You are on page 1of 8

J Artif Organs (2010) 13:189–196

DOI 10.1007/s10047-010-0518-8

ORIGINAL ARTICLE

A new pulse duplicator with a passive fill ventricle


for analysis of cardiac dynamics
Yoshimasa Yokoyama • Osamu Kawaguchi •

Tadahiko Shinshi • Ulrich Steinseifer •


Setsuo Takatani

Received: 15 January 2010 / Accepted: 31 August 2010 / Published online: 28 September 2010
Ó The Japanese Society for Artificial Organs 2010

Abstract A new pulse duplicator was designed for mock ventricle is applicable in simulating the dynamics of
evaluation of the performance of ventricular assist devices the normal heart and the sick heart. The P–V diagram
through pressure–volume (P–V) diagrams of the native changes seen with rotary blood pump assistance revealed
heart. A linear drive system in combination with a pusher- changes similar to those reported by other workers. The
plate mechanism was designed as a drive system to effects of the ventricular assist device, either pulsatile or
implement the passive fill mechanism during diastole of the continuous flow, on cardiac dynamics can be easily simu-
mock ventricle. The compliances of the native heart during lated with this system to derive design criteria for clinical
both diastole and systole were simulated by placing a circulatory assist devices.
ventricle sack made of soft latex rubber in a sealed
chamber and by varying the air-to-fluid volume ratio inside Keywords Pulse duplicator  P–V diagram  Heart
the chamber. The ratio of the capacities of the systemic function  Arterial compliance  Ventricular assist device
venous and pulmonary circuits was adjusted to properly (VAD)  Emax
reflect the effects of volume shift between them. As the air-
to-fluid volume ratio was varied from 1:12.3 to 1:1.58, the
contractility of the ventricle expressed by Emax varied from Introduction
1.75 to 0.56 mmHg/ml with the mean V0 of 4.58 ml closely
mimicking those of native hearts (p \ 0.05). Because the The pulse duplicator can be used to design and evaluate
Emax value of the normal human heart ranges from 1.3 to ventricular assist devices or heart valve prostheses before
1.6, with a value below 1.0 indicating heart failure, the animal studies and clinical trials. The pulse duplicator must
thus represent physiological characteristics of the native
heart as well as the circulatory system. One pioneering
Y. Yokoyama  S. Takatani (&)
Department of Artificial Organs, system is the mock loop of the Helmholtz Institute Aachen
Institute of Biomaterials and Bioengineering, (HIA) developed by Reul et al. in 1975 [1], which com-
Tokyo Medical and Dental University, 2-3-10 Surugadai, prises a hydraulic pump, a chamber, a Windkessel com-
Kanda, Chiyoda-ku, Tokyo 101-0062, Japan
pliance, and a resistance element. Because the pulsatile
e-mail: takatani.ao@tmd.ac.jp
flow generated by a hydraulic pump is affected by the
O. Kawaguchi compliance, resistance, and inertia elements of the system
Department of Cardiovascular Surgery, external to the heart, the coupling between the ventricular
Toyoda Kosei Hospital, Toyota, Aichi, Japan
and arterial systems in the HIA pulse duplicator was
T. Shinshi accurately designed to evaluate heart valve prostheses [2].
Institute of Precision Engineering, In simulation of cardiac dynamics, in 1998 Ferrari et al.
Tokyo Institute of Technology, Yokohama, Japan showed how to vary ventricular pressure–volume
(P–V) diagrams and Emax (the index to indicate the cardiac
U. Steinseifer
AME Helmholtz Institute of Biomedical Engineering, elasticity [3]) by controlling the end-systolic and end-dia-
RWTH Aachen, Aachen, Germany stolic volumes of the mock ventricle and effective arterial

