Back to Book/course

Clinical ECG Interpretation

0% Complete
0/0 Steps
  1. Introduction to ECG Interpretation
    6 Chapters
  2. Arrhythmias and arrhythmology
    24 Chapters
  3. Myocardial Ischemia & Infarction
    22 Chapters
  4. Conduction Defects
    11 Chapters
  5. Cardiac Hypertrophy & Enlargement
    5 Chapters
  6. Drugs & Electrolyte Imbalance
    3 Chapters
  7. Genetics, Syndromes & Miscellaneous
    7 Chapters
  8. Exercise Stress Testing (Exercise ECG)
    6 Chapters
Section 6, Chapter 2
In Progress

ECG changes caused by antiarrhythmic drugs, beta blockers & calcium channel blockers

Section Progress
0% Complete

The effect of antiarrhythmic drugs, beta-blockers and calcium channel blockers on rhythm, conduction and ECG waveforms

Although the purpose of antiarrhythmic drugs is to control arrhythmias, these medications may also cause arrhythmias and confusing ECG changes. ECG changes and arrhythmias caused by digoxin were discussed previously. Below follows a rather detailed declaration of ECG changes, arrhythmias and conduction defects that occur due to antiarrhythmic drugs, beta blockers and calcium channel blockers (inhibitors). The reader will notice that most of these drugs are contraindicated in patients with structural heart disease, as well as patients with reduced left ventricular function. This is because these patients are at particularly high risk of developing life-threatening arrhythmias.

Antiarrhythmic drugs

Disopyramide

Indications

Effects of disopyramide on ECG, heart rhythm and conduction

Effect on sinoatrial (SA) nodeSA node function may become worse in patients with established SA node disease (sinus node dysfunction, sick sinus syndrome)
P-waveNo effect.
AV system (AV node, His bundle, Purkinje system)Preexisting AV block, bundle branch block or fascicular block may become worse. Particularly, the degree of AV block may increase.
QRS complexQRS duration becomes prolonged.
ST segmentST segment depression may develop.
T-waveT-wave may diminish in amplitude.
U-waveNo effect
QT (QTc) intervalQT and QTc interval becomes prolonged.
ArrhythmiaDisopyramide may provoke or aggravate any ventricular arrhythmia, such as ventricular tachycardia, ventricular fibrillation, torsade de pointes etc). Hypokalemia is likely to predispose to the pro-arrhythmic effects of disopyramide. Structural heart disease also increases the risk of developing arrhythmias during disopyramide treatment.

Propafenone and flecainide

Propafenone and flecainide are both class I antiarrhythmic drugs and share several characteristics.

Indications, propafenone

  • Prophylaxis and treatment of life-threatening ventricular tachyarrhythmias. Propafenone is usually not the first-line therapy in this patient category.
  • Prophylaxis and treatment of symptomatic paroxysmal supraventricular tachyarrhythmia in patients without evidence of structural heart disease. Propafenone is usually not the first-line therapy in this patient category.

Indications, flecainide

  • Cardioversion of atrial fibrillation in patients without structural heart disease (reduced left ventricular function is considered a structural heart disease).
  • AVNRT, AVRT (WPW syndrome) and other conditions involving an accessory pathway.
  • Paroxysmal atrial fibrillation in patients with severe symptoms, provided that first-line therapies have failed and the patient does not have structural heart disease or reduced left ventricular function.
  • Persistent or non-persistent ventricular tachycardia or frequent premature ventricular contractions that cause pronounced symptoms and other therapies have failed. Patients with structural heart disease or reduced left ventricular function are not eligible.

Effects of propafenone and flecainide on ECG, heart rhythm and conduction

Effect on sinoatrial (SA) nodeFlecainide has no effect on the activity in the SA node. Propafenone may decrease automaticity in the SA node and thereby lower heart rate.
P-waveNo effect.
AV system (AV node, His bundle, Purkinje system)PR interval is prolonged. AV block occurs occasionally.
QRS complexQRS duration is prolonged.
ST segmentNo effect.
T-waveNo effect.
U-waveNo effect.
QT (QTc) intervalMay be prolonged.
ArrhythmiaFlecainide may induce Brugada syndrome in individuals with underlying genetic susceptibility. If ECG changes consistent with Brugada syndrome develop during treatment with flecainide, the drug must be withdrawn immediately

Amiodarone

Amiodarone is the most potent antiarrhythmic drug available. ECG changes develop gradually and may come to full expression first after 6 weeks treatment. The main electrophysiological effect of amiodarone is lengthening of the refractory period.

Indications

  • Serious ventricular or supraventricular tachycardia owing to WPW syndrome, atrial flutter or atrial fibrillation. Amiodarone is only considered after failure of first-line choices. Catheter ablation is generally considered before considering amiodarone.

