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			Dopamine and dobutamine are used for
                short-term inotropic support of the failing
                heart.
			
			Dobutamine is less arrhythmogenic and
                produces less tachycardia compared to endogenous
                catecholamines or isoproterenol. 
		Dobutamine: 
            
			
			Dobutamine is a racemate that binds to
                and activates beta-1 and beta-2 adrenoceptor
                subtypes. The (-) enantiomer stimulates alpha 1
                and alpha 2 receptors, but this effect in humans
                appear negated by binding of the inactive (+)
                enantiomer. Therefore the positive inotropic
                action mediated by beta receptor activation
                predominates.
			
			Dobutamine does not activate dopamine
                receptors and therefore does not increase renal
                blood flow.
			
			Because of its vasodilator properties,
                dobutamine's positive inotropism is accompanied
                by a decrease in afterload. For this reason
                dobutamine is favored over dopamine for most
                advanced heart failure patients who have not
                improved with digoxin, diuretics, and vasodilator
                therapy. 
		Dopamine
		  
            
			
			
			Dopamine has limited
                utility in patents with left ventricular
                dysfunction. It often produces tachycardia which
                may increase left ventricular work. 
			
			
			Dopamine-induced
                vasodilation is mediated by direct stimulation of
                D1 and D2 post-synaptic dopamine receptors.
                Vasodilation of renal vasculature is noteworthy
                and may benefit patients with marginal GFR due to
                poor renal perfusion. |