123
190 J Artif Organs (2010) 13:189–196

elastance (Ea). The model was used to predict changes in Materials and methods
cardiac chamber volume when ventricular assist devices
were used to support the failing ventricle [4]. For dynamic Mock circulation system
evaluation of left heart assist devices, the system developed
by Pantalos et al. and Koenig et al. in 2004 mimicked the The configuration of the newly designed mock circulation
normal and failing heart characteristics by utilizing pneu- system are shown in Fig. 1. The system comprises a ven-
matically operated ventricles that were controlled via a tricular model denoted , an arterial system model `, a
feedback mechanism [5–7]. In 2008, Colacino et al. [8]. venous system reservoir ´, a centrifugal pump representing
developed a mock circulation system by use of a mathe- the right heart ˆ, and a pulmonary venous compliance ˜; a
matical technique, which added resistive and inductive venous system reservoir and pulmonary venous compliance
terms to the classical Suga–Sagawa elastance model [9] for are opened to atmosphere in order to remove the effect of
the whole cardiac cycle. arterial pulsatility. The system is instrumented with ultra-
Although the literature is filled with abundant reports, a sonic flow probes at the inlet and outlet ports (Transonic
common and major drawback of the mock circulatory Systems, NY, USA) of the left ventricle and pressure
systems reported above, however, is the active fill mech- transducers (Edwards Lifesciences, CA, USA) with mea-
anism in the ventricle as a result of the use of pneumati- surement points depicted in Fig. 1. Pressure and flow rate are
cally operated blood pumps. The native heart passively fills recorded from which P–V diagrams are constructed on a
with the preload pressure during the diastolic phase, fol- digital oscilloscope (Yokogawa Denshikiki, Tokyo, Japan).
lowed by active contraction. Takatani et al. [10] in 1981 For simulating left ventricular assistance, a continuous flow
reported use of passive-fill ventricles to simulate total cir- pump (Gyrop Pump C1E3, Kyocera, Kyoto, Japan) is con-
culation, where the elastance of the left and right hearts nected from the apex of the ventricular model to the simu-
was represented by the pusher-plate type blood pumps lated aorta (Þ in Fig. 1); it is clamped at A in Fig. 1 while
vented to the atmosphere. Although excellent sensitivity to the performance of the ventricular model is evaluated.
filling pressure during diastole was shown with the vented
system, alteration in the P–V diagrams was difficult to Passive fill ventricle
achieve once the pump design was fixed with the vented
pump system. The passive-fill ventricular model is shown in Fig. 2. A
To improve the performance of pulse duplicators, ventricular sack (` in Fig. 2) made with latex rubber and
particularly the ventricular performance, the pulse dupli- with an unstretched volume of 100 ml was placed inside a
cator designed in this study incorporates a servomotor sealed chamber containing a mixture of air and fluid ( in
coupled with a pusher-plate actuation-decoupling mecha- Fig. 2); it has a u28 mono-leaflet tilting disk Bjork Shiley
nism to implement passive filling of the ventricle. A valve (Shiley, Irvine, CA, USA) in its inlet port and a u25
ventricle sack fabricated with latex rubber was placed bi-leaflet SJM regent valve (St Jude Medical, NJ, USA) in
inside a sealed chamber containing a mixture of air and the outlet port. The air-to-fluid volume ratio was adjusted
fluid to achieve physiological levels of cardiac elastance to control ventricular elastance during systole and diastole.
and to express various levels of contractility, denoted
Emax, by varying the air-to-fluid volume ratio. An appro-
priate combination of the Windkessel compliance of the
systemic, venous, and pulmonary systems, and the inertia
effects in the arterial system as proposed by Reul et al.
[1]. were incorporated into the system to obtain physio-
logical arterial pressure waveforms. Furthermore, to
properly couple the mock ventricle with the external cir-
cuit, a left–right heart output balance mechanism was
implemented using an appropriate ratio of the systemic to
pulmonary venous compliance.
This study validated the performance of a newly
developed pulse duplicator with a passive fill ventricle
having adjustable P–V relationships, its performance to Fig. 1 Configuration of a mock circulation system comprising a left
control cardiac contractility Emax by simply varying the ventricular model , an arterial system model `, a venous system
reservoir ´ (diameter of cross section u10), a centrifugal pump
air-to-fluid volume ratio inside the LV chamber, and
simulating the right heart ˆ, pulmonary circuit reservoir ˜ (diameter
P–V diagram changes during left heart bypass using a rotary of cross section is u14), and gyro pump (C1E3) Þ. The figure
blood pump. indicates the measurement point of pressure and flow rate

123
J Artif Organs (2010) 13:189–196 191

uncompressed air volume VAir Unload was established


with the left atrial pressure PLA of 10 mmHg. Since the air-
to-fluid volume ratio inside the chamber determined the
E(t)Air, it changed as the elastance of the E(t)LV varied.

