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Related Concept Videos

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

Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers

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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,...
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Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers01:12

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers

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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...
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Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers01:24

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers

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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...
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Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers01:20

Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers

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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...
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Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

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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...
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Disturbances in Heart Rhythm01:29

Disturbances in Heart Rhythm

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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...
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Laser-Induced Action Potential-Like Measurements of Cardiomyocytes on Microelectrode Arrays for Increased Predictivity of Safety Pharmacology
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How to Prescribe Drugs With an Identified Proarrhythmic Liability.

Munveer Thind1, Ignacio Rodriguez2,3, Sam Kosari4

  • 1Lankenau Institute for Medical Research, Philadelphia, Pennsylvania, USA.

Journal of Clinical Pharmacology
|November 20, 2019
PubMed
Summary

Drug-induced proarrhythmia, including torsades de pointes (TdP), can cause serious cardiac events. Understanding drug risks and patient factors is crucial for safe prescribing and preventing TdP.

Keywords:
QT intervalcardiac safetydrug-drug interactionsdrug-induced proarrhythmiaelectrocardiogram monitoringelectrolyte monitoringpredisposing clinical risk factorstorsades de pointes

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Area of Science:

  • Clinical Pharmacology
  • Cardiology
  • Pharmacology

Background:

  • Drug-induced proarrhythmia is a significant concern, potentially leading to fatal arrhythmias like torsades de pointes (TdP).
  • Various drug classes can prolong cardiac repolarization, increasing TdP risk.
  • Identifying susceptible patients and understanding drug liability are essential for clinical practice.

Purpose of the Study:

  • To educate medical students and residents on drug-induced proarrhythmia and torsades de pointes (TdP).
  • To explain the mechanism of action for drugs prolonging repolarization.
  • To guide prescribers in assessing patient risk and managing potential TdP events.

Main Methods:

  • Review of pharmacological mechanisms of drug-induced proarrhythmia.
  • Analysis of drug prescribing information for proarrhythmic liability.
  • Description of patient clinical characteristics associated with TdP susceptibility.
  • Outline of interventions for managing TdP.
  • Inclusion of clinical vignettes for practical illustration.

Main Results:

  • Drugs prolonging the cardiac repolarization period are a common cause of TdP.
  • Prescribing information often details proarrhythmic risks.
  • Certain patient factors increase susceptibility to TdP.
  • Dose adjustments and monitoring can mitigate risks.
  • Prompt intervention is necessary if TdP occurs.

Conclusions:

  • Prescribers must understand drug benefit-risk profiles and patient factors to prevent TdP.
  • Awareness of drug-induced proarrhythmia mechanisms and clinical manifestations is vital.
  • Effective management strategies exist for TdP, emphasizing risk assessment and monitoring.