TY - JOUR
T1 - Hemodynamic effects of direct biventricular compression studied in isovolumic and ejecting isolated canine hearts
AU - Artrip, John H.
AU - Wang, Jie
AU - Leventhal, Andrew R.
AU - Tsitlik, Joshua E.
AU - Levin, Howard R.
AU - Burkhoff, Daniel
PY - 1999/4/27
Y1 - 1999/4/27
N2 - Background - Biventricular direct cardiac compression (DCC) can potentially support the failing heart without the complications associated with a blood/device interface. The effect of uniform DCC on left and right ventricular performance was evaluated in 7 isolated canine heart preparations. Methods and Results - A computer-controlled afterload system either constrained the isolated heart to contract isovolumically or simulated hemodynamic properties of physiological ejection. Biventricular DCC was provided by a chamber surrounding the heart that allowed adjustment of the compression pressure, onset time, and duration. Through a series of ventricular preloads, the effect of DCC on the end-systolic pressure-volume relationship (ESPVR) was evaluated under isovolumic and ejecting conditions. Under both conditions, DCC shifted the ESPVR of the left and fight ventricles upward by an amount approximately equal to the compression pressure. The augmentation of end-systolic pressure for each initial preload tested, however, was less under ejecting conditions, because reductions in end- systolic and end-diastolic volumes occurred with ejection. Nevertheless, the net effect was to increase stroke volume. Measurement of Ṁ(O2) demonstrated that at a given ventricular volume, Ṁ(O2) did not change with DCC; however, peak ventricular pressure increased substantially, so that the effective pressure-volume area increased. Conclusions - Biventricular DCC can augment end-systolic pressure with no added costs of Ṁ(O2). Under ejecting conditions, this augmentation of ventricular contracting ability manifests as increases in stroke volume. Thus, DCC represents a feasible alternative form of ventricular assist, and devices that support the heart in this manner should be further explored.
AB - Background - Biventricular direct cardiac compression (DCC) can potentially support the failing heart without the complications associated with a blood/device interface. The effect of uniform DCC on left and right ventricular performance was evaluated in 7 isolated canine heart preparations. Methods and Results - A computer-controlled afterload system either constrained the isolated heart to contract isovolumically or simulated hemodynamic properties of physiological ejection. Biventricular DCC was provided by a chamber surrounding the heart that allowed adjustment of the compression pressure, onset time, and duration. Through a series of ventricular preloads, the effect of DCC on the end-systolic pressure-volume relationship (ESPVR) was evaluated under isovolumic and ejecting conditions. Under both conditions, DCC shifted the ESPVR of the left and fight ventricles upward by an amount approximately equal to the compression pressure. The augmentation of end-systolic pressure for each initial preload tested, however, was less under ejecting conditions, because reductions in end- systolic and end-diastolic volumes occurred with ejection. Nevertheless, the net effect was to increase stroke volume. Measurement of Ṁ(O2) demonstrated that at a given ventricular volume, Ṁ(O2) did not change with DCC; however, peak ventricular pressure increased substantially, so that the effective pressure-volume area increased. Conclusions - Biventricular DCC can augment end-systolic pressure with no added costs of Ṁ(O2). Under ejecting conditions, this augmentation of ventricular contracting ability manifests as increases in stroke volume. Thus, DCC represents a feasible alternative form of ventricular assist, and devices that support the heart in this manner should be further explored.
KW - Heart failure
KW - Heart-assist device
KW - Hemodynamics
KW - Physiology
KW - Ventricles
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U2 - 10.1161/01.CIR.99.16.2177
DO - 10.1161/01.CIR.99.16.2177
M3 - Article
C2 - 10217660
AN - SCOPUS:0033609107
SN - 0009-7322
VL - 99
SP - 2177
EP - 2184
JO - Circulation
JF - Circulation
IS - 16
ER -