Coupling between the mock ventricle, aortic system,


and left atrial system

The pressure change of the mock ventricle, LVP, is


expressed as a function of the compliance of the sack CSack,
the air inside the chamber, CAir, and the ventricle volume,
LVV, as follows:
1 LVV  LVVUnload
LVP ¼ ðLVV  LVVUnload Þ ¼ ; ð4Þ
CV CAir þ CSack
where LVVUnload is the unstressed sack volume, and CV is
the compliance of the ventricle, expressed as the sum of
Fig. 2 Schematic diagram of the left ventricular model. It comprises CAir and CSack.
a compression chamber containing air and tap water  (diameter Equation 5 expresses the flow dynamics during systolic
of cross section u140), a left ventricular sack `, a pusher plate ´, phase, with PVentricular_wall representing the pressure
a linear guide servo motor ˆ, and mechanical valves ˜
applied to the sack by the actuator. RdirAo and RCV are the
A servomotor coupled with a linear actuator (RCS2; IAI, resistances to flow through the aortic valve and inside the
Shizuoka, Japan) (ˆ in Fig. 2) was used to compress the air mock ventricle, respectively, LV is the inertia effect, and
and water mixture via a polyethylene pusher-plate (´ in fAo_Outlet is the flow through the aortic valve.
Fig. 2). The actuator contacts the pusher-plate during sys- dfAo Outlet
tole to compress the ventricle sack by compression of the PVentricular wall  LVP ¼ Lv þ RdirAo fAo Outlet
dt
air inside the chamber, and during diastole the actuator was þ RCV fAo Outlet ; ð5Þ
rapidly retracted to decouple from the pusher-plate,
enabling the ventricle to relax and to fill passively with the where
preload pressure; the stroke displacement of the linear PVentricular wall
FT
¼ PServo Motor ¼ SChamber ¼ ðmWater þmTest Fluid ÞaServo Motor
SChamber
servo actuator was set at 24 mm; the displacement and air-
In Eq. 5, PServo Motor is the pressure generated by the
to-water ratio were experimentally determined on cardiac
servo motor, FT the force transmitted by the servo motor to
output as 5.0 l/min.
the chamber with a cross sectional area of SChamber, mWater
Generally, the ventricular elastance E(t)LV is known to
and mTest Fluid the mass of the fluid inside the chamber and
vary during the cardiac cycle and the maximum of E(t)LV
test fluid inside the duplicator, respectively, and aServo Motor
named as Emax is independent of the preload and afterload as
the acceleration of the linear actuator. By substituting LVP
reported by Suga et al. [9]. E(t)LV is expressed in terms of the
from Eq. 4 into Eq. 5, we obtain the relationship between
left ventricular pressure, LVP, and volume, LVV, by the
the linear actuator compression force, FT, mock ventricle
equation:
volume changes, the inertia effect of the ventricle, air
EðtÞLV ¼ LVP=ðLVV  V0 Þ; ð1Þ compliance, sack compliance, aortic flow resistance, and
flow into the aortic system:
where V0 is the intersection of the ESPVR (end systolic
 
pressure–volume relationship) with the volume axis. LVVSystole  LVVUnload
Likewise, the time-varying elastance of the air inside the PServo Motor 
ðCAir þ CSack Þ
LV chamber ( in Fig. 2), E(t)Air, can be expressed by the dfAo Outlet
equations: ¼ LV þ RdirAo fAo Oulet þ RCV fAo Outlet ð6Þ
dt
PAir Unload The ventricular volume change during the systolic phase,
VAir ¼ VAir Unload ð2Þ
PAir LVVSystole, is expressed by Eq. 7, where LVVEnd Diastole is
EðtÞAir ¼ PAir =VAir ; ð3Þ the end-diastolic ventricular volume.
EndZSystole
where VAir and PAir are the time-dependent volume
and pressure of the air inside the LV chamber. To calculate LVVSystole ¼ LVVEnd Diastole  fAo Outlet dt ð7Þ
VAir by use of Eq. 2, PAir Unload was measured when each End Diastole

