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cpt code for gc chlamydia urine test labcorp

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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. It is very essential to screen, and diagnose chlamydia in order to prevent its spread and possible long-term complications. Chlamydia Trachomatis And Neisseria Gonorrhoeae Detection - Test Code. Do not touch the soft tip or lay the swab down. Female patients should not cleanse the labial area prior to providing the specimen. Carefully break the swab shaft at the scoreline using care to avoid splashing of contents. Physicians and other persons responsible for ordering clinical tests should be familiar with the following. Test code 16505- Chlamydia trachomatis RNA, TMA, Rectal Test code 70048- Chlamydia trachomatis RNA, TMA, Throat Test code 16504- Neisseria gonorrhoeae RNA, TMA, Rectal Test code 70049- Neisseria gonorrhoeae RNA, TMA, Throat Question 1 Which Specimen Types Are Suitable For C Trachomatis And N Gonorrhoeae Nucleic Acid Amplification Tests ThinPrep 3000 System Operator's Manual Addendum, 70557-001-B001 Rev A. Female patients should not cleanse the labial area prior to providing the specimen. Chlamydia A common STI caused by the bacteria, Chlamydia trachomatis. In some cases, additional time should be 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/. 17. Store the aliquot in Aptima tube at 15C to 30C for transport to LabCorp. 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. It also states that women are more prone to be re-infected, if their partner is not getting tested and treated properly. 14. 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). (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. Direct patient to provide a first-catch urine (approximately 20 mL to 30 mL of the initial urine stream) into a urine collection cup free of any preservatives. 91448. 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). Turnaround time is defined as the usual number of days from the date of pickup of a specimen for CPT: 87491; 87591 Print Share Include LOINC in print Expected Turnaround Time 2 - 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. 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. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Discard this swab. Test Code M14 Chlamydia/GC PCR, Urine Important Note. Cover the bench with clean, plastic-backed absorbent laboratory bench covers. Your risk of infertility increases if you delay treatment. Other types of chlamydia tests are available but are rarely used given the accuracy and availability of NAAT. Testing schedules may vary. Webcpt code for gc chlamydia urine test labcorp. 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. Test Code M14 Chlamydia/GC PCR, Urine Important Note. Transport and store urine refrigerated. 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. 15. 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. Gently rotate the swab clockwise for 10 to 30 seconds in the endocervical canal to ensure adequate sampling. Add urine to the Aptima Combo 2 urine collection device. Option 2: Urine Specimen: The patient should not have urinated for at least one hour prior to specimen collection. If reflex testing is performed, additional charges/CPT code(s) may apply. If youve been in a long-term, monogamous sexual relationship the same partner, you should still test for STDs once a year. Brush/spatula technique: Insert the brush into the endocervical canal until only the bottommost fibers are exposed. CPT Disclaimer. If negative results from the specimen do not fit with the clinical impression, a new specimen may be necessary. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Tightly screw on the cap. A full range of tests for STI screening and confirmation are available from ACL Laboratories. Chlamydia trachomatis : Symptoms, Diagnosis and Treatments. 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 First-void urine in Aptima urine transport, 2 mL aliquot of a 20 to 30 mL urine collection. 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. Specify the exact specimen source/origin (eg, endocervical). If an at-home chlamydia test returns positive results, a doctor may suggest confirmation testing with a laboratory-based method. Female patients should not cleanse the labial area prior to providing the specimen. These types of testing are sensitive to even very small amounts of bacterial DNA. Remove the cap from the swab specimen transport tube and immediately place the specimen collection swab into the transport tube. Chlamydia/N. 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. Withdraw the swab carefully. 2023 Laboratory Corporation of America Holdings. Although the findings were not statistically significant, positivity appeared to. 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. 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. CPT Description. 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 ThinPrep Liquid Pap specimen for Pap smear processing. Kilpatrick SJ, Papile LA, Macones GA, eds. All Rights Reserved. Remove the cap from the swab specimen transport tube and immediately place the specimen collection swab into the transport tube. Serum specimen: Usual blood collection technique. 