Respiratory pathogen panel labcorp

Expected Turnaround Time. 2 - 5 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. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

Pseudomonas bacteria are everywhere. They live on plants, in water and soil, and on humans. In most cases, coming in contact with these germs is uneventful or mildly irritating, bu...9. The BioFire RP2.1 Bordetella pertussis (ptxP) assay can also amplify pertussis toxin pseudogene sequences when present in B. bronchiseptica and B parapertussis. Cross-reactivity was observed only at high concentration (e.g. > 1.2E+09 CFU/mL). 10. The FilmArray RP2.1 Human Rhinovirus/Enterovirus assay may amplify off-target sequences found in ...At-Home Stool Collection. How soon can I expect to receive my kit? How do I track my kit? How do I register my kit? Where do I find the barcode? Does the kit expire? What should I do if I sent my kit to the lab before registering it? What preparation is required for stool sample collection? How do I collect my stool sample?Isolation and identification (additional CPT code) of aerobic bacteria considered pathogenic in the lower respiratory tract of patients with cystic fibrosis. Susceptibilities are performed, at an additional charge, where appropriate. Anaerobic culture is not appropriate from expectorated sputum. See specific requirements in Fungus (Mycology ...Test Code RPP Respiratory Pathogen Panel Patient Preparation. No special patient preparation required. Minimum Volume. Nasopharyngeal swab. ... Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Portions ©2024 Mayo Foundation for Medical Education and Research.The Pneumonia Panel should be considered in the following situations: 1) Patients with severe CAP (admitted to ICU, respiratory failure, etc.). 2) CAP patients on expanded-spectrum therapy (vancomycin, cefepime, etc.). 3) Patients not responding to typical therapy. 4) Patients with hospital-acquired or ventilator-associated pneumonia.Our real-time PCR-based respiratory pathogen panel (RPP) is a sensitive, syndromic, flexible-content solution for detecting respiratory pathogens in less than 12 hours. Our Open Array solution will catch up to 35 different bacterial and viral pathogens, including COVID-19.The LabCorp 2019 Novel Coronavirus (COVID-19), NAA Test is for Use by Clinicians with Patients Who Meet COVID-19 Evaluation Criteria. BURLINGTON, N.C.--(BUSINESS WIRE)-- LabCorp® (NYSE: LH), a leading global life sciences company that is deeply integrated in guiding patient care, is making its LabCorp 2019 Novel Coronavirus (COVID-19), NAA test available today, beginning at 6 p.m. ET, for ...

LabCorp’s Respiratory Pathogen Profile, PCR (139650) utilizing the BioFire PCR methodology to improve speed and versatility of testing. Respiratory Pathogen Profile, PCR (139650) Rapid and accurate identification of the causative agent of upper respiratory tract infections may improve patientAnaerobic infection is most commonly associated with operations involving opening or manipulating the bowel or a hollow viscus (eg, appendectomy, cholecystectomy, colectomy, gastrectomy, bile duct exploration, etc). The ratio of anaerobes to facultative species is normally about 10:1 in the mouth, vagina, and sebaceous glands and at least 1000: ...Economic Advantages. Syndromic testing with a gastrointestinal PCR panel can provide economic benefits for laboratories and healthcare organizations. The BioFire GI Panel is intended to be used with the BioFire ® FilmArray ® Torch in moderate complexity settings. This GI pathogen panel does not require a high level of skill to perform and only involves 2 minutes of laboratorian hands-on time.Respiratory Pathogen Panel. 24 hrs/day, 7 days a week, including holidays. 3 hours (upon receipt in laboratory) includes all of the analytes below. When ordered as Cascading. positive for influenza. If negative for influenza, all of the. additional analytes will be reported. If a test is positive for.Call Us Today! only you hotel valencia tripadvisor which of the following best describes advisory opinions

Use. Detect possible allergic responses to various substances in the environment (see Test Includes) and evaluate for hay fever, asthma, atopic eczema, and respiratory allergy. The quantitative allergen-specific IgE test is indicated (1) to determine whether an individual has elevated allergen-specific IgE antibodies; (2) if specific allergic ...Respiratory pathogen panels can identify the genetic material of common disease-carrying pathogens in a single sample, making it easier for doctors and lab technicians to provide patients with diagnoses. A medical professional may spot only one microbe with traditional testing but can detect multiple pathogens with a respiratory panel.The Pathogens Panel measures pathogenic organisms that are known to cause hospital-acquired infections (HAI) (such as C. difficile or norovirus ), foodborne illnesses (such as E. coli or Salmonella), and common causes of diarrhea (such as Campylobacte r, Shigella, and rotavirus A ). This panel measures viral causes of gastroenteritis ..."The addition of these tests further enhances ViroMed's comprehensive respiratory pathogen test menu," noted Myla Lai-Goldman, M.D., Executive Vice President, Chief Scientific Officer and Medical Director of LabCorp. ... Further information on potential factors that could affect LabCorp's financial results is included in the …Marcy-l'Étoile (France), April 13, 2023 - bioMérieux, a world leader in the field of in vitro diagnostics, has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the fast and accurate multiplex PCR*-based BIOFIRE ® SPOTFIRE ® Respiratory (R) Panel Mini. bioMérieux will immediately apply for Clinical Laboratory Improvement Amendments (CLIA) waiver for the test.