123
192 J Artif Organs (2010) 13:189–196

The relationship among the mock ventricular pressure, Variation of Emax as a function of air-to-fluid volume ratio
its volume, and the preload changes during the diastolic
phase is expressed by Eq. 8, where RdirLA represents The elastance E(t)LV defined by Eq. 1 usually takes the
the forward resistance of the mitral valve against the flow, maximum value Emax at the end systole and is modified as
PAir Diastole the air pressure inside the chamber, and fLA_Inlet LVPEnd Systole/(LVVEnd Systole – V0).
the flow through the inlet mitral valve. This study examines the hypothesis that the air-to-fluid
dfLA Inlet volume ratio in the LV chamber referring to Fig. 2 alters
PAir Diastole  LVP ¼ Lv þ RdirLA fLA Inlet the contractility of the mock ventricle expressed by Emax.
dt
þ RCV fLA Inlet ð8Þ Experimentally, the compliance effect was simulated as the
air-to-fluid volume ratio in the chamber was varied from
The ventricular volume change during diastole, 300:3700 (1:12.3), to 600:3400 (1:5.67), 750:3350 (1:4.47),
LVVDiastole, is expressed by Eq. 9 900:3200 (1:3.56), 1050:2050 (1:1.95), 1200:1900 (1:1.58),
EndZDiastole and 1350:1750 (1:1.30) ml. From the P–V diagrams, the
LVVDiastole ¼ LVVEnd Ssystle þ fLA Inlet dt; ð9Þ variation in the index Emax and the value of V0 were
End Systole
derived while the mean AoP was varied (60, 80 and
100 mmHg). Also, the elastance changes of the air inside
where LVVEnd Systole is the end-systolic ventricular volume. the chamber, expressed as E(t)Air max, were obtained from
An important factor for simulation of the total circu- Eqs. 2 and 3. The Emax derived from the P–V diagrams was
lation is appropriate coupling between the systemic and correlated against the E(t)Air max values.
pulmonary circuits in controlling the left and right heart
output and preload changes that occur secondary to Effects on P–V diagrams of rotary pump assistance
changes in the output of each heart. The arterial system
comprises an aortic system and a downstream arterial Finally, the clamp on the outflow port of the Gyro Pump C1E3
system in which each component is represented by was released to evaluate its effects on the ventricular
inertia elements and Windkessel compliance with an dynamics. The bypass flow rate was varied from 3.0 to
adjustable resistance. The centrifugal pump (BP-X80; 4.0 l/min to obtain effects on the P–V diagrams of the mock
Medtronic, MN, USA) was used to represent the pump ventricle; the bypass conditions that set 3.0 and 4.0 l/min
function of the right heart. The rotational speed was mean support rate as 60 and 80%, respectively, but the
experimentally set 1,500 rpm in order that the average total flow for each bypass condition were approximately
water head of the venous system reservoir (´ in Fig. 1) 5.0 l/min.
and pulmonary compliance (˜ in Fig. 1) did not vary
when the air-to-water volume ratio or the arterial resis- Statistical analysis
tance were not changed. For fixing the rotational speed,
the output of the BP-X80 responds to changes in the The results were expressed as mean ± SD (standard
head pressure, i.e. the pulmonary pressure minus the deviation) and statistical significance was tested by the
right atrial pressure. Furusato et al. [11] reported a standard Student’s t test with p value less than 0.05.
technique incorporating a centrifugal blood pump
between two tanks that was adapted to another mock
circulatory system in order to reproduce the inflow Results
restriction of heart failure. The systemic to pulmonary
venous system capacity ratio was fixed to 2:1 by the P–V diagram, Emax, and ELV(t) versus air-to-fluid
cross sectional area of the reservoirs [12]. volume ratio of the LV chamber

Validation of the mock circulation system Figure 3a–c shows the hydrodynamics of the pulse dupli-
cator showing waveforms of mock ventricular pressure
To validate the performance of the pulse duplicator, we LVP, aortic pressure AoP, preload pressure, mock ven-
evaluated changes in the P–V diagram and in heart con- tricular volume LVV, and cardiac output for mean AoP of
tractility, expressed in terms of Emax, as the air-to-fluid 60, 80, and 100 mmHg. The air-to-fluid volume ratio in the
volume ratio in the chamber was varied. Finally, a rotary LV chamber was 1:5.67. Figure 4 shows the variations in
blood pump was placed from the apex of the mock ven- the P–V diagrams with the changes in the air-to-fluid vol-
tricle to the aorta to assess the feasibility of the mock ume ratio. The mean ± SD of Emax decreased from
circulatory system for evaluation of the ventricular assist 1.75 ± 0.015 to 1.42 ± 0.019, 1.06 ± 0.025, 0.89 ±
pumps. 0.005, 0.77 ± 0.002, 0.56 ± 0.003, and to 0.44 ± 0.015 as

