Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Control systems for the electric heart.

R K White1, D B Olsen

  • 1Division of Artificial Organs, University of Utah, Salt Lake City 84103-1414.

Artificial Organs
|October 1, 1991
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Achievement of Target Gain Larger than Unity in an Inertial Fusion Experiment.

Physical review letters·2024
Same author

Lawson Criterion for Ignition Exceeded in an Inertial Fusion Experiment.

Physical review letters·2022
Same author

Long-acting formulations for the treatment of latent tuberculous infection: opportunities and challenges.

The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease·2018
Same author

Prototype Continuous Flow Ventricular Assist Device Supported on Magnetic Bearings.

Artificial organs·2017
Same author

Fine structure of swarmers of Cladophora and Chaetomorpha : III. Wall synthesis and development.

Planta·2014
Same author

The death crisis and pastoral counseling.

Journal of religion and health·2013
Same journal

Large-Eddy Simulation of the FDA Benchmark Blood Pump: Validation Against Experiments and Implications for Turbulent Flow Mechanisms.

Artificial organs·2026
Same journal

The Warm Revolution: A Meta-Analysis of DCD Versus DBD Liver Transplant Outcomes in the Normothermic Machine Perfusion Era.

Artificial organs·2026
Same journal

Toward Optimal Remote Monitoring in LVAD Recipients: Remaining Challenges Beyond Feasibility.

Artificial organs·2026
Same journal

Advancing Organ Preservation and Perfusion: Introducing the International Society of Organ Preservation and Perfusion Therapy (ISOPPT).

Artificial organs·2026
Same journal

Short Inter-Treatment Interval Treatment With Artificial Liver Support System Reduces 90-Day Transplant-Free Mortality in Patients With Hepatitis B Virus-Related Acute-On-Chronic Liver Failure: A Retrospective Observational Study.

Artificial organs·2026
Same journal

Extracorporeal Albumin Dialysis (OPAL) as Novel Therapeutic Bridging Option in Posthepatectomy Liver Failure.

Artificial organs·2026
See all related articles

Predicting and controlling cardiac output (CO) in total artificial heart (TAH) recipients remains challenging. Current TAH systems struggle to integrate physiological data for optimal blood flow regulation, highlighting a need for improved control strategies.

Area of Science:

  • Biomedical Engineering
  • Cardiovascular Physiology
  • Medical Device Technology

Background:

  • Accurate prediction and control of cardiac output (CO) in total artificial heart (TAH) recipients have evolved significantly.
  • Early TAH models featured limited control and fixed pumping parameters.
  • Modern TAH systems require complex interactions between blood volume and electric pumps for organ perfusion.

Purpose of the Study:

  • To review the evolution of methods for predicting and controlling cardiac output in TAH recipients.
  • To identify the limitations of current TAH control strategies.
  • To highlight the lack of consensus on appropriate physiological parameters for TAH regulation.

Main Methods:

  • Review of historical and current methodologies for TAH control.

Related Experiment Videos

  • Analysis of electromechanical systems and their integration with physiological feedback.
  • Examination of attempts to link end-organ function to TAH control.
  • Main Results:

    • Past TAH models had minimal control mechanisms.
    • Current advanced TAH devices necessitate intricate communication for maintaining blood flow.
    • Attempts to quantify end-organ flow, metabolic changes, and oxygen delivery for TAH control have been unsuccessful.
    • Existing devices focus on predicting CO via preload and afterload monitoring.
    • No consensus exists on which in vivo physiological parameters should regulate TAH output.

    Conclusions:

    • The precise control of cardiac output in TAH recipients remains a significant clinical challenge.
    • Current TAH technologies face difficulties in integrating comprehensive physiological feedback for optimal regulation.
    • Further research is needed to establish consensus on physiological parameters for effective TAH control.