Course Content
01. Why Antiarrhythmic Drugs Are High-Risk Drugs
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02. Normal Cardiac Conduction
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03. ECG Intervals: What Drugs Change
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04. Ventricular Action Potential and Ion Currents
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05. Nodal Action Potential and Autonomic Control
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06. Mechanisms of Arrhythmogenesis
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07. First Clinical Decision: Stable or Unstable?
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08. Vaughan Williams Classification
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09. Class I Shared Biophysics
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10. Class I Subgroups: Kinetics and ECG Effects
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11. Class IA: Quinidine, Procainamide, Disopyramide
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12. Class IB: Lidocaine and Mexiletine
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13. Class IC: Flecainide, Propafenone, and CAST
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14. Class II: Beta Blockers
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15. Class IV: Non-DHP Calcium Channel Blockers
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16. Adenosine: The AV Node Reset Drug
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17. Class III: Potassium Channel Blockers
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18. Reverse Use-Dependence
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19. Amiodarone: Broad-Spectrum Multi-Channel Drug
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20. Amiodarone Toxicity and Monitoring
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21. Other Class III and Amiodarone-Related Drugs
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22. Magnesium, Electrolytes, and Torsades
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23. Digoxin: AV Nodal Drug and Toxicity Trap
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24. Bradyarrhythmia Pharmacology
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25. Atrial Fibrillation and Flutter: Framework
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26. WPW and Pre-Excited Atrial Fibrillation
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27. PSVT: AV Node-Dependent Tachycardia
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28. Wide-Complex Tachycardia and Ventricular Tachycardia
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29. Comparative Safety Matrix
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30. Final Board-Ready Drug Selection Map
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