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The following recommendations are made for efficient and cost-effective diagnosis of diarrheal disease in patients admitted with gastroenteritis. • Submit one or two specimens per diarrheal illness immediately. Consider requesting the EIA for Giardia (see Giardia lamblia, EIA and Ova and Parasites Examination [188110] or Giardia lamblia ...Background: The multiplex polymerase chain reaction Respiratory Pathogen Panel (RPP) has been utilized at Jersey Shore University Medical Center for the diagnosis of infants with fever of unknown source whose rapid RSV and/or influenza testing were negative. However, the value of RPP testing in terms of medical care and …Call Us Today! only you hotel valencia tripadvisor which of the following best describes advisory opinionsMarcy-l'Étoile (France), April 13, 2023 - bioMérieux, a world leader in the field of in vitro diagnostics, has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the fast and accurate multiplex PCR*-based BIOFIRE ® SPOTFIRE ® Respiratory (R) Panel Mini. bioMérieux will immediately apply for Clinical Laboratory Improvement Amendments (CLIA) waiver for the test.

Women's wellness. Patient Provider. No matching entries. Explore Labcorp's diagnostic testing by disease or condition for key treatment areas and specialties.Labcorp test details for Allergen Profile with Component Reflexes, Respiratory-Area 19 Skip to main content Close Menu. Logins. Individuals & Patients. Find a Lab View ... Panel 606578: 606645: E220-IgE Fel d 2: kU/L: 19732-7: Reflex Table for E001-IgE Cat Dander; Order Code Order NameAsthma allergy testing options. If a respiratory allergy is suspected, you can order a single respiratory profile with reflex components with a single blood draw for patients 3 months of age and older. The Labcorp Regional Respiratory Allergen Profiles test for clinically relevant inhalant allergens such as pollen, mold, dust mites, insect ...Refrigerate immediately. Throat swab: Carefully rub the posterior wall of the nasopharynx with a dry, sterile swab. Avoid touching the tongue or buccal mucosa. Place swab in viral transport tube. Feces: Collect 4 to 8 g of feces (about the size of a thumbnail) and place in a clean, screw-cap container.The Luminex® NxTAG® Respiratory Pathogen Panel (NxTAG RPP) is an IVD-cleared assay for the simultaneous detection and identification of nucleic acids from 18 respiratory viruses and 2 (or 3 outside of the U.S.) atypical bacterial pathogens in nasopharyngeal swabs. Its scalability allows concurrent testing of up to 96 samples in a single batch.Viral transport medium acceptable for collection of influenza specimens in 1 mL or 3 mL volumes can be used to transport swabs for COVID-19 testing. For swabs in saline: OP, NP or anterior nasal swabs may be placed in 1 to 3 mL of sterile saline (0.85 to 0.9%) in a sterile screw cap container. Do not use vacutainer or "pop-top" tubes.FACT SHEET FOR HEALTHCARE PROVIDERS. Laboratory Corporation of America (Labcorp) May 17, 2022 Labcorp Seasonal Respiratory Virus RT-PCR Test Coronavirus Disease 2019 (COVID-19) should be made by a healthcare provider and follow current CDC guidelines. Results (positive and negative) for influenza and/or RSV should be interpreted with caution ...Viral transport medium acceptable for collection of influenza specimens in 1 mL or 3 mL volumes can be used to transport swabs for COVID-19 testing. For swabs in saline: OP, NP or anterior nasal swabs may be placed in 1 to 3 mL of sterile saline (0.85 to 0.9%) in a sterile screw cap container. Do not use vacutainer or "pop-top" tubes.