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. All Rights Reserved. Withdraw the swab carefully. Direct patient to provide a first-catch urine (approximately 20 mL to 30 mL of the initial urine stream) into a urine collection cup free of any preservatives. Using a pipetting device with an aerosol barrier tip, immediately withdraw a 1 mL aliquot from the ThinPrep vial. Tightly screw on the cap. All Rights Reserved. These facilities are private, comfortable and test for diseases other than STDs. testing to when the result is released to the ordering provider. 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. Turnaround time is defined as the usual number of days from the date of pickup of a specimen for 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. testing to when the result is released to the ordering provider. Start: Nov 27, 2022 Get Offer. 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. Testing schedules may vary. Routine chemistry and bacterial or fungal culture require use of the clean catch midstream collection technique. Discard this swab. Withdraw the swab carefully; avoid contact with the vaginal mucosa. 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. It works differently than a bacterial culture. 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. 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. 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. This type of test detects the genetic material of Chlamydia trachomatis. Chlamydia trachomatis and Neisseria gonorrhoeae infections should be diagnosed by using nucleic acid amplification tests (NAATs) because their sensitivity and specificity are high and they are. For more information, please contact ReproSource at 1.800.667.8893 or visit ReproSource.com/Contact . People at risk of getting chlamydia need to be tested, regularly. All in on place. 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. 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/. Gently invert the tube two to three times to ensure complete mixing of the specimen. Summary and Explanation of the Test . 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 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. Label each Aptima tube with the appropriate specimen label. Patient self-collection instructions: Partially open the package. Male urethral swab: The patient should not have urinated for at least one hour prior to specimen collection. To reduce the chance of contaminating other specimens, work with one ThinPrep Liquid Pap specimen at a time. The final volume must be between the two black lines on the device (about 2 mL). Direct the patient to collect the first 15 50 mL of the initial urine stream in the cup provided On a LabCorp bill, does Chlamydia/GC Amplification mean the presence of Chlamydia or a test for it? Carefully break the swab shaft at the scoreline using care to avoid splashing of contents. Tightly screw on the cap. . 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. 3. Both chlamydia and gonorrhea show the same symptoms. allowed for additional confirmatory or additional reflex tests. Note: Specimens cannot be collected and used for Chlamydia/Neisseria and routine chemistry or urine culture. Remove the swab. Remove the swab. 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 and Research. 91448. Test code 70048- Chlamydia trachomatis RNA, TMA, Throat Test code 16504- Neisseria gonorrhoeae RNA, TMA, Rectal Test code 70049- Neisseria gonorrhoeae RNA, TMA, Throat You May Like: Causes Of Chlamydia In Females Urine Testing Vs Bacterial Culture Urine testing is currently primarily used to detect bacterial STIs. 7. Note: Specimen collected in Aptima PCR Urine media contain a preservative and are stable for 30 days. Urine samples must be transported to the laboratory at 4C to 30C within 24 hours of specimen To easily check for chlamydia from the comfort of home, simply collect a urine sample and send it to a lab with prepaid shipping using the Everlywell at-home Gonorrhea and Chlamydia test kit. This makes chlamydia a widespread sexually transmitted disease. Remove the swab. Rapid chlamydia tests are typically performed on urine samples or swabs of fluid taken from the vagina or cervix. 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. It has not been cleared or approved by the US Food and Drug Administration (FDA). The final volume must be between the two black lines on the device (about 2 mL). 2020. Tightly screw on the cap. Negative; no Chlamydia trachomatis or Neisseria gonorrhoeae detected. Tests are available to detect chlamydia at home. Browse records in Test Code. 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. Guidelines for Perinatal Care. Screening and Referral Algorithm for Hepatitis B Virus (HBV) Infection Among Pregnant Women. This can be done using a process called ligase chain reaction or with other DNA amplification techniques. The FDA has determined that such clearance or approval is not necessary. Sometimes, this may lead to infertility . CPT Code a. The chlamydia test can identify bacteria causing this infection. Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. Nucleic acid amplification testing is recommended for detection of Chlamydia trachomatis from endocervical or urethral specimens. 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. 87491: Infectious Agent Detection by Nucleic Acid (DNA or RNA), Chlamydia . Put on clean gloves before proceeding to specimen transfer. download here chlamydia gc screening requisition form supply order form of america llc home healthcare supply Chlamydia/N. 