VisionQuest Biomedical Inc — Department of Health and Human Services SBIR Phase II: M

Description

DESCRIPTION provided by applicant This Phase II project is motivated by current issues associated with screening for retinopathy of prematurity ROP ROP is the leading cause of blindness in infants In recent years the number of infants at risk for ROP has been increasing In the United States the rate of prematurity has risen from of all births in to in for a total of over preterm births Preterm neonate disease management depends largely on timely screening and intervention Unfortunately low reimbursement levels for ROP screening insufficient equipment for ROP screening in remote locations and long term exposure to medical malpractice actions make it difficult to provide appropriate care to neonates at risk To mitigate these problems VisionQuest Biomedical LLC and its collaborators Oakland University MI and the Retina Institute of South Texas RIST will demonstrate and test NeoScan a family of software products aimed at improving the management and detection of ROP NeoScan consists of two products NeoScan Assist and NeoScan Detect NeoScan Assist is aimed at increasing the productivity and reducing the variability in interpretation by th neonatal healthcare providers through accurate quantification of vasculature tortuosity and caliber factors that have been demonstrated to correlate with the presence of advanced stages of ROP The objectives of NeoScan Assist are to reduce variability in the diagnosis of advanced stages of ROP and to provide a tool for accurate screening and staging of ROP in neonates NeoScan Detect is aimed at automatically identifying infants that need further examination by an ophthalmologist The objectives of this project will be accomplished through three specific aims In Aim we will finalize the product development of NeoScan Assist by productizing the methods developed during Phase I of this project In Aim a prospective clinical study will be performed to evaluate the effectiveness of NeoScan Assist and to provide data for validation of NeoScan Detect In Aim we will demonstrate the image processing techniques that will be part of NeoScan Detect At the end of this Phase II project we will be ready to submit an FDA k market clearance for NeoScan Assist and in parallel with that submission we will perform a clinical trial to demonstrate the safety and effectiveness of NeoScan Detect in preparation for an FDA market clearance submission of that product PUBLIC HEALTH RELEVANCE Retinopathy of prematurity ROP is a disease that affects low birth weight infants and is the leading cause of blindness in children worldwide In this project we will demonstrate NeoScan a family of software products aimed at improving the management and detection of ROP This project is relevant to public health because it addresses the need of providing better and more widespread eye care to preterm infants thus improving their health outcomes and potentially preventing blindness