Use. Detect possible allergic responses to various substances in the environment (see Test Includes) and evaluate for hay fever, asthma, atopic eczema, and respiratory allergy. The quantitative allergen-specific IgE test is indicated (1) to determine whether an individual has elevated allergen-specific IgE antibodies; (2) if specific allergic ...

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC; 500918: Pathology Report: 500920. 22633-2: 500918: Pathology Report: 500943Jul 11, 2021 · A respiratory pathogen panel test must not be unbundled and billed as individual components regardless of the fact that the panel reports multiple individual pathogens and/or targets. The term "panel" refers to all respiratory pathogens tested in the outpatient setting on a single date of service from a single biologic specimen, not ordered as ... The newest panel from GenMark Dx, the ePlex Respiratory Pathogen Panel 2 (RP2), which added the SARS-CoV-2 target to the RP was also evaluated for NPS. Verification of the performance of the ePlex RP for both NPS and BAL showed 93.3 % and 84.9 % total agreement with the NxTAG-RPP respectively. An overall comparison of the …The NxTAG Respiratory Pathogen Panel requires only minutes of hands-on time, with no upstream reagent preparation. A simplified workflow allows extracted samples to be added directly to pre-plated ...Stool for bacterial culture and enterohemorrhagic E coli Shiga toxin by EIA should be submitted in the C&S transport vial. Only a thumbnail-size portion of stool, about 1 g or 1 mL, should be added to the vial. Overfilling the vial will reduce recovery of stool pathogens. Specimens from sources, such as genital, stool, urine, and upper and ...Respiratory Pathogen Panel. GTR Test ID Help Each Test is a specific, orderable test from a particular laboratory, and is assigned a unique GTR accession number. The format is GTR00000001.1, with a leading prefix 'GTR' followed by 8 digits, a period, then 1 or more digits representing the version. When a laboratory updates a registered test, a ...The Luminex® NxTAG® Respiratory Pathogen Panel (NxTAG RPP) is an IVD-cleared assay for the simultaneous detection and identification of nucleic acids from 18 respiratory viruses and 2 (or 3 outside of the U.S.) atypical bacterial pathogens in nasopharyngeal swabs. Its scalability allows concurrent testing of up to 96 samples in a single batch.Coding Guidance. Notice: It is not appropriate to bill Medicare for services that are not covered (as described by the entire LCD) as if they are covered. When billing for non-covered services, use the appropriate modifier. A respiratory pathogen panel test is a single service with a single unit of service (UOS=1).The NxTAG® Respiratory Pathogen Panel (US-IVD) enables your laboratory to simultaneously detect 20 respiratory pathogens in a single closed tube system, and ...

