Safety profile and hemodynamic responses to beta-adrenergic stimulation by dobutamine in heart transplant patients

K O Akosah1, B Denlinger, P K Mohanty

  • 1Gundersen Lutheran Heart Institute, La Crosse, WI 54601, USA.

Chest
|December 14, 1999
PubMed

Insights

Heart transplant patients show an augmented heart rate response to dobutamine stress echocardiography (DSE). This heightened response, despite similar blood pressure changes, may increase myocardial oxygen demand and risk of ischemia.

Area of Science:

  • Cardiology
  • Transplant Medicine
  • Diagnostic Imaging

Background:

  • Dobutamine stress echocardiography (DSE) is utilized for coronary artery disease screening post-heart transplantation and for identifying cardiac event risks.
  • The safety of high-dose dobutamine in heart transplant recipients, particularly concerning the influence of cardiac denervation, requires systematic evaluation.

Purpose of the Study:

  • To systematically examine the safety profile and hemodynamic responses to escalating dobutamine doses in heart transplant patients.
  • To determine the influence of cardiac denervation on these responses compared to innervated control subjects.

Main Methods:

  • Assessed hemodynamic responses, heart rate (HR), and arterial blood pressure (BP) indexes (mean arterial pressure, systolic BP [SBP], diastolic BP [DBP], pulse pressure) to dobutamine.
  • Studied 87 heart transplant patients and compared results with 97 nontransplant patients serving as innervated controls.

Main Results:

  • Heart transplant patients exhibited significantly higher baseline and peak HR responses compared to nontransplant patients (p < 0.001).
  • SBP was lower in heart transplant patients at baseline and peak, while baseline DBP was higher (p < 0.02).
  • The decrease in DBP was similar in both groups; however, heart transplant patients showed a leftward-shifted HR dose-response curve with higher absolute HR and rates of increase.

Conclusions:

  • Heart transplant patients demonstrate an augmented chronotropic response to dobutamine infusion.
  • The observed increase in myocardial oxygen demand and potential decrease in coronary perfusion pressure may contribute to ischemic abnormalities detected via echocardiography.
Abstract

Related Concept Videos

Heart Failure Drugs: &#946;-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation, vasodilation, and...
Adrenergic Antagonists: Pharmacological Actions of &#946;-Receptor Blockers01:27

Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers

β-receptor blockers significantly impact the cardiovascular system by counteracting catecholamine-induced sympathetic responses. These medications decrease heart rate, contractility, and cardiac output, potentially leading to cardiac depression, life-threatening bradycardia, and death. Therapeutically, β-blockers function as mild antihypertensives and are utilized in treating angina pectoris and cardiac arrhythmias. However, nonselective β-blockers inhibit β2-receptors in bronchial smooth...
Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
Adrenergic Receptors: &#946; Subtype01:26

Adrenergic Receptors: β Subtype

β-adrenoceptors have varied sensitivities towards adrenaline, noradrenaline, and isoprenaline. The order of agonist potency is as follows:
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors have equal affinities for...
Antiarrhythmic Drugs: Class II Agents as &#946;-Adrenergic Blockers01:24

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers

Adrenergic stimulation generally impacts cardiac rate and rhythm. Specifically, stimulation of the β-adrenoceptors triggers an increase in intracellular calcium ion influx and pacemaker currents, which may cause arrhythmias. Catecholamines like adrenaline also demonstrate β2-adrenoceptor-mediated hypokalemia, impacting cardiac action potential and disrupting the normal cardiac rhythm. Class II antiarrhythmic drugs are β-adrenoceptor antagonists or β-blockers, which indirectly block calcium...
Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...