123
J Artif Organs (2010) 13:189–196 193

Fig. 3 Wave forms obtained for LVP, AoP, LVV, preload, and cardiac output at Emax = 1.42 and mean AoP of a 60, b 80 and c100 mmHg

the air-to-fluid volume ratio was varied from 1:13.3, to of 0.6 and with the bypass flow rate varying from 3.0 to
1:6.66, 1:5.55, 1:4.55, 1:3.0, 1:2.56, and to 1:2.27. 4.0 l/min.
The elastance E(t)LV, as derived by use of Eq. 1, for the
data of Fig. 4 is shown in Fig. 5. The statistical signifi-
cance of differences among Emax of E(t)LV was evaluated Discussion
as 0.001. The difference among them was significantly
small with p \ 0.05. A new pulse duplicator with a passive fill ventricle was
Therefore, the relationship between E(t)Air max and designed to implement cardiac dynamics as evaluated by
Emax shows that Emax can be set with the control of E(t)Air use of P–V diagrams. We were successful in obtaining
(Fig. 6). As the air volume decreased, E(t)Air max and Emax physiological P–V diagrams of the heart. Successful
both increased, from 0.072 to 0.713 and from 0.521 to duplication of the physiological P–V diagrams relies on
1.921, respectively, with the regression line between three key elements:
them expressed by the quadratic equation y = 2.33x2 ?
1 a passive fill mechanism of the mock ventricle;
3.86x ? 0.35 (r2 = 0.9846).
2 compliant characteristics of the mock ventricle during
systole and diastole; and
Effects of the rotary blood pump assistance
3 proper adjustment of the circuit elements in both
on P–V diagrams
systemic and pulmonary systems.
Figure 7 shows the alterations in the P–V diagrams when a In order to mimic the passive fill mechanism of the
rotary blood pump assisted the failing heart with the Emax native heart during diastole, first of all a linear drive system

123
194 J Artif Organs (2010) 13:189–196

Fig. 4 Variation of pressure–volume diagram and Emax with air- Fig. 7 Alterations in the P–V diagrams when the rotary blood pump
to-fluid volume ratio. For these air-to-fluid volume ratios, the values was connected; the three diagrams are heart failure mode
of Emax were: 1.75, `1.52, ´1.06, ˆ0.89, ˜0.77, Þ0.56, and (Emax = 0.6 mmHg/ml) with clamped bypass, and heart failure mode
þ0.44. The ESPVR lines connecting the end-systolic points of the with the bypass flow of 3.0 and 4.0 l/min
pressure–volume diagrams showed decrease in the slope of Emax as
the air-to-fluid volume ratio was increased
pusher-plate position using a laser light displacement sen-
sor (LB-60; Keyence, Osaka, Japan), a linear actuator was
rapidly retracted decoupling from the pusher-plate.
A large-orifice 28 mm mono-leaflet valve placed in the
inlet of the left ventricular model minimized resistance to
filling. A similar mechanism was reported by Takatani
et al. in 1981 [10] where a Hall-effect pusher-plate position
signal was used for feedback control of both left and right
hearts in the full-fill and full-eject modes.
Second, the compliant characteristics of the ventricle
during both diastole and systole were implemented by
placing a 100 ml sack made of soft latex rubber in the
Fig. 5 Variation of E(t)LV calculated from the P–V diagram in Fig. 4. chamber that contained a variable volume percentage of
Emax are 1.75, `1.52, ´1.06, ˆ0.89, ˜0.77, and Þ0.56 sealed air and water. The air inside the chamber was
compressed during ejection before transmitting the applied
force by the linear actuator to the mock ventricle, while
pressure and volume changes of the air during diastole
assisted mimicking of the filling characteristics of the
native heart. The timing of the ventricular ejection, and
hence the time of the volume change of the ventricle sack,
was detected from the flow waveform monitored in the
aorta. The P–V diagrams for the air-to-fluid volume ratio
1:5.67 yielded the Emax of 1.56 with the V0 of 4.5 ml,
irrespective of the aortic pressure change, confirming
similar characteristics as those of the native hearts.
The third key factor in duplicating physiological
P–V relationships was utilization of properly designed
circuit elements. A 28 mm inflow valve and a 25 mm
outflow valve were used to couple the mock ventricle with
the atrial reservoir and aortic system with low resistance to
fill and eject. The compliance in each element and fluid
Fig. 6 E(t)Air max versus Emax of the mock ventricle could be inertia force were properly adjusted to ensure physiological
expressed by the quadratic equation y = 2.33x2 ? 3.86x ? 0.35; the
correlation coefficient was enough strong at r2 = 0.9846 pressure and flow wave forms. The ratio of the capacities of
the systemic venous and pulmonary circuits was adjusted
in combination with a pusher-plate actuation-decoupling to 2:1 so as to appropriately reflect the effects of volume
mechanism was incorporated in the cardiac chamber. shift between the systemic and pulmonary circuits. In
After completion of each ejection as determined from a particular, the effects of the preload changes, which reflect

