TY - JOUR
T1 - Direct myocardial effects of OPC-18790 in human heart failure
T2 - Beneficial effects on contractile and diastolic function demonstrated by intracoronary infusion with pressure-volume analysis
AU - MacGowan, Guy A.
AU - Haber, Howard L.
AU - Douglas Cowart, T.
AU - Tedesco, Christine
AU - Wu, Clarence
AU - Feldman, Marc D.
N1 - Copyright:
Copyright 2007 Elsevier B.V., All rights reserved.
PY - 1998/5
Y1 - 1998/5
N2 - Objectives. We sought to determine the precise myocardial effects of OPC-18790 as demonstrated by intracoronary administration. Background. Although previous studies have determined the cardiovascular effects of a novel intravenous inotrope, OPC-18790, the observed benefits on contractile and diastolic function may have been confounded by the marked changes in peripheral loading associated with this drug when given intravenously. Methods. Eight heart failure patients received intracoronary OPC-18790 at 31.25 μg/min for 20 min, and then at 62.5 μg/min for another 20 min. Hemodynamic variables and pressure-volume indexes using the conductance catheter method were determined at baseline and then after the two doses. Results. There were no significant effects on heart rate, cardiac output or loading conditions, including afterload as determined by systemic vascular resistance and arterial elastance (E(a)) and preload as determined by end- diastolic volume (EDV). There were significant increases in end-systolic elastance (E(es)) from 0.74 ± 0.11 to 0.90 ± 0.16 mm Hg/ml at 31.25 μg/min and to 1.37 ± 033 mm Hg/ml at 62.5 μg/min (p < 0.05 by analysis of variance [ANOVA]). Diastolic function improved, as determined by the time constant for isovolumetric relaxation tau, which decreased significantly from baseline to 31.25 μg/min (94 ± 9 to 79 ± 9 ms, p < 0.05), and did not shorten further at 62.5 μg/min (78 ± 8 ms, p = NS). There were significant decreases in fight atrial pressure (9 ± 1 to 7 ± 1 mm Hg, p < 0.01 by ANOVA) and mean pulmonary artery wedge pressure (21 ± 3 to 16 ± 2 mm Hg, p < 0.05 by ANOVA). This fall in filling pressures was not accompanied by any change in EDV. Inspection of the diastolic portion of the pressure-volume curve confirmed a downward shift consistent with pericardial release in five of the eight patients. Conclusions. Intracoronary administration of OPC-18790 demonstrates that the direct myocardial effects of this agent include a modest increase in inotropy and improvement in diastolic function, both of which occur without increases in heart rate, indicating that this agent may be beneficial for the intravenous treatment of congestive heart failure.
AB - Objectives. We sought to determine the precise myocardial effects of OPC-18790 as demonstrated by intracoronary administration. Background. Although previous studies have determined the cardiovascular effects of a novel intravenous inotrope, OPC-18790, the observed benefits on contractile and diastolic function may have been confounded by the marked changes in peripheral loading associated with this drug when given intravenously. Methods. Eight heart failure patients received intracoronary OPC-18790 at 31.25 μg/min for 20 min, and then at 62.5 μg/min for another 20 min. Hemodynamic variables and pressure-volume indexes using the conductance catheter method were determined at baseline and then after the two doses. Results. There were no significant effects on heart rate, cardiac output or loading conditions, including afterload as determined by systemic vascular resistance and arterial elastance (E(a)) and preload as determined by end- diastolic volume (EDV). There were significant increases in end-systolic elastance (E(es)) from 0.74 ± 0.11 to 0.90 ± 0.16 mm Hg/ml at 31.25 μg/min and to 1.37 ± 033 mm Hg/ml at 62.5 μg/min (p < 0.05 by analysis of variance [ANOVA]). Diastolic function improved, as determined by the time constant for isovolumetric relaxation tau, which decreased significantly from baseline to 31.25 μg/min (94 ± 9 to 79 ± 9 ms, p < 0.05), and did not shorten further at 62.5 μg/min (78 ± 8 ms, p = NS). There were significant decreases in fight atrial pressure (9 ± 1 to 7 ± 1 mm Hg, p < 0.01 by ANOVA) and mean pulmonary artery wedge pressure (21 ± 3 to 16 ± 2 mm Hg, p < 0.05 by ANOVA). This fall in filling pressures was not accompanied by any change in EDV. Inspection of the diastolic portion of the pressure-volume curve confirmed a downward shift consistent with pericardial release in five of the eight patients. Conclusions. Intracoronary administration of OPC-18790 demonstrates that the direct myocardial effects of this agent include a modest increase in inotropy and improvement in diastolic function, both of which occur without increases in heart rate, indicating that this agent may be beneficial for the intravenous treatment of congestive heart failure.
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U2 - 10.1016/S0735-1097(98)00105-3
DO - 10.1016/S0735-1097(98)00105-3
M3 - Article
C2 - 9581731
AN - SCOPUS:0032080525
VL - 31
SP - 1344
EP - 1351
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
SN - 0735-1097
IS - 6
ER -