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Economic Advantages. Syndromic testing with a gastrointestinal PCR panel can provide economic benefits for laboratories and healthcare organizations. The BioFire GI Panel is intended to be used with the BioFire ® FilmArray ® Torch in moderate complexity settings. This GI pathogen panel does not require a high level of skill to perform and only involves 2 minutes of laboratorian hands-on time.Solar Panel Cleaning Agents - Solar panel cleaning agents help ensure that the panels are working efficiently. Visit HowStuffWorks to learn about solar panel cleaning agents. Adver...The current algorithm for the laboratory diagnosis of RTIs relies on multiple approaches including gold-standard conventional methods, among which the traditional …Place the swab into VTM/UTM and cap tightly. Anterior nasal swab: Insert the tip of the swab into one nostril. The swab does not need to be inserted far. Insert just until the tip of the swab is no longer visible. Rotate the swab in a circle around the entire edge of your nostril at least three times. Repeat with the second nostril.Introduction: Successful treatment outcomes for viral respiratory tract infections presenting from primary health care to quaternary hospitals will only be achieved with rapid, sensitive and specific identification of pathogens to allow effective pathogen-specific antiviral therapy and infection control measures.. Areas covered: This review aims to explore the different point-of-care tests ...Respiratory virus testing algorithms. (A) All patients with ILI are tested using an influenza A/B test. (B) All patients with ILI are tested with a respiratory pathogen panel. (C) Patients with ILI are tested with an influenza A/B test and, if the results are negative, then reflex testing with a respiratory pathogen panel is performed.Clinical Significance. Respiratory Pathogen Panel - The detection and identification of specific pathogen nucleic acids from individuals exhibiting signs and symptoms of respiratory infection aids in proper diagnosis. The Respiratory Pathogen Panel (37444) is used for the detection of the following respiratory viruses and bacterial pathogens:The GT-Research Panel (RUO) is a multiplexed molecular reagent kit that contains all primers, probes, and controls for the detection of SARS-CoV-2, Influenza A & B, and RSV. Get the information needed to help analyze the distribution of SARS-CoV-2, flu, and RSV nucleic acid. The assay incorporates an optimized SARS-CoV-2 target (SC2) to ...Viral transport medium acceptable for collection of influenza specimens in 1 mL or 3 mL volumes can be used to transport swabs for COVID-19 testing. For swabs in saline: OP, NP or anterior nasal swabs may be placed in 1 to 3 mL of sterile saline (0.85 to 0.9%) in a sterile screw cap container. Do not use vacutainer or "pop-top" tubes.RESPIRATORY PATHOGEN PANEL,NAAT. Test Code: LAB1307 ... (PCR) panel for the diagnosis of respiratory tract infections. Sensitivity exceeds the sensitivity of DFA or culture. Specificity >99%.Due to the sensitivity and specificity of the technology, when this test is ordered, there is no need to order either respiratory viral DFA or culture. ... ….

Then, it will be more cost-effective to request the respiratory pathogen panel," Dr. Yao says. He notes that the standalone RSV test requires a nasal pharyngeal swab. The four-target test can be performed with a variety of specimens, including nasal pharyngeal swabs, throat swabs or nasal mid-turbinate swabs, as well as lower …Respiratory pathogen panel tests are laboratory tests used to identify the presence of specific viruses and bacteria in the respiratory tract, which is comprised of the nose, mouth, throat, and lungs. While many respiratory infections go away on their own, there are cases where typical treatments for a respiratory infection are ineffective.RESPIRATORY PATHOGEN PANEL 2.1, NAT: Test Code: 2133795: Alias: LAB15035 Respiratory pathogen panel PCR RPP: ... Respiratory pathogens cause acute local and systemic disease of varying severity, with the most severe cases occurring in children, the elderly and immunocompromised individuals. Due to the similarity of diseases caused by many ...The Labcorp Seasonal Respiratory Virus RT-PCR DTC Test is a direct to consumer product intended for the simultaneous qualitative detection and differentiation of RNA from SARS-CoV-2, Influenza AThe ePlex® Respiratory Pathogen Panel (RP panel) is a novel molecular based assay, developed by GenMark Diagnostics Inc. (Carlsbad, California), to be performed within a single cartridge for the ...Economic Advantages. Syndromic testing with a gastrointestinal PCR panel can provide economic benefits for laboratories and healthcare organizations. The BioFire GI Panel is intended to be used with the BioFire ® FilmArray ® Torch in moderate complexity settings. This GI pathogen panel does not require a high level of skill to perform and only involves 2 minutes of laboratorian hands-on time.The