123
J Artif Organs (2010) 13:189–196 195

changes in the filling characteristics and pump output of the whether pulsatile or continuous flow, can be easily simu-
mock ventricle were expressed using a constant-flow right lated with this system from which design criteria for
heart represented by a centrifugal blood pump. These fill- efficient circulatory assist devices may be derived before
ing and ejection characteristics controlled through feed- in-vivo verification in animals. More interesting studies
back mechanism of the pulse duplicator were instrumental from the point of understanding the interaction between the
in duplicating physiological pressure and flow waveforms cardiac system and the mechanical circulatory support
from which physiological P–V diagrams were derived. devices can be promoted by utilizing the newly designed
Variations in the air-to-fluid volume ratio inside the pulse duplicator system.
ventricle chamber from 1:12.3, to 1:5.67, 1:4.47, 1:3.56,
1:1.95 and to 1:1.58 resulted in appropriate Emax changes
from 1.75 to 0.56. The increase in the air volume inside the Conclusion
chamber reduced the compliant characteristics of the
ventricle exhibiting a lower contractile strength. The larger A newly designed pulse duplicator system yielded physi-
the air volume, the lower was the Emax or the less the ological P–V diagrams with Emax values ranging from 0.5
contractile strength of the ventricle. The maximum elas- through 1.75, simulate those of the normal heart and the
tic property of the air inside the chamber, expressed as sick heart. The newly designed pulse duplicator is appli-
E(t)Air max, correlated with the Emax derived from the cable to studying the interaction between the native heart
P–V diagrams with correlation coefficient of r2 = 0.9846. and continuous or pulsatile ventricular assist devices before
Although the value of V0 remained fairly constant until the animal studies and clinical trial.
Emax decreased to 0.5, further reduction in the Emax sec-
ondary to increase in the V0 value, deviated from the native Acknowledgments The authors would like to thank the Tokyo
heart characteristics. Because the Emax value of the normal Institute of Technology, Center for Precise Fabrication Technology,
human heart ranges from 1.3 to 1.6, with a value below 1.0 for constructing the hydraulic system essential for the conduct of this
investigation. This study was partially supported by a grant-in-aid
indicating heart failure [9, 12, 13], the newly developed from Japan Society for Promotion of Science Basic Science Research
pulse duplicator may be applicable to simulation of the B #18300149 (PI: Professor Setsuo Takatani).
dynamics of the normal heart as well as the sick heart.
Because the characteristics of P–V diagram of this dupli-
cator are similar to those of other systems [4–6, 8] and References
ESPVRs in Fig. 4 showed Emax varied when V0 does not
change [4–6, 8, 14, 15], this pulse duplicator can simulate 1. Reul H, Minamitani H, Runge J. A hydraulic analog of the sys-
temic and pulmonary circulation for testing artificial hearts.
the mechanical character of the ventricle similar to the Proceeding ESAO2 (1975);120–27.
Suga-Sagawa elastance model [9]. 2. Medeart D, Schmitz C, Rau G, Reul H. Design and in vitro
The P–V diagram changes seen with rotary blood pump performance of a novel bileaflet mechanical heart valve pros-
assistance revealed similar changes in the P–V diagrams thesis. Int J Artif Organs. 2005;28:256–63.
3. Maughan WL, Burkhoff D, Sunagawa K. Left ventricular inter-
reported by other workers [16]. When the clamp on the action with arterial load studied in isolated canine heart. Am J
cannula connected from the apex of the ventricle to the Physiol. 1983;245:H773–80.
assist device was released, the end diastolic volume 4. Ferrari G, De Lazzari C, Mimmo R, Tosti G, Ambrosi D, Gor-
decreased, peak LVP increased, and the ejection time czynska K. A computer controlled mock circulatory system for
mono- and biventricular assist device testing. Int J Artif Organs.
period revealed by the P–V diagrams (Fig. 7) shortened 1998;21:26–36.
and the area inside the P–V diagram was reduced in 5. Pantalos GM, Koenig SC, Gillars KJ, Giridharan GA, Ewert DL.
comparison with the non-assisted P–V diagram. This is Characterization of an adult mock circulation for testing for
because the rotary blood pump continually drained fluid cardiac support devices. ASAIO J. 2004;50(1):37–46.
6. Koenig SC, Pantalos GM, Gillars KJ, Ewert DL, Litwak KN,
from the ventricular model during the period of isovolumic Etoch SW. Hemodynamic and pressure–volume responses to
contraction and relaxation; 146 ml end diastolic LVV was continuous and pulsatile ventricular assist in adult mock circu-
shifted to 131 (3.0 l/min) and 114 (4.0 l/min) ml, and lation. ASAIO J. 2004;50:15–24.
69 mmHg peak LVP to 104 (3.0 l/min) and 80 (4.0 l/min) 7. Schroeder MJ, Perrault B, Ewert DL, Koenig SC. HEART: an
automated beat-to-beat cardiovascular analysis package using
mmHg. Thus, the pulse duplicator can represent not only Matlab. Comput Biol Med. 2004;34(5):371–88.
recovery of LVV and LVP, but the ventricular pumping 8. Colacino FM, Moscato F, Piedimonte F, Danieli G, Nicosia S,
mechanism and the change of cardiac external work Arabia M. A modified elastance model to control mock ventricles
dependent on drainage by ventricular assist devices. Also, in real time: numerical and experimental validation. ASAIO J.
2008;54:563–73.
although negative pressure was found in Fig. 4, it is not 9. Suga H, Sagawa K. Instantaneous pressure–volume relationships
considered a large problem to evaluate the ventricular and their ratio in the excised supported canine left ventricle. Circ
assist device. The effects of the ventricular assist devices, Res. 1974;35:117–26.

