Why the study?
Does a 24-hour infusion of milrinone improve hemodynamic parameters more effectively than dobutamine in patients with acute congestive heart failure following acute myocardial infarction?
Does a 24-hour infusion of milrinone improve hemodynamic parameters more effectively than dobutamine in patients with acute congestive heart failure following acute myocardial infarction?
Short-term infusion of milrinone provides a more rapid and greater reduction in pulmonary capillary wedge pressure compared to dobutamine in patients with acute heart failure post-myocardial infarction.
May favor milrinone over dobutamine for acute hemodynamic relief post-MI; extends limited RCT data on inotrope selection in decompensated HF.
The purpose of this study was to compare the hemodynamic and clinical effects of milrinone, a vasodilating and positive inotropic agent, with those of dobutamine in patients with congestive heart failure (CHF) following acute myocardial infarction (AMI). Thirty-three patients in Killip classification II or III within 12 h to 5 days after AMI were randomized in a multicenter, open-label clinical trial to receive a 24-h infusion of milrinone or dobutamine. Drugs were titrated to achieve at least a 30% increase in cardiac index (CI) from mean baseline or at least a 25% decrease in mean pulmonary capillary wedge pressure (MPCWP) from baseline. Both drugs improved CI, MPCWP, and other hemodynamic parameters. Criteria for decrease in MPCWP were met by 94% (15/16) of the milrinone-treated patients and 57% (8/14) of dobutamine-treated patients (p = 0.03). Both groups met the minimum efficacy criterion for CI. Maximal reduction in MPCWP over 0-3 h was greater in the milrinone group (-53.2%) than in the dobutamine group (-31.0%; p < or = 0.01); reductions were sustained over 24 h. Both drugs improved echocardiographic global ejection fraction and were generally well tolerated. The short-term infusion of milrinone may have a role in the management of CHF following AMI, especially when the aim is the rapid reduction of pulmonary congestion.
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Karlsberg et al. (1996) studied this question.
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