Differential effects of milrinone and dobutamine on right ventricular preload, afterload and systolic performance in congestive heart failure secondary to ischemic or idiopathic dilated cardiomyopathy

To compare the effects of intravenous dobutamine and milrinone on right ventricular (RV) systolic function, 14 patients with severe congestive heart failure underwent simultaneous radionuclide-hemodynamic study. Patients were randomized to receive intravenous milrinone (50 μg/kg bolus then 0.5 μg/kg...

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Veröffentlicht in:The American journal of cardiology 1987-12, Vol.60 (16), p.1329-1333
Hauptverfasser: Eichhorn, Eric J., Konstam, Marvin A., Weiland, David S., Roberts, David J., Martin, Tami T., Stransky, Nicholas B., Salem, Deeb N.
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container_end_page 1333
container_issue 16
container_start_page 1329
container_title The American journal of cardiology
container_volume 60
creator Eichhorn, Eric J.
Konstam, Marvin A.
Weiland, David S.
Roberts, David J.
Martin, Tami T.
Stransky, Nicholas B.
Salem, Deeb N.
description To compare the effects of intravenous dobutamine and milrinone on right ventricular (RV) systolic function, 14 patients with severe congestive heart failure underwent simultaneous radionuclide-hemodynamic study. Patients were randomized to receive intravenous milrinone (50 μg/kg bolus then 0.5 μg/kg/ min) or dobutamine (2.5 to 15 μg/kg/min) to achieve equal increases in cardiac output. Both drugs significantly improved cardiac performance, with identical 24% increases in mean cardiac index (p < 0.05 vs baseline; difference not significant for milrinone vs dobutamine) and no change in heart rate. Neither drug substantially altered RV preload, as reflected by mean right atrial pressure and RV end-diastolic volume. Both drugs caused similar increases in RV ejection fraction (mean ± standard deviation; dobutamine: 0.32 ± 0.09 to 0.40 ± 0.11; p < 0.05; milrinone: 0.35 ± 0.19 to 0.43 ± 0.21; p < 0.05) resulting from reductions in RV end-systolic volume. RV afterload reduction contributed substantially to drug effect on RV systolic performance in patients treated with milrinone but not those treated with dobutamine. With doses effecting equal increases in cardiac index and RV systolic performance, pulmonary artery end-systolic pressure was significantly reduced by milrinone (40 ± 12 to 33 ± 12 mm Hg; p < 0.05), but not by dobutamine. Thus, in patients with congestive heart failure milrinone's effect on RV systolic function is explainable, at least in part, by RV afterload reduction, whereas RV inotropic augmentation contributed more strongly to dobutamine's effect.
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With doses effecting equal increases in cardiac index and RV systolic performance, pulmonary artery end-systolic pressure was significantly reduced by milrinone (40 ± 12 to 33 ± 12 mm Hg; p &lt; 0.05), but not by dobutamine. 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With doses effecting equal increases in cardiac index and RV systolic performance, pulmonary artery end-systolic pressure was significantly reduced by milrinone (40 ± 12 to 33 ± 12 mm Hg; p &lt; 0.05), but not by dobutamine. Thus, in patients with congestive heart failure milrinone's effect on RV systolic function is explainable, at least in part, by RV afterload reduction, whereas RV inotropic augmentation contributed more strongly to dobutamine's effect.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Cardiomyopathy, Dilated - complications</subject><subject>Cardiotonic agents</subject><subject>Cardiovascular system</subject><subject>Dobutamine - therapeutic use</subject><subject>Female</subject><subject>Heart - physiopathology</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - etiology</subject><subject>Heart Failure - physiopathology</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Milrinone</subject><subject>Pharmacology. 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Patients were randomized to receive intravenous milrinone (50 μg/kg bolus then 0.5 μg/kg/ min) or dobutamine (2.5 to 15 μg/kg/min) to achieve equal increases in cardiac output. Both drugs significantly improved cardiac performance, with identical 24% increases in mean cardiac index (p &lt; 0.05 vs baseline; difference not significant for milrinone vs dobutamine) and no change in heart rate. Neither drug substantially altered RV preload, as reflected by mean right atrial pressure and RV end-diastolic volume. Both drugs caused similar increases in RV ejection fraction (mean ± standard deviation; dobutamine: 0.32 ± 0.09 to 0.40 ± 0.11; p &lt; 0.05; milrinone: 0.35 ± 0.19 to 0.43 ± 0.21; p &lt; 0.05) resulting from reductions in RV end-systolic volume. RV afterload reduction contributed substantially to drug effect on RV systolic performance in patients treated with milrinone but not those treated with dobutamine. With doses effecting equal increases in cardiac index and RV systolic performance, pulmonary artery end-systolic pressure was significantly reduced by milrinone (40 ± 12 to 33 ± 12 mm Hg; p &lt; 0.05), but not by dobutamine. Thus, in patients with congestive heart failure milrinone's effect on RV systolic function is explainable, at least in part, by RV afterload reduction, whereas RV inotropic augmentation contributed more strongly to dobutamine's effect.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>3687783</pmid><doi>10.1016/0002-9149(87)90616-3</doi><tpages>5</tpages></addata></record>
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subjects Adult
Aged
Biological and medical sciences
Cardiomyopathy, Dilated - complications
Cardiotonic agents
Cardiovascular system
Dobutamine - therapeutic use
Female
Heart - physiopathology
Heart Failure - drug therapy
Heart Failure - etiology
Heart Failure - physiopathology
Hemodynamics - drug effects
Humans
Male
Medical sciences
Middle Aged
Milrinone
Pharmacology. Drug treatments
Pyridones - therapeutic use
Systole - drug effects
title Differential effects of milrinone and dobutamine on right ventricular preload, afterload and systolic performance in congestive heart failure secondary to ischemic or idiopathic dilated cardiomyopathy
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