123
196 J Artif Organs (2010) 13:189–196

10. Takatani S, Harasaki H, Suwa S, Murabaryashi S, Sukalac R, 13. Guyton AC, Hall JE. Textbook of medical physiology, 11th edn.
Jacobs G, Kiraly R, Nose Y. Pusher-Plate Type TAH system Pennsylvania: Elsevier Saunders; 2006. p. 111–3.
operated in the left and right free-running variable rate mode. 14. Maughan WL, Sunagawa K, Burkhoff D, Sagawa K. Effect of
Artif Organs. 1981;5(2):132–42. arterial impedance changes on the end-systolic pressure–volume
11. Furusato M, Shima T, Kokuzawa Y, Ito K, Tanaka T, Iwasaki K, relation. Circ Res. 1984;54:595–602.
Qian Y, Umezu M, Yan Z, Zhu L. A reproduction of inflow 15. Baloa LA, Boston JR, Antaki F. Elastance-based control of a
restriction in the mock circulatory system to evaluate a hydro- mock circulatory system. Ann Biomed Eng. 2001;29:244–51.
dynamic performance of a ventricular assist device in practical 16. Moscato F, Vollkron M, Bergmeister H, Wieselthaler G, Leonard
conditions. Life Syst Model Simul. 2007;4689:553–8. E, Schima H. Left ventricular pressure–volume loop analysis
12. Guyton AC, Hall JE. Textbook of medical physiology, 11th edn. during continuous cardiac assist in acute animal trials. Artif
Pennsylvania: Elsevier Saunders; 2006. p. 171–2. Organs. 2007;31:369–76.

123

You might also like