BIOFIRE RP Panel* resulted in avoidance of antibiotics in 23% of pediatric patients tested.9 Reduce Length of Stay The hospital length of stay was nearly 5 days less for febrile infants with a positive BIOFIRE RP Panel* result compared to those with a negative result.4 Panel Information BIOFIRE Respiratory Pathogen Trends (RP2.1)10Today, FDA authorized the Labcorp Seasonal Respiratory Virus RT-PCR DTC Test, the first direct-to-consumer (non-prescription) multi-analyte COVID-19 test authorized by FDA. Respiratory pathogen panel labcorp, Additional Information. Mycoplasma pneumoniae infection is acquired via the respiratory route from small-particle aerosols or large droplets of secretions. The organism can penetrate the mucociliary barrier of respiratory epithelium and produce cellular injury and ciliostasis that may account for the prolonged cough observed clinically., The Ontario Respiratory Virus Tool provides comprehensive epidemiological information on respiratory virus activity in Ontario, including COVID-19, influenza, RSV, and other respiratory viruses. Explore respiratory virus data including case trends, outcomes (hospital bed occupancy, ICU bed occupancy, and deaths), laboratory testing, and outbreaks., the collection of LabCorp's 2019 Novel Coronavirus (COVID-19) assay [139900] from the anterior nares (nasal collection). Orders for other respiratory viral testing panels or assays will NOT be accepted when samples are collected using this COVID-19 collection kit. These other respiratory pathogens require collection using an, Call Us Today! only you hotel valencia tripadvisor which of the following best describes advisory opinions, Respiratory pathogen panel testing simplifies the process by screening numerous bacteria and viruses from a single sample. So, what is a respiratory pathogen panel? TOPLAB ® gives an overview of the …, 2019 Novel Coronavirus. COVID-19. Respiratory Viral panel. SARS-CoV-2. Special Instructions. Please note: Labcorp does not currently collect specimens for this test. …, Use. Detect possible allergic responses to various substances in the environment (see Test Includes) and evaluate for hay fever, asthma, atopic eczema, and respiratory allergy. The quantitative allergen-specific IgE test is indicated (1) to determine whether an individual has elevated allergen-specific IgE antibodies; (2) if specific allergic ..., Labcorp Patient™ is your partner in managing your health. Our easy and secure Labcorp patient account allows you to get lab results, track your health history, manage appointments and pay bills—all in one place. Thinking about growing your family? Meet the Ovia apps. Get daily, personalized family health support and resources to guide you ..., When ordered as Respiratory Virus panel, Epic LAB8656 this test includes all of the analytes below. When ordered as Cascading Respiratory Virus Panel, Epic LAB8657 this test will terminate if positive for influenza. ... PCR amplification; ePlex Respiratory Pathogen Panel. CPT Code: 0115U. Alphabetic main page. Updated: 2023/01/04 16:35:50., Collection. Female: Do not use lubricant on speculum. Cervical mucus should be removed first before inserting swab into endocervical canal, move swab from side to side allowing several seconds for absorption of organisms by the swab. Return swab to the transport tube and label. Male: Using small wire swab, gently scrape the anterior urethral ..., 1. Introduction. Epidemics of different respiratory infectious agents occur simultaneously each winter season or at intervals of several years. Viruses are most frequently involved (Esposito et al., 2013), but atypical bacterial pathogens, mainly Mycoplasma pneumoniae, can also play a role (Principi and Esposito, 2013, Brown et al., 2016).When available, the etiologic diagnosis of a ..., Use. Detect possible allergic responses to various substances in the environment (see Test Includes) and evaluate for hay fever, asthma, atopic eczema, and respiratory allergy. The quantitative allergen-specific IgE test is indicated (1) to determine whether an individual has elevated allergen-specific IgE antibodies; (2) if specific allergic ... , Changes and New Tests Explore the most recent updates to our Laboratory Test Directory in one convenient location. Review important information about upcoming or current Hotlines, CPT code changes, new tests, and immediate activations. Test Resources Find general guidance on ARUP specimen preparation and handling, specimen …, Respiratory Pathogen Panel. GTR Test ID Help: GTR000593026.5. Last updated: 2023-07-13. Test version history. Clinical microbial test Help for Mycoplasma …, Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC; 648014: Allergen Profile, Food-Basic: 602444: Class Description: N/A: 648014, Vacutainer® gray-top urine culture transport tube with preservative (preferred). If less than 4 mL of urine is collected, usually from pediatric and geriatric patients or from a catheter, submit refrigerated in a sterile, screw cap container or tube. Do