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Pulse Oximeter for Newborn Screening

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41HD079051-01A1
Agency Tracking Number: R41HD079051
Amount: $326,224.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: NICHD
Solicitation Number: PA12-089
Solicitation Year: 2013
Award Year: 2013
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
2520 W 237TH ST
TORRANCE, CA 90505-5217
United States
DUNS: 33449757
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 (424) 263-6310
Business Contact
Phone: (424) 263-6313
Research Institution
UNIVERSITY OF CALIFORNIA LOS ANGELES Office of Contract and Grant Administration 11000 Kinross Avenue, Suite 211
LOS ANGELES, CA 90095-2000
United States

 () -
 Nonprofit College or University

DESCRIPTION (provided by applicant): Congenital heart diseases (CHD) are the most common serious congenital anomalies and the leading cause of death due to birth defects. Clinical practice relying on physical examination of the newborn before discharge from the nursery often misses newborns with critical CHD (CCHD), which can lead to death or long-term morbidities. Using pulse oximetry (PO) can improve clinical examination by detecting CCHD that would otherwise be missed. In September 2011, DHHS decided toadd pulse oximetry screening in the right hand and one foot for CCHD detection to the Recommended Uniform Screening Panel. Hospitals throughout the US are now working expeditiously to implement PO screening programs so that all newborns will have PO screening prior to nursery discharge. However, there is no PO device for newborns and many are concerned about the high false screening rates and cost using current pulse oximeters. The goal of this project is to develop a pulse oximeter for newborn screening (PONS) that has many advantages: 1) simple to use thus reducing training time and cost; 2) much shorter procedure time; 3) better signal quality from multiple sensors; 4) lower cost from lower false positive rate and elimination of disposable sensors; less patient distress. We aim to develop a PONS prototype with multiple sensors for newborn screening. Our PONS device will slip over the infant's hand or foot, and a unique combination of algorithms and sensor placement will provide accurate, reproducible, SpO2reading in less than two minutes. A single use interior cover of the device will be used to prevent infection, enhance signal acquisition, and reduce the cost of screening. After initial bench top testing, safety and efficacy, the PONS will be evaluatedin 5 adults first, then in 5 newborns with co-oximetry validation. We will then conduct a clinical effectiveness study on newborns to benchmark PONS readings against conventional readings with a commercial pulse oximeter. We will recruit 100 newborns fromthe nursery at Harbor-UCLA Medical Center. All newborns will have pulse oximeter checks by a commercial device and the PONS at 24 hours of life. The primary expected outcome is a reduction of total procedure time with the PONS device. We will also comparethe following parameters-SpO2, signal quality, time for signal acquisition, cost, and user feedback. In Phase II of this project, the Phase I clinical will be used to re-engineer th device and conduct a clinical trial evaluating the cost-effectiveness ofthe PONS for CCHD detection in newborns during Phase II. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: Many infants born with critical congenital heart disease (CCHD), missed by routine clinical examination, die soon after hospital dischargeor suffer from long term complications. It is mandated by CDC that all newborns should undergo pulse oximetry screening of the right hand and one foot after 24 hours of life and before nursery discharge in order to detect CCHD. We aim to develop a pulse oximeter designed specifically for newborn screening that is accurate, convenient to use and cost-saving.

* Information listed above is at the time of submission. *

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