SBIR/STTR Research Award

Cardiac Monitor for VA ECMO Pediatric and Neonatal Patients

Award identifier 8d88702cd88c96135a15885145e5a2cbae200a7ad963dd74d95cc4a90d440de7Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,396,363

Program and phase

SBIR · Phase II

Award year

2019

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
TRANSONIC SYSTEMS, INC.
Proposal award date
2019-09-01
Contract end date
2021-08-31
UEI
JYLFZBGCEVB6
Solicitation number
PA16-302
Topic code
NHLBI

Research abstract

7. PROJECT SUMMARY/ABSTRACT Venoarterial Extracorporeal Membrane Oxygenation (VA ECMO) is a way to provide cardiac and pulmonary support to patients without other alternatives. This form of life support is vital to pediatric and neonatal patients. As with any life support, there are serious complications that occur. These complications including bleeding, thrombosis, and infection become more frequent the longer a patient is on ECMO. Therefore a method that would allow physicians to determine the cardiac status of these patients to know when to take them off VA ECMO would be very valuable. The long term objective of this project is to provide the first noninvasive bedside Cardiac Monitor for automatic/manual cardiac output and blood volume assessment for VA ECMO pediatric and neonatal patients. Unlike existing technology, this device will be allow for frequent measurements and will be suitable for use on infants and children. This device will consist of two ultrasound sensors that get clamped onto the ECMO tubing. Measurements are made by injecting saline into the ECMO circuit. Cardiac output and blood volume measurements are calculated using the ultrasound dilution curves produced. These values will be displayed on a monitor for the physician to see and determine the appropriate course of action for the patient. Based on preliminary work and the prototype software, algorithms for determining cardiac output and blood volume will be tested in an in-vitro model. Animal studies will be performed on 6-8 newborn lambs at the Animal Research Facility at Children’s National Medical Center to compare measurement techniques to be used to optimize the software. Phase I work will end with a preliminary study on 4-8 patients to collect feasibility data. In preparation for the clinical study in Phase II, necessary modifications will be made to the software and hardware. Clinical testing will be performed at the Children’s National Medical Center and the Children’s Hospital of Philadelphia on 40-48 neonatal and pediatric patients on VA ECMO. With the data acquired through clinical testing, the software will be optimized to yield highly accurate and reproducible measurements. Finally, preparation will begin for submission to the FDA for medical device clearance.8. PROJECT NARRATIVE A bedside noninvasive Cardiac Monitor for venoarterial extracorporeal membrane oxygenation (VA ECMO) would allow physicians to routinely determine the cardiac status of patients to know when they are ready to be taken off. This will help to reduce the serious and fatal complications patients experience due to prolonged time on VA ECMO.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

22 SBIR/STTR records share this UEI (1987–2020). Reported award amounts total $8,451,413. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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