not submit low volume urine specimens in underfilled gray top tubes., All allergens are reported down to a cutoff level of 0.10 kU/L. The significance of allergen specific IgE levels between 0.10 and 0.35 kU/L remains undefined. Cumulative levels of multiple allergen specific IgE antibodies may have an additive effect in producing clinical symptoms. Individual allergen specific IgE antibody levels may not always ..., The respiratory pathogens panel can detect a wide range of respiratory pathogens, including respiratory syncytial virus (RSV), influenza viruses, rhinovirus, adenovirus, coronavirus, Mycoplasma pneumoniae, Chlamydia pneumoniae, and more. The test usually takes a few hours to complete, and the results are typically available within a …, As of November 17, 2020, the current average time to deliver results for COVID-19, Flu & RSV combined testing is 1-3 days from the date of specimen pickup. Delivered to the ordering physician's EMR or Labcorp Link. Labcorp’s COVID-19 PCR test has not been FDA cleared or approved, has been authorized by FDA under an Emergency Use Authorization ..., All allergens are reported down to a cutoff level of 0.10 kU/L. The significance of allergen specific IgE levels between 0.10 and 0.35 kU/L remains undefined. Cumulative levels of multiple allergen specific IgE antibodies may have an additive effect in producing clinical symptoms. Individual allergen specific IgE antibody levels may not always ..., How much do solar panels cost — and are they worth the money? Our guide will help you decide if a solar system is worth the expense. Expert Advice On Improving Your Home Videos Lat..., Listed below are the potential results of the pneumonia panel and specific therapy recommendations based upon Nebraska Medicine-specific antibiogram data (respiratory tract-specific and overall antibiogram). Previous respiratory culture results and antibiotic allergies should be taken into account when making therapy decisions., Call Us Today! only you hotel valencia tripadvisor which of the following best describes advisory opinions, Labcorp test details for Sexually Transmitted Infections (STI ... Screen for and diagnose sexually transmitted infections and blood borne pathogens including syphilis, hepatitis B virus (HBV), hepatitis C virus (HCV), and HIV. ... Some of the assays in this panel have not been FDA cleared or approved for the screening of blood or plasma donors ..., Detect possible allergic responses to various substances in the environment (see Test Includes) and evaluate for hay fever, asthma, atopic eczema, and respiratory allergy. The quantitative allergen-specific IgE test is indicated (1) to determine whether an individual has elevated allergen-specific IgE antibodies; (2) if specific allergic ... , Negative results combined with respiratory illness may be due to pathogens not detected by this panel. Repeat testing should not be performed on specimens collected less than 7 days apart. For SARS-CoV-2 results from this assay, if repeat testing is considered within a 7-day period after an initial negative SARS-CoV-2 result, consider ordering ..., Smears made from fresh whole capillary (fingerstick) blood and/or capillary blood in EDTA (Microtainer™), or 3 to 5 mL fresh whole venous blood in EDTA, Labcorp’s COVID-19 PCR test has not been FDA cleared or approved, has been authorized by FDA under an Emergency Use Authorization (EUA), and has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. The test is only authorized for the duration of the declaration that circumstances ..., Laboratory testing for other pathogens from PUIs (including testing for influenza, RSV, respiratory pathogen panel, etc.) should not be delayed. In order to provide adequate infection control, please notify AEL in advance of sending specimens from a PUI for COVID-19. A separate specimen(s) will be required., TRUPCR® Respiratory Pathogen Panel Kit is based on amplification of conserved region of the microbial genome. There is a multiplexing reaction running in parallel in each tubes to detect different targets with the help of four different dyes (FAM/Green, Yellow/HEX/VIC, Orange/ROX/TEX Red & Red/Cy5)., The Sanity-2 Respiratory Pathogen Panel (RPP4) is a multiplex real-time, reverse transcriptase polymerase chain reaction (RT-PCR) test intended for the in vitro qualitative detection and differentiation of influenza A, influenza B, respiratory syncytial virus (RSV) and SARS-CoV-2 viral RNA in nasopharyngeal swab (NPS), oropharyngeal swab …, Respiratory Pathogen Panel. Qualitative multiplexed nucleic acid-based in vitro diagnostic test. Detect and differentiate 17 pathogens and subtypes from one sample, all-in-one test., This GI profile is a multiplexed nucleic acid test intended for the simultaneous qualitative detection and identification of nucleic acids from multiple bacteria, viruses and parasites directly from stool samples in Cary-Blair transport media obtained from individuals with signs and/or symptoms of gastrointestinal infection.