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Updated: Jun 15, 2026

Use of Two Intracorporeal Ventricular Assist Devices As a Total Artificial Heart

Use of Two Intracorporeal Ventricular Assist Devices As a Total Artificial Heart

Published on: May 11, 2018

Are ventricular assist devices underutilized?

Andrew J Boyle¹

¹Division of Cardiology, Aurora St Luke's Medical Center, Milwaukee, Wisconsin 53215, USA. andrew.boyle@aurora.org

Journal of Cardiac Surgery

|March 6, 2010

Summary

This summary is machine-generated.

Newer ventricular assist devices (VADs) promise improved reliability and function. Expanding mechanical circulatory support (MCS) requires enhanced technology, better patient selection, and broader access for advanced heart failure patients.

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Last Updated: Jun 15, 2026

Use of Two Intracorporeal Ventricular Assist Devices As a Total Artificial Heart

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Published on: May 11, 2018

Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock

Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock

Published on: June 12, 2021

Area of Science:

Cardiology
Biomedical Engineering
Heart Failure Management

Background:

Continuous flow ventricular assist devices (VADs) represent a significant advancement in mechanical circulatory support (MCS).
Current VAD technology faces challenges in durability and reliability, limiting patient eligibility and outcomes.
The development of next-generation VADs aims to overcome these limitations.

Purpose of the Study:

To analyze the critical factors influencing the expansion of the mechanical circulatory support (MCS) field.
To highlight the role of technological advancements and improved patient selection in VAD therapy.
To discuss the necessary improvements for broader adoption and enhanced patient quality of life.

Main Methods:

Review of current literature on VAD technology and clinical trials.
Analysis of factors impacting patient selection and outcomes in advanced heart failure.
Discussion of the requirements for FDA approval and commercialization of new VADs.

Main Results:

Next-generation continuous flow VADs show potential for enhanced durability and reliability.
Improvements in functional capacity and quality of life are crucial for expanding the VAD patient pool.
Optimized patient selection is key to improving outcomes and increasing MCS accessibility.

Conclusions:

Advancements in VAD technology and reliability are pivotal for the future of MCS.
Enhanced training, wider geographical availability, and refined patient selection criteria are essential for expanding VAD therapy.
Successful implementation of these factors will broaden the MCS patient population and improve overall patient care.