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Rapid Ebola Test Could Play Key Role in Efforts to End Lingering Outbreak

Lead author of research showing the test's accuracy to discuss findings at 2015 AACC Annual Meeting

Dedicated to achieving better health through laboratory medicine, the American Association for Clinical Chemistry, AACC, brings together more than 50,000 clinical laboratory professionals, physicians, research scientists, and business leaders from around the world focused on clinical chemistry, molecular diagnostics, mass spectrometry, translational medicine, lab management, and other areas of breaking laboratory science. Since 1948, AACC has worked to advance the common interests of the field, providing programs that advance scientific collaboration, knowledge, expertise, and innovation. For more information, visit www.aacc.org.

News provided by

AACC

Jul 27, 2015, 10:30 ET

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ATLANTA, July 27, 2015 /PRNewswire-USNewswire/ -- Research presented at the 2015 AACC Annual Meeting & Clinical Lab Expo will expand on the studies that led to a fingerprick Ebola test becoming the first and only rapid diagnostic for this disease to receive approval from the World Health Organization (WHO). This test could prove vital to breaking Ebola's grip on West Africa by identifying suspected Ebola cases within minutes, and enabling healthcare workers to isolate and treat these patients much faster than is currently possible.

More than 11,000 people have died since the Ebola epidemic began in March 2014, and though cases have been declining, the international emergency response that the outbreak prompted has not been able to drive the virus back underground. The fight against the disease achieved a significant victory in May, when Liberia—one of the nations hardest hit by the virus—was declared Ebola-free by WHO. Less than 2 months after this win, however, new cases of the disease were discovered in the country. The first of these was a 17-year-old boy who was misdiagnosed with malaria and who, before passing away, came into contact with at least 102 people who may have caught the disease from him. This case tragically illustrates the need for a fast way to accurately identify Ebola cases so that patients get the care they need and transmission can be halted.

The Viral Hemorrhagic Fever Consortium, which is led by Tulane University and the diagnostic company Corgenix, has developed such a rapid test for Ebola. Called the ReEBOV Antigen Rapid Test Kit, this test uses a few drops of blood and the same technology used in at-home pregnancy tests to provide results in 15 minutes. In comparison, the current gold standard test for Ebola, qRT-PCR, can take up to a day to return a diagnosis.

Matt Boisen, Program Director of Infectious Diseases and Emerging Technologies at Corgenix and Development Director of In Vitro Diagnostics at the Viral Hemorrhagic Fever Consortium, will present the findings of two studies by WHO and Corgenix, respectively, demonstrating ReEBOV's efficacy at the 2015 AACC Annual Meeting. The WHO study, conducted in Ebola-hotspot Sierra Leone, compares ReEBOV's performance with that of qRT-PCR. By testing 292 stored patient samples with both methods, researchers found that ReEBOV performed nearly as well as the gold standard, and agreed with qRT-PCR on 91.8% of infected samples and 84.6% of non-infected samples. ReEBOV's accuracy was also recently confirmed by a third separate study published in The Lancet. This means that ReEBOV could be used as a complement to qRT-PCR, enabling healthcare workers to act immediately on potential Ebola cases without having to wait for the qRT-PCR results to come in.

"All three studies—our internal emergency use authorization study, the WHO study, and The Lancet paper—show that the rapid test can provide a plus 90 percent accuracy when paired with the PCR test," said Boisen. "This really establishes that the rapid test can be used as a triage method to quickly provide patient results that can later be confirmed by PCR. This represents a breakthrough in the detection of Ebola for this and future Ebola virus outbreaks."

Session Information
AACC annual meeting registration is free for members of the media. Reporters can register online here: https://www.xpressreg.net/register/aacc075/media/landing.asp 

Session 32104: Clinical Outcome-Focused Patient Care
Monday, July 27
10:30 a.m. – Noon
Room B314
Georgia World Congress Center
Atlanta

About the 2015 AACC Annual Meeting & Clinical Lab Expo
AACC's annual meeting offers 5 days packed with opportunities to learn about exciting science from July 26–30. Plenary sessions feature expert presentations on using tumor DNA in the blood to diagnose and monitor cancer, reducing the risk of heart disease, transparency in healthcare delivery, the latest advances that could lead to a cure for HIV, and new tests and treatment for infection.

At the AACC Clinical Lab Expo, more than 700 exhibitors will fill the show floor of Atlanta's convention center, Georgia World Congress Center, with displays of the latest diagnostic technology, including but not limited to mobile health, molecular diagnostics, mass spectrometry, point-of-care, and automation.

About AACC
Dedicated to achieving better health through laboratory medicine, AACC brings together more than 50,000 clinical laboratory professionals, physicians, research scientists, and business leaders from around the world focused on clinical chemistry, molecular diagnostics, mass spectrometry, translational medicine, lab management, and other areas of progressing laboratory science. Since 1948, AACC has worked to advance the common interests of the field, providing programs that advance scientific collaboration, knowledge, expertise, and innovation. For more information, visit www.aacc.org.

Logo - http://photos.prnewswire.com/prnh/20130701/PH41045LOGO

Christine DeLong
AACC
Manager, Communications & PR
(p) 202.835.8722
[email protected]

Molly Polen
AACC
Director of Communications & PR
(p) 202.420.7612
(c) 703.598.0472
[email protected]

SOURCE AACC

Related Links

http://www.aacc.org

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