Positive Clinical Study Results for BSP’s HyperQ Technology will be reported in American Journal of Cardiology
November 16, 2011 – Biological Signal Processing (BSP), which develops and manufactures products for the non-invasive, accurate diagnosis of coronary artery disease (CAD), recently announced the successful completion of a comprehensive clinical research study evaluating the performance of the company’s HyperQ technology in diagnosing CAD. An article describing the study and its results was accepted for publication in the American Journal of Cardiology.
The study recruited 996 patients and compared the clinical performance of HyperQ vs. conventional electrocardiogram (ECG) for the detection of CAD, using nuclear imaging as the gold standard. The study was conducted in two major medical centers in Israel – Assuta Medical Center and Sheba Medical Center, and was headed by Tali Sharir, M.D., and professor Pierre Chouraqui. The major finding reported by the researchers is a 30 percent improvement in the sensitivity of the HyperQ analysis in the detection of CAD when compared to conventional stress ECG. HyperQ analysis also had a lower false alarm rate compared to conventional stress ECG.
The results of this study were also recently presented, together with additional HyperQ related clinical evidence, at a meeting and hearing of the Medicare Evidence Development & Coverage Advisory Committee (MEDCAC) in the United States. The MEDCAC meeting on November 9th was convened in order to consider and make recommendations on the use of new ECG signal analysis technologies to detect CAD, and regarding their inclusion in the coverage policies. MEDCAC is an advisory committee, commissioned by to CMS (Centers for Medicare & Medicaid Services) – the organization responsible for the determination of the services and medical products that will be reimbursed by Medicare and Medicaid, also heavily weighing in on the coverage policies of private insurers in the United States. The MEDCAC committee concluded its discussions with a recommendation encouraging the CMS to include new signal analysis technologies, that are U.S. Food and Drug Administration (FDA) cleared and have shown sufficient clinical evidence, in the coverage policies for cardiac care and diagnosis.
"Appearing before MEDCAC committee is an important milestone in the process of obtaining reimbursement for our products in the U.S.," says Amir Beker, M.D., chairman of BSP, who presented at the hearing. He added, "This endeavor is also backed by a HyperQ large-scale clinical study in three leading U.S. medical centers, The Cleveland Clinic, University of Virginia medical center and Minneapolis Heart Institute Foundation, to collect clinical and economic data in support of BSP's reimbursement campaign in the U.S."
For more information: www.bspmedical.com