254 IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, VOL. 57, NO. 2, FEBRUARY 2010
Parameter-Optimized Model of Cardiovascular–
Rotary Blood Pump Interactions
Einly Lim, Socrates Dokos, Shaun L. Cloherty, Member, IEEE, Robert F. Salamonsen,
David G. Mason, John A. Reizes, and Nigel H. Lovell
∗
, Senior Member, IEEE
Abstract—A lumped parameter model of human
cardiovascular–implantable rotary blood pump (iRBP) in-
teraction has been developed based on experimental data recorded
in two healthy pigs with the iRBP in situ. The model includes
descriptions of the left and right heart, direct ventricular
interaction through the septum and pericardium, the systemic
and pulmonary circulations, as well as the iRBP. A subset of
parameters was optimized in a least squares sense to faithfully
reproduce the experimental measurements (pressures, flows and
pump variables). Our fitted model compares favorably with our
experimental measurements at a range of pump operating points.
Furthermore, we have also suggested the importance of various
model features, such as the curvilinearity of the end systolic
pressure–volume relationship, the Starling resistance, the suction
resistance, the effect of respiration, as well as the influence of
the pump inflow and outflow cannulae. Alterations of model
parameters were done to investigate the circulatory response to
rotary blood pump assistance under heart failure conditions. The
present model provides a valuable tool for experiment designs,
as well as a platform to aid in the development and evaluation of
robust physiological pump control algorithms.
Index Terms—Heart failure, heart–pump interaction model, im-
plantable rotary blood pump (iRBP), ventricular assist devices.
I. INTRODUCTION
I
MPLANTABLE rotary blood pumps (iRBPs) have potential
as bridge-to-transplantation and destination therapy devices
for end-stage heart failure patients. However, insensitivity of
iRBPs to preload, overpumping, or underpumping may endan-
ger implant recipients if pump control is not properly imple-
mented. This is further complicated by the remaining intrinsic
ventricular function, which is dependent on residual contractil-
Manuscript received February 19, 2009; revised May 12, 2009. First
published September 18, 2009; current version published January 20, 2010.
Asterisk indicates corresponding author.
E. Lim and S. Dokos are with the Graduate School of Biomedical Engineer-
ing, University of New South Wales, Sydney, N.S.W. 2052, Australia (e-mail:
z3179719@student.unsw.edu.au; s.dokos@unsw.edu.au).
S. L. Cloherty is with the Research School of Biology, Australian National
University, Canberra, A.C.T., Australia (e-mail: shaun.cloherty@anu.edu.au).
R. F. Salamonsen is with the Cardiothoracic Intensive Care, Alfred Hospital,
Melbourne, Vic., Australia, and also with Monash University, Melbourne, Vic.
3800, Australia (e-mail: r.salamonsen@alfred.org.au).
D. G. Mason is with the School of Information Technology and Electri-
cal Engineering, University of Queensland, Brisbane, Qld., Australia (e-mail:
mason@itee.uq.edu.au).
J. A. Reizes is with the School of Mechanical and Manufacturing Engineer-
ing, University of New South Wales, Sydney, N.S.W. 2052, Australia, and also
with the Faculty of Engineering, University of Technology Sydney, Sydney,
N.S.W. 2000, Australia.
∗
N. H. Lovell is with the Graduate School of Biomedical Engineering,
University of New South Wales, Sydney, N.S.W. 2052, Australia (e-mail:
n.lovell@unsw.edu.au).
Digital Object Identifier 10.1109/TBME.2009.2031629
ity and venous return, causing the pump differential pressure
(head) to vary with each heart beat.
Interaction between iRBPs and the cardiovascular system
(CVS) may be partially explored through in vivo animal studies.
However, such studies are inconclusive at present due to limi-
tations in animal models of heart failure and complexity of the
experimental procedures [1]. Numerical models, able to simu-
late the response of the human CVS in the presence of an iRBP,
can provide additional insights into the dynamics of the assisted
circulation. Such models also offer an excellent platform for
the development and evaluation of robust physiological pump
control algorithms by easily allowing reproducible numerical
experiments under identical conditions.
Various heart–pump interaction computational models have
been described in the literature, with varying degrees of com-
plexity depending on their purpose [1]–[3]. However, previous
work has not focused on fitting the entire waveforms (the mean
and complete dynamics of the waveforms) to actual experimen-
tal measurements and examining the dynamics of the responses
during various pumping state transitions in a quantitative sense.
This is despite the fact that dangerous pump operating con-
ditions, including suction/ventricular collapse and back flow
are closely related to the transient dynamics rather than mean
hemodynamic values [4]. In recent experiments, a number of
commonly accepted phenomena have been challenged. These
include the insufficiency of the widely used time-varying elas-
tance theory [5], the question of the interpretability of the well-
established end systolic pressure–volume relationship (ESPVR)
under left ventricular (LV) assist device (LVAD) assist [6], and
the significant increase of mean aortic pressure with progressive
LVAD unloading [7].
The aim of the present study is to develop a heart–pump
interaction model, taking into careful consideration various dis-
crepancies between experimental findings and model simulation
results. A number of important features, including curvilinear-
ity of the ESPVR, the Starling resistance, respiration effect, and
suction and pump cannulae have been included and tested for
their significance. Our model is validated using data collected
from in vivo animal experiments, mock-loop experiments as
well as other published data.
II. METHODS
A. Animal Experiments
The VentrAssist iRBP (Ventracor Ltd., Sydney, Australia)
was acutely implanted in two healthy, anaesthetized, open-chest
pigs supported by mechanical ventilation. The inflow cannula
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