Effects of amiodarone on ECG, heart rhythm and conduction

Effect on sinoatrial (SA) nodeDecreases automaticity in the SA node. Sinus bradycardia is a common side effect.
P-waveNo effect.
AV system (AV node, His bundle, Purkinje system)No significant effect besides prolongation of PR interval.
QRS complexMay be prolonged.
ST segmentNo effect.
T-waveMay become wider.
U-waveMay become more pronounced.
QT (QTc) intervalBecomes prolonged.
ArrhythmiaSinus bradycardia is very common. Approximately 1% to 5% develops torsade de pointes due to QT prolongation.

Sotalol

Sotalol is a class III antiarrhythmic drug that also exerts beta blocking effect (it inhibits beta adrenergic stimulation). Sotalol should not be confused with conventional beta blockers (which have no effect on heart rhythm), because the drug has profound pro-arrhythmic effects owing to its prolongation of the QT interval.

Indications

  • Prophylaxis and treatment (also in acute setting) of ventricular tachyarrhythmias.
  • Prophylaxis and treatment (also in acute setting) of supraventricular tachyarrhythmias.
  • Rhythm control in atrial fibrillation (or atrial flutter) after return to sinus rhythm.

Effects of sotalol on ECG, heart rhythm and conduction

Effect on sinoatrial (SA) nodeDecreases automaticity in the SA node. Sinus bradycardia may occur.
P-waveNo effect.
AV system (AV node, His bundle, Purkinje system)No significant effect besides prolongation of PR interval.
QRS complexNo effect.
ST segmentNo effect.
T-waveNo effect.
U-waveNo effect.
QT (QTc) intervalBecomes prolonged. Normally the prolongation ranges between 20 and 100 milliseconds.
ArrhythmiaQT prolongation may cause torsade de pointes (polymorphic ventricular tachycardia). The risk is particularly high at low heart rates.

Beta blockers

Beta blockers reduce the effect of catecholamines on the heart. This results in negative inotropic effect (decreased contractility), negative bathmotropic effect (decreased cellular excitability) and negative chronotropic effect (decreased heart rate). Decreased heart rate will prolong diastole, which improves myocardial perfusion (the ventricles [particularly the left ventricle] are perfused during diastole). The negative inotropic effect (meaning that the contractility is diminished) results in decreased myocardial oxygen consumption, which is beneficial.

Although beta blockers do not exert any direct antiarrhythmic effect, they may reduce the incidence of arrhythmias by blocking the pro-arrhythmic effect of catecholamines. For example, beta blockers have an astonishing effect in reducing the incidence of ventricular tachycardia among patients with congenital LQTS (long QT syndrome); these patients are very sensitive to catecholamines.

Indications

Effects of beta blockers on ECG, heart rhythm and conduction

Effect on sinoatrial (SA) nodeDecreases automaticity in the SA node. Sinus rate is decreased.
P-waveNo effect.
AV system (AV node, His bundle, Purkinje system)PR interval may be prolonged. Development of AV block indicates underlying AV node disease (which will typically become clinically overt sooner or later).
QRS complexNo effect.
ST segmentNo effect.
T-waveNo effect.
U-waveNo effect.
QT (QTc) intervalMay become shortened.
ArrhythmiaHas no pro-arrhythmic effects. The most clinically relevant rhythm effect is the slowing of heart rate and particularly ventricular rate. First line therapy in patients with atrial fibrillation and atrial flutter.

Calcium channel blockers

Verapamil and diltiazem are the most widely used calcium channel blockers.

Indications

Effects of verapamil and diltiazem on ECG, heart rhythm and conduction

Effect on sinoatrial (SA) nodeNo effect unless there is underlying SA node disease (sinus node dysfunction). In case there is sinus node dysfunction, calcium channel blockers may cause sinus bradycardia or even sinus arrest.
P-waveNo effect.
AV system (AV node, His bundle, Purkinje system)PR interval becomes prolonged, but second- and third-degree AV block is uncommon unless there is pre-existing AV nodal disease.
QRS complexNo effect.
ST segmentNo effect.
T-waveNo effect.
U-waveNo effect.
QT (QTc) intervalMay become shortened.
ArrhythmiaHas no pro-arrhythmic effects. The most clinically relevant rhythm effect is the slowing of heart rate and particularly ventricular rate. Second line therapy in patients with atrial fibrillation and atrial flutter. Must never be used in atrial fibrillation with concomitant pre-excitation (WPW syndrome), as discussed previously.

References

Chou’s Electrocardiography in Clinical Practice by Surawicz B, Knilans T.

Clinical Arrhythmology and Electrophysiology: A Companion to Braunwald’s Heart Disease by Zipes D et al.

Electrophysiological disorders of the heart by Camm AJ et al.

Marriott’s Practical Electrocardiography by Wagner GS et al.

CONTINUE LEARNING

Evidence-based Cardiovascular Medicine.

Peer-Reviewed Courses.

Trusted by experts worldwide.

Join our newsletter and get a free ECG Pocket Guide

ECG pocket guide
Subscription Form

Start learning now