that your doctor would send you to test for various other issues such as allergies or cholesterol. allowed for additional confirmatory or additional reflex tests. Transfer enough urine with pipet into the tube provided in the Aptima PCR Urine Sample Packet. Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. Direct patient to provide a first-catch urine (approximately 20 to 30 mL of the initial urine stream) into a urine collection cup free of any preservatives. If a positive result is obtained for either Chlamydia trachomatis or Neisseria gonorrhoeae, testing for Trichomonas vaginalis is performed. Discard the collection device. 2. Chlamydia and gonorrhea urine tests are widely available. Turnaround time is defined as the usual number of days from the date of pickup of a specimen for For oral, anal, or rectal sourcessee test code CTGCO. 2021 Laboratory Corporation of America Holdings and Lexi-Comp Inc. All Rights Reserved. 87491: Infectious Agent Detection by Nucleic Acid (DNA or RNA), Chlamydia trachomatis, Amplified Probe Technique : CHLAMYDIA AND GC DNA URINE; CHLAMYDIA AND GC NON-CERVICAL; Portions 2023 Mayo Foundation for Medical Education . CPT Description. All in on place. 008128: GC (Neisseria gonorrhoeae) Culture Only | Labcorp Specimen Details LOINC Back to Top GC ( Neisseria gonorrhoeae) Culture Only TEST: 008128 CPT: 87081 Print Share Include LOINC in print Synonyms Neisseria gonorrhoeae Culture Culture for Neisseria gonorrhoeae Only Culture for GC Only Genital Culture (GC) Only Gonorrhea Culture 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; <15 mL urine submitted in sterile container; receipt of urine in sterile container >24 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 nonGen-Probe swab submitted in Aptima transport device; wooden-shaft 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; UTM-RT; SurePath vial, Diagnosis of Chlamydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis infections. Instead of trying to grow bacteria, these tests just look for bacterial DNA. Are samples other than genital samples, such as throat and rectal swabs, acceptable for C trachomatis and N gonorrhoeae NAATs? Start: Nov 27, 2022 Get Offer. 2. Because many people who are infected with gonorrhea do not have any noticeable symptoms, a number of health organizations recommend regular gonorrhea screening for certain adolescents and adults between the ages of 15 and 65, including. allowed for additional confirmatory or additional reflex tests. WebCPT Code.CPT Description.CPT Disclaimer. Female patients should not cleanse the labial area prior to providing the specimen. Clinical Significance Immediately place the swab into the transport tube, and carefully break the swab shaft against the side of the tube. But, only half of these cases are reported to the CDC. Female patients should not cleanse the labial area prior to providing the specimen. Discard this swab. 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. This test may exhibit interference when sample is collected from a person who is consuming a supplement with a high dose of biotin (also termed as vitamin B7 or B8, vitamin H, or coenzyme R). I looked up/Googled health codes and 74.5 stands. Gently rotate the swab clockwise for 10 to 30 seconds in the endocervical canal to ensure adequate sampling. 30 days (stability provided by manufacturer or literature reference). Other types of chlamydia tests are available but are rarely used given the accuracy and availability of NAAT. 19. Vaginal, endocervical, or male urethral swab, first-void urine (patient should not have urinated for one hour prior to specimen collection), or cervical cells in liquid cytology vial. Withdraw the swab carefully; avoid contact with the vaginal mucosa. 1. testing to when the result is released to the ordering provider.