Dobutamine, an inotropic agent, chosen to address neurohormonal response in subclinical hemodynamic deterioration, administered at 5 μg/kg/min to mitigate tachyarrhythmia risk. Patients receive 24-h IV infusion of dobutamine or placebo, with potential dose reduction for persistent tachyarrhythmia. Primary endpoint is between-group difference in peak proBNP within 48 h. Secondary endpoints include hemodynamic function, pulse rate, blood pressure, and biomarkers. Trial powered to show 30% reduction in proBNP levels with 88 patients, with 100 patients enrolled to account for dropouts.