LifeBelt CPR: Combined Thoracic and Sternal Compression

Information

  • Research Project
  • 6641971
  • ApplicationId
    6641971
  • Core Project Number
    R41HL071378
  • Full Project Number
    1R41HL071378-01A1
  • Serial Number
    71378
  • FOA Number
    PA-01-54
  • Sub Project Id
  • Project Start Date
    5/5/2003 - 21 years ago
  • Project End Date
    4/30/2004 - 20 years ago
  • Program Officer Name
    DESVIGNE-NICKENS, PATRICE
  • Budget Start Date
    5/5/2003 - 21 years ago
  • Budget End Date
    4/30/2004 - 20 years ago
  • Fiscal Year
    2003
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    -
Organizations

LifeBelt CPR: Combined Thoracic and Sternal Compression

[unreadable] DESCRIPTION (provided by applicant): [unreadable] In the United States, more than 250,000 persons annually experience out-of-hospital sudden cardiac death (SCD). However, few, approximately 4%, are revived with standard CPR and advanced life support interventions and survive to be discharged from the hospital. Successful restoration of cardiac function after SCD is dependent on early electrical defibrillation in patients found to be in ventricular fibrillation (VF) and early provision of effective artificial circulation and ventilation, i.e., CPR. However, standard CPR, as currently practiced, provides only 10-20% of normal cardiac output. The purpose of this project is to evaluate the effectiveness of a new manual CPR device that provides sequential thoracic and sternal (cardiac) compression. The specific aims of the project include defining the mechanism of blood flow produced by the device, measuring intravascular pressures, blood flow, and ventilation during prolonged CPR with the device, and evaluating short-term outcome when the device is compared to standard manual CPR. All studies will be undertaken in the research laboratory and design modifications of the device will be made based upon laboratory observations. The mechanism of blood flow will be assessed with pressure synchronized cine-angiography, transesophageal 2-D Doppler echocardiography, and high-fidelity hemodynamic measurements. Cardiac output, coronary perfusion pressure, and ventilation produced by the device will be evaluated in an animal model of VF cardiac arrest and resuscitation. The new CPR device will be compared to conventional manual CPR with a study end-point of short-term outcome and survival for three hours. The long-term objective of the project is the production of a simple manual CPR device that will produce greater blood flow than standard CPR, negate the need for mouth-to-mouth ventilation, and that can be used by the lay person with minimal instruction. The device could easily be deployed with existing automatic external defibrillators (AEDs), which provide brief and simple audio instruction regarding use. Use of early and effective CPR with the new device preceding or following early defibrillation attempts by lay persons (public access defibrillation) could result in more lives saved. [unreadable] [unreadable]

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R41
  • Administering IC
    HL
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    151452
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    837
  • Ed Inst. Type
  • Funding ICs
    NHLBI:151452\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    DECA-MEDICS, INC.
  • Organization Department
  • Organization DUNS
    102349441
  • Organization City
    COLUMBUS
  • Organization State
    OH
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    43212
  • Organization District
    UNITED STATES