Popular Articles
Cellulite Cream

Turkish Ministry Of Health Purchases Two CyberKnife(R) Systems
Accuray Incorporated (Nasdaq: ARAY), a global leader in the field of radiosurgery, announced that the Turkish Ministry of Health has purchased two CyberKnife(R) Robotic Radiosurgery Systems for installation in Ankara and Istanbul, Turkey.
generic viagra online
South London Healthcare Trust Announces Partnership With NHS Institute For Innovation And Improvement In Its Drive For Clinical Excellence
South London Healthcare NHS Trust (SLHT) is delighted to announce a new partnership with the NHS Institute for Innovation and Improvement as part of the trust"s drive for
News of the day
Quality Of Care Delivery In Colorectal Cancer Improved By Educational Initiatives
A study of targeted educational initiatives between the clinical staff at Fox Chase Cancer Center and the hospitals within their Partners program suggest that educational interventions by academic cancer centers can improve quality of care for cancer patients at community hospitals. The study, to be presented at the 2009 Annual Meeting of the American Society of Clinical Oncology, looked specifically at the number of lymph nodes that were surgically removed in colorectal cancer patients at Fox Chase"s partner hospitals and the impact that educational initiatives by clinical staff had on improving the number of nodes removed.
Endocrinology

Luminex Receives FDA Clearance For An Update To The XTAG(R) Respiratory Viral Panel Package Insert

Luminex Corporation (NASDAQ: LMNX), the worldwide leader in multiplexed solutions, today announced that the U.S. Food and Drug Administration (FDA) has cleared labeling updates for the company"s xTAG® Respiratory Viral Panel (RVP) to include data about the performance of the test in humans infected with the pandemic strain of influenza A, 2009 influenza A/H1N1, which is sometimes referred to as "swine flu." The test"s labeling has been updated to include information from two new studies that demonstrate that xTAG RVP can be an effective aid in the detection of 2009 Influenza A/HIN1, but cannot identify the hemagglutinin gene of the 2009 Influenza A/H1N1 in clinical specimens. "The studies now referenced in the xTAG RVP package insert demonstrate that the test can help determine if a patient is carrying a typical, seasonal respiratory virus or an unsubtypeable flu A virus," said Patrick J. Balthrop, president and chief executive officer of Luminex. "The xTAG RVP test can be a critical first line of defense in virus surveillance and in separating patients with more common respiratory infections from novel cases." xTAG RVP was first cleared by the FDA in January 2008. It is the only commercially available test that can simultaneously detect 12 respiratory viruses and subtypes, including influenza A with subtyping, at the DNA/RNA level. xTAG RVP was designed to detect the matrix gene that is shared across several influenza A strains, including 2009 influenza A/H1N1. In contrast, it does not detect the hemagglutinin gene of the 2009 Influenza A/H1N1 strain; whereas, it detects the hemagglutinin gene of seasonal strains of H1N1 and H3N2. This design enables xTAG RVP to provide 3 types of results for patients infected with influenza A: 1) influenza A-H1; 2) influenza A-H3; 3) influenza A-unsubtypeable. The xTAG RVP package insert has been updated to reference two recent publications of studies led by Dr. Christine Ginocchio, Director of Microbiology, Virology and Molecular Diagnostics at North Shore-LIJ Health System Laboratories: - "Evaluation of Multiple Test Methods for the Detection of the Novel 2009 Influenza A (H1N1) during the New York City Outbreak."1 This study evaluated the performance of a variety of diagnostic tests, including xTAG RVP, for 2009 Influenza A/H1N1 surveillance. A total of 2,715 patient samples were tested by xTAG RVP and 1,265 of these were positive for influenza A. Of the 1,265, 1,108 were influenza A-unsubtypeable, 151 were influenza A-H3, and 6 were influenza A-H1. Of the 1,108 flu A unsubtypeable samples tested by the x TAG RVP, all were confirmed to be the 2009 Influenza A/H1N1 with the CDC rRT-PCR assay for the 2009 Influenza A/H1N1. - "Likelihood that an unsubtypeable Influenza A result in the Luminex xTAG Respiratory Virus Panel is indicative of novel A/H1N1 (swine-like) influenza."2 In this study, which was carried out during the 2009 Influenza A/H1N1 (swine flu) outbreak in New York, 1,382 patient samples were initially tested with a variety of methods including rapid antigen tests, direct immunofluorescence, and rapid virus culture. Samples that tested positive for Influenza A with any of these methods, or derived from patients with a high potential to be infected with the 2009 Influenza A/H1N1 strain, were further tested with xTAG RVP. A total of 201 samples were identified as Flu A positive by xTAG RVP: 2 influenza A-H1, 58 influenza A-H3, 141 influenza A-unsubtypeable. Frozen residual portions were available for 101 of the 141 unsubtypeable samples tested on xTAG RVP and were forwarded to the Laboratory of Viral Diseases (Albany, NY) for further testing with the CDC rRT-PCR assay for 2009 Influenza A/H1N1 (swine flu). A total of 99 of the 101 specimens tested with the CDC assay were identified as positive for 2009 Influenza A/H1N1 (CThttp://www.luminexcorp.com/rvp. 1 Ginocchio C.C., Zhang F., et al (2009). "Evaluation of Multiple Test Methods for the Detection of the Novel 2009 Influenza A (H1N1) during the New York City Outbreak." J Clin Virol. (in press) 2 Ginocchio C.C. and St. George K (2009) "Likelihood that an unsubtypeable Influenza A result in the Luminex xTAG Respiratory Virus Panel is indicative of novel A/H1N1 (swine-like) influenza." J Clin Microbiol. J. Clin. Microbiol. 47(7): 1027-1029. Luminex Corporation


Add your comment:
Name:
Site address: http://
Your message:
Enter today\\\\'s date, 2 digits
(spam protection):