Novel rate control strategy with landiolol in patients with cardiac dysfunction and atrial fibrillation

Teruhiko Imamura1, Koichiro Kinugawa1

  • 1Second Department of Internal Medicine, Toyama University, Toyama, Japan.

ESC Heart Failure
|July 16, 2020
PubMed

Insights

Landiolol offers a safer and more effective way to control tachycardia in acute heart failure patients with atrial fibrillation compared to digoxin. This ultra-short-acting beta-blocker is increasingly recommended in Japan for improved cardiac care.

Area of Science:

  • Cardiology
  • Pharmacology

Background:

  • Acute heart failure patients often experience tachycardia with atrial fibrillation, lacking definitive safe treatment options.
  • Digoxin, a previous first-choice, has slow onset and risks, especially in chronic kidney disease.
  • Landiolol, an ultra-short-acting beta-blocker with high beta-1 selectivity, is a newer therapeutic option.

Purpose of the Study:

  • To review the use of landiolol in patients with cardiac dysfunction and tachycardia due to atrial fibrillation.
  • To evaluate landiolol's efficacy and safety compared to existing treatments.

Main Methods:

  • Review of randomized control trials involving landiolol.
  • Analysis of updated clinical guidelines.
  • Assessment of current practical applications of landiolol in Japan.

Main Results:

  • The Japan Landiolol vs. Digoxin (J-Land) study showed landiolol's superior tachycardia control over digoxin in atrial fibrillation with left ventricular dysfunction.
  • Japanese heart failure guidelines now recommend landiolol (Class IIa, Level B) for rate control in acute heart failure with atrial fibrillation.
  • Landiolol is used in Japan for rate control, even in advanced heart failure patients on inotropes.

Conclusions:

  • Landiolol is an effective and increasingly utilized option for managing tachycardia in atrial fibrillation patients with cardiac dysfunction.
  • Further research is needed to fully understand the benefits of rapid and safe rate control with landiolol.

Related Concept Videos

Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers01:22

Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers

Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
2.5K
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...
1.1K
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
277
Antiarrhythmic Drugs: Class II Agents as β-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...
1.2K
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers01:20

Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers

Class IV antiarrhythmic drugs, such as verapamil and diltiazem, block calcium channels. They primarily affect the heart, slowing the conduction in calcium-dependent tissues like the SA and AV nodes. These drugs manage reentrant supraventricular tachycardia (SVT) and reduce ventricular rate in atrial flutter/fibrillation.
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
1.4K
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers01:12

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers

Class III antiarrhythmic drugs are a group of medications that can prolong action potentials in the heart. They achieve this by blocking potassium channels or enhancing inward currents from sodium channels. However, these drugs have a unique property of "reverse use-dependence," which is most pronounced at slower heart rates and can lead to torsades de pointes—a specific type of arrhythmia. However, it is essential to note that excessive QT interval prolongation—a measure of...
1.7K