[Pharmacological cardioversion with intravenous propafenone in atrial fibrillation]

E Velázquez Rodríguez1, C Cancino Rodríguez, S Arias Estrada

  • 1Unidad Coronaria, HCN PEMEX, México, D.F.

Archivos Del Instituto De Cardiologia De Mexico
|August 10, 2000
PubMed

Insights

Intravenous propafenone effectively converts recent-onset atrial fibrillation, including Wolff-Parkinson-White syndrome, to sinus rhythm. Its efficacy is limited in chronic atrial fibrillation, but it safely reduces heart rate and pre-excitation intervals.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Pharmacology

Background:

  • Atrial fibrillation (AF) is a common arrhythmia.
  • Effective treatments for AF conversion are crucial.
  • Propafenone is an antiarrhythmic drug with Class Ic properties.

Purpose of the Study:

  • To assess the efficacy and safety of intravenous propafenone for converting recent-onset and chronic atrial fibrillation.
  • To evaluate propafenone's effects in patients with and without structural heart disease, and those with Wolff-Parkinson-White syndrome.

Main Methods:

  • 46 patients with recent-onset or chronic AF received intravenous propafenone (2 mg/kg over 15 minutes).
  • Continuous electrocardiographic monitoring was employed.
  • Efficacy was measured by successful conversion to sinus rhythm and time to conversion.

Main Results:

  • Successful conversion to sinus rhythm was achieved in 87.5% of patients with recent-onset AF and 83.3% with Wolff-Parkinson-White syndrome.
  • Conversion was less effective in chronic AF (37.5%).
  • Propafenone reduced heart rate and increased pre-excited R-R intervals, with minimal adverse effects (dizziness, hypotension, conduction disturbances) in one patient.

Conclusions:

  • Intravenous propafenone is effective and safe for converting recent-onset AF and AF associated with ventricular preexcitation.
  • Efficacy is significantly lower in chronic atrial fibrillation.
  • Propafenone demonstrates favorable electrophysiological effects in specific patient groups.

Related Concept Videos

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 the heart's...
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...
Disturbances in Heart Rhythm01:29

Disturbances in Heart Rhythm

Arrhythmia or dysrhythmia refers to an abnormal heart rhythm caused by a defect in the heart's conduction system. It can cause the heart to beat irregularly, too quickly, or too slowly, leading to symptoms like chest pain, shortness of breath, and fainting. Factors such as stress, caffeine, alcohol, nicotine, cocaine, certain drugs, congenital defects, diseases, and electrolyte abnormalities can trigger arrhythmias.
Arrhythmias are categorized by their speed, rhythm, and origin. A slow heart...
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...
Cardiopulmonary Resuscitation IV: Pharmacological Management01:25

Cardiopulmonary Resuscitation IV: Pharmacological Management

Pharmacologic intervention is crucial in treating cardiac arrest patients during ACLS or Advanced Cardiovascular Life Support. The ACLS algorithms guide the administration of specific drugs based on the patient's cardiac arrest rhythm, which includes pulseless ventricular tachycardia (VT), ventricular fibrillation (VF), asystole, and pulseless electrical activity (PEA).EpinephrineIndication: Epinephrine is the first-line drug for all cardiac arrest rhythms.Mechanism of Action: Epinephrine...
ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias01:25

ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias

Arrhythmia is a condition characterized by an irregular heart rhythm, with ECG changes that differ based on its origin and nature. The types of arrhythmias discussed below include atrial, junctional, and ventricular arrhythmias.Atrial ArrhythmiasPremature Atrial Complexes (PACs): PACs are early atrial beats caused by stress, caffeine, alcohol, electrolyte imbalances, hypoxia, hyperthyroidism, or certain medications (e.g., bronchodilators and decongestants). The ECG shows early P waves with an...