The Influence of Different Operating Conditions on the Blood Damage of a Pulsatile Ventricular Assist Device

ASAIO J. 2015 Nov-Dec;61(6):656-63. doi: 10.1097/MAT.0000000000000261.

Abstract

Because of pulsatile blood flow's benefit for myocardial recovery, perfusion of coronary arteries and end organs, pulsatile ventricular assist devices (VADs) are still widely used as paracorporeal mechanical circulatory support devices in clinical applications, especially in pediatric heart failure patients. However, severe blood damage limits the VAD's service period. Besides optimizing the VAD geometry to reduce blood damage, the blood damage may also be decreased by changing the operating conditions. In this article, a pulsatile VAD was used to investigate the influence of operating conditions on its blood damage, including hemolysis, platelet activation, and platelet deposition. Three motion profiles of pusher plate (sine, cosine, and polynomial), three stroke volumes (ejection fractions) (56 ml [70%], 42 ml [52.5%], and 28 ml [35%]), three pulsatile rates (75, 100, and 150 bpm), and two assist modes (copulsation and counterpulsation) were implemented respectively in VAD fluid-structure interaction simulations to calculate blood damage. The blood damage indices indicate that cosine motion profile, higher ejection fraction, higher pulsatile rate, and counterpulsation can decrease platelet deposition whereas increase hemolysis and platelet activation, and vice versa. The results suggest that different operating conditions have different effects on pulsatile VAD's blood damage and may be beneficial to choose suitable operating condition to reduce blood damage in clinical applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Assisted Circulation / methods*
  • Computer Simulation
  • Heart Failure / surgery*
  • Heart-Assist Devices / adverse effects*
  • Hemolysis / physiology
  • Humans
  • Models, Biological
  • Platelet Activation / physiology
  • Pulsatile Flow
  • Rabbits
  • Thrombosis / etiology
  • Thrombosis / physiopathology*