BEARINGLES DISPOSABLE CENTRIFUGAL BLOOD PUMP

Information

  • Research Project
  • 2771456
  • ApplicationId
    2771456
  • Core Project Number
    R44HL055037
  • Full Project Number
    5R44HL055037-03
  • Serial Number
    55037
  • FOA Number
  • Sub Project Id
  • Project Start Date
    8/1/1995 - 28 years ago
  • Project End Date
    8/31/1999 - 24 years ago
  • Program Officer Name
  • Budget Start Date
    9/15/1998 - 25 years ago
  • Budget End Date
    8/31/1999 - 24 years ago
  • Fiscal Year
    1998
  • Support Year
    3
  • Suffix
  • Award Notice Date
    9/7/1998 - 25 years ago
Organizations

BEARINGLES DISPOSABLE CENTRIFUGAL BLOOD PUMP

The duration of use of the present generation of disposable centrifugal blood pumps has been limited to 1 to 2 days due to the propensity for thrombus formation around the central bearing and/or shaft seals need to maintain rotor stability. For many patients undergoing short term post-cardiotomy support, duration of support up to two weeks is desirable for heart recovery. To eliminate the bearing problem, we have demonstrated in Phase I the operation of a non-contact, passively operated bearing using permanent magnet configurations for maintaining angular and radial stability of the rotor and hydrostatic pressure distribution over the surfaces of the rotor for axial stability. The pump configuration is compatible with the use of currently available external rotor drive units. Such a device is amenable to cardiac support without the use of anticoagulation. In the Phase H program, a comprehensive design optimization of the non-contact bearing, flow around the bearing, and pump configuration will be tested. Following this effort, non- contact bearing centrifugal pumps will be fabricated and tested in vitro for device performance, and tested in vivo to demonstrate minimal hemolysis and its anti-thrombogenic characteristics. PROPOSED COMMERCIAL APPLICATIONS The potential application of the device is in approximately 300,000 cardiac surgery cases per year in the US which require cardiopulmonary bypass. The proposed device 'will be particularly appropriate for use in those patients requiring circulatory support extending beyond a few hours, into the range of a few weeks. These cases number approximately 10,000 to 20,000 annually in the US.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R44
  • Administering IC
    HL
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    837
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ZRG7
  • Study Section Name
  • Organization Name
    ABIOMED, INC.
  • Organization Department
  • Organization DUNS
    050636737
  • Organization City
    DANVERS
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    01923
  • Organization District
    UNITED STATES