Infertility affects one out of every 6 couples and about 7.3 million women and their partners in the U.S..The demand for assisted reproduction tools and procedures is growing worldwide. This growth is occurring despite the significant cost per IVF cycle and the low success rate, with approximately one-third of cycles resulting in a live birth. This necessitates the transfer of multiple embryos and/or conducting multiple cycles, leading to greater physical, emotional, practical and financial costs, before determining if pregnancy can be achieved.
About the Early Embryo Viability Assessment ( Eeva) Test
The Eeva test provides IVF clinicians with predictive information about the embryo's development potential to help improve embryo selection. Eeva's proprietary software automatically analyzes embryo development against scientifically and clinically validated cell-division parameters conceived by researchers at Stanford University in the US. With results from the Eeva test, IVF teams now have predictive and objective information to combine morphological assessment to help improve the embryo selection decision. The Eeva Test was validated in a prospective, multi-centre, 54-patient clinical trial with 758 embryos. Embryologists using Eeva were significantly able to improve their ability to identify non-viable embryos relative to traditional methods alone. Additionally, Eeva was able to increase the consistency of embryo assessment across embryologists. Results of this study were presented in July 2012 at the European Society of Human Reproduction and Embryology (ESHRE) Annual Meeting and published by Conaghan et al in Fertility and Sterility, May 2013.
Eeva is currently CE Marked and available for use in the EU and is pending FDA clearance in the United States . For a full list of clinics offering the Eeva test please visit http://www.eevaivf.com or follow us on Twitter @EevaIVF.About Auxogyn