SBIR/STTR Research Award

Development of Percutaneous DLC for Total Cavo pulmonary Assistance

Award identifier 352915486050776a6b48cc1bd083f09fc023343abd4ae17f9560b405b2f32ea3Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,000,521

Program and phase

SBIR · Phase II

Award year

2016

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
W-Z BIOTECH LLC
Proposal award date
2016-08-15
Contract end date
2018-07-31
UEI
RK1ZDCXE3LJ7
Solicitation number
PA15-269
Topic code
NHLBI

Research abstract

DESCRIPTION provided by applicant The Fontan procedure or total cavopulmonary connection TCPC is a standard palliative surgery for patients with complex single ventricle congenital heart anomalies TCPC connects the inferior and superior vena cava IVC and SVC directly to the right pulmonary artery bypassing the heart The single ventricle is then reserved for pumping oxygenated blood to the systemic circulation The Fontan procedure has benefited thousands of patients but the Fontan circulation fails years later with relatively high mortality The failing Fontan circulation causes end organ dysfunction due to venous blood congestion from elevated central venous pressure and low arterial blood perfusion from low cardiac output The only effective option for the failing Fontan patient is heart transplant but most of these patients are too sick to be transplant candidates Cavopulmonary assist CPA is needed to pump venous blood from SVC IVC through the Fontan connection to reverse failing Fontan pathophysiology Our ultimate goal is to create a convenient and secure connection between the TCPC and the blood pump establishing an ambulatory percutaneous CPA system Our enabling technology is one of the worldandapos s most complex double lumen cannula DLC Through only one percutaneous venous cannulation this DLC can easily connect the TCPC to a commercial blood pump without major surgery This CPA system will bridge the failing Fontan patient to heart transplant recovery and or further reconstructive heart surgery In ou phase I study the working prototype demonstrated up to l min blood flow in our sheep model and completely reversed failing Fontan circulation n achieving total CPA In this Phase II SBIR we will optimize the design based on our Phase I results and fabricate a final commercial quality CPA DLC prototype for bench test and day survival in vivo studies Specific Aim To design and fabricate a percutaneous DLC for ambulatory CPA application Two thin membrane umbrellas are designed on the DLC to prevent infusion flow recirculation ensuring efficient and reliable performance These umbrellas do not block the blood flow from SVC and IVC to pulmonary artery guaranteeing safety if the CPA system malfunctions Two infusion openings guide separate blood flow to each umbrella eliminating blood stagnancy and associated thrombosis formation Particle image velocimetry PIV validated CFD will be used to optimize the design for maximum performance and minimal thrombotic potential Specific Aim To test the CPA DLC prototype in a simulated mock loop bench test Bench testing will include performance reliability evaluation one month durability test and PIV flow study Specific Aim To test the CPA DLC prototype in our TCPC sheep model Short term in vivo studies N will test CPA DLC feasibility performance and reliability Long term day in vivo studies N will test performance reliability durability and biocompatibility Although the CPA DLC market is small the impact on the patients that need CPA is significant PUBLIC HEALTH RELEVANCE We are proposing to develop a percutaneous cavo pulmonary assist system to bridge the patients with failing Fontan circulation for recovery reconstructive surgery and heart transplantation

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

10 SBIR/STTR records share this UEI (2011–2024). Reported award amounts total $6,885,758. 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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