BEDSIDE SYSTEM FOR COMBINED RNA AND PACIN HEART FAILURE

Information

  • Research Project
  • 6337390
  • ApplicationId
    6337390
  • Core Project Number
    R43HL065963
  • Full Project Number
    1R43HL065963-01A1
  • Serial Number
    65963
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/27/2001 - 24 years ago
  • Project End Date
    5/31/2004 - 21 years ago
  • Program Officer Name
    CHEUNG, GEOFFREY P.
  • Budget Start Date
    9/27/2001 - 24 years ago
  • Budget End Date
    5/31/2004 - 21 years ago
  • Fiscal Year
    2001
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    9/26/2001 - 24 years ago

BEDSIDE SYSTEM FOR COMBINED RNA AND PACIN HEART FAILURE

DESCRIPTION (Provided by Applicant): One of the most significant current health care challenges is treatment of heart failure (HF). There are approximately 5 million Americans currently diagnosed with this condition, and there are 400,000-700,000 new cases annually. The direct costs of treatment are estimated at $10-$38 billion with the majority of this cost attributable to patients with New York Heart Association Class III or IV disease. Much of this cost is a result of repeat hospitalization, which occurs in many cases because of inappropriate therapeutic drug regimen. This proposal seeks to develop a technology for combined bedside radionuclide angiography (RNA) and pulmonary artery catheterization (PAC) that can be employed in this population at reasonable cost in the CCU. By merging RNA and PAC, this system will yield LV and RV ejection fractions, right heart, pulmonary, and left atrial pressures, cardiac output, stroke volume, wall motion, pulmonary blood volume, and, most significantly, absolute RV and LV volume curves, so that pressure-volume relations can be examined. By providing this wealth of additional clinical data, which can be obtained repeatedly at low cost through use of a short-lived radiotracer, this system will enable much more thorough evaluation of such patients, including quantitative examination of the effects of interventions, such as dobutamine and IV diuretics, as well as assessments of response to therapeutic dose levels. It will therefore lead to improved diagnosis, allow drug dose levels to be more accurately determined, and improve prognostic assessment. Since much of the cost of this disease is attributable to the need for repeated hospitalization of decompensated patients, substantial reduction of overall cost can be realized. Improved prognostic evaluation can also have a profound benefit by more accurately identifying patients who are suitable for heart transplantation and/or coronary artery bypass. PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R43
  • Administering IC
    HL
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    100000
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    837
  • Ed Inst. Type
  • Funding ICs
    NHLBI:100000\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    PROPORTIONAL TECHNOLOGIES, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    HOUSTON
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    77054
  • Organization District
    UNITED STATES