cpt code for gc chlamydia urine test labcorp

testing to when the result is released to the ordering provider. allowed for additional confirmatory or additional reflex tests. In some cases, additional time should be Accessed March 2022 at https://www.hhs.gov/sites/default/files/STI-National-Strategic-Plan-2021-2025.pdf. Trichomoniasis urine tests are also available, but they are less common. Turnaround time is defined as the usual number of days from the date of pickup of a specimen for Female patients should not cleanse the labial area prior to providing the specimen. 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. Swirl the brush vigorously to release additional material. AAP Committee on Fetus and Newborn and ACOG Committee on Obstetric Practice. CPT Code: 87491, 87591. 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/. female and male urine specimens. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. These facilities are private, comfortable and test for diseases other than STDs. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Chlamydia Trachomatis And Neisseria Gonorrhoeae Detection - Test Code. Lab/Phone: 330-543-8576 TAT: 4 hours if specimen is received when test is being run Additional Info: Positive results are called and reported to the Ohio Department of Health (ODH). Offer. Ct/GC: Option 1: Gen-Probe Aptima endocervical or vaginal swab. These instructions include the following statement. Dispose of the pipette tip into a biohazard bag containing absorbent material soaked with bleach. The people you see wont know for what you are getting tested for. U.S. Department of Health and Human Service. 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. Slowly rotate the brush to turn in one direction. Provide patient with a sterile, plastic, preservative-free, screw cap specimen collection cup. The fluid level must fall between the 2 black lines on the urine transport tube. For men, first-catch urine is the recommended. Although the clinical significance of oropharyngeal C trachomatis infection is unclear and routine oropharyngeal screening for CT is not recommended, available evidence suggests oropharyngeal C trachomatis can be sexually transmitted to genital sites therefore, per the 2015 guidelines on sexually transmitted diseases, oropharyngeal C trachomatis should be treated with appropriate antimicrobials.4. testing to when the result is released to the ordering provider. The LabCorp Test Menu is a page at LabCorp. 5. 1. As such, health plan access, test ordering, and billing processes may differ from those of Quest Diagnostics. It can be performed using a urine sample or swab of fluid taken from a site of potential infection such as the urethra, vagina, rectum, or eye. Which specimen types are suitable for C trachomatis and N gonorrhoeae nucleic acid amplification tests (NAATs)? Traditionally, NAAT takes a day or more to provide results, but there have also been rapid chlamydia tests developed using NAAT methods. Most persons with C trachomatis detected at oropharyngeal sites do not have oropharyngeal symptoms. Chlamydia trachomatis is a type of gram-negative bacteria that is responsible for causing Chlamydia infection. 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. Carefully break the swab shaft at the scoreline using care to avoid splashing of the contents. The final volume must be between the two black lines on the device (about 2 mL). Read Also: Over The Counter Drugs For Chlamydia, Labcorps test menu provides a comprehensive list of specialty and general laboratory testing services. 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. Assay interference may be observed in the presence of blood, mucin, bilirubin, or Vagisil feminine powder with urine specimens. Quest; LabCorp; Buy LabCorp: $99.00 . Female patients should not cleanse the labial area prior to providing the specimen. 8th edition, September 2017. When your order from Health Testing Centers there is no need to visit a std clinic, neighborhood health center or public health clinic. 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. Routine chemistry and bacterial or fungal culture require use of the clean catch midstream collection technique. 2. (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. Chlamydia and gonorrhea urine tests are widely available. Option 2: Urine Specimen: The patient should not have urinated for at least one hour prior to specimen collection. ThinPrep 2000 System Operator's Manual Addendum, 70983-001-B001 Rev A. Testing schedules may vary. Note: Specimens cannot be collected and used for Chlamydia/Neisseria and routine chemistry or urine culture. I looked up/Googled health codes and 74.5 stands. 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/. Do not touch the soft tip or lay the swab down. Discard this swab. Testing schedules may vary. It is recommended to ask all patients who may be indicated for this test about biotin supplementation. 2023 Laboratory Corporation of America Holdings. The final volume must be between the two black lines on the device (about 2 mL). Insert the specimen collection swab (blue-shaft swab in the package with the green printing) 2 to 4 cm into the urethra. CPT Code (s) Collect Serum Separator Tube (SST) or plain red-top tube Specimen Preparation Separate from cells ASAP or within 2 hours of collection. Some of the assays in this panel have not been FDA cleared or approved for the screening of blood or plasma donors, nor have assay performance characteristics been established for immunocompromised or immunosuppressed patients, cord blood, or patients less than 2 years of age. Serum specimen: Usual blood collection technique. Chlamydia trachomatis and Neisseria gonorrhoeae (CTNG) by Transcription-Mediated Amplification (TMA) with Reflex to CT/NG Confirmation 2011164 Copy Utility Click to copy Test Number / Name Choose the Right Test ARUP Consult assists with test selection and interpretation Sexually Transmitted Infections Go to ARUP Consult Example Reports Negative 8. Hemolysis; lipemia; received outside of specimen and/or storage and/or labeling requirements; aliquot received for HIV testing; specimen in expired transport or incorrect transport device; specimens with inappropriate source for test requested; Aptima urine transport >30 days from collection; Aptima urine transport with incorrect specimen volume; Aptima swab transport >60 days from collection; Aptima swab specimen without a swab; cleaning swab (white-shaft swab) in Aptima swab transport; Aptima transport device with multiple swabs. 2021 Laboratory Corporation of America Holdings and Lexi-Comp Inc. All Rights Reserved. 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. Many people with chlamydia have no symptoms. If a positive result is obtained for either Chlamydia trachomatis or Neisseria gonorrhoeae, testing for Trichomonas vaginalis is performed. Test Code M14 Chlamydia/GC PCR, Urine Important Note. 4. Gently rotate the swab clockwise for 10 to 30 seconds in the endocervical canal to ensure adequate sampling. 9. Chlamydia/gonococcus Naa With Reflex To Test Code M14 Chlamydia/GC PCR, Urine Important Note. This bacterial infection is mostly common among young adults who are sexually active. Reference Values: . PID sometimes causes your reproductive organs to swell, triggering chronic pelvic pain and making it difficult to conceive. For bacterial infections, such as gonorrhea, syphilis or Chlamydia, those indicators would be bacteria in urine samples. Ct/GC: Option 2: Urine Specimen: The patient should not have urinated for at least one hour prior to specimen collection. 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. 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/. Add urine to the Aptima Combo 2 urine collection device. If youve recently tested positive for chlamydia or gonorrhea, complete the treatment, then test again after 3 months to ensure the treatment was successful. As a final step, twirl the brush between the thumb and forefinger vigorously to further release cellular material. Tightly screw on the cap. 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. 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. This infection can be spread by either vaginal, anal or oral sex. 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. Male urethral swab: The patient should not have urinated for at least one hour prior to specimen collection. Please provide SERVICE AREA INFORMATION to find available tests you can order. Physicians and other persons responsible for ordering clinical tests should be familiar with the following. 2. Uncap the vial and place it on the work surface with the threads facing up. Washington, DC. Sometimes, this may lead to infertility . There is no evidence of degradation of cytology results by aliquot removal, however, this cannot be ruled out for all specimens. 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. Kilpatrick SJ, Papile LA, Macones GA, eds. Enhancing Outcomes: Universal Screening for Chlamydia and Gonorrhea, Microbiology Specimen Collection and Transport Guide, Protect Your Patients From the Consequences of Untreated Chlamydia, Gonorrhea, and Trichomonas: Easily Detected and Easily Treated, The Most Accurate Results Come From the Best Specimens, Trichomonas vaginalis: Detect More Infections With Nucleic Acid Amplification, Endocervical, vaginal, 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, One swab (endocervical, vaginal, or urethral), 2 mL of a 20 mL to 30 mL urine collection, or entire liquid cytology vial, One swab (endocervical, vaginal, or urethral), 2 mL of a 15 mL urine collection, or entire liquid cytology vial, Gen-Probe Aptima swab or Aptima urine specimen transport; ThinPrep liquid cytology vial, Option 1: Gen-Probe Aptima Endocervical, Male Urethral, or Vaginal Swab. See test code CTGCU for urine sources and CTGCO for non-FDA approved sources (oral, anal, or rectal swabs). Hepatitis B. CDC website: www.cdc.gov/hepatitis/hbv/index.htm. 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. 2015 the icd 9 code sets used to report medical diagnoses and inpatient procedures will be replaced by icd 10 code . Ordering Restrictions may apply. Browse our menu of tests. Urine samples must be transported to the laboratory at 4C to 30C within 24 hours of specimen Good laboratory practices should be followed to avoid introducing contaminants into either the PreservCyt sample vial (ThinPrep vial) or the aliquot. Both men and women can experience fertility problems after a chlamydia infection. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Patient self-collection: Partially open the package of the Gen-Probe Aptima vaginal swab kit. You should get tested for STDs, including chlamydia and gonorrhea, before and after every sexual encounter with new partners. Mycoplasma genitalium. Aliquots must be transferred to the Aptima tube within seven days of collection. Chlamydia trachomatis. Female patients should NOT cleanse the labial area prior to specimen collection.