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. In some cases, additional time should be 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. No Chlamydia trachomatis or Neisseria gonorrhoeae detected. Recap the swab specimen transport tube tightly. Urine testing is currently primarily used to detect bacterial STIs. Tightly screw on the cap. 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. Add urine to the Aptima COMBO 2 urine collection device. For more information, please view the literature below. Note: Client must clearly label the site/source of each Chlamydia/Gonococcus Nucleic Acid Amplification specimen. Prior to sampling the patient should not have urinated for at least 1 hour. ThinPrep 2000 System Operator's Manual Addendum, 70983-001-B001 Rev A. Discard the collection device. Quest Diagnostics offers throat- and anal -based testing: You May Like: Causes Of Chlamydia In Females, Introduction. mass effect 2 console commands list. 11. Also Known As: Chlamydia/Gonococcus, Amplicor PCR; Chlamydia . 0 . 1. Instead of trying to grow bacteria, these tests just look for bacterial DNA. Remove the cap from the swab specimen transport tube and immediately place the specimen collection swab into the specimen transport tube. Retrieve ThinPrep vials that are to have aliquots removed. Vortex the ThinPrep vial for 8 to 12 seconds at high speed. 2021 Laboratory Corporation of America Holdings and Lexi-Comp Inc. All Rights Reserved. Withdraw the swab carefully; avoid contact with the vaginal mucosa. There is no evidence of degradation of cytology results by aliquot removal, however, this cannot be ruled out for all specimens. CPT Code (s): 87481 (x 2), 87491, 87591, 87661, 87798 (x 3) Collection Procedure: Vaginal Swab: Collect a vaginal fluid sample using a 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. It affects both men and women, of all ages. Offer. Although much less commonly used, cell cultures can help diagnose a chlamydia infection. Remove the cap from the swab specimen transport tube and immediately place the specimen collection swab into the transport tube. It isnt me. Many people with chlamydia have no symptoms. Withdraw the swab carefully; avoid contact with the vaginal mucosa. gonorrhoeae and T. vaginalis RNA, Qualitative, TMA, Pap Vial - Diagnosis of the three most common sexually transmitted infections. Schillie S, Vellozzi C, Reingold A, et al. Trichomoniasis urine tests are also available, but they are less common. ChlamidiaExplained.com is a one-stop resource for everything you wanted to know about chlamidia symptoms and treatments. For men, first-catch urine is the recommended. Because cytology/HPV testing and STD testing address different clinical questions, aliquot removal may not be suitable for all clinical situations. All Rights Reserved. You should get tested for STDs, including chlamydia and gonorrhea, before and after every sexual encounter with new partners. 2021 Laboratory Corporation of America Holdings and Lexi-Comp Inc. All Rights Reserved. In some cases, additional time should be If the soft tip is touched, the swab is laid down, or the swab is dropped, use a new Aptima swab specimen collection kit. Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. The Gonorrhea test is essential in screening, diagnosing and evaluating the treatment plan of a gonorrhea infection. The final volume must be between the two black lines on the device (about 2 mL). 2. When your order from Health Testing Centers there is no need to visit a std clinic, neighborhood health center or public health clinic. A chlamydia or gonorrhea infection may cause inflammation or scarring of the reproductive organs. 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. 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. 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. Do not touch the soft tip or lay the swab down. Even better, they do not require a live bacterial sample. testing to when the result is released to the ordering provider. 5. For more information, please view the literature below. Recap the swab specimen transport tube tightly. Insert the specimen collection swab (blue-shaft swab in the package with green printing) into the endocervical canal. Obtain an adequate sample from the ectocervix using a plastic spatula. 2023 Laboratory Corporation of America Holdings. For women, yearly screening is recommended if you are sexually active and younger than age 25, or 25 or older and at increased risk for chlamydia infection when you are pregnant or considering pregnancy. 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. The purpose of gonorrhea testing is to detect a gonorrhea infection. Carefully break the swab shaft at the scoreline using care to avoid splashing of the contents. Top 3Reference Laboratory Test Catalogs for MiscellaneousLab TestOrders: As of 23 February 2023, NorDx is transitioning to Aptima collection devices for this test. Wipe down work surfaces and pipettors with 1:1 bleach:water solution. Insert the specimen collection swab (blue-shaft swab in the package with green printing) into the endocervical canal. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. 13. (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. In order to minimize the potential for cross contamination, aliquot removal should be performed in an appropriate location outside an area where amplification is performed..

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