SBIR-STTR Award

A comparison of doppler cardiac output determination
Award last edited on: 3/1/2007

Sponsored Program
SBIR
Awarding Agency
NIH : NHLBI
Total Award Amount
$50,000
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Emily Johnson

Company Information

Cardiac Screening Partners (AKA: Cardionics)

910 Bay Star Boulevard
Webster, TX 77598
   (281) 488-5901
   keithj@cardionics.com
   www.cardionics.com
Location: Single
Congr. District: 22
County: Harris

Phase I

Contract Number: 1R43HL034249-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1985
Phase I Amount
$50,000
Cardionics, Inc of Houston, Texas is currently providing a relatively inexpensive portable pulsed Doppler (PD) ultrasonic unit that noninvasively measures cardiac output (CO) in humans. Using thermodilution as the invasive standard for CO determination, this study will compare the relative reliabilities and accuracies of the PD device (CardioFlo_) and a commercially available continuous wave Doppler unit (CWD) (Ultracom_). The specific objectives of this study are 1. to determine whether this simple noninvasive device can accurately and reliably measure CO and 2. to investigate possible design improvements that can be incorporated into a subsequent model.We will address the relative accuracies of several methods of obtaining and processing Doppler spectral signals. Quadrature outputs will be recorded and subsequently analyzed through computer-based fast Fourier transform (FFT) and analog offset zerocrosser (ZC) units. Paired comparisons will be: 1. PD vs. CWD; 2. baseband ZC vs. FFT; 3. baseband ZC vs. offset ZC; 4. analog or digital integration of the entire cardiac cycle vs. Ieft ventricular ejection period only; 5. analog temporal mean of consecutive cycles vs. operator selected cycles.Phase II of this study will incorporate the results of Phase I into an improved CardioFlo_ unit which should have widespread commercial applications in clinical and research settings where CO is needed but the cost and risks of traditional invasive methods are not justified.National Heart, Lung, and Blood Institute (NHLBI)

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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