One of the major maladaptive changes after a major heart attack or cardiac event is an initial decline in pumping capacity of the heart leading to activation of a variety of compensatory mechanisms, and subsequently a phenomenon known as cardiac or left ventricular remodeling, i.e., a geometrical change in the architecture of the left ventricle. Evidence suggests that the local mechanical environment governs remodeling processes. Thus, in order to control two important mechanical parameters, cardiac size and cardiac output, we have developed a minimally invasive direct cardiac contact device capable of providing two actions simultaneously: (1) adjustable cardiac support to modulate cardiac size and (2) synchronous active assist to modulate cardiac output. As a means of enabling experiments to determine the role of these mechanical parameters in reverse remodeling or ventricular recovery, the device was further designed to (1) be deployed via minimally invasive surgical procedures, (2) allow uninhibited motion of the heart, (3) remain in place about the heart via an intrinsic pneumatic attachment, and (4) provide direct cardiac compression without aberrantly inverting the curvature of the heart. These actions and features are mapped to particular design solutions and assessed in an acute implantation in an ovine model of acute heart failure (esmolol overdose). The passive support component was used to effectively shift the EDPVR leftward, i.e., counter to the effects of disease. The active assist component was used to effectively decompress the constrained heart and restore lost cardiac output and stroke work in the esmolol failure model. It is expected that such a device will provide better control of the mechanical environment and thereby provide cardiac surgeons a broader range of therapeutic options and unique intervention possibilities.
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December 2011
Research Papers
Assessment of Minimally Invasive Device That Provides Simultaneous Adjustable Cardiac Support and Active Synchronous Assist in an Acute Heart Failure Model
Michael R. Moreno,
Michael R. Moreno
Department of Biomedical Engineering,
e-mail: michael.moreno@tamu.edu
Texas A&M University, College Station
, TX 77843-3120; CorInnova Incorporated, College Station, TX 77845
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Saurabh Biswas,
Saurabh Biswas
Department of Biomedical Engineering,
Texas A&M University
, College Station, TX 77843-3120
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Lewis D. Harrison,
Lewis D. Harrison
CorInnova Incorporated
, College Station, TX 77845
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Guilluame Pernelle,
Guilluame Pernelle
CorInnova Incorporated
, College Station, TX 77845
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Matthew W. Miller,
Matthew W. Miller
Texas A&M Institute for Preclinical Studies, Texas A&M University
, College Station, TX 77843; Department of Small Animal Clinical Sciences, College of Veterinary Medicine, Texas A&M University, College Station, TX 77943-4474
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Theresa W. Fossum,
Theresa W. Fossum
Texas A&M Institute for Preclinical Studies, Texas A&M University
, College Station, TX 77843; Department of Small Animal Clinical Sciences, College of Veterinary Medicine, Texas A&M University, College Station, TX 77943-4474
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David A. Nelson,
David A. Nelson
Texas A&M Institute for Preclinical Studies, Texas A&M University
, College Station, TX 77843
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John C. Criscione
John C. Criscione
Department of Biomedical Engineering,
Texas A&M University
, College Station, TX 77843-3120; CorInnova Incorporated, College Station, TX 77845
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Michael R. Moreno
Department of Biomedical Engineering,
Texas A&M University, College Station
, TX 77843-3120; CorInnova Incorporated, College Station, TX 77845e-mail: michael.moreno@tamu.edu
Saurabh Biswas
Department of Biomedical Engineering,
Texas A&M University
, College Station, TX 77843-3120
Lewis D. Harrison
CorInnova Incorporated
, College Station, TX 77845
Guilluame Pernelle
CorInnova Incorporated
, College Station, TX 77845
Matthew W. Miller
Texas A&M Institute for Preclinical Studies, Texas A&M University
, College Station, TX 77843; Department of Small Animal Clinical Sciences, College of Veterinary Medicine, Texas A&M University, College Station, TX 77943-4474
Theresa W. Fossum
Texas A&M Institute for Preclinical Studies, Texas A&M University
, College Station, TX 77843; Department of Small Animal Clinical Sciences, College of Veterinary Medicine, Texas A&M University, College Station, TX 77943-4474
David A. Nelson
Texas A&M Institute for Preclinical Studies, Texas A&M University
, College Station, TX 77843
John C. Criscione
Department of Biomedical Engineering,
Texas A&M University
, College Station, TX 77843-3120; CorInnova Incorporated, College Station, TX 77845J. Med. Devices. Dec 2011, 5(4): 041008 (9 pages)
Published Online: November 28, 2011
Article history
Received:
January 29, 2011
Revised:
July 9, 2011
Online:
November 28, 2011
Published:
November 28, 2011
Citation
Moreno, M. R., Biswas, S., Harrison, L. D., Pernelle, G., Miller, M. W., Fossum, T. W., Nelson, D. A., and Criscione, J. C. (November 28, 2011). "Assessment of Minimally Invasive Device That Provides Simultaneous Adjustable Cardiac Support and Active Synchronous Assist in an Acute Heart Failure Model." ASME. J. Med. Devices. December 2011; 5(4): 041008. https://doi.org/